US20120093922A1 - Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same - Google Patents
Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same Download PDFInfo
- Publication number
- US20120093922A1 US20120093922A1 US13/124,628 US201013124628A US2012093922A1 US 20120093922 A1 US20120093922 A1 US 20120093922A1 US 201013124628 A US201013124628 A US 201013124628A US 2012093922 A1 US2012093922 A1 US 2012093922A1
- Authority
- US
- United States
- Prior art keywords
- pat
- epa
- composition
- inhibitor
- per
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 0 *OC([3*])O[1*].[1*]OCCC Chemical compound *OC([3*])O[1*].[1*]OCCC 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
- A61K31/202—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids having three or more double bonds, e.g. linolenic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/155—Amidines (), e.g. guanidine (H2N—C(=NH)—NH2), isourea (N=C(OH)—NH2), isothiourea (—N=C(SH)—NH2)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
- A61K31/222—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin with compounds having aromatic groups, e.g. dipivefrine, ibopamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
- A61K31/23—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin of acids having a carboxyl group bound to a chain of seven or more carbon atoms
- A61K31/232—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin of acids having a carboxyl group bound to a chain of seven or more carbon atoms having three or more double bonds, e.g. etretinate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/337—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
- A61K31/366—Lactones having six-membered rings, e.g. delta-lactones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/397—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/405—Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/22—Heterocyclic compounds, e.g. ascorbic acid, tocopherol or pyrrolidones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/34—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/127—Liposomes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4841—Filling excipients; Inactive ingredients
- A61K9/4858—Organic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/12—Antidiuretics, e.g. drugs for diabetes insipidus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/06—Antiarrhythmics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2121/00—Preparations for use in therapy
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/74—Synthetic polymeric materials
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
Definitions
- Cardiovascular disease is one of the leading causes of death in the United States and most European countries. It is estimated that over 70 million people in the United States alone suffer from a cardiovascular disease or disorder including but not limited to high blood pressure, coronary heart disease, dyslipidemia, congestive heart failure and stroke.
- the present invention provides a pharmaceutical composition
- EPA comprises eicosapentaenoic acid ethyl ester.
- the composition contains substantially no amount of docosahexaenoic acid or derivative thereof (e.g. ethyl-DHA), if any.
- the present invention provides methods of treating and/or preventing a cardiovascular-related disease comprising administering to a subject in need thereof a pharmaceutical composition or composition(s) comprising EPA and optionally one or more additional cardiovascular agents.
- the EPA and additional cardiovascular agent(s) can be co-formulated as a single dosage unit or can be formulated as two to a plurality of dosage units for coordinated, combination or concomitant administration.
- FIG. 1 shows effects of EPA, DHA and Combination Treatment on membrane lipid peroxidation at cholesterol-to-phospholipid ratio of 1.0.
- FIG. 2 shows effects of EPA, DHA and Combination Treatment on membrane lipid peroxidation at cholesterol-to-phospholipid ratio of 0.5.
- FIG. 3 shows cholesterol-dependent effects of EPA, DHA and Combination Treatment on membrane lipid peroxidation.
- FIG. 4 EPA, DHA or EPA/DHA with atorvastatin (10:1 Mole Ratio) on lipid peroxide levels in cholesterol enriched membranes (1:1 cholesterol-to-phospholipid ratio).
- compositions of the invention comprise EPA as an active ingredient.
- EPA refers to eicosapentaenoic acid (e.g. eicosa-5,8,11,14,17-pentaenoic acid) and/or a pharmaceutically acceptable ester, derivative, conjugate or salt thereof, or mixtures of any of the foregoing.
- pharmaceutically acceptable in the present context means that the substance in question does not produce unacceptable toxicity to the subject or interaction with other components of the composition.
- the EPA comprises all-cis eicosa-5,8,11,14,17-pentaenoic acid.
- the EPA is in the form of an eicosapentaenoic acid ester (also referred to herein as E-EPA or ethyl-EPA).
- the EPA comprises a C 1 -C 5 alkyl ester of EPA.
- the EPA comprises, eicosapentaenoic acid methyl ester, eicosapentaenoic acid propyl ester, or eicosapentaenoic acid butyl ester.
- the EPA comprises all-cis eicosa-5,8,11,14,17-pentaenoic acid ethyl ester.
- the EPA comprises lithium EPA, mono, di- or triglyceride EPA or any other ester or salt of EPA, or the free acid form of EPA.
- the EPA may also be in the form of a 2-substituted derivative or other derivative which slows down its rate of oxidation but does not otherwise change its biological action to any substantial degree.
- EPA present in a composition of the invention comprises ultra-pure EPA.
- ultra-pure as used herein with respect to EPA refers to a composition comprising at least 96% by weight EPA (as the term “EPA” is defined and exemplified herein).
- Ultra-pure EPA can comprise even higher purity EPA, for example at least 97% by weight EPA or at least 98% by weight EPA, wherein the EPA is any form of EPA as set forth herein.
- Ultra-pure EPA can further be defined (e.g. impurity profile) by any of the description of EPA provided herein.
- the EPA comprises an EPA-Fatty Acid conjugate wherein EPA is conjugated to another molecule of EPA or to another fatty acid.
- the EPA-Fatty Acid conjugate comprises a diester formed between EPA and EPA or between EPA a second fatty acid as shown in structures (I) and (II).
- R 1 is a fatty acid acyl group derived from EPA and R 2 is selected from H, a fatty acid acyl of 12 to 30 carbon atoms with two or more cis or trans double bonds and fatty alcohol groups of 12 to 30 carbon atoms, the same or different than R 1 .
- R 1 and R 2 may both be derived from EPA (EPA-EPA) or one may be derived from EPA and the second from a different fatty acid (EPA-Fatty acid), for example gamma-linolenic acid, dihomo-gamma-linolenic acid, arachidonic acid, adrenic acid, stearidonic acid, docosapentaenoic acid n-3, etc.).
- R 3 is generally either hydrogen, fully hydrocarbon, or containing heteroatoms, and in one embodiment is a C 1 -C 4 alkyl group.
- Synthesis of a diester conjugate can be accomplished according to methods well known in the art, including for example, using metals, metal-chlorides, or organic acids as catalysts; using fatty acid chlorides such as EPA-chloride, ⁇ -linolenic acid chloride (GLA-chloride), dihomo- ⁇ -linolenic acid chloride (DGLA-chloride), linoleic acid chloride (LA-chloride), arachidonic acid chloride (AA-chloride), conjugated linoleic acid chloride (cLA-chloride), ALA-chloride, STA-chloride, ETA-chloride, DPA-chloride, etc.; and the use of immobilized enzymes as catalysts.
- fatty acid chlorides such as EPA-chloride, ⁇ -linolenic acid chloride (GLA-chloride), dihomo- ⁇ -linolenic acid chloride (DGLA-chloride), linoleic
- composition of the present invention includes a mixture of EPA-Fatty Acid diesters.
- compositions of the present invention include less than 20% EPA-DHA conjugate, less than 15% EPA-DHA conjugate, less than 10% EPA-DHA conjugate, less than 9% EPA-DHA conjugate, less than 8% EPA-DHA conjugate, less than 7% EPA-DHA conjugate, less than 6% EPA-DHA conjugate, less than 5% EPA-DHA conjugate, less than 4% EPA-DHA conjugate, less than 3% EPA-DHA conjugate, less than 2% EPA-DHA conjugate, less than 1% EPA-DHA conjugate, less than 0.5% EPA-DHA conjugate, or less than 0.1% EPA-DHA conjugate, by weight.
- a composition of the present invention includes at least 96% EPA-Fatty acid conjugate (e.g. EPA-EPA), at least 97% EPA-Fatty acid conjugate, at least 98% EPA-Fatty acid conjugate, or at least 99% EPA-Fatty acid conjugate.
- EPA-EPA EPA-Fatty acid conjugate
- 97% EPA-Fatty acid conjugate at least 97% EPA-Fatty acid conjugate
- 98% EPA-Fatty acid conjugate or at least 99% EPA-Fatty acid conjugate.
- a composition of the present invention contains no more than 10%, no more than 9%, no more than 8%, no more than 7%, no more than 6%, no more than 5%, no more than 4%, no more than 3%, no more than 2%, no more than 1%, or no more than 0.6%, no more than 0.5%, no more than 0.4%, no more than 0.3%, no more than 0.2, or no more than 0.1% of any EPA-Fatty Acid conjugate other than EPA-EPA diester.
- EPA is present in a composition of the invention in an amount of about 50 mg to about 5000 mg, about 75 mg to about 2500 mg, or about 100 mg to about 1000 mg, for example about 75 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about 600 mg, about 625 mg, about 650 mg, about 675 mg, about 700 mg, about 725 mg, about 750 mg, about 775 mg, about 800 mg, about 825 mg, about 850 mg, about 875 mg, about 900 mg, about 925 mg, about 950 mg, about 975 mg, about 1000 mg, about 1025 mg, about 1050 mg, about 1075 mg, about 1100 mg, about 1025 mg, about 1050 mg, or about 100
- a composition of the invention contains not more than about 10%, not more than about 9%, not more than about 8%, not more than about 7%, not more than about 6%, not more than about 5%, not more than about 4%, not more than about 3%, not more than about 2%, not more than about 1%, or not more than about 0.5%, by weight of total fatty acids, docosahexaenoic acid or derivative thereof such as ethyl-DHA (E-DHA), if any.
- E-DHA ethyl-DHA
- a composition of the invention contains substantially no docosahexaenoic acid or derivative thereof such as E-DHA.
- a composition of the invention contains no docosahexaenoic acid or E-DHA.
- EPA represents at least about 60%, at least about 70%, at least about 80%, at least about 90%, at least about 95%, at least about 97%, at least about 98%, at least about 99%, or 100%, by weight, of all fatty acids present in a composition of the invention.
- a composition of the invention contains less than 30%, less than 20%, less than 10%, less than 9%, less than 8%, less than 7%, less than 6%, less than 5%, less than 4%, less than 3%, less than 2%, less than 1%, less than 0.5% or less than 0.25%, by weight of the total composition or by weight of the total fatty acid content, of any fatty acid other than EPA, or derivative thereof.
- Illustrative examples of a “fatty acid other than EPA” include linolenic acid (LA) or derivative thereof such as ethyl-linolenic acid, arachidonic acid (AA) or derivative thereof such as ethyl-AA, docosahexaenoic acid (DHA) or derivative thereof such as ethyl-DHA, alpha-linolenic acid (ALA) or derivative thereof such as ethyl-ALA, stearadonic acid (STA) or derivative thereof such as ethyl-SA, eicosatrienoic acid (ETA) or derivative thereof such as ethyl-ETA and/or docosapentaenoic acid (DPA) or derivative thereof such as ethyl-DPA.
- LA linolenic acid
- AA arachidonic acid
- DHA docosahexaenoic acid
- ALA alpha-linolenic acid
- STA stearad
- a composition of the invention has one or more of the following features: (a) eicosapentaenoic acid ethyl ester represents at least 96%, at least 97%, or at least 98%, by weight, of total fatty acids present in the composition; (b) the composition contains not more than 4%, not more than 3%, or not more than 2%, by weight, of total fatty acids other than eicosapentaenoic acid ethyl ester; (c) the composition contains not more than 0.6%, 0.5%, or 0.4% of any individual fatty acid other than eicosapentaenoic acid ethyl ester; (d) the composition has a refractive index (20° C.) of about 1 to about 2, about 1.2 to about 1.8 or about 1.4 to about 1.5; (e) the composition has a specific gravity (20° C.) of about 0.8 to about 1.0, about 0.85 to about 0.95 or about 0.9 to about 0.92; (f) the composition
- a composition useful in accordance with the invention comprises, consists essentially of or consists of at least 95% ethyl eicosapentaenoate (EPA-E), about 0.2% to about 0.5% ethyl octadecatetraenoate (ODTA-E), about 0.05% to about 0.25% ethyl nonaecapentaenoate (NDPA-E), about 0.2% to about 0.45% ethyl arachidonate (AA-E), about 0.3% to about 0.5% ethyl eicosatetraenoate (ETA-E), and about 0.05% to about 0.32% ethyl heneicosapentaenoate (HPA-E), each by weight of total fatty acids present in the composition.
- the composition is present in a capsule shell.
- the capsule shell contains no chemically modified gelatin.
- compositions useful in accordance with the invention comprise, consist essentially of, or consist of at least 95%, 96% or 97%, ethyl eicosapentaenoate, about 0.2% to about 0.5% ethyl octadecatetraenoate, about 0.05% to about 0.25% ethyl nonaecapentaenoate, about 0.2% to about 0.45% ethyl arachidonate, about 0.3% to about 0.5% ethyl eicosatetraenoate, and about 0.05% to about 0.32% ethyl heneicosapentaenoate, each by weight of all fatty acids present in the composition.
- the composition contains not more than about 0.06%, about 0.05%, or about 0.04%, by weight of total fatty acids present, DHA or derivative there of such as ethyl-DHA.
- the composition contains substantially no or no amount of DHA or derivative thereof such as ethyl-DHA.
- the composition further optionally comprises one or more antioxidants (e.g. tocopherol) in an amount of not more than about 0.5% or not more than 0.05%.
- the composition comprises about 0.05% to about 0.4%, for example about 0.2% by weight tocopherol.
- about 500 mg to about 1 g of the composition is provided in a capsule shell.
- the capsule shell contains no chemically modified gelatin.
- compositions useful in accordance with the invention comprise, consist essentially of, or consist of at least 96% ethyl eicosapentaenoate, about 0.22% to about 0.4% ethyl octadecatetraenoate, about 0.075% to about 0.20% ethyl nonaecapentaenoate, about 0.25% to about 0.40% ethyl arachidonate, about 0.3% to about 0.4% ethyl eicosatetraenoate and about 0.075% to about 0.25% ethyl heneicosapentaenoate, each by weight of total fatty acids present in the composition.
- the composition contains not more than about 0.06%, about 0.05%, or about 0.04%, by weight of total fatty acids present, DHA or derivative there of such as ethyl-DHA. In one embodiment the composition contains substantially no or no amount of DHA or derivative there of such as ethyl-DHA.
- the composition further optionally comprises one or more antioxidants (e.g. tocopherol) in an amount of not more than about 0.5% or not more than 0.05%. In another embodiment, the composition comprises about 0.05% to about 0.4%, for example about 0.2% by weight tocopherol.
- the invention provides a dosage form comprising about 500 mg to about 1 g of the foregoing composition in a capsule shell. In one embodiment, the dosage form is a gel- or liquid-containing capsule and is packaged in blister packages of about 1 to about 20 capsules per sheet.
- compositions useful in accordance with the invention comprise, consist essentially of or consist of at least 96%, 97% or 98%, by weight, ethyl eicosapentaenoate, about 0.25% to about 0.38% by weight ethyl octadecatetraenoate, about 0.10% to about 0.15% by weight ethyl nonaecapentaenoate, about 0.25% to about 0.35% by weight ethyl arachidonate, about 0.31% to about 0.38% by weight ethyl eicosatetraenoate, and about 0.08% to about 0.20% ethyl heneicosapentaenoate, each by weight of all fatty acids present in the composition.
- the composition contains not more than about 0.06%, about 0.05%, or about 0.04%, by weight of all fatty acids present, DHA or derivative there of such as ethyl-DHA. In one embodiment the composition contains substantially no or no amount of DHA or derivative there of such as ethyl-DHA.
- the composition further optionally comprises one or more antioxidants (e.g. tocopherol) in an amount of not more than about 0.5% or not more than 0.05%. In another embodiment, the composition comprises about 0.05% to about 0.4%, for example about 0.2% by weight tocopherol.
- the invention provides a dosage form comprising about 500 mg to about 1 g of the foregoing composition in a capsule shell. In another embodiment, the capsule shell contains no chemically modified gelatin.
- a composition (or co-administration regimen) of the invention comprises one or more additional cardiovascular agents.
- the one or more additional cardiovascular agents can be co-formulated with EPA or can be co-administered with EPA.
- the interchangeable terms “cardiovascular agent” or “cardiovascular drug” herein refer to a drug or agent that is capable of treating, preventing, or reducing the risk of developing a cardiovascular disease or disorder, or a risk factor or symptom thereof, in a subject.
- Cardiovascular agents herein can include, without limitation, cholesterol and triglyceride modulating agents, agents that treat coronary artery disease, agents that treat hypertension or pulmonary arterial hypertension, agents that treat arterial fibrillation or arrhythmia, agents that treat stroke, agents that treat myocardial ischemia and/or agents that treat thrombosis.
- Non-limiting examples of classes from which cardiovascular agents suitable for use in accordance with the present invention can be selected include: Acyl-coenzyme A: cholesterol acyltransferase (ACAT) inhibitors including selective inhibitors of ACAT-1, ACAT-2 as well as dual inhibitors of ACAT-1 and ACAT-2, alpha-adrenergic blocking drugs (alpha-blockers), alpha/beta blockers, angiotensin-converting enzyme (ACE) inhibitors, aldosterone antagonists, angiotensin II receptor antagonists, anti-arrhythmics, anticoagulants, antiplatelet agents, apolipoprotein A-1 (apoA-1) mimetics, beta-blockers, bile acid sequestrants, calcium-channel blockers, ApoB cholesteryl ester transfer protein (CETP) inhibitors, cholesterol absorption inhibitors, diuretics, dyslipidemia agents, endothelin receptor antagonists, fibrates, 3-hydroxy-3-methyl-glutaryl-coenzyme A (HMG-CoA
- ACAT Acyl-CoA cholesteryl acyl transferase
- CI-1011 Avasimibe, Pfizer
- CS-505 Pactimibe sulfate, Sankyo Pharma
- One or more ACAT inhibitors are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 1 mg to about 1000 mg, for example about 1 mg, about 5 mg, about 10 mg, about 20 mg, about 30 mg, about 40 mg, about 50 mg, about 60 mg, about 70 mg, about 80 mg, about 90 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 266 mg, about 275 mg, about 300 mg, about 324 mg, about 325 mg, about 330 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about 600 mg, about 625 mg, about 650 mg, about 675 mg, about 700 mg, about 725 mg, about 750 mg, about 775 mg, about 800 mg, about 825 mg,
- Angiotensin I converting enzyme (“ACE”) converts angiontensin I to angiotensin II and inhibits bradykinin. Because increased angiotensin II and decreased bradykinin levels both promote a variety of cardiovascular diseases and disorders, agents that inhibit ACE are useful in preventing or treating cardiovascular-related diseases such as hypertension, heart failure, diabetic neuropathy, and type 2 diabetes.
- suitable ACE inhibitors include captopril, enalapril, enaliprilat, trandolapril, moexipril, ramipril, quinapril, perindopril, lisinopril, benazepril, fosinopril, or combinations thereof.
- One or more ACE inhibitors are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 0.5 mg to about 50 mg, for example about 0.5 mg, about 0.75 mg, about 1 mg, about 1.25 mg, about 2 mg, about 2.5 mg, about 3 mg, about 4 mg, about 5 mg, about 6 mg, about 7 mg, about 7.5 mg, about 8 mg, about 9 mg, about 10 mg, about 11 mg, about 12 mg, about 13 mg, about 14 mg, about 15 mg, about 16 mg, about 17 mg, about 18 mg, about 19 mg, about 20 mg, about 21 mg, about 22 mg, about 23 mg, about 24 mg, about 25 mg, about 26 mg, about 27 mg, about 28 mg, about 29 mg, about 30 mg, about 31 mg, about 32 mg, about 33 mg, about 34 mg, about 35 mg, about 36 mg, about 37 mg, about 38 mg, about 39 mg, about 40 mg, about 41 mg, about 42 mg, about 43 mg, about
- Aldosterone is a steroidal hormone that contributes to hypertension by inhibiting kidney function. Agents that compete with aldosterone for mineralo-corticoid receptors are therefore useful in preventing or treating hypertension.
- suitable aldosterone agents include eplerenone and aldactone, or combinations thereof.
- Aldosterone antagonists are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 5 mg to about 100 mg, for example about 5 mg, about 10 mg, about 12 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 55 mg, about 60 mg, about 65 mg, about 70 mg, about 75 mg, about 80 mg, about 85 mg, about 90 mg, about 95, or about 100 mg.
- Alpha blockers also called adrenergic alpha-antagonists, compete with adrenaline binding at ⁇ -adrenoreceptors. Adrenaline binding at such receptors leads to vasoconstriction and therefore hypertension. Agents that compete with adrenaline or block ⁇ -adrenoreceptors are therefore useful in preventing or treating hypertension.
- suitable alpha blockers include doxazosin, methyldopa, clonidine, prazosin, terazosin, or combinations thereof.
- Alpha blockers are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 0.02 mg to about 0.5 mg, for example about 0.02 mg, about 0.03 mg, about 0.04 mg, about 0.05 mg, about 0.06 mg, about 0.07 mg, about 0.08 mg, about 0.09 mg, about 0.1 mg, about 0.2 mg, about 2.5 mg, about 0.3 mg, about 3.5 mg, about 0.4 mg, about 4.5 mg, or about 0.5 mg; in an amount of about 0.5 mg to about 15 mg, for example about 0.5 mg, about 0.75 mg, about 1 mg, about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 6 mg, about 7 mg, about 8 mg, about 9 mg, about 10 mg, about 11 mg, about 12 mg, about 13 mg, about 14 mg, or about 15 mg; or in an amount of about 100 mg to about 500 mg, for example about 100 mg, about 125 mg, about 150 mg, about 175 mg, about
- alpha/beta blockers are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 1 mg to about 25 mg, for example about 1 mg, about 2 mg, about 3 mg, about 3.125 mg, about 4 mg, about 5 mg, about 6 mg, about 6.25 mg, about 7 mg, about 8 mg, about 9 mg, about 10 mg, about 11 mg, about 12 mg, about 13 mg, about 14 mg, about 15 mg, about 16 mg, about 17 mg, about 18 mg, about 19 mg, about 20 mg, about 21 mg, about 22 mg, about 23 mg, about 24, or about 25 mg.
- a non-limiting example of an alpha/beta blocker is carvedilol.
- Angiotensin II receptor antagonists alternately called angiotensin receptor blockers, ARBs, AT 1 -receptor antagonists, or sartans, are useful in treating hypertension, congestive heart failure, and various other diseases and disorders.
- angiotensin II receptor antagonists include candesartan, irbesartan, olmesartan, losartan, valsartan, telmisartan, eprosartan, or combinations thereof.
- One or more angiotensin II receptor antagonists are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 1 mg to about 100 mg, for example about 1 mg, about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 6 mg, about 7 mg, about 8 mg, about 9 mg, about 10 mg, about 12 mg, about 15 mg, about 16 mg, about 20 mg, about 24 mg, about 25 mg, about 28 mg, about 30 mg, about 32 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 55 mg, about 60 mg, about 65 mg, about 70 mg, about 75 mg, about 80 mg, about 85 mg, about 90 mg, about 95 mg, about 100 mg; in an amount of about 40 mg to about 320 mg, for example, about 40 mg, about 60 mg, about 80 mg, about 100 mg, about 120 mg, about 140 mg, about 160 mg, about 180 mg, about 200 mg, about 220 mg, about 240 mg
- Anti-arrhythmic drugs act to correct an irregular heartbeat and/or slow a heart that is beating too rapidly.
- suitable anti-arrhythmic agents include adenosine, amiodarone, digoxin, disopyramide, flecamide, lidocaine, mexiletine, procainamide, quinidine gluconate, propafenone hydrochloride, tocamide, or combinations thereof.
- One or more anti-arrhythmics are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 0.1 mg to about 1500 mg, about 1 mg to about 1200 mg, or about 5 mg to about 1000 mg, for example about 0.1 mg, about 0.5 mg, about 0.75 mg, about 1 mg, about 5 mg, about 6 mg, about 10 mg, about 20 mg, about 30 mg, about 40 mg, about 50 mg, about 60 mg, about 70 mg, about 80 mg, about 90 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 266 mg, about 275 mg, about 300 mg, about 324 mg, about 325 mg, about 330 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about 600 mg, about 625
- one or more anti-arrhythmics can be present in an amount of about 1 mg per mL to about 500 mg per mL, for example about 1 mg per mL, about 2 mg per mL, about 3 mg per mL, about 4 mg per mL, about 5 mg per mL, about 6 mg per mL, about 10 mg per mL, about 25 mg per mL, about 50 mg per mL, about 75 mg per mL, about 80 mg per mL, about 100 mg per mL, about 125 mg per mL, about 150 mg per mL, about 175 mg per mL, about 200 mg per mL, about 225 mg per mL, about 250 mg per mL, about 275 mg per mL, about 300 mg per mL, about 325 mg per mL, about 350 mg per mL, about 375 mg per mL, about 400 mg per mL, about 425 mg per mL, about 450 mg per mL,
- an anti-arrhythmics is present in an amount of about 0.01% to about 5%, for example about 0.01%, about 0.02%, about 0.03%, about 0.04%, about 0.05%, about 0.06%, about 0.07%, about 0.08%, about 0.09%, about 0.1%, about 0.2%, about 0.3%, about 0.4%, about 0.5%, about 0.6%, about 0.7%, about 0.8%, about 0.9%, about 1%, about 1.1%, about 1.2%, about 1.3%, about 1.4%, about 1.5%, about 1.6%, about 1.7%, about 1.8%, about 1.9%, about 2%, about 2.1%, about 2.2%, about 2.3%, about 2.4%, about 2.5%, about 2.6%, about 2.7%, about 2.8%, about 2.9%, about 3%, about 3.1%, about 3.2%, about 3.3%, about 3.4%, about 3.5%, about 3.6%, about 3.7%, about 3.8%, about 3.9%, about 4%, about 4.1%, about 4.2%, about 4.3%, about 4.4%, about 4.5%, about 4.5%, about
- Antiplatelet agents inhibit platelet aggregation and therefore combat thrombus development.
- Non-limiting examples of antiplatelet agents include adeparin, aspirin, clopidogrel, danaparoid, deltaparin, denaparoid, ticlopidine, cilostazol, abciximab, eptifibatide, tirofiban, defibrotide, enoxaparin, dipyridamole, tinzaparin, or combinations thereof.
- One or more antiplatelet agents are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 10 mg to about 100 mg, for example about 10 mg, about 12.5 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 55 mg, about 60 mg, about 65 mg, about 70 mg, about 75 mg, about 80 mg, about 85 mg, about 90 mg, about 95 mg, or about 100 mg; in an amount of about 50 mg to about 300 mg, for example about 50 mg, about 75 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, or about 300 mg.
- one or more antiplatelet agents are present in an amount of about 25 ⁇ g per mL to about 50 ⁇ g per mL, for example about 25 ⁇ g per mL, about 30 ⁇ g per mL, about 35 ⁇ g per mL, about 40 ⁇ g per mL, about 45 ⁇ g per mL, or about 50 ⁇ g per mL; or in an amount of about 1 mg per mL to about 2 mg per mL, for example about 1 mg per mL, about 1.25 mg per mL, about 1.50 mg per mL, about 1.75, or about 2 mg per mL.
- Apolipoprotein A-1 (“apoA-1”) is the primary protein component of serum HDL cholesterol.
- apoA-1 mimetics include ETC-216, ETC-588-liposome, ETC-642, trimeric apoA-1, CSL-111, APP018, reverse D-4F, or combinations thereof.
- One or more apoA-1 mimetics are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 0.1 mg to about 1500 mg, about 1 mg to about 1200 mg, or about 5 mg to about 1000 mg, for example about 0.1 mg, about 0.5 mg, about 0.75 mg, about 1 mg, about 5 mg, about 6 mg, about 10 mg, about 20 mg, about 30 mg, about 40 mg, about 50 mg, about 60 mg, about 70 mg, about 80 mg, about 90 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 266 mg, about 275 mg, about 300 mg, about 324 mg, about 325 mg, about 330 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about 600 mg, about 6
- Beta blockers block responses to the beta nerve receptor which tends to slow heart rate and lower blood pressure.
- suitable beta blockers include acebutolol, atenolol, metoprolol, nadolol, nebivolol, pindolol, propranolol, or combinations thereof.
- One or more beta blockers are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 1 mg to about 1000 mg, about 1 mg to about 750 mg, or about 1 mg to about 500 mg, for example about 1 mg, about 2 mg, about 2.5 mg, about 3 mg, about 4 mg, about 5 mg, about 10 mg, about 20 mg, about 25 mg, about 30 mg, about 40 mg, about 50 mg, about 60 mg, about 70 mg, about 80 mg, about 90 mg, about 100 mg, about 120 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, or about 500 mg.
- Bile acid sequestrants interrupt the enterohepatic circulation of bile acids by binding bile acid components in the gastrointestinal tract, rendering them unabsorbable thereafter. Bile acid sequestrants are thus useful in preventing or treating hyperlipidemia, among other diseases and disorders.
- Non-limiting examples of bile acid sequestrants include colesevelam Hcl, colestipol, locholest and cholestyramine or combinations thereof.
- One or more bile acid sequestrants are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 4 mg to about 32 mg, for example about 4 mg, about 8 mg, about 12 mg, about 16 mg, about 24 mg, about 32 mg; or in an amount of about 300 mg to about 4000 mg, for example about 300 mg, about 325 mg, about 350 mg, about 400 mg, about 450 mg, about 500 mg, about 550 mg, about 600 mg, about 625 mg, about 650 mg, about 700 mg, about 750 mg, about 800 mg, about 900 mg, about 1000 mg, about 1250 mg, about 1500 mg, about 1750 mg, about 2000 mg, about 2250 mg, about 2500 mg, about 2750 mg, about 3000 mg, about 3250 mg, about 3500 mg, about 3750, or about 4000 mg.
- Calcium channel blockers are useful in preventing or treating hypertension by their vasodilating action.
- Non-limiting examples of calcium channel blockers include nicardipine, diltiazem, clevidipine butyrate, isradipine, nimodipine, nisoldipine, verapamil, and amlodipine besylate, or combinations thereof.
- Non-limiting examples of combination calcium channel blockers include amlodipine, olmesartan, valsartan, or combinations thereof.
- One or more calcium channel blockers are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 1 mg to about 10 mg, for example about 1 mg, about 2 mg, about 2.5 mg, about 3 mg, about 4 mg, about 5 mg, about 6 mg, about 7 mg, about 8 mg, about 9 mg, or about 10 mg; in an amount of about 5 mg to about 34 mg, for example about 5 mg, about 6 mg, about 7 mg, about 8 mg, about 8.5 mg, about 9 mg, about 10 mg, about 15 mg, about 17.5 mg, about 20 mg, about 22.5 mg, about 25 mg, about 25.5 mg, about 27.5 mg, about 30 mg, about 32.5, or about 34 mg; in an amount of about 10 mg to about 60 mg, for example about 10 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 55 mg, or about 60 mg; in an amount of about 20
- one or more calcium channel blockers is present in an amount of about 0.05 mg per mL to about 2.5 mg per mL, for example about 0.05 mg per mL, about 0.1 mg per mL, about 0.2 mg per mL, about 0.3 mg per mL, about 0.4 mg per mL, about 0.5 mg per mL, about 0.6 mg per mL, about 0.7 mg per mL, about 0.8 mg per mL, about 0.9 mg per mL, about 1.0 mg per mL, about 1.25 mg per mL, about 1.5 mg per mL, about 1.75 mg per mL, about 2.0 mg per mL, about 2.25 mg per mL, or about 2.5 mg per mL.
- CETP Cholesteryl ester transfer protein
- One or more CETP inhibitors are present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount sufficient to provide the subject with a dose of about 25 mg per kg body weight (“mg per kg”) to about 100 mg per kg, for example about 25 mg per kg, about 30 mg per kg, about 35 mg per kg, about 40 mg per kg, about 45 mg per kg, about 50 mg per kg, about 55 mg per kg, about 60 mg per kg, about 65 mg per kg, about 70 mg per kg, about 75 mg per kg, about 80 mg per kg, about 85 mg per kg, about 90 mg per kg, about 95 mg per kg, or about 100 mg per kg.
- mg per kg body weight
- one or more CETP inhibitors are present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 100 mg to about 10 g, about 500 mg to about 9 g, or about 750 mg to about 5 g.
- Cholesterol absorption inhibitors reduce the cholesterol content of chylomicrons and chylomicron remnants by preventing the uptake of micellar cholesterol from the small intestine. As a result, less cholesterol is delivered to the liver and thereby reduces LDL.
- Non-limiting examples of cholesterol absorption inhibitors include ezetimibe and simvastatin, or combinations thereof.
- One or more cholesterol absorption inhibitors are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 1 mg to about 10 mg, for example about 1 mg, about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 6 mg, about 7 mg, about 8 mg, about 9 mg, or about 10 mg; or in an amount of about 10 to about 80 mg, for example about 10 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 55 mg, about 60 mg, about 65 mg, about 70 mg, about 75 mg, or about 80 mg.
- Diuretics increase urination rates forcing diuresis. Some diuretics also provide antihypertensive effects. Non-limiting examples of diuretics include hydrochlorothiazide, torsemide, ethacrynic acid, furosemide, triamterene, indapamide, chlorothiazide sodium, aliskiren, or combinations thereof.
- One or more diuretics are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of: (a) about 0.25 mg to about 2.5 mg, for example about 0.25 mg, about 0.5 mg, about 0.75 mg, about 1 mg, about 1.25 mg, about 1.5 mg, about 1.75 mg, about 2 mg, about 2.25 mg, or about 2.5 mg; (b) in an amount of about 5 mg to about 25 mg, for example about 5 mg, about 10 mg, about 12.5 mg, about 15 mg, about 17.5 mg, about 20 mg, about 22.5 mg, or about 25 mg; (c) in an amount of about 2 mg to about 100 mg, for example about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 7.5 mg, about 10 mg, about 12.5 mg, about 15 mg, about 17.5 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 55 mg, about 60 mg, about 65
- Dyslipidemia is a class of diseases that includes hyperlipidemia.
- Fredrickson's Type I dyslipidemia (sometimes referred to as Buerger-Gruetz syndrome, primary hyperlipoproteinaemia, or familial hyperchylomicronemia) is characterized by elevated cholesterol levels, subjects with Fredrickson's Type IIa dyslipidemia (also known as familial hypercholesterolemia) exhibit elevated LDL levels.
- Those with Fredrickson's Type IIb dyslipidemia familial combined hyperlipoproteinemia (FCH) or secondary combined hyperlipoproteinemia
- FCH familial hyperlipoproteinemia
- Fredrickson's Type III dyslipidemia (sometimes called beta disease or dysbetalipoproteinemia) features elevated intermediate density lipoproteins (“IDL”), while Fredrickson's Type IV dyslipidemics (sometimes called “pure hypertriglyceridemics”) have elevated VLDL levels. Subjects with Fredrickson's Type V dyslipidemia have increased VLDL and chylomicron levels.
- dyslipidemia agents include Angpt14 antibody, APA-01 (Phosphagenics), CRD-5 (ImaSight), NCX6560 (NicOx), PCSK9 RNAi (Alnylam), recombinant apoA-1 (SemBio Sys Genetics), anti-oxLDL (Genentech), APL180 (Novartis), APP018 (D4F) (Novartis), CER-002 (Cerenis Therapeutics), CP-800,569 (Pfizer), GSK-256073 (GlaxoSmithKline), MB07811 (Metabasis), PF-3185043 (Pfizer), R7232 (Roche), rilapladib (GlaxoSmithKline), RVX-208 (Resverlogix), Sobetirome (QRX-431 (QuatRx)), anacetrapib (Merk), CSL111 (CSL Limited), darapladib (Grk), C
- One or more dyslipidemia agents are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 1 mg to about 1000 mg, for example about 1 mg, about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 6 mg, about 7 mg, about 8 mg, about 9 mg, about 10 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 43 mg, about 45 mg, about 48 mg, about 50 mg, about 54 mg, about 55 mg, about 60 mg, about 65 mg, about 67 mg, about 70 mg, about 75 mg, about 80 mg, about 85 mg, about 87 mg, about 90 mg, about 95 mg, about 100 mg, about 105 mg, about 107 mg, about 110 mg, about 115 mg, about 120 mg, about 125 mg, about 130 mg, about 134 mg, about 135 mg, about 140 mg, about 145 mg, about 150 mg, about 155 mg, about 160 mg,
- Endothelin-1 at endothelin-A (ETA) or endothelin-B (ETB) receptors causes pulmonary vasoconstriction.
- Endothelin receptor antagonists compete with endothelin-1 binding, thereby attenuating pulmonary vasoconstriction. Endothelin receptor antagonists, therefore, are useful in treating pulmonary hypertension.
- Non-limiting examples of endothelin receptor antagonists include ambrisentan, bosentan, volibris, thelin, or combinations thereof.
- One or more endothelin receptor antagonists are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 1 mg to about 10 mg, for example about 1 mg, about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 6 mg, about 7 mg, about 8 mg, about 9 mg, or about 10 mg; in an amount of about 50 mg to about 250 mg, for example about 50 mg, about 75 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, or about 250 mg.
- HMG-CoA reductase (also known as HMGR) converts HMG-CoA (3-hydroxy-3-methyl-glutaryl-co enzyme A) to mevalonic acid (3,5-dihydroxy-3-methyl-pentanoic acid) along the metabolic pathway that produces cholesterol.
- HMG-CoA reductase inhibitors also called statins, inhibit HMG-CoA reductase and thereby reduce cholesterol production.
- HMG-CoA reductase inhibitors are useful in treating a variety of cardiovascular diseases and disorders including, for example, hypercholesterolemia, hyperlipidemia, mixed dyslipidemia, hypertriglyceridemia, atherosclerosis.
- HMG-CoA reductase inhibitors include lovastatin, lovastatin+niacin, mevastatin, pitavastatin, pravastatin, rosuvastatin, fluvastatin, atorvastatin, atorvastatin+amlodipine besylate, simvastatin, simvistatin+niacin, ezetimibe, and pravastatin, among others.
- HMG-CoA reductase inhibitors are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 1 mg to about 1000 mg, for example about 1 mg, about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 6 mg, about 7 mg, about 8 mg, about 9 mg, or about 10 mg; about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 55 mg, about 60 mg, about 65 mg, about 70 mg, about 75 mg, about 80 mg, about 90 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 5
- LCAT Lecithin-cholesterol acyltransferase
- LCAT activators are therefore useful in reducing serum HDL levels and treating or preventing atherosclerosis.
- Non-limiting examples of LCAT activators include LCAT enzyme, recombinant LCAT, genetic therapy agents that include a nucleic acid sequence coding for expression of LCAT, estrogens, estrogen analogs, and combinations thereof for example as disclosed in U.S. Pat. No. 6,635,614 incorporated by reference herein in its entirety.
- LCAT activators are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount sufficient to raise the serum LCAT level of the subject to a desired level.
- Subjects with abnormally low LCAT serum levels may be administered an amount of a composition of the invention comprising EPA and LCAT enzyme, estrogen, estrogen analogs, or combinations thereof sufficient to raise the subject's serum LCAT level to normal levels, typically about 5 ⁇ g per mL or greater.
- subjects with about normal LCAT serum levels may be treated with a composition of the invention comprising EPA and LCAT enzyme, estrogen, estrogen analogs, or combinations thereof in an amount sufficient to raise the LCAT serum level to about 6 ⁇ g per mL or more, about 7 ⁇ g per mL or more, about 8 ⁇ g per mL or more, about 9 ⁇ g per mL or more, or about 10 ⁇ g per mL or more.
- LDL receptors are cell surface proteins. Along with adaptin, LDL receptors bind free LDL cholesterol to form clathrin-coated vesicles, reducing serum LDL levels. Thus, agents that induce LDL receptors further reduce serum LDL levels and are useful in preventing or treating atherosclerosis.
- a non-limiting example of LDL receptor is lactacystin.
- One or more LDL receptor inducers are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 1 mg to about 1000 mg, for example about 1 mg, about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 6 mg, about 7 mg, about 8 mg, about 9 mg, or about 10 mg about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 55 mg, about 60 mg, about 65 mg, about 70 mg, about 75 mg, about 80 mg, about 90 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about 600 mg,
- compositions of the invention may comprise one or more lipoprotein-associated phospholipase A2 (Lp-PLA2) inhibitors.
- Lp-PLA2 hydrolyzes oxidized phospholipids in LDL cholesterols. High levels of Lp-PLA2 seem to trigger a cascade of inflammatory events in atherosclerosis and an increased risk of stroke.
- Lp-PLA2 inhibitors therefore, are useful in slowing or preventing development of atherosclerosis.
- Non-limiting examples of Lp-PLA2 inhibitors include rilapladib, darapladib, and combinations thereof.
- One or more Lp-PLA2 inhibitors are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 1 mg to about 1000 mg, for example about 1 mg, about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 6 mg, about 7 mg, about 8 mg, about 9 mg, or about 10 mg; about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 55 mg, about 60 mg, about 65 mg, about 70 mg, about 75 mg, about 80 mg, about 90 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about
- 5-lipoxygenase inhibitors are useful in accordance with various embodiments of the invention.
- Non-limiting examples of 5-lipixygenase inhibitors include VIA-2291, MK-886, CMI 977, ABT-761, ZD2138, lonapalene, zileuton, 5-LO inhibitor 6, L-739,010, CGS 22745, SC 45662, and combinations thereof.
- One or more 5-lipoxygenase inhibitors are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 0.01 mg to about 2500 mg, about 0.1 mg to about 1500 mg, about 1 mg to about 1200 mg, or about 5 mg to about 1000 mg, for example about 0.1 mg, about 0.5, about 0.75 mg, about 1 mg, about 5 mg, about 10 mg, about 20 mg, about 30 mg, about 40 mg, about 50 mg, about 60 mg, about 70 mg, about 80 mg, about 90 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about 600 mg, about 625 mg, about 650 mg,
- Microsomal triglyceride transfer protein (“MTTP” or “MTP”) is a heterodimeric protein involved in lipoprotein assembly. MTP inhibitors are thus useful in slowing or preventing the production of lipoproteins and therefore cardiovascular diseases and disorders.
- MTP inhibitors include SLx-4090, AEGR-733, implitapide, BMS-200150, CP-346086, JTT-130, dirlotapide, and combinations thereof.
- one or more MTP inhibitors are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount sufficient to provide the subject with a dose of about 1 ⁇ g per kg of body weight ( ⁇ g per kg) to about 100 ⁇ g per kg, for example about 25 ⁇ g per kg, about 30 ⁇ g per kg, about 35 ⁇ g per kg, about 40 ⁇ g per kg, about 45 ⁇ g per kg, about 50 ⁇ g per kg, about 55 ⁇ g per kg, about 60 ⁇ g per kg, about 65 ⁇ g per kg, about 70 ⁇ g per kg, about 75 ⁇ g per kg, about 80 ⁇ g per kg, about 85 ⁇ g per kg, about 90 ⁇ g per kg, about 95 ⁇ g per kg, or about 100 ⁇ g per kg.
- one or more MTP inhibitors are present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 30 ⁇ g to about 20 mg, about 50 ⁇ g to about 15 mg, or about 70 ⁇ g to about 10 mg.
- one or more MTP inhibitors are present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 0.01 mg to about 2500 mg, about 0.1 mg to about 1500 mg, about 1 mg to about 1200 mg, or about 5 mg to about 1000 mg, for example about 0.1 mg, about 0.5, about 0.75 mg, about 1 mg, about 5 mg, about 10 mg, about 20 mg, about 30 mg, about 40 mg, about 50 mg, about 60 mg, about 70 mg, about 80 mg, about 90 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about 600 mg, about 625 mg, about 650 mg, about 6
- Peroxisome proliferator-activated receptors are nuclear receptor proteins regulating the expression of genes by acting as transcription factors in combination with the retinoid X receptor (“RXR”). Agents that inhibit or activate PPARs are therefore useful in modifying the expression of certain genes including, for example, genes associated with metabolic disorders such as hypercholesterolemia.
- PPAR agonists and activators include fenofibrate, bezafibrate, ciprofibrate, clofibrate, gemfibrozil, CER-002, rosiglitazone, GW501516, RWJ 800025, KD-3010, and combinations thereof.
- One or more PPAR agonists and/or activators are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 0.5 mg to about 4 mg, for example about 0.5 mg, about 0.75 mg, about 1 mg, about 1.25 mg, about 1.5 mg, about 1.75 mg, about 2 mg, about 2.25 mg, about 2.5 mg, about 2.75 mg, about 3 mg, about 3.25 mg, about 3.5 mg, about 3.75 mg, or about 4 mg; or in an amount of about 20 mg to about 120 mg, for example about 20 mg, about 30 mg, about 40 mg, about 50 mg, about 60 mg, about 70 mg, about 80 mg, about 90 mg, about 100 mg, about 110 mg, or about 120 mg.
- sPLA2 inhibitors are suitable for use in accordance with various embodiments of the present invention.
- Non-limiting examples of sPLA2 inhibitors include LY 333013, varespladib, WA8242A, WA8242A 2 , WA8242B, A-0001, A-0002 and combinations thereof.
- One or more sPLA2 inhibitors are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 0.01 mg to about 2500 mg, about 0.1 mg to about 1500 mg, about 1 mg to about 1200 mg, or about 5 mg to about 1000 mg, for example about 0.1 mg, about 0.5, about 0.75 mg, about 1 mg, about 5 mg, about 10 mg, about 20 mg, about 30 mg, about 40 mg, about 50 mg, about 60 mg, about 70 mg, about 80 mg, about 90 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about 600 mg, about 625 mg, about 650 mg, about 6
- Squalene epoxidase also called squalene monooxygenase, catalyzes the oxidation of squalene in the cholesterol biosynthesis pathway.
- agents that inhibit squalene epoxidase are useful in preventing or slowing the cholesterol production.
- Non-limiting examples of squalene epoxidase inhibitors include terbinafine, naftifine, amorolfine, butenafine, FR194738, NB-598, resveratrol (trans-3,4′,5-trihydroxystilbene), epigallocatechin-3-O-gallate, S-allylcysteine, selenocysteine, alliin, diallyl trisulfide, diallyl disulfide, and combinations thereof.
- One or more squalene epoxidase inhibitors are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 100 mg to 250 mg, for example about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, or about 250 mg; or in an amount of about 0.5% to about 5%, by weight of the composition, for example about 0.5%, about 0.75%, about 1%, about 1.25%, about 1.5%, about 1.75%, about 2%, about 2.25%, about 2.5%, about 2.75%, about 3%, about 3.25%, about 3.5%, about 3.75%, about 4%, about 4.25%, about 4.5%, about 4.75%, or about 5%, by weight.
- Thrombolytic agents dissolve blood clots. Thrombolytic agents are therefore useful in treating cardiovascular diseases and disorders including, for example, deep vein thrombosis, pulmonary embolism, ischemic complications, unstable angina, myocardial infarction, and venous thromboembolism, among others.
- Non-limiting examples of thrombolytic agents include fondoparinux, dalteparin, enoxaparin, apixaban, PD-348292, and combinations thereof.
- One or more thrombolytic agents are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount sufficient to provide a dosage of about 0.5 mg per kg of body weight (“mg per kg”) to about 40 mg per kg, for example about 0.5 mg per kg, about 1 mg per kg, about 2 mg per kg, about 3 mg per kg, about 4 mg per kg, about 5 mg per kg, about 6 mg per kg, about 7 mg per kg, about 8 mg per kg, about 9 mg per kg, about 10 mg per kg, about 11 mg per kg, about 12 mg per kg, about 13 mg per kg, about 14 mg per kg, about 15 mg per kg, about 16 mg per kg, about 17 mg per kg, about 18 mg per kg, about 19 mg per kg, about 20 mg per kg, about 21 mg per kg, about 22 mg per kg, about 23 mg per kg, about 24 mg per kg, about 25 mg per kg, about 26 mg per kg, about 27 mg per kg, about 28 mg per kg, about 29
- one or more thrombolytic agents are present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 0.5 mg to about 2.5 mg, for example 0.5 mg, about 0.75 mg, about 1 mg, about 1.25 mg, about 1.5 mg, about 1.75 mg, about 2 mg, about 2.25 mg, or about 2.5 mg; or in an amount sufficient to provide about 60 international units per kg of body weight (“IU per kg”) to about 240 IU per kg, for example 60 IU per kg, about 70 IU per kg, about 80 IU per kg, about 90 IU per kg, about 100 IU per kg, about 110 IU per kg, about 120 IU per kg, about 130 IU per kg, about 140 IU per kg, about 150 IU per kg, about 160 IU per kg, about 170 IU per kg, about 180 IU per kg, about 190 IU per kg, about 200 IU per kg, about 210 IU per kg, about 220 IU per kg, about 230
- cardiovascular agents are also useful in preventing, inhibiting, or treating cardiovascular diseases or disorders.
- Non-limiting examples of other cardiovascular agents include gemfibrozil, niaspan, orlistat, GFT14, AZD-2479, ETC-1001, and combinations thereof.
- cardiovascular agent(s) can be present in a composition of the invention (or may be co-administered with EPA according to other embodiments of the invention) in an amount corresponding to the recommended or suggested dosage for the particular cardiovascular agent(s).
- the cardiovascular agent(s) may be present in a composition of the invention (or may be co-administered with EPA according to other embodiments of the invention) in an amount less than the recommended or suggested dosage for the particular cardiovascular agent(s).
- a composition of the invention may comprise EPA and one or more of these other cardiovascular agents in an amount of about 5 mg to about 1500 mg for example about 10 mg, about 20 mg, about 30 mg, about 40 mg, about 50 mg, about 60 mg, about 70 mg, about 80 mg, about 90 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 266 mg, about 275 mg, about 300 mg, about 324 mg, about 325 mg, about 330 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about 600 mg, about 625 mg, about 650 mg, about 675 mg, about 700 mg, about 725 mg, about 750 mg, about 775 mg, about 800 mg, about 825 mg, about 850 mg, about 875 mg, about 900 mg, about 925 mg, about 950 mg, about 975 mg,
- Cardiocascular agents can have multiple modes of action and can be described under one or more headings.
- Salts, hydrates, solvate, esters, amides, enantiomers, isomers, tautomers, polymorphs, prodrugs, and derivatives of any of the foregoing drugs may be used in accordance with the invention and may be prepared using standard procedures known to those skilled in the art of synthetic organic chemistry. See, e.g., March, Advanced Organic Chemistry: Reactions, Mechanisms and Structure, 4th Ed. (New York: Wiley-Interscience, 1992); Leonard et al., Advanced Practical Organic Chemistry (1992); Howarth et al., Core Organic Chemistry (1998); and Weisermel et al., Industrial Organic Chemistry (2002).
- “Pharmaceutically acceptable salts,” or “salts,” include the salt of a drug prepared from formic, acetic, propionic, succinic, glycolic, gluconic, lactic, malic, tartaric, citric, ascorbic, glucuronic, maleic, fumaric, pyruvic, aspartic, glutamic, benzoic, anthranilic, mesylic, stearic, salicylic, p-hydroxybenzoic, phenylacetic, mandelic, embonic, methanesulfonic, ethanesulfonic, benzenesulfonic, pantothenic, toluenesulfonic, 2-hydroxyethanesulfonic, sulfanilic, cyclohexylaminosulfonic, algenic, beta-hydroxybutyric, galactaric and galacturonic acids.
- acid addition salts are prepared from the free base forms using conventional methodology involving reaction of the free base with a suitable acid.
- suitable acids for preparing acid addition salts include both organic acids, e.g., acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, malic acid, malonic acid, succinic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid, and the like, as well as inorganic acids, e.g., hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like.
- base addition salts are prepared from the free acid forms using conventional methodology involving reaction of the free acid with a suitable base.
- an acid addition salt is reconverted to the free base by treatment with a suitable base.
- the acid addition salts are halide salts, which are prepared using hydrochloric or hydrobromic acids.
- the basic salts are alkali metal salts, e.g., sodium salt.
- a base addition salt is reconverted to the free acid by treatment with a suitable acid.
- EPA and one or more cardiovascular agent(s) are present in a composition of the invention, or are co-administered in a weight ratio of EPA:cardiovascular agent of about 1:1000 to about 1000:1, about 1:500 to about 500:1, about 1:100 to about 100:1, about 1:50 to about 50:1, about 1:25 to about 25:1, about 1:10 to about 10:1, about 1:5 to about 5:1, about 1:4 to about 4:1 about 1:3 to about 3:1, about 1:2 to about 2:1 or about 1:1.
- the present invention provides a method of treating a cardiovascular-related disease as defined herein, for example dyslipidemia or hyperlipidemia, in an HIV positive subject.
- the method comprises co-administration, or concomitant administration, of a composition or compositions as disclosed herein with one or more HIV-1 protease inhibitors.
- HIV-1 protease inhibitors include amprenavir, fosamprenavir, indinavir, lopinavir, nelfinavir, ritonavir and saquinavir.
- HIV-1 protease inhibitors are typically present in a composition of the invention (or co-administered with EPA according to other embodiments of the invention) in an amount of about 100 mg to about 2500 mg, for example about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 300 mg, about 350 mg, about 400 mg, about 450 mg, about 500 mg, about 550 mg, about 600 mg, about 625 mg, about 650 mg, about 700 mg, about 800 mg, about 900 mg, about 1000 mg, about 1100 mg, about 1200 mg, about 1250 mg, about 1300 mg, about 1400 mg, about 1500 mg, about 1600 mg, about 1700 mg, about 1800 mg, about 1825 mg, about 1900 mg, about 2000 mg, about 2100 mg, about 2200 mg, about 2300 mg, about 2400 mg, or about 2500 mg; in an amount of about 200 mg to about 1000 mg, for example about 200 mg, about 300 mg, about 400 mg, about 500
- compositions of the invention are orally deliverable.
- oral administration include any form of delivery of a therapeutic agent or a composition thereof to a subject wherein the agent or composition is placed in the mouth of the subject, whether or not the agent or composition is swallowed.
- oral administration includes buccal and sublingual as well as esophageal administration.
- compositions of the invention are in the form of solid dosage forms.
- suitable solid dosage forms include tablets (e.g. suspension tablets, bite suspension tablets, rapid dispersion tablets, chewable tablets, melt tablets, effervescent tablets, bilayer tablets, etc), caplets, capsules (e.g. a soft or a hard gelatin capsule filled with solid and/or liquids), powder (e.g. a packaged powder, a dispensable powder or an effervescent powder), lozenges, sachets, cachets, troches, pellets, granules, microgranules, encapsulated microgranules, powder aerosol formulations, or any other solid dosage form reasonably adapted for oral administration.
- EPA and/or any other desired cardiovascular agent(s) can be co-formulated in the same dosage unit, or can be individually formulated in separate dosage units.
- dose unit and “dosage unit” herein refer to a portion of a pharmaceutical composition that contains an amount of a therapeutic agent suitable for a single administration to provide a therapeutic effect. Such dosage units may be administered one to a plurality (i.e. 1 to about 10, 1 to 8, 1 to 6, 1 to 4 or 1 to 2) of times per day, or as many times as needed to elicit a therapeutic response.
- a composition of the invention comprises one or more cardiovascular agents dispersed or suspended in EPA, wherein the dispersion or suspension is present in a capsule (for example gelatin or HPMC capsule), sachet, or other dosage form or carrier as described herein.
- the dispersion or suspension is substantially uniform.
- the EPA is present in a first dosage unit, for example a suspension in a capsule
- the cardiovascular agent is present in second dosage unit, for example a tablet.
- any desired additional cardiovascular agent can be present in a third composition.
- composition(s) of the invention can be in the form of liquid dosage forms or dose units to be imbibed directly or they can be mixed with food or beverage prior to ingestion.
- suitable liquid dosage forms include solutions, suspension, elixirs, syrups, liquid aerosol formulations, etc.
- compositions of the invention upon storage in a closed container maintained at room temperature, refrigerated (e.g. about 5 to about 5-10° C.) temperature, or frozen for a period of about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 months, exhibit at least about 90%, at least about 95%, at least about 97.5%, or at least about 99% of the active ingredient(s) originally present therein.
- the invention provides a pharmaceutical composition
- EPA and a cardiovascular agent (fill) encapsulated in a capsule shell, wherein the fill has a baseline peroxide value not greater than about 10 Meq/kg, about 9 Meq/kg, about 8 Meq/kg, about 7 Meq/kg, about 6 Meq/kg, about 5 Meq/kg, about 4 Meq/kg, about 3 Meq/kg or about 2 Meq/kg, wherein upon storage of the composition at 23° C.
- the ultra-pure EPA has a second peroxide value not greater than about 25 Meq/kg, about 24 Meq/kg, about 23 Meq/kg, about 22 Meq/kg, about 21 Meq/kg, about 20 Meq/kg, about 19 Meq/kg, about 18 Meq/kg, about 17 Meq/kg, about 16 Meq/kg, about 15 Meq/kg, about 14 Meq/kg, about 13 Meq/kg, about 12 Meq/kg, about 11 Meq/kg, about 10 Meq/kg, about 9 Meq/kg, about 8 Meq/kg, about 7 Meq/kg, about 6 Meq/kg, about 5 Meq/kg, about 4 Meq/kg, about 3 Meq/kg or about 2 Meq/kg.
- Degradation products can alter a composition's efficacy, for example by delivering less active ingredient to a subject than recommended.
- Degradation products for new drugs above certain thresholds should be reported to the Food & Drug Administration (FDA) in accordance with current Guidance Documents. Degradation products above a certain threshold amount should be identified. A degradation product is “identified” when its structural characterization has been achieved. Degradation products above a certain amount should be qualified. A degradation product is “qualified” when its biological safety is acquired and evaluated.
- compositions of the invention with a maximum daily dose of less than or equal to 1 gram, upon storage under light, heat, humidity, acid/base hydrolytic, and/or oxidative conditions contain less than about 0.1% of any degradation product not reported to the Food and Drug Administration (FDA).
- compositions of the invention with a maximum daily dose of greater than 1 gram, upon storage under light, heat, humidity, acid/base hydrolytic, and/or oxidative conditions contain less than about 0.05% of any degradation product not reported to the FDA.
- compositions of the invention with a maximum daily dose of less than 1 mg, upon storage under light, heat, humidity, acid/base hydrolytic, and/or oxidative conditions contain less than about 1% of any unidentified degradation product. In another embodiment, compositions of the invention with a maximum daily dose of less than 1 mg, upon storage under light, heat, humidity, acid/base hydrolytic, and/or oxidative conditions, contain less than about 5 ⁇ g of any unidentified degradation product.
- compositions of the invention with a maximum daily dose of 1 mg to 10 mg, upon storage under light, heat, humidity, acid/base hydrolytic, and/or oxidative conditions, contain less than about 0.5% of any unidentified degradation product.
- compositions of the invention with a maximum daily dose of 1 mg to 10 mg, upon storage under light, heat, humidity, acid/base hydrolytic, and/or oxidative conditions contain less than about 20 ⁇ g of any unidentified degradation product.
- compositions of the invention with a maximum daily dose of 10 mg to 2 g, upon storage under light, heat, humidity, acid/base hydrolytic, and/or oxidative conditions contain less than about 0.2% of any unidentified degradation product.
- compositions of the invention with a maximum daily dose of 10 mg to 2 g, upon storage under light, heat, humidity, acid/base hydrolytic, and/or oxidative conditions contain less than about 2 mg of any unidentified degradation product.
- compositions of the invention with a maximum daily dose of greater than 2 g upon storage under light, heat, humidity, acid/base hydrolytic, and/or oxidative conditions, contain less than about 0.1% of any unidentified degradation product.
- compositions of the invention with a maximum daily dose of less than 10 mg, upon storage under light, heat, humidity, acid/base hydrolytic, and/or oxidative conditions contain less than about 1% of any unqualified degradation product. In another embodiment, compositions of the invention with a maximum daily dose of less than 10 mg, upon storage under light, heat, humidity, acid/base hydrolytic, and/or oxidative conditions, contain less than about 50 ⁇ g of any unqualified degradation product.
- compositions of the invention with a maximum daily dose of 10 mg to 100 mg, upon storage under light, heat, humidity, acid/base hydrolytic, and/or oxidative conditions contain less than about 0.5% of any unqualified degradation product.
- compositions of the invention with a maximum daily dose of 10 mg to 100 mg, upon storage under light, heat, humidity, acid/base hydrolytic, and/or oxidative conditions contain less than about 200 ⁇ g of any unqualified degradation product.
- compositions of the invention with a maximum daily dose of 100 mg to 2 g, upon storage under light, heat, humidity, acid/base hydrolytic, and/or oxidative conditions contain less than about 0.2% of any unqualified degradation product.
- compositions of the invention with a maximum daily dose of 100 mg to 2 g, upon storage under light, heat, humidity, acid/base hydrolytic, and/or oxidative conditions contain less than about 3 mg of any unqualified degradation product.
- compositions of the invention with a maximum daily dose of greater than 2 g upon storage under light, heat, humidity, acid/base hydrolytic, and/or oxidative conditions, contain less than about 0.15% of any unqualified degradation product.
- compositions of the invention comprise a stabilizing agent that suppresses, prevents, hinders, or otherwise attenuates the decomposition of the active ingredient(s) during storage.
- oxidative decomposition of EPA in compositions of the invention may be prevented or attenuated by the presence of antioxidants.
- suitable antioxidants include tocopherol, lecithin, citric acid and/or ascorbic acid.
- One or more antioxidants, if desired, are typically present in a composition in an amount of about 0.01% to about 0.1%, by weight, or about 0.025% to about 0.05%, by weight.
- compositions of the invention optionally comprise one or more pharmaceutically acceptable excipients.
- pharmaceutically acceptable excipient herein means any substance, not itself a therapeutic agent, used as a carrier or vehicle for delivery of a therapeutic agent to a subject or added to a pharmaceutical composition to improve its handling or storage properties or to permit or facilitate formation of a unit dose of the composition, and that does not produce unacceptable toxicity or interaction with other components in the composition.
- compositions of the invention optionally comprise one or more pharmaceutically acceptable diluents as excipients.
- suitable diluents illustratively include, either individually or in combination, lactose, including anhydrous lactose and lactose monohydrate; starches, including directly compressible starch and hydrolyzed starches (e.g., CelutabTM and EmdexTM); mannitol; sorbitol; xylitol; dextrose (e.g., CereloseTM 2000) and dextrose monohydrate; dibasic calcium phosphate dihydrate; sucrose-based diluents; confectioner's sugar; monobasic calcium sulfate monohydrate; calcium sulfate dihydrate; granular calcium lactate trihydrate; dextrates; inositol; hydrolyzed cereal solids; amylose; celluloses including microcrystalline cellulose, food grade sources of ⁇ - and amorphous cellulose (e.g.,
- compositions of the invention optionally comprise one or more pharmaceutically acceptable disintegrants as excipients.
- Suitable disintegrants include, either individually or in combination, starches, including sodium starch glycolate (e.g., ExplotabTM of PenWest) and pregelatinized corn starches (e.g., NationalTM 1551, NationalTM 1550, and ColocornTM 1500), clays (e.g., VeegumTM HV), celluloses such as purified cellulose, microcrystalline cellulose, methylcellulose, carboxymethylcellulose and sodium carboxymethylcellulose, croscarmellose sodium (e.g., Ac-Di-SolTM of FMC), alginates, crospovidone, and gums such as agar, guar, xanthan, locust bean, karaya, pectin and tragacanth gums.
- Such disintegrants if present, typically comprise in total about 0.2% to about 30%, about 0.2% to about 10%, or about 0.2% to about 5%, of the total weight
- compositions of the invention optionally comprise one or more antioxidants.
- antioxidants include sodium ascorbate and vitamin E (tocopherol).
- One or more antioxidants, if present, are typically present in a composition of the invention in an amount of about 0.001% to about 5%, about 0.005% to about 2.5%, or about 0.01% to about 1%, by weight.
- compositions of the invention optionally comprise one or more pharmaceutically acceptable binding agents or adhesives as excipients.
- binding agents and adhesives can impart sufficient cohesion to a powder being tableted to allow for normal processing operations such as sizing, lubrication, compression and packaging, but still allow the tablet to disintegrate and the composition to be absorbed upon ingestion.
- Suitable binding agents and adhesives include, either individually or in combination, acacia; tragacanth; sucrose; gelatin; glucose; starches such as, but not limited to, pregelatinized starches (e.g., NationalTM 1511 and NationalTM 1500); celluloses such as, but not limited to, methylcellulose and carmellose sodium (e.g., TyloseTM); alginic acid and salts of alginic acid; magnesium aluminum silicate; PEG; guar gum; polysaccharide acids; bentonites; povidone, for example povidone K-15, K-30 and K-29/32; polymethacrylates; HPMC; hydroxypropylcellulose (e.g., KlucelTM); and ethylcellulose (e.g., EthocelTM).
- Such binding agents and/or adhesives if present, constitute in total about 0.5% to about 25%, about 0.75% to about 15%, or about 1% to about 10%, of the total weight of the composition.
- compositions of the invention optionally comprise one or more pharmaceutically acceptable wetting agents as excipients.
- surfactants that can be used as wetting agents in compositions of the invention include quaternary ammonium compounds, for example benzalkonium chloride, benzethonium chloride and cetylpyridinium chloride, dioctyl sodium sulfosuccinate, polyoxyethylene alkylphenyl ethers, for example nonoxynol 9, nonoxynol 10, and octoxynol 9, poloxamers (polyoxyethylene and polyoxypropylene block copolymers), polyoxyethylene fatty acid glycerides and oils, for example polyoxyethylene (8) caprylic/capric mono- and diglycerides (e.g., LabrasolTM of Gattefossé), polyoxyethylene (35) castor oil and polyoxyethylene (40) hydrogenated castor oil; polyoxyethylene alkyl ethers, for example polyoxyethylene (20) cetostearyl ether
- compositions of the invention optionally comprise one or more pharmaceutically acceptable lubricants (including anti-adherents and/or glidants) as excipients.
- suitable lubricants include, either individually or in combination, glyceryl behapate (e.g., CompritolTM 888); stearic acid and salts thereof, including magnesium (magnesium stearate), calcium and sodium stearates; hydrogenated vegetable oils (e.g., SterotexTM); colloidal silica; talc; waxes; boric acid; sodium benzoate; sodium acetate; sodium fumarate; sodium chloride; DL-leucine; PEG (e.g., CarbowaxTM 4000 and CarbowaxTM 6000); sodium oleate; sodium lauryl sulfate; and magnesium lauryl sulfate.
- Such lubricants if present, constitute in total about 0.1% to about 10%, about 0.2% to about 8%, or about 0.25% to about
- Suitable anti-adherents include talc, cornstarch, DL-leucine, sodium lauryl sulfate and metallic stearates.
- Talc is an anti-adherent or glidant used, for example, to reduce formulation sticking to equipment surfaces and also to reduce static in the blend. Talc, if present, constitutes about 0.1% to about 10%, about 0.25% to about 5%, or about 0.5% to about 2%, of the total weight of the composition.
- Glidants can be used to promote powder flow of a solid formulation. Suitable glidants include colloidal silicon dioxide, starch, talc, tribasic calcium phosphate, powdered cellulose and magnesium trisilicate.
- compositions of the present invention optionally comprise one or more flavoring agents, sweetening agents, and/or colorants.
- Flavoring agents useful in the present invention include, without limitation, acacia syrup, alitame, anise, apple, aspartame, banana, Bavarian cream, berry, black currant, butter, butter pecan, butterscotch, calcium citrate, camphor, caramel, cherry, cherry cream, chocolate, cinnamon, citrus, citrus punch, citrus cream, cocoa, coffee, cola, cool cherry, cool citrus, cyclamate, cylamate, dextrose, eucalyptus, eugenol, fructose, fruit punch, ginger, glycyrrhetinate, glycyrrhiza (licorice) syrup, grape, grapefruit, honey, isomalt, lemon, lime, lemon cream, MagnaSweet®, maltol, mannitol, maple, menthol, mint, mint cream, mixed berry, nut, orange
- Sweetening agents that can be used in the present invention include, for example, acesulfame potassium (acesulfame K), alitame, aspartame, cyclamate, cylamate, dextrose, isomalt, MagnaSweet®, maltitol, mannitol, neohesperidine DC, neotame, Prosweet® Powder, saccharin, sorbitol, stevia, sucralose, sucrose, tagatose, thaumatin, xylitol, and the like.
- Flavoring agents, sweetening agents, and/or colorants can be present in compositions of the invention in any suitable amount, for example about 0.01% to about 10%, about 0.1% to about 8%, or about 1% to about 5%, by weight.
- compositions of the invention optionally comprise a suspending agent.
- suitable suspending agents include silicon dioxide, bentonite, hydrated aluminum silicate (e.g. kaolin) and mixtures thereof.
- One or more suspending agents are optionally present in compositions of the invention in a total amount of about 0.01% to about 3.0%, about 0.1% to about 2.0%, or about 0.25% to about 1.0%, by weight
- excipients can have multiple roles as is known in the art.
- starch can serve as a filler as well as a disintegrant.
- the classification of excipients above is not to be construed as limiting in any manner. Excipients categorized in any manner may also operate under various different categories of excipients as will be readily appreciated by one of ordinary skill in the art.
- compositions of the invention are useful for treatment and/or prevention of a cardiovascular-related disease.
- cardiovascular-related disease herein refers to any disease or disorder of the heart or blood vessels (i.e. arteries and veins) or any symptom thereof, or any disease or condition that causes or contributes to a cardiovascular disease.”
- cardiovascular-related diseases and disorders include acute cardiac ischemic events, acute myocardial infarction, angina, angina pectoris, arrhythmia, atrial fibrulation, atherosclerosis, arterial fibrillation, cardiac insufficiency, cardiovascular disease, chronic heart failure, chronic stable angina, congestive heart failure, coronary artery disease, coronary heart disease, deep vein thrombosis, diabetes, diabetes mellitus, diabetic neuropathy, diastolic dysfunction in subjects with diabetes mellitus, edema, essential hypertension, eventual pulmonary embolism, fatty liver disease, heart disease, heart failure, homozygous familial hypercholesterolemia (HoFH)
- treatment in relation a given disease or disorder, includes, but is not limited to, inhibiting the disease or disorder, for example, arresting the development of the disease or disorder; relieving the disease or disorder, for example, causing regression of the disease or disorder; or relieving a condition caused by or resulting from the disease or disorder, for example, relieving, preventing or treating symptoms of the disease or disorder.
- prevention in relation to a given disease or disorder means: preventing the onset of disease development if none had occurred, preventing the disease or disorder from occurring in a subject that may be predisposed to the disorder or disease but has not yet been diagnosed as having the disorder or disease, and/or preventing further disease/disorder development if already present.
- compositions of the present invention can be co-administered or administered concomitantly with one or more additional cardiovascular agents.
- co-administered refers to, for example, administration of two or more agents (e.g., EPA or a derivative thereof and a cardiovascular agent) at the same time, in the same dosage unit, one immediately after the other, within five minutes of each other, within ten minutes of each other, within fifteen minutes of each other, within thirty minutes of each other, within one hour of each other, within two hours of each other, within four hours of each other, within six hours of each other, within twelve hours of each other, within one day of each other, within one week of each other, within two weeks of each other, within one month of each other, within two months of each other, within six months of each other, within one year of each other, etc.
- agents e.g., EPA or a derivative thereof and a cardiovascular agent
- the present invention provides a method of treating a cardiovascular-related disease comprising administering to a subject in need thereof a composition or compositions comprising EPA and one or more additional cardiovascular agents (either as a single dosage unit or as multiple dosage units), wherein one or more lipid parameters are improved by comparison with lipid parameters achieved by the additive effects of the individual treatments.
- the subject or subject group upon treatment in accordance with the present invention, for example over a period of about 1 to about 200 weeks, about 1 to about 100 weeks, about 1 to about 80 weeks, about 1 to about 50 weeks, about 1 to about 40 weeks, about 1 to about 20 weeks, about 1 to about 15 weeks, about 1 to about 12 weeks, about 1 to about 10 weeks, about 1 to about 5 weeks, about 1 to about 2 weeks or about 1 week, the subject or subject group exhibits one or more of the following outcomes:
- methods of the present invention comprise measuring baseline levels of one or more markers set forth in (a)-(y) above prior to dosing the subject or subject group.
- the methods comprise administering a composition as disclosed herein to the subject after baseline levels of one or more markers set forth in (a)-(y) are determined, and subsequently taking an additional measurement of said one or more markers.
- the subject or subject group upon treatment with a composition of the present invention, for example over a period of about 1 to about 200 weeks, about 1 to about 100 weeks, about 1 to about 80 weeks, about 1 to about 50 weeks, about 1 to about 40 weeks, about 1 to about 20 weeks, about 1 to about 15 weeks, about 1 to about 12 weeks, about 1 to about 10 weeks, about 1 to about 5 weeks, about 1 to about 2 weeks or about 1 week, the subject or subject group exhibits any 2 or more of, any 3 or more of, any 4 or more of, any 5 or more of, any 6 or more of, any 7 or more of, any 8 or more of, any 9 or more of, any 10 or more of, any 11 or more of, any 12 or more of, any 13 or more of, any 14 or more of, any 15 or more of, any 16 or more of, any 17 or more of, any 18 or more of, any 19 or more of, any 20 or more of, any 21 or more of, any 22 or more of, any 23 or more, any 24 or more, or all 25 of outcomes (a
- the subject or subject group upon treatment with a composition of the present invention, for example over a period of about 1 to about 200 weeks, about 1 to about 100 weeks, about 1 to about 80 weeks, about 1 to about 50 weeks, about 1 to about 40 weeks, about 1 to about 20 weeks, about 1 to about 15 weeks, about 1 to about 10 weeks, about 1 to about 5 weeks, about 1 to about 2 weeks or about 1 week, the subject or subject group exhibits one or more of the following outcomes:
- methods of the present invention comprise measuring baseline levels of one or more markers set forth in (a)-(y) prior to dosing the subject or subject group. In another embodiment, the methods comprise administering a composition as disclosed herein to the subject after baseline levels of one or more markers set forth in (a)-(y) are determined, and subsequently taking a second measurement of the one or more markers as measured at baseline for comparison thereto.
- the subject or subject group upon treatment with a composition of the present invention, for example over a period of about 1 to about 200 weeks, about 1 to about 100 weeks, about 1 to about 80 weeks, about 1 to about 50 weeks, about 1 to about 40 weeks, about 1 to about 20 weeks, about 1 to about 15 weeks, about 1 to about 12 weeks, about 1 to about 10 weeks, about 1 to about 5 weeks, about 1 to about 2 weeks or about 1 week, the subject or subject group exhibits any 2 or more of, any 3 or more of, any 4 or more of, any 5 or more of, any 6 or more of, any 7 or more of, any 8 or more of, any 9 or more of, any 10 or more of, any 11 or more of, any 12 or more of, any 13 or more of, any 14 or more of, any 15 or more of, any 16 or more of, any 17 or more of, any 18 or more of, any 19 or more of, any 20 or more of, any 21 or more of, any 22 or more of, any 23 or more of, any 24 or more of, or all 25 of outcomes
- Parameters (a)-(y) can be measured in accordance with any clinically acceptable methodology.
- triglycerides, total cholesterol, HDL-C and fasting blood sugar can be sample from serum and analyzed using standard photometry techniques.
- VLDL-TG, LDL-C and VLDL-C can be calculated or determined using serum lipoprotein fractionation by preparative ultracentrifugation and subsequent quantitative analysis by refractometry or by analytic ultracentrifugal methodology.
- Apo A1, Apo B and hsCRP can be determined from serum using standard nephelometry techniques.
- Lipoprotein (a) can be determined from serum using standard turbidimetric immunoassay techniques.
- LDL particle number and particle size can be determined using nuclear magnetic resonance (NMR) spectrometry.
- Remnants lipoproteins and LDL-phospholipase A2 can be determined from EDTA plasma or serum and serum, respectively, using enzymatic immunoseparation techniques.
- Oxidized LDL, intercellular adhesion molecule-1 and interleukin-2 levels can be determined from serum using standard enzyme immunoassay techniques. These techniques are described in detail in standard textbooks, for example Tietz Fundamentals of Clinical Chemistry, 6 th Ed. (Burtis, Ashwood and Borter Eds.), WB Saunders Company.
- the present invention provides a method of blood lipid therapy comprising administering to a subject in need thereof 1 to a plurality of dosage units comprising a composition or compositions as disclosed herein.
- the subject being treated has a baseline triglyceride level, prior to treatment with a composition of the present invention, greater than or equal to about 150 mg/dl, greater than or equal to about 175 mg/dl, greater than or equal to about 250 mg/dl, or greater than or equal to about 500 mg/dl, for example about 200 mg/dl to about 2000 mg/dl, about 300 to about 1800 mg/dl, or about 500 mg/dl to about 1500 mg/dl.
- methods of the present invention comprise measuring baseline levels of one or more markers set forth in (a)-(y) prior to dosing the subject or subject group. In another embodiment, the methods comprise administering a composition as disclosed herein to the subject after baseline levels of one or more markers set forth in (a)-(y) are determined, and subsequently taking a second measurement of the one or more markers as measured at baseline for comparison thereto.
- the present invention provides a method of treating or preventing primary hypercholesteremia and/or mixed dyslipidemia (Fredrickson Types IIa and IIb) in a subject in need thereof, comprising administering to the subject a composition or compositions comprising EPA and one or more additional cardiovascular agents (either as a single dosage unit or as multiple dosage units) as disclosed herein.
- the present invention provides a method of reducing triglyceride levels in a subject or subjects when treatment with a statin or niacin extended-release monotherapy is considered inadequate (Frederickson type IV hyperlipidemia).
- Statin or niacin extended-release monotherapy is considered inadequate when, for example, the subject's non-HDL-C level is not lowered or is not lowered to the degree desired, the subject's LDL-C level is not improved or is not improved to the degree desired, the subject's HDL-C level is not improved or is not improved to the degree desired, and/or the subject's triglyceride level is not improved or is not improved to the degree desired.
- the present invention provides a method of treating or preventing nonfatal myocardial infarction, comprising administering to the subject a composition or compositions comprising EPA and one or more additional cardiovascular agents (either as a single dosage unit or as multiple dosage units) as disclosed herein.
- the present invention provides a method of treating or preventing risk of recurrent nonfatal myocardial infarction in a subject with a history of myocardial infarction, comprising administering to the subject a composition or compositions comprising EPA and one or more additional cardiovascular agents (either as a single dosage unit or as multiple dosage units) as disclosed herein.
- the present invention provides a method of slowing progression of or promoting regression of atherosclerotic disease in a subject in need thereof, comprising administering to the subject a composition or compositions comprising EPA and one or more additional cardiovascular agents (either as a single dosage unit or as multiple dosage units) as disclosed herein.
- the present invention provides a method of treating obesity in a subject in need thereof, comprising administering to a subject in need thereof a composition or compositions comprising EPA and one or more additional cardiovascular agents (either as a single dosage unit or as multiple dosage units) as disclosed herein.
- the present invention provides a method of treating or preventing very high serum triglyceride levels (e.g. Types IV and V hyperlipidemia) in a subject in need thereof, comprising administering to the subject a composition or compositions comprising EPA and one or more additional cardiovascular agents (either as a single dosage unit or as multiple dosage units) as disclosed herein.
- very high serum triglyceride levels e.g. Types IV and V hyperlipidemia
- the present invention provides a method of treating subjects having very high serum triglyceride levels (e.g. greater than 1000 mg/dl or greater than 2000 mg/dl) and that are at risk of developing pancreatitis, comprising administering to the subject a composition or compositions comprising EPA and one or more additional cardiovascular agents (either as a single dosage unit or as multiple dosage units) as disclosed herein.
- very high serum triglyceride levels e.g. greater than 1000 mg/dl or greater than 2000 mg/dl
- additional cardiovascular agents either as a single dosage unit or as multiple dosage units
- the present invention provides a method of preventing recurrence of stroke, comprising administering to a subject with a history of stroke a composition or compositions comprising EPA and one or more additional cardiovascular agents (either as a single dosage unit or as multiple dosage units) as disclosed herein.
- the present invention provides a method of preventing onset and/or recurrence of cardiovascular events in a subject who has escaped the unstable period after cardiovascular angioplasty, comprising administering to the subject a composition or compositions comprising EPA and one or more additional cardiovascular agents (either as a single dosage unit or as multiple dosage units) as disclosed herein.
- the present invention provides a method of reducing Apo-B and non-HDL cholesterol levels in a subject group with a baseline LDL-cholesterol level of at least 100 mg/dl, a baseline non-HDL-cholesterol level of at least 130 mg/dl and a baseline triglyceride level of at least 200 mg/dl, and reducing the Apo-B and the non-HDL-cholesterol level of the subject group by administering a composition or compositions comprising EPA and one or more additional cardiovascular agents (either as a single dosage unit or as multiple dosage units) as disclosed herein to members of the subject group.
- the invention provides a method of reducing Apo-B levels in a subject group, comprising measuring LDL-cholesterol, non-HDL-cholesterol, and triglyceride levels in subjects, providing a subject group with a baseline LDL-cholesterol level of at least 100 mg/dL, a baseline non-HDL-cholesterol level of at least 130 mg/dL, and a baseline triglyceride level of at least 200 mg/dL, and reducing the Apo-B levels of the subject group by administering to members of the subject group a composition or compositions comprising EPA and one or more additional cardiovascular agents (either as a single dosage unit or as multiple dosage units) as disclosed herein in an amount effective to reduce the Apo-B levels of the subject group in a statistically significant amount as compared to a control treatment, wherein an increase or statistically significant increase of LDL-cholesterol level is avoided.
- the invention provides a method of reducing Apo-B levels in a subject group, comprising providing a subject group with a baseline LDL-cholesterol level of at least 100 mg/dL, a baseline non-HDL-cholesterol level of at least 130 mg/dL, and a baseline triglyceride level of at least 200 mg/dL, reducing the Apo-B levels of the subject group by administering to members of the subject group a composition or compositions comprising EPA and one or more additional cardiovascular agents (either as a single dosage unit or as multiple dosage units) as disclosed herein in an amount effective to reduce the Apo-B levels of the subject group in a statistically significant amount as compared to a control treatment, and determining the reduction in the Apo-B levels of the subject group.
- a composition of the invention is administered to a subject in an amount sufficient to provide a daily EPA dose of about 1 mg to about 10,000 mg, 25 about 5000 mg, about 50 to about 3000 mg, about 75 mg to about 2500 mg, or about 100 mg to about 1000 mg, for example about 75 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about 600 mg, about 625 mg, about 650 mg, about 675 mg, about 700 mg, about 725 mg, about 750 mg, about 775 mg, about 800 mg, about 825 mg, about 850 mg, about 875 mg, about 900 mg, about 925 mg, about 950 mg, about 975 mg, about 1000 mg, about 1025 mg, about 10
- the EPA and optional one or more additional cardiovascular agents can be administered as a co-formulated single dosage unit, or as individual dosage units. Where the EPA and optional one or more additional cardiovascular agents are co-administered as separate dosage units, each dosage unit can be administered to a subject at substantially the same or substantially different times.
- each dosage unit can be administered to the subject within a period of about 24 hours, 18 hours, 12 hours, 10 hours, 8 hours, 6 hours, 4 hours, 2 hours, 1 hour, or 0.5 hours.
- the EPA and one or more optional cardiovascular agents can be administered sequentially.
- EPA can be administered to a subject as a sole agent during an EPA loading period.
- the loading period can be, for example, 1 day, 2 days, 4 days, 6 days, 2 weeks, 3 weeks, 4 weeks, 5 weeks, 6 weeks, 7 weeks, 8 weeks, 9 weeks or 10 weeks.
- one or more additional cardiovascular agents can be initiated together with current EPA administration or in place of EPA treatment.
- EPA is administered to a subject in the morning, for example from about 4 am to about 10 am, about 5 am to about 9 am, or about 6 am to about 8 am
- the optional one or more cardiovascular agents are administered to the subject in the afternoon or evening, for example from about 1 pm to about 11 pm, about 2 pm to about 10 pm, or about 3 pm to about 9 pm, or vice versa.
- the invention provides the use of EPA and one or more cardiovascular agents in the manufacture of a medicament for treatment or prevention of a cardiovascular-related disease such as hypertriglyceridemia, hypercholesterolemia, mixed dyslipidemia, coronary heart disease, vascular disease, stroke, atherosclerosis, arrhythmia, hypertension, myocardial infarction, and other cardiovascular events.
- a cardiovascular-related disease such as hypertriglyceridemia, hypercholesterolemia, mixed dyslipidemia, coronary heart disease, vascular disease, stroke, atherosclerosis, arrhythmia, hypertension, myocardial infarction, and other cardiovascular events.
- the composition contains not more than 10% DHA, if any. In another embodiment, the composition contains substantially no or no DHA.
- the invention provides a pharmaceutical composition comprising EPA and one or more cardiovascular agents for the treatment and/or prevention of a cardiovascular-related disease, wherein the composition contains not more than 10% DHA, if any. In a related embodiment, the composition contains substantially no DHA or no DHA.
- a subject being treated with a composition or regimen set forth herein is a diabetic or pre-diabetic subject.
- any of the methods disclosed herein are used in treatment or prevention of a subject or subjects that consume a traditional Western diet.
- the methods of the invention include a step of identifying a subject as a Western diet consumer or prudent diet consumer and then treating the subject if the subject is deemed to consume a Western diet.
- the term “Western diet” herein refers generally to a typical diet consisting of, by percentage of total calories, about 45% to about 50% carbohydrate, about 35 to about 40% fat, and about 10% to about 15% protein.
- a Western diet may further be characterized by relatively high intakes of red and processed meats, sweets, refined grains, and desserts, for example where half or more or 70% or more calories come from these sources.
- EPA and DHA were tested individually at a fixed concentration of 10.0 ⁇ M or in combination at 5.65 ⁇ M and 4.35 ⁇ M (EPA and DHA, respectively), which is a mole ratio of 1.3:1.
- LOOH lipid peroxide
- C/P cholesterol-to-phospholipid
- Levels of lipid hydroperoxides were also measured for EPA, DPH and EPA/DPH in cholesterol-enriched membrane prepared in the absence and presence of atorvastatin.
- 1,2-Dilinoleoyl-3-sn-phosphatidylcholine was obtained from Avanti Polar Lipids (Alabaster, Ala.) and stored in chloroform (25 mg/ml) at ⁇ 80° C. until use. Cholesterol obtained and stored in chloroform (10 mg/ml) at ⁇ 20° C.
- CHOD-iodide color reagent was prepared according to a procedure modified from El-Saadani et al. (El-Saadani M, Esterbauer H, El-Sayed M, Goher M, Nassar A Y, Jurgens G.
- Atorvastatin was prepared in ethanol just prior to experimental use and added together with component lipids containing fixed amounts of EPA, DPH or EPA/DPH at equimolar levels. The compounds and lipids were added in combination during membrane sample preparation to ensure full incorporation into the lipid bilayers.
- Membrane samples consisting of DLPC ⁇ cholesterol, with cholesterol-to-phospholipid (C/P) mole ratios ranging from 0.5 to 1.5, were prepared as follows. Component lipids (in chloroform) were transferred to 13 ⁇ 100 mm test tubes and shell-dried under a steady stream of nitrogen gas while vortex mixing. The lipid was co-dried with EPA, DPH or EPA/DPH prepared in the absence or presence of the atorvastatin at equimolar levels.
- C/P cholesterol-to-phospholipid
- lipid membrane samples were subjected to time-dependent autoxidation by incubating at 37° C. in an uncovered, shaking water bath. Small aliquots of each sample were removed at 24 h intervals and combined with 1.0 ml of active CHOD-iodide color reagent. To ensure spectrophotometric readings within the optimum absorbance range, sample volumes taken for measurement of lipid peroxide formation were adjusted for length of peroxidation and range between 100 and 10 ⁇ l. Test samples were immediately covered with foil and incubated at room temperature for >4 h in the absence of light. Absorbances were measured against a CHOD blank at 365 nm using a Beckman DU-640 spectrophotometer.
- the CHOD colorimetric assay is based on the oxidation of iodide (I ⁇ ) by lipid hydroperoxides (LOOH) and proceeds according to the following reaction scheme:
- the quantity of triiodide anion (I 3 ⁇ ) liberated in this reaction is directly proportional to the amount of lipid hydroperoxides present in the membrane sample.
- the molar absorptivity value ( ⁇ ) of I 3 ⁇ is 2.46 ⁇ 10 4 M ⁇ 1 cm ⁇ 1 at 365 nm.
- Results are shown in FIGS. 1-4 .
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Emergency Medicine (AREA)
- Obesity (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Endocrinology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Molecular Biology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Child & Adolescent Psychology (AREA)
- Virology (AREA)
- Biomedical Technology (AREA)
- Hospice & Palliative Care (AREA)
- Biochemistry (AREA)
- Inorganic Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Oncology (AREA)
- Psychiatry (AREA)
- Gastroenterology & Hepatology (AREA)
- Vascular Medicine (AREA)
- AIDS & HIV (AREA)
- Communicable Diseases (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13/124,628 US20120093922A1 (en) | 2009-04-29 | 2010-04-29 | Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US17375909P | 2009-04-29 | 2009-04-29 | |
US13/124,628 US20120093922A1 (en) | 2009-04-29 | 2010-04-29 | Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same |
PCT/US2010/032948 WO2010127099A2 (en) | 2009-04-29 | 2010-04-29 | Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same |
Publications (1)
Publication Number | Publication Date |
---|---|
US20120093922A1 true US20120093922A1 (en) | 2012-04-19 |
Family
ID=43032772
Family Applications (27)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US13/124,628 Abandoned US20120093922A1 (en) | 2009-04-29 | 2010-04-29 | Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same |
US13/266,085 Active 2031-07-14 US11033523B2 (en) | 2009-04-29 | 2010-04-29 | Pharmaceutical compositions comprising EPA and a cardiovascular agent and methods of using the same |
US13/417,899 Active 2030-05-04 US8563608B2 (en) | 2009-04-29 | 2012-03-12 | Methods for lowering triglycerides without raising LDL-C levels in a subject on concomitant statin therapy |
US13/418,591 Abandoned US20120172432A1 (en) | 2009-04-29 | 2012-03-13 | Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same |
US13/540,319 Active US8618166B2 (en) | 2009-04-29 | 2012-07-02 | Methods of treating mixed dyslipidemia |
US13/758,332 Abandoned US20130195972A1 (en) | 2009-04-29 | 2013-02-04 | Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same |
US13/898,447 Active US8691871B2 (en) | 2009-04-29 | 2013-05-20 | Methods of treating mixed dyslipidemia |
US13/898,457 Active US8680144B2 (en) | 2009-04-29 | 2013-05-20 | Methods of treating mixed dyslipidemia |
US14/175,602 Active US9056088B2 (en) | 2009-04-29 | 2014-02-07 | Pharmaceutical compositions comprising fatty acids |
US14/175,515 Abandoned US20140155455A1 (en) | 2009-04-29 | 2014-02-07 | Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same |
US14/536,161 Active 2030-12-23 US10888537B2 (en) | 2009-04-29 | 2014-11-07 | Pharmaceutical compositions comprising omega-3 fatty acids |
US14/704,329 Active US9855237B2 (en) | 2009-04-29 | 2015-05-05 | Methods of treating mixed dyslipidemia |
US15/273,430 Active US10220013B2 (en) | 2009-04-29 | 2016-09-22 | Methods of treating mixed dyslipidemia |
US15/725,617 Active US10265287B2 (en) | 2009-04-29 | 2017-10-05 | Methods of reducing triglycerides and LDL-C |
US16/179,763 Active US10940131B2 (en) | 2009-04-29 | 2018-11-02 | Methods of treating mixed dyslipidemia |
US16/284,543 Active US10624870B2 (en) | 2009-04-29 | 2019-02-25 | Methods of treating mixed dyslipidemia |
US16/389,317 Active US10792267B2 (en) | 2009-04-29 | 2019-04-19 | Methods of treating mixed dyslipidemia |
US16/709,492 Active US10987331B2 (en) | 2009-04-29 | 2019-12-10 | Methods of treating mixed dyslipidemia |
US17/027,069 Active US11154526B2 (en) | 2009-04-29 | 2020-09-21 | Methods of treating mixed dyslipidemia |
US17/127,652 Pending US20210113509A1 (en) | 2009-04-29 | 2020-12-18 | Methods of treating mixed dyslipidemia |
US17/127,398 Pending US20210100765A1 (en) | 2009-04-29 | 2020-12-18 | Methods of treating mixed dyslipidemia |
US17/127,354 Pending US20210100764A1 (en) | 2009-04-29 | 2020-12-18 | Methods of treating mixed dyslipidemia |
US17/208,091 Pending US20210212974A1 (en) | 2009-04-29 | 2021-03-22 | Methods of treating mixed dyslipidemia |
US17/393,213 Abandoned US20210379002A1 (en) | 2009-04-29 | 2021-08-03 | Methods of treating mixed dyslipidemia |
US17/457,160 Active US11400069B2 (en) | 2009-04-29 | 2021-12-01 | Methods of treating mixed dyslipidemia |
US17/457,126 Active US11690820B2 (en) | 2009-04-29 | 2021-12-01 | Methods of treating mixed dyslipidemia |
US17/725,357 Pending US20220241234A1 (en) | 2009-04-29 | 2022-04-20 | Methods of treating mixed dyslipidemia |
Family Applications After (26)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US13/266,085 Active 2031-07-14 US11033523B2 (en) | 2009-04-29 | 2010-04-29 | Pharmaceutical compositions comprising EPA and a cardiovascular agent and methods of using the same |
US13/417,899 Active 2030-05-04 US8563608B2 (en) | 2009-04-29 | 2012-03-12 | Methods for lowering triglycerides without raising LDL-C levels in a subject on concomitant statin therapy |
US13/418,591 Abandoned US20120172432A1 (en) | 2009-04-29 | 2012-03-13 | Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same |
US13/540,319 Active US8618166B2 (en) | 2009-04-29 | 2012-07-02 | Methods of treating mixed dyslipidemia |
US13/758,332 Abandoned US20130195972A1 (en) | 2009-04-29 | 2013-02-04 | Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same |
US13/898,447 Active US8691871B2 (en) | 2009-04-29 | 2013-05-20 | Methods of treating mixed dyslipidemia |
US13/898,457 Active US8680144B2 (en) | 2009-04-29 | 2013-05-20 | Methods of treating mixed dyslipidemia |
US14/175,602 Active US9056088B2 (en) | 2009-04-29 | 2014-02-07 | Pharmaceutical compositions comprising fatty acids |
US14/175,515 Abandoned US20140155455A1 (en) | 2009-04-29 | 2014-02-07 | Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same |
US14/536,161 Active 2030-12-23 US10888537B2 (en) | 2009-04-29 | 2014-11-07 | Pharmaceutical compositions comprising omega-3 fatty acids |
US14/704,329 Active US9855237B2 (en) | 2009-04-29 | 2015-05-05 | Methods of treating mixed dyslipidemia |
US15/273,430 Active US10220013B2 (en) | 2009-04-29 | 2016-09-22 | Methods of treating mixed dyslipidemia |
US15/725,617 Active US10265287B2 (en) | 2009-04-29 | 2017-10-05 | Methods of reducing triglycerides and LDL-C |
US16/179,763 Active US10940131B2 (en) | 2009-04-29 | 2018-11-02 | Methods of treating mixed dyslipidemia |
US16/284,543 Active US10624870B2 (en) | 2009-04-29 | 2019-02-25 | Methods of treating mixed dyslipidemia |
US16/389,317 Active US10792267B2 (en) | 2009-04-29 | 2019-04-19 | Methods of treating mixed dyslipidemia |
US16/709,492 Active US10987331B2 (en) | 2009-04-29 | 2019-12-10 | Methods of treating mixed dyslipidemia |
US17/027,069 Active US11154526B2 (en) | 2009-04-29 | 2020-09-21 | Methods of treating mixed dyslipidemia |
US17/127,652 Pending US20210113509A1 (en) | 2009-04-29 | 2020-12-18 | Methods of treating mixed dyslipidemia |
US17/127,398 Pending US20210100765A1 (en) | 2009-04-29 | 2020-12-18 | Methods of treating mixed dyslipidemia |
US17/127,354 Pending US20210100764A1 (en) | 2009-04-29 | 2020-12-18 | Methods of treating mixed dyslipidemia |
US17/208,091 Pending US20210212974A1 (en) | 2009-04-29 | 2021-03-22 | Methods of treating mixed dyslipidemia |
US17/393,213 Abandoned US20210379002A1 (en) | 2009-04-29 | 2021-08-03 | Methods of treating mixed dyslipidemia |
US17/457,160 Active US11400069B2 (en) | 2009-04-29 | 2021-12-01 | Methods of treating mixed dyslipidemia |
US17/457,126 Active US11690820B2 (en) | 2009-04-29 | 2021-12-01 | Methods of treating mixed dyslipidemia |
US17/725,357 Pending US20220241234A1 (en) | 2009-04-29 | 2022-04-20 | Methods of treating mixed dyslipidemia |
Country Status (16)
Country | Link |
---|---|
US (27) | US20120093922A1 (ru) |
EP (4) | EP3791880A1 (ru) |
KR (1) | KR101357438B1 (ru) |
CN (4) | CN102413825A (ru) |
AU (1) | AU2010241567B2 (ru) |
BR (1) | BRPI1014405A2 (ru) |
CA (1) | CA2759176C (ru) |
CO (1) | CO6470839A2 (ru) |
HK (1) | HK1202795A1 (ru) |
MX (3) | MX2011011517A (ru) |
MY (2) | MY173994A (ru) |
NZ (6) | NZ734905A (ru) |
RU (5) | RU2624506C2 (ru) |
SG (1) | SG175390A1 (ru) |
WO (1) | WO2010127099A2 (ru) |
ZA (1) | ZA201107623B (ru) |
Cited By (99)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20120302639A1 (en) * | 2011-02-16 | 2012-11-29 | Pivotal Therapeutics Inc. | Omega 3 formulations for treatment of risk factors for cardiovascular disease and protection against sudden death |
US20130040927A1 (en) * | 2011-02-16 | 2013-02-14 | Pivotal Therapeutics Inc. | Cholesterol absorption inhibitor and omega 3 fatty acids for the reduction of cholesterol and for the prevention or reduction of cardiovascular, cardiac and vascular events |
WO2013192109A1 (en) * | 2012-06-17 | 2013-12-27 | Matinas Biopharma, Inc. | Omega-3 pentaenoic acid compositions and methods of use |
WO2014084433A1 (ko) * | 2012-11-30 | 2014-06-05 | 경상대학교 산학협력단 | 퍼옥시좀 증식인자 활성화 수용체 델타 작용물질을 유효성분으로 함유하는 심근경색후 심근상처치유 촉진용 조성물 |
WO2014143272A1 (en) * | 2013-03-13 | 2014-09-18 | Matinas Biopharma Inc. | Omega-3 pentaenoic acid compositions and methods of use |
US9056088B2 (en) | 2009-04-29 | 2015-06-16 | Amarin Pharmaceuticals Ireland Limited | Pharmaceutical compositions comprising fatty acids |
US20150164850A1 (en) * | 2013-10-10 | 2015-06-18 | Amarin Pharmaceuticals Ireland Limited | Compositions and Methods for Lowering Triglycerides Without Raising LDL-C Levels in a Subject on Concomitant Statin Therapy |
US9060982B2 (en) | 2009-04-29 | 2015-06-23 | Amarin Pharmaceuticals Ireland Limited | Stable pharmaceutical composition and methods of using same |
US9096537B1 (en) | 2014-12-31 | 2015-08-04 | Mahesh Kandula | Compositions and methods for the treatment of mucositis |
US9102649B1 (en) | 2014-09-29 | 2015-08-11 | Mahesh Kandula | Compositions and methods for the treatment of multiple sclerosis |
US9108942B1 (en) | 2014-11-05 | 2015-08-18 | Mahesh Kandula | Compositions and methods for the treatment of moderate to severe pain |
US9150557B1 (en) | 2014-11-05 | 2015-10-06 | Cellix Bio Private Limited | Compositions and methods for the treatment of hyperglycemia |
US9175008B1 (en) | 2014-11-05 | 2015-11-03 | Cellix Bio Private Limited | Prodrugs of anti-platelet agents |
US9174931B2 (en) | 2013-06-04 | 2015-11-03 | Cellix Bio Private Limited | Compositions for the treatment of diabetes and pre-diabetes |
US9173877B1 (en) | 2014-11-05 | 2015-11-03 | Cellix Bio Private Limited | Compositions and methods for the treatment of local pain |
US9187427B2 (en) | 2012-08-03 | 2015-11-17 | Cellix Bio Private Limited | N-substituted nicotinamide compounds and compositions for the treatment migraine and neurologic diseases |
US9206111B1 (en) | 2014-12-17 | 2015-12-08 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurological diseases |
US9227974B2 (en) | 2012-05-23 | 2016-01-05 | Cellex Bio Private Limited | Compositions and methods for the treatment of respiratory disorders |
US9233161B2 (en) | 2012-05-10 | 2016-01-12 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurological conditions |
US9242939B2 (en) | 2012-05-10 | 2016-01-26 | Cellix Bio Private Limited | Compositions and methods for the treatment of respiratory disorders |
US9255154B2 (en) | 2012-05-08 | 2016-02-09 | Alderbio Holdings, Llc | Anti-PCSK9 antibodies and use thereof |
US9266823B2 (en) | 2012-05-08 | 2016-02-23 | Cellix Bio Private Limited | Compositions and methods for the treatment of parkinson's disease |
US9273061B2 (en) | 2012-05-10 | 2016-03-01 | Cellix Bio Private Limited | Compositions and methods for the treatment of chronic pain |
US9284287B1 (en) | 2014-11-05 | 2016-03-15 | Cellix Bio Private Limited | Compositions and methods for the suppression of carbonic anhydrase activity |
US9283201B2 (en) | 2013-03-14 | 2016-03-15 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for treating or preventing obesity in a subject in need thereof |
US9290486B1 (en) | 2014-11-05 | 2016-03-22 | Cellix Bio Private Limited | Compositions and methods for the treatment of epilepsy |
US9302016B2 (en) | 2012-03-30 | 2016-04-05 | Sancilio & Company, Inc. | Omega-3 fatty acid ester compositions |
US9303038B2 (en) | 2011-09-06 | 2016-04-05 | Cellix Bio Private Limited | Compositions and methods for the treatment of epilepsy and neurological diseases |
US9309233B2 (en) | 2012-05-08 | 2016-04-12 | Cellix Bio Private Limited | Compositions and methods for the treatment of blood clotting disorders |
US9315461B2 (en) | 2012-05-10 | 2016-04-19 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurologic diseases |
US9315478B2 (en) | 2012-05-10 | 2016-04-19 | Cellix Bio Private Limited | Compositions and methods for the treatment of metabolic syndrome |
US9321775B2 (en) | 2012-05-10 | 2016-04-26 | Cellix Bio Private Limited | Compositions and methods for the treatment of moderate to severe pain |
US9321716B1 (en) | 2014-11-05 | 2016-04-26 | Cellix Bio Private Limited | Compositions and methods for the treatment of metabolic syndrome |
US9333187B1 (en) | 2013-05-15 | 2016-05-10 | Cellix Bio Private Limited | Compositions and methods for the treatment of inflammatory bowel disease |
US9339484B2 (en) | 2012-05-10 | 2016-05-17 | Cellix Bio Private Limited | Compositions and methods for the treatment of restless leg syndrome and fibromyalgia |
US9346742B2 (en) | 2012-05-10 | 2016-05-24 | Cellix Bio Private Limited | Compositions and methods for the treatment of fibromyalgia pain |
US9394288B2 (en) | 2012-05-10 | 2016-07-19 | Cellix Bio Private Limited | Compositions and methods for the treatment of asthma and allergy |
US9399634B2 (en) | 2012-05-07 | 2016-07-26 | Cellix Bio Private Limited | Compositions and methods for the treatment of depression |
US9403857B2 (en) | 2012-05-10 | 2016-08-02 | Cellix Bio Private Limited | Compositions and methods for the treatment of metabolic syndrome |
US9403826B2 (en) | 2012-05-08 | 2016-08-02 | Cellix Bio Private Limited | Compositions and methods for the treatment of inflammatory disorders |
US9434704B2 (en) | 2012-05-08 | 2016-09-06 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurological degenerative disorders |
US9434729B2 (en) | 2012-05-23 | 2016-09-06 | Cellix Bio Private Limited | Compositions and methods for the treatment of periodontitis and rheumatoid arthritis |
US9452151B2 (en) | 2013-02-06 | 2016-09-27 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing apolipoprotein C-III |
US9480651B2 (en) | 2012-03-30 | 2016-11-01 | Sancilio & Company, Inc. | Omega-3 fatty acid ester compositions unitary pharmaceutical dosage forms |
US9492409B2 (en) | 2012-05-23 | 2016-11-15 | Cellix Bio Private Limited | Compositions and methods for the treatment of local pain |
US9498461B2 (en) | 2012-05-23 | 2016-11-22 | Cellix Bio Private Limited | Compositions and methods for the treatment of inflammatory bowel disease |
US9499526B2 (en) | 2012-05-10 | 2016-11-22 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurologic diseases |
US9499527B2 (en) | 2012-05-10 | 2016-11-22 | Cellix Bio Private Limited | Compositions and methods for the treatment of familial amyloid polyneuropathy |
US9522884B2 (en) | 2012-05-08 | 2016-12-20 | Cellix Bio Private Limited | Compositions and methods for the treatment of metabolic disorders |
US9573927B2 (en) | 2012-05-10 | 2017-02-21 | Cellix Bio Private Limited | Compositions and methods for the treatment of severe pain |
US9580383B2 (en) | 2012-05-23 | 2017-02-28 | Cellix Bio Private Limited | Compositions and methods for the treatment of multiple sclerosis |
US9603826B2 (en) | 2012-06-29 | 2017-03-28 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject on statin therapy |
US9624492B2 (en) | 2013-02-13 | 2017-04-18 | Amarin Pharmaceuticals Ireland Limited | Compositions comprising eicosapentaenoic acid and mipomersen and methods of use thereof |
US9624168B2 (en) | 2012-09-06 | 2017-04-18 | Cellix Bio Private Limited | Compositions and methods for the treatment inflammation and lipid disorders |
US9642915B2 (en) | 2012-05-07 | 2017-05-09 | Cellix Bio Private Limited | Compositions and methods for the treatment of neuromuscular disorders and neurodegenerative diseases |
US9662307B2 (en) | 2013-02-19 | 2017-05-30 | The Regents Of The University Of Colorado | Compositions comprising eicosapentaenoic acid and a hydroxyl compound and methods of use thereof |
US9670153B2 (en) | 2012-09-08 | 2017-06-06 | Cellix Bio Private Limited | Compositions and methods for the treatment of inflammation and lipid disorders |
US9725404B2 (en) | 2014-10-27 | 2017-08-08 | Cellix Bio Private Limited | Compositions and methods for the treatment of multiple sclerosis |
US9738631B2 (en) | 2012-05-07 | 2017-08-22 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurological disorders |
US9765020B2 (en) | 2012-05-23 | 2017-09-19 | Cellix Bio Private Limited | Dichlorophenyl-imino compounds and compositions, and methods for the treatment of mucositis |
US9771355B2 (en) | 2014-09-26 | 2017-09-26 | Cellix Bio Private Limited | Compositions and methods for the treatment of epilepsy and neurological disorders |
US9814733B2 (en) | 2012-12-31 | 2017-11-14 | A,arin Pharmaceuticals Ireland Limited | Compositions comprising EPA and obeticholic acid and methods of use thereof |
US9827219B2 (en) | 2012-01-06 | 2017-11-28 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering levels of high-sensitivity C-reactive protein (HS-CRP) in a subject |
US9909178B2 (en) | 2013-03-27 | 2018-03-06 | Hoffmann-La Roche Inc. | Dalcetrapib for therapeutic use |
US9932294B2 (en) | 2014-12-01 | 2018-04-03 | Cellix Bio Private Limited | Compositions and methods for the treatment of multiple sclerosis |
US10172818B2 (en) | 2014-06-16 | 2019-01-08 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing or preventing oxidation of small dense LDL or membrane polyunsaturated fatty acids |
WO2019008101A1 (en) | 2017-07-06 | 2019-01-10 | Evonik Technochemie Gmbh | ENTERICALLY COATED SOLID DOSAGE FORM COMPRISING AMINO ACIDS SALTS OF OMEGA-3 FATTY ACIDS |
US10208014B2 (en) | 2014-11-05 | 2019-02-19 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurological disorders |
WO2019034698A1 (en) | 2017-08-15 | 2019-02-21 | Evonik Technochemie Gmbh | TABLET WITH HIGH ACTIVE INGREDIENT CONTENT OF OMEGA-3 FATTY ACID AMINO ACID SALTS |
US10227301B2 (en) | 2015-01-06 | 2019-03-12 | Cellix Bio Private Limited | Compositions and methods for the treatment of inflammation and pain |
US10287528B2 (en) | 2012-03-30 | 2019-05-14 | Micelle Biopharma, Inc. | Omega-3 fatty acid ester compositions |
US10314803B2 (en) | 2008-09-02 | 2019-06-11 | Amarin Pharmaceuticals Ireland Limited | Pharmaceutical composition comprising eicosapentaenoic acid and nicotinic acid and methods of using same |
US10406130B2 (en) | 2016-03-15 | 2019-09-10 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing or preventing oxidation of small dense LDL or membrane polyunsaturated fatty acids |
US10434141B2 (en) | 2016-05-31 | 2019-10-08 | Abcentra, Llc | Methods for treating systemic lupus erythematosus with an anti-apolipoprotein B antibody |
US10493058B2 (en) | 2009-09-23 | 2019-12-03 | Amarin Pharmaceuticals Ireland Limited | Pharmaceutical composition comprising omega-3 fatty acid and hydroxy-derivative of a statin and methods of using same |
US10537544B2 (en) | 2011-11-07 | 2020-01-21 | Amarin Pharmaceuticals Ireland Limited | Methods of treating hypertriglyceridemia |
US10561631B2 (en) | 2014-06-11 | 2020-02-18 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing RLP-C |
US10584385B2 (en) | 2014-07-30 | 2020-03-10 | Hoffmann-La Roche Inc. | Genetic markers for predicting responsiveness to therapy with HDL-raising or HDL mimicking agent |
US10668042B2 (en) | 2018-09-24 | 2020-06-02 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of cardiovascular events in a subject |
CN111712240A (zh) * | 2017-12-06 | 2020-09-25 | 巴斯夫股份公司 | 用于治疗非酒精性脂肪性肝炎的脂肪酸衍生物 |
US10842768B2 (en) | 2009-06-15 | 2020-11-24 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides |
US10858422B2 (en) | 2016-05-31 | 2020-12-08 | Abcentra, Llc | Methods for treating systemic lupus erythematosus with an anti-apolipoprotein B antibody |
US10888539B2 (en) | 2013-09-04 | 2021-01-12 | Amarin Pharmaceuticals Ireland Limited | Methods of treating or preventing prostate cancer |
US10894027B2 (en) | 2012-03-30 | 2021-01-19 | Micelle Biopharma, Inc. | Sickle cell disease treatment utilizing omega-3 fatty acids |
WO2021023857A1 (en) | 2019-08-08 | 2021-02-11 | Evonik Operations Gmbh | Solubility enhancement of poorly soluble actives |
WO2021023849A1 (en) | 2019-08-08 | 2021-02-11 | Evonik Operations Gmbh | Down streaming process for the production of polyunsaturated fatty acid salts |
US10966968B2 (en) | 2013-06-06 | 2021-04-06 | Amarin Pharmaceuticals Ireland Limited | Co-administration of rosiglitazone and eicosapentaenoic acid or a derivative thereof |
US10966951B2 (en) | 2017-05-19 | 2021-04-06 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides in a subject having reduced kidney function |
US11058661B2 (en) | 2018-03-02 | 2021-07-13 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides in a subject on concomitant statin therapy and having hsCRP levels of at least about 2 mg/L |
US11141399B2 (en) | 2012-12-31 | 2021-10-12 | Amarin Pharmaceuticals Ireland Limited | Methods of treating or preventing nonalcoholic steatohepatitis and/or primary biliary cirrhosis |
US11179362B2 (en) | 2012-11-06 | 2021-11-23 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides without raising LDL-C levels in a subject on concomitant statin therapy |
US20220016025A1 (en) * | 2020-07-08 | 2022-01-20 | Vinayak Dinesh DENDUKURI | Formulations of nebivolol |
WO2022032077A3 (en) * | 2020-08-06 | 2022-03-10 | Redux Therapeutics, Llc | Compositions and methods for treating metabolic dysregulation |
US11291643B2 (en) | 2011-11-07 | 2022-04-05 | Amarin Pharmaceuticals Ireland Limited | Methods of treating hypertriglyceridemia |
US11547710B2 (en) | 2013-03-15 | 2023-01-10 | Amarin Pharmaceuticals Ireland Limited | Pharmaceutical composition comprising eicosapentaenoic acid and derivatives thereof and a statin |
US11712428B2 (en) | 2010-11-29 | 2023-08-01 | Amarin Pharmaceuticals Ireland Limited | Low eructation composition and methods for treating and/or preventing cardiovascular disease in a subject with fish allergy/hypersensitivity |
US11712429B2 (en) | 2010-11-29 | 2023-08-01 | Amarin Pharmaceuticals Ireland Limited | Low eructation composition and methods for treating and/or preventing cardiovascular disease in a subject with fish allergy/hypersensitivity |
WO2024102429A1 (en) * | 2022-11-10 | 2024-05-16 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing risks of cardiovascular events in subjects with low baseline epa:aa ratio |
US11986452B2 (en) | 2021-04-21 | 2024-05-21 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of heart failure |
Families Citing this family (47)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101444489B1 (ko) | 2007-02-01 | 2014-09-24 | 리스버로직스 코퍼레이션 | 심혈관 질환을 예방 및 치료하기 위한 화합물 |
JP5795304B2 (ja) | 2009-03-18 | 2015-10-14 | レスバーロジックス コーポレイション | 新規抗炎症剤 |
PT2421533T (pt) | 2009-04-22 | 2019-01-21 | Resverlogix Corp | Novos agentes anti-inflamatórios |
US8492108B2 (en) * | 2009-06-12 | 2013-07-23 | Bruce J. Auerbach | Methods of treating anemia and red blood cell dysfunction with lecithin cholesterol acyltransferase |
CN102770126A (zh) * | 2010-02-25 | 2012-11-07 | 百时美施贵宝公司 | 阿哌沙班制剂 |
WO2012063272A1 (en) | 2010-11-12 | 2012-05-18 | Gentium S.P.A. | Defibrotide for use in prophylaxis and/or treatment of graft versus host disease (gvhd). |
CN103237542A (zh) * | 2010-12-08 | 2013-08-07 | 霍夫曼-拉罗奇有限公司 | 达塞曲匹的脂质体制剂 |
US20120178813A1 (en) | 2011-01-12 | 2012-07-12 | Thetis Pharmaceuticals Llc | Lipid-lowering antidiabetic agent |
US9119826B2 (en) * | 2011-02-16 | 2015-09-01 | Pivotal Therapeutics, Inc. | Omega 3 fatty acid for use as a prescription medical food and omega 3 fatty acid diagniostic assay for the dietary management of cardiovascular patients with cardiovascular disease (CVD) who are deficient in blood EPA and DHA levels |
CA2851996C (en) * | 2011-11-01 | 2020-01-07 | Resverlogix Corp. | Pharmaceutical compositions for substituted quinazolinones |
PT2800563T (pt) | 2012-01-06 | 2018-11-07 | Chrysalis Pharma Ag | Composições enriquecidas com dpa de ácidos gordos omega-3 polinsaturados sob a forma de ácido livre |
KR20150028233A (ko) | 2012-05-07 | 2015-03-13 | 옴테라 파마슈티칼스, 인크. | 스타틴 및 오메가-3 지방산의 조성물 |
CN110079580B (zh) * | 2012-06-22 | 2022-12-06 | 真蒂奥姆责任有限公司 | 用于测定去纤维蛋白多核苷酸的生物活性的基于优球蛋白的方法 |
US8765811B2 (en) | 2012-07-10 | 2014-07-01 | Thetis Pharmaceuticals Llc | Tri-salt form of metformin |
US9382187B2 (en) | 2012-07-10 | 2016-07-05 | Thetis Pharmaceuticals Llc | Tri-salt form of metformin |
BR112015000368A2 (pt) * | 2012-07-10 | 2017-06-27 | Thetis Pharmaceuticals Llc | forma de tri-sais de metformina |
WO2014011895A2 (en) * | 2012-07-11 | 2014-01-16 | Thetis Pharmaceuticals Llc | High solubility acid salts, intravenous dosage forms, nutrition supplementation and methods of use thereof |
WO2014041445A2 (en) * | 2012-09-13 | 2014-03-20 | Mahesh Kandula | Compositions and methods for the treatment of hypertension and management of diabetic kidney disease |
CN103768023B (zh) * | 2012-10-23 | 2016-12-07 | 北京泰德制药股份有限公司 | 一种考来维仑的干混悬剂及其制备方法 |
US10123986B2 (en) | 2012-12-24 | 2018-11-13 | Qualitas Health, Ltd. | Eicosapentaenoic acid (EPA) formulations |
US9629820B2 (en) | 2012-12-24 | 2017-04-25 | Qualitas Health, Ltd. | Eicosapentaenoic acid (EPA) formulations |
SG11201504641SA (en) * | 2012-12-24 | 2015-07-30 | Qualitas Health Ltd | Eicosapentaenoic acid (epa) formulations |
WO2014134466A1 (en) * | 2013-03-01 | 2014-09-04 | Amarin Pharmaceuticals Ireland Limited. | Co-administration of atorvastatin and ethyl eicosapentaenoic acid or a derivative thereof |
ES2770667T3 (es) * | 2013-06-27 | 2020-07-02 | Roche Innovation Ct Copenhagen As | Oligómeros antisentido y conjugados que se dirigen a PCSK9 |
JPWO2015005393A1 (ja) * | 2013-07-09 | 2017-03-02 | 日本水産株式会社 | 大動脈瘤の予防または治療剤および容器詰飲食品 |
CN103690960A (zh) * | 2013-12-18 | 2014-04-02 | 北京科源创欣科技有限公司 | 甲磺酸洛美他派药物组合物及制备方法 |
US10272058B2 (en) * | 2014-03-20 | 2019-04-30 | Cymabay Therapeutics, Inc. | Treatment of intrahepatic cholestatic diseases |
CA2947741A1 (en) | 2014-05-05 | 2015-11-12 | Thetis Pharmaceuticals Llc | Compositions and methods relating to ionic salts of peptides |
US9242008B2 (en) | 2014-06-18 | 2016-01-26 | Thetis Pharmaceuticals Llc | Mineral amino-acid complexes of fatty acids |
DK3157936T3 (en) | 2014-06-18 | 2019-02-04 | Thetis Pharmaceuticals Llc | MINERAL AMINO ACID ACID COMPLEXES OF ACTIVE SUBSTANCES |
CN104069117A (zh) * | 2014-07-03 | 2014-10-01 | 滨州医学院 | 安普那韦在制备预防或治疗缺血性心脑血管疾病的药物中的应用 |
AU2015327928A1 (en) | 2014-10-03 | 2017-05-04 | Nanotics, Llc | Compositions and methods for inhibiting the biological activity of soluble biomolecules |
EP3026122A1 (en) | 2014-11-27 | 2016-06-01 | Gentium S.p.A. | Cellular-based method for determining the potency of defibrotide |
EP3268007B1 (en) | 2015-03-13 | 2022-11-09 | Resverlogix Corp. | Compositions and therapeutic methods for the treatment of complement-associated diseases |
US10183044B2 (en) | 2015-05-15 | 2019-01-22 | P Tech, Llc | Systems and methods for thrombosis prevention |
CN108135850A (zh) | 2015-07-29 | 2018-06-08 | 纳米提克斯有限责任公司 | 用于清除可溶性生物分子的模块化组合物及其相关方法 |
WO2017083397A1 (en) * | 2015-11-09 | 2017-05-18 | Cayo Max A | Cardiac glycosides for the treatment of hypercholesterolemia |
KR102437682B1 (ko) | 2016-06-03 | 2022-08-29 | 테티스 파마수티컬스 엘엘씨 | 특화된 사전 해소 매개체의 염에 관한 조성물 및 방법 |
EP3565604A4 (en) | 2017-01-04 | 2020-09-09 | Nanotics, LLC | ELIMINATING PARTICLE ASSEMBLY PROCESSES |
CN107029208A (zh) * | 2017-06-13 | 2017-08-11 | 江苏黄河药业股份有限公司 | 一种治疗心血管疾病的赖诺普利复方制剂及其制备方法 |
SG11202006601VA (en) | 2018-01-12 | 2020-08-28 | Metimedi Pharmaceuticals Co Ltd | Methods of treating chronic inflammatory diseases |
CN108904807A (zh) * | 2018-07-27 | 2018-11-30 | 舟山三合生物科技有限公司 | 二甲双胍复配组合物及其应用 |
US11452599B2 (en) | 2019-05-02 | 2022-09-27 | Twelve, Inc. | Fluid diversion devices for hydraulic delivery systems and associated methods |
US20220233542A1 (en) * | 2019-06-05 | 2022-07-28 | University Of Georgia Research Foundation | Compositions and methods for preventing or treating human immunodeficiency virus associated pulmonary arterial hypertension |
US11452690B1 (en) | 2021-01-27 | 2022-09-27 | ECI Pharmaceuticals, LLC | Oral liquid compositions comprising amlodipine besylate and methods of using the same |
KR102543789B1 (ko) * | 2021-03-08 | 2023-06-20 | 주식회사 온코크로스 | 토르세미드 및 크로몰린을 포함하는 대사질환 예방 또는 치료용 조성물 |
KR20240054775A (ko) | 2022-10-19 | 2024-04-26 | 김학수 | 니들 펀칭을 통한 부직포 패널의 제조시스템 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6620821B2 (en) * | 2000-06-15 | 2003-09-16 | Bristol-Myers Squibb Company | HMG-CoA reductase inhibitors and method |
US8410086B2 (en) * | 2009-06-15 | 2013-04-02 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides |
Family Cites Families (725)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US568822A (en) | 1896-10-06 | Lamp-wick and art of producing same | ||
US624012A (en) | 1899-05-02 | Stenciling or decorative device | ||
US482828A (en) | 1892-09-20 | Locomotive | ||
AU527784B2 (en) | 1978-05-26 | 1983-03-24 | Bang, Hans Olaf Dr. | Treatment of thromboembolic conditions withall-z)-5, 8, 11, 14, 17-eicosapentaenoic acid |
JPS57112593A (en) | 1980-12-26 | 1982-07-13 | Koken Boring Machine Co | Lathe drill |
US4377526A (en) | 1981-05-15 | 1983-03-22 | Nippon Suisan Kaisha, Ltd. | Method of purifying eicosapentaenoic acid and its esters |
CA1239587A (en) | 1983-10-24 | 1988-07-26 | David Rubin | Combined fatty acid composition for lowering blood cholestrol and triglyceride levels |
US4526902A (en) | 1983-10-24 | 1985-07-02 | Century Laboratories, Inc. | Combined fatty acid composition for treatment or prophylaxis of thrombo-embolic conditions |
US4933351A (en) | 1983-10-31 | 1990-06-12 | Merck Frosst Canada, Inc. | Benzofuran 2-carbox amides useful as inhibitors of leukoriene biosynthesis |
US4663347A (en) | 1983-10-31 | 1987-05-05 | Merck Frosst Canada, Inc. | Benzofuran 2-carboxylic acid esters useful as inhibitors of leukotriene biosynthesis |
US4822803A (en) | 1983-10-31 | 1989-04-18 | Merck Frosst Canada, Inc. | Benzofuran 2-carboxylic acid hydrazides useful as inhibitors of leukotriene biosynthesis |
US4745127A (en) | 1983-10-31 | 1988-05-17 | Merck Frosst Canada, Inc. | Benzyl esters of benzofuran-2-carboxylic acids useful as inhibitors of leukotriene biosynthesis |
US4673684A (en) | 1984-04-04 | 1987-06-16 | Terumo Corporation | Amide derivatives and 5-lipoxygenase inhibitors containing the same as an active ingredient |
JPS6135356A (ja) | 1984-07-27 | 1986-02-19 | Nippon Oil & Fats Co Ltd | 血液脂質脂肪酸の分析方法 |
US4728735A (en) | 1984-10-15 | 1988-03-01 | Merck & Co., Inc. | 10,11-dihydro-dibenzo-[b,f][1,4]-thiazepin derivatives |
GB8505285D0 (en) | 1985-03-01 | 1985-04-03 | Beecham Group Plc | Compounds |
US4624964A (en) | 1985-03-27 | 1986-11-25 | E. I. Du Pont De Nemours And Company | Aryl oxo-alkynoates as 5-lipoxygenase inhibitors |
ZA863425B (en) | 1985-05-08 | 1988-01-27 | Du Pont | 2-substituted-1-naphthols as 5-lipoxygenase inhibitors |
US4803279A (en) | 1985-05-23 | 1989-02-07 | Smithkline Beckman Corporation | 1.4-dihydro-4-pyridyl-substituted imidazo (2,1-b) thiazoles and the corresponding thiazines. |
US5008390A (en) | 1985-05-23 | 1991-04-16 | Smithkline Beckman Corporation | Compounds for preparing 6-phenyl-2,3-dihydroimidazo[2,1-b]-thiazoles and corresponding thiazines |
US4786755A (en) | 1985-06-03 | 1988-11-22 | Warner-Lambert Company | Diphenic acid monoamides |
US4602023A (en) | 1985-06-03 | 1986-07-22 | Warner-Lambert Company | Diphenic acid monoamides |
GB8515522D0 (en) | 1985-06-19 | 1985-07-24 | Beecham Group Plc | Compounds |
EP0347509A1 (en) | 1988-06-21 | 1989-12-27 | Century Laboratories Inc. | A process of extraction and purification of polyunsaturated fatty acids from natural sources |
EP0246245A1 (en) | 1985-09-20 | 1987-11-25 | The Upjohn Company | 1,4-naphthalenediol and 1,4-hydroquinone derivatives |
US4939169A (en) | 1985-09-20 | 1990-07-03 | The Upjohn Company | 1,4-naphthalenediol and 1,4-hydroquinone derivatives |
JPS6272657A (ja) | 1985-09-27 | 1987-04-03 | Terumo Corp | アミド誘導体およびこれを含有する5−リポキシゲナ−ゼ作用阻害剤 |
US4694018A (en) | 1985-11-29 | 1987-09-15 | G. D. Serale & Co. | Substituted 1,5-diphenyl-2-pyrrolepropionic acids and derivatives |
US4719218A (en) | 1985-12-12 | 1988-01-12 | Smithkline Beckman Corporation | Pyrrolo[1,2-a]imidazole and pyrrolo[1,2-a]pyridine derivatives and their use as 5-lipoxygenase pathway inhibitor |
US5134150A (en) | 1985-12-12 | 1992-07-28 | Smithkline Beecham Corporation | Inhibition of the 5-lipoxygenase pathway |
US4847270A (en) | 1985-12-12 | 1989-07-11 | Smithkline Beckman Corporation | Inhibition of the 5-lipoxygenase pathway utilizing certain 2,2'-alkyldiyl bis(thio)bis-imidazoles and derivatives |
US4728656A (en) | 1985-12-12 | 1988-03-01 | Smithkline Beckman Corporation | 2,2-alkyldiylbis(thio)bis(imidazoles) useful for inhibition of the 5-lipoxygenase pathway |
US4686231A (en) | 1985-12-12 | 1987-08-11 | Smithkline Beckman Corporation | Inhibition of 5-lipoxygenase products |
US4751310A (en) | 1985-12-12 | 1988-06-14 | Smithkline Beckman Corporation | Inhibition of the 5-lipoxygenase pathway |
US4755524A (en) | 1986-01-31 | 1988-07-05 | G. D. Searle & Co. | Novel phenolic thioethers as inhibitors of 5-lipoxygenase |
US4711903A (en) | 1986-01-31 | 1987-12-08 | G. D. Searle & Co. | Phenolic thioethers as inhibitors of 5-lipoxygenase |
IE59813B1 (en) | 1986-05-09 | 1994-04-06 | Warner Lambert Co | Styryl pyrazoles, isoxazoles and analogs thereof having activity as 5-lipoxy-genase inhibitors and pharmaceutical compositions containing them |
US4794114A (en) | 1986-08-19 | 1988-12-27 | Smithkline Beckman Corporation | Inhibition of interleukin-1 production by monocytes and/or macrophages |
US4672075A (en) | 1986-08-26 | 1987-06-09 | E. R. Squibb & Sons | 7-Oxabicyclo(2.2.1)heptane hydroxamic acid derivatives useful as antiinflammatory, antiasthma and antipsoriatic agents |
US4920098A (en) | 1986-09-17 | 1990-04-24 | Baxter International Inc. | Nutritional support or therapy for individuals at risk or under treatment for atherosclerotic vascular, cardiovascular, and/or thrombotic diseases |
US4695586A (en) | 1986-09-23 | 1987-09-22 | E. R. Squibb & Sons, Inc. | 7-oxabicyclo(2.2.1)heptane-based derivatives useful as antiinflammatory, antiasthma and antipsoratic agents |
US4695585A (en) | 1986-09-23 | 1987-09-22 | E. R. Squibb & Sons, Inc. | 7-oxabicyclo(2.2.1)heptane analogs useful as inhibitors of 5-lipoxygenase and cyclooxygenase |
DE3789435T2 (de) | 1986-12-26 | 1994-10-20 | Sagami Chem Res | Verfahren zur Herstellung von Eicosapentaensäure. |
US4861798A (en) | 1986-12-29 | 1989-08-29 | Bristol-Myers Company | Lipoxygenase inhibitory compounds |
US4731382A (en) | 1986-12-29 | 1988-03-15 | Bristol-Myers Company | Lipoxygenase inhibitory phenylalkanohydroxamic acids |
JPS63185390A (ja) | 1987-01-27 | 1988-07-30 | Suntory Ltd | 藻類によるエイコサペンタエン酸の製造方法 |
US5250565A (en) | 1987-02-10 | 1993-10-05 | Abbott Laboratories | Indole-,benzofuran-,and benzothiophene-containing lipoxygenase-inhibiting compounds |
US4877881A (en) | 1987-04-06 | 1989-10-31 | Warner-Lambert Company | Process of preparing pyrazoles, isoxazoles and analogs thereof having activity as 5-lipoxygenase inhibitors |
US4889941A (en) | 1987-04-23 | 1989-12-26 | Fisons Corporation | Synthetic flavonoids as inhibitors of leukotrienes and 5-lipoxygenase |
US5252333A (en) | 1987-04-27 | 1993-10-12 | Scotia Holdings Plc | Lithium salt-containing pharmaceutical compositions |
US5036105A (en) | 1987-05-07 | 1991-07-30 | G. D. Searle & Co. | 5-lipoxygenase inhibitors |
US4801611A (en) | 1987-05-07 | 1989-01-31 | G. D. Searle & Co. | 5-lipoxygenase inhibitors |
US5162365A (en) | 1987-05-07 | 1992-11-10 | G. D. Searle & Co. | 5-lipoxygenase inhibitors |
GB8711802D0 (en) | 1987-05-19 | 1987-06-24 | Fujisawa Pharmaceutical Co | Dithioacetal compounds |
US4835189A (en) | 1987-06-05 | 1989-05-30 | G. D. Searle & Co. | Phenolic thioalkylamides as inhibitors of 5-lipoxygenase |
US4835190A (en) | 1987-06-05 | 1989-05-30 | G. D. Searle & Co. | Phenolic thioethers as inhbitors of 5-lipoxygenase |
US5198468A (en) | 1987-06-24 | 1993-03-30 | Efamol Holdings Plc | Essential fatty acid composition |
US4970210A (en) | 1987-07-17 | 1990-11-13 | Abbott Laboratories | Triazinone lipoxygenase compounds |
US5086052A (en) | 1987-07-17 | 1992-02-04 | Abbott Laboratories | Substituted 1,4,5,6-tetrahydro-2H-pyridazin-3-one and -3-thione compounds having lipoxygenase inhibitory activity |
US4843095A (en) | 1987-08-07 | 1989-06-27 | Century Laboratories, Inc. | Free fatty acids for treatment or propyhlaxis of rheumatoid arthritis arthritis |
FR2621038B1 (fr) | 1987-09-28 | 1989-12-29 | Rhone Poulenc Sante | Derives d'alcadienes, leurs preparations, les medicaments les contenant et produits intermediaires |
WO1989003375A1 (en) | 1987-10-16 | 1989-04-20 | Terumo Kabushiki Kaisha | Isoprenoid derivatives and pharmaceutical preparation containing same |
US6166031A (en) | 1987-10-19 | 2000-12-26 | Pfizer Inc, | Substituted tetralins, chromans and related compounds in the treatment of asthma |
US5059609A (en) | 1987-10-19 | 1991-10-22 | Pfizer Inc. | Substituted tetralins, chromans and related compounds in the treatment of asthma, arthritis and related diseases |
CA1334975C (en) | 1987-11-13 | 1995-03-28 | James H. Holms | Furan and pyrrole containing lipoxygenase inhibiting compounds |
JPH01149764A (ja) | 1987-12-07 | 1989-06-12 | Green Cross Corp:The | ビス−s−アルキルベンゼン誘導体 |
CA1331757C (en) | 1988-02-29 | 1994-08-30 | Janssen Pharmaceutica Naamloze Vennootschap | 5-lipoxygenase inhibiting 4-(4-phenyl-1-piperazinyl)phenols |
US4943587A (en) | 1988-05-19 | 1990-07-24 | Warner-Lambert Company | Hydroxamate derivatives of selected nonsteroidal antiinflammatory acyl residues and their use for cyclooxygenase and 5-lipoxygenase inhibition |
US5112868A (en) | 1988-05-19 | 1992-05-12 | Warner-Lambert Company | Hydroxamate derivatives of selected nonsteroidal antiinflammatory acyl residues having cyclooxygenase and 5-lipoxygenase inhibition |
US5232939A (en) | 1988-07-26 | 1993-08-03 | Sankyo Company Limited | Use of imidazopyrazole derivatives as analgesics and anti-inflammatory agents |
US5665752A (en) | 1988-07-26 | 1997-09-09 | Sankyo Company, Limited | Use of imidazopyrazole derivatives as analgesics and anti-inflammatory agents |
US5354768A (en) | 1988-07-26 | 1994-10-11 | Sankyo Company, Limited | Use of imidazopyrazole derivatives as analgesics and anti-inflammatory agents |
US5260294A (en) | 1988-08-09 | 1993-11-09 | Hoffman-La Roche Inc. | Chromanes and their pharmaceutical compositions and methods |
GB8819110D0 (en) | 1988-08-11 | 1988-09-14 | Norsk Hydro As | Antihypertensive drug & method for production |
CA1338683C (en) | 1988-09-13 | 1996-10-29 | Efamol Holdings Plc | Fatty acid therapy and compositions |
GB2223943A (en) | 1988-10-21 | 1990-04-25 | Tillotts Pharma Ag | Oral disage forms of omega-3 polyunsaturated acids |
US5066658A (en) | 1988-11-10 | 1991-11-19 | Ortho Pharmaceutical Corporation | Substituted hydroxyureas |
US5155122A (en) | 1988-11-29 | 1992-10-13 | Warner-Lambert Company | 3,5-di-tertiary-butyl-4-hydroxyphenyl-1,3,4-thiadiazoles, and oxadiazoles and 3,5-di-tertiary-butyl-4-hydroxy-phenyl-1,2,4-thiadazoles, oxadiazoles and triazoles as antiinflammatory agents |
US5256680A (en) | 1988-11-29 | 1993-10-26 | Warner-Lambert Company | 3,5-di-tertiary-butyl-4-hydroxyphenyl-1,3,4-thiadiazoles, and oxadiazoles and 3,5-di-tertiary-butyl-4-hydroxy-phenyl-1,2,4-thiadazoles, oxadiazoles and triazoles as antiinflammatory agents |
US5068251A (en) | 1988-12-16 | 1991-11-26 | Abbott Laboratories | Lipoxygenase inhibiting compounds |
US4935243A (en) | 1988-12-19 | 1990-06-19 | Pharmacaps, Inc. | Chewable, edible soft gelatin capsule |
IL92620A0 (en) | 1988-12-23 | 1990-08-31 | Ici Pharma | Cycloalkane derivatives |
US5234950A (en) | 1988-12-23 | 1993-08-10 | Imperial Chemical Industries Plc | Tetrahydrofuran derivatives |
US5145860A (en) | 1989-01-05 | 1992-09-08 | Fujisawa Pharmaceutical Co., Ltd. | Thiazole compounds and pharmaceutical composition comprising the same |
US5229386A (en) | 1989-01-05 | 1993-07-20 | Fujisawa Pharmaceutical Co., Ltd. | Thiazole compounds, processes for the preparation thereof and pharmaceutical composition comprising the same |
US5217971A (en) | 1989-01-05 | 1993-06-08 | Fujisawa Pharmaceutical Co., Ltd. | Thiazole compounds and pharmaceutical composition comprising the same |
JP2839276B2 (ja) | 1989-01-23 | 1998-12-16 | 日本分光工業株式会社 | 超臨界流体抽出・分離方法及び装置 |
US5217977A (en) | 1989-02-28 | 1993-06-08 | Imperial Chemical Industries Plc | Heterocyclic cycloalkanes |
US5457130A (en) | 1989-03-20 | 1995-10-10 | Cancer Research Campaign Technology Limited | Eicosapentaenoic acid used to treat cachexia |
GB8906369D0 (en) | 1989-03-20 | 1989-05-04 | Tisdale Michael J | Eicosapentaenoic acid |
US5298512A (en) | 1989-04-07 | 1994-03-29 | Pfizer Inc. | Substituted chromans and their use in the treatment of asthma, arthritis and related diseases |
WO1990012006A1 (en) | 1989-04-07 | 1990-10-18 | Pfizer Inc. | Substituted 1-[3-(heteroarylmethoxy)phenyl]alkanols and related compounds in the treatment of asthma, arthritis and related diseases |
US5300655A (en) | 1989-04-18 | 1994-04-05 | Pfizer Inc. | 2-carboxy-thiophene derivatives |
US5047554A (en) | 1989-04-18 | 1991-09-10 | Pfizer Inc. | 3-substituted-2-oxindole derivatives |
US5006549A (en) | 1989-05-24 | 1991-04-09 | Merck & Co., Inc. | Novel 7-aroyl-4-hydroxy-3-methyl-benzofurans as dual inhibitors of cyclooxygenase and 5-lipoxygenase |
US5066668A (en) | 1989-06-09 | 1991-11-19 | Warner-Lambert Co. | Triazole derivatives of fenamates as antiinflammatory agents |
US4962119A (en) | 1989-06-09 | 1990-10-09 | Warner-Lambert Company | Triazole derivatives of fenamates as antiinflammatory agents |
US5384318A (en) | 1989-06-22 | 1995-01-24 | Pfizer Inc. | Substituted sulfonamides and related compounds in the treatment of asthma, arthritis and related diseases |
ES2057415T3 (es) | 1989-07-26 | 1994-10-16 | Ici Plc | Derivados biciclicos. |
US4975457A (en) | 1989-09-25 | 1990-12-04 | Merck & Co., Inc. | Trans 2,3-disubstituted-2,3-dihydro-5-hydroxy-benzofurans as inhibitors of leukotriene biosynthesis |
US4978679A (en) | 1989-09-25 | 1990-12-18 | Merck & Co., Inc. | 6- and/or 7-substituted-1,2,3,4,4A,9B-hexahydro-8-hydroxydibenzofuran-3-ols as inhibitors of leukotriene biosynthesis |
GB9018134D0 (en) | 1989-09-29 | 1990-10-03 | Ici Plc | Heterocyclic derivatives |
JPH03148217A (ja) | 1989-11-02 | 1991-06-25 | Terumo Corp | フエノキシプロピルアミン誘導体またはその塩ならびにこれらを含有する抗潰瘍剤 |
US5504108A (en) | 1990-01-12 | 1996-04-02 | The Ohio State University Research Foundation | Optically pure 4-aryl-2-hydroxytetronic acids |
US5093356A (en) | 1990-01-16 | 1992-03-03 | Merck Frosst Canada, Inc. | Indenyl hydroxamic acids and hydroxy ureas as inhibitors of 5-lipoxygenase |
US5036067A (en) | 1990-03-14 | 1991-07-30 | Merck & Co., Inc. | Dibenzoheterocyclic hydroxamic acids and hydroxy ureas as inhibitors of 5-lipoxygenase |
US5143928A (en) | 1990-03-27 | 1992-09-01 | Warner-Lambert Company | 3,5-di-tertiarybutyl-4-hydroxyphenylmethylene derivatives of 2-substituted thiazolidinones, oxazolidinones, and imidazolidinones as antiinflammatory agents |
US5234937A (en) | 1990-03-27 | 1993-08-10 | Warner-Lambert Company | 3,5-di-tertiary-butyl-4-hydroxphenyl oxazolyl methanones and related compounds as antiinflammatory agents |
US5234939A (en) | 1990-03-27 | 1993-08-10 | Warner-Lambert Company | 3,5-di-tertiary-butyl-4-hydroxyphenyl imidazolyl methanones and related compounds as antiinflammatory agents |
US5086064A (en) | 1990-03-27 | 1992-02-04 | Warner-Lambert Company | 3,5-di-tertiary-butyl-4-hydroxyphenyl thiazolyl, oxazolyl, and imidazolyl methanones and related compounds as antiinflammatory agents |
US5102897A (en) | 1990-03-27 | 1992-04-07 | Warner-Lambert Company | 3,5-ditertiarybutyl-4-hydroxyphenyl, 1,3,4-thiadiazoles and oxadiazoles linked by carbon, oxygen, and sulfur residues |
DK95490D0 (da) | 1990-04-18 | 1990-04-18 | Novo Nordisk As | Fremgangsmaade til fremstilling af triglycerid og triglyceridsammensaetning |
AU649673B2 (en) | 1990-04-30 | 1994-06-02 | Isis Pharmaceuticals, Inc. | Oligonucleotide modulation of arachidonic acid metabolism |
CA2043615C (en) | 1990-06-04 | 2001-08-14 | Kazuhiko Hata | Method of producing eicosapentaenoic acid or the ester derivative thereof |
GB9012651D0 (en) | 1990-06-06 | 1990-07-25 | Efamol Holdings | Essential fatty acid treatment |
US5254581A (en) | 1990-06-21 | 1993-10-19 | Imperial Chemical Industries Plc | Pyran derivatives and their use as inhibitors of 5-lipoxygenase |
AU637500B2 (en) | 1990-06-21 | 1993-05-27 | Zeneca Limited | Bicyclic heterocyclic compounds |
IE911853A1 (en) | 1990-06-21 | 1992-01-01 | Ici Plc | Heterocyclene derivatives |
US5064851A (en) | 1990-07-24 | 1991-11-12 | Pfizer Inc. | 3-(1-substituted-pyrazoyl)-2-oxindole derivatives, compositions and use |
EP0547090B1 (en) | 1990-09-07 | 1995-03-01 | G.D. Searle & Co. | Phenolic thioetheramides as 5-lipoxygenase inhibitors |
JPH04134077A (ja) | 1990-09-21 | 1992-05-07 | Taiho Yakuhin Kogyo Kk | イソオキサゾール化合物 |
US5811432A (en) | 1990-11-09 | 1998-09-22 | Pfizer Inc | Azaoxindole derivatives |
JP3103588B2 (ja) | 1990-11-16 | 2000-10-30 | 持田製薬株式会社 | リポプロテイン(a)低下剤 |
US5248682A (en) | 1991-01-31 | 1993-09-28 | Warner-Lambert Company | 2-substituted-4,6-di-tertiary-butyl-5-hydroxy-1,3-pyrimidines useful as antiinflammatory agents |
US5177079A (en) | 1991-01-31 | 1993-01-05 | Warner-Lambert Company | 2-substituted-4,6-di-tertiarybutyl-5-hydroxy-1,3-pyrimidines useful as antiinflammatory agents |
EP0505122A1 (en) | 1991-03-21 | 1992-09-23 | Zeneca Limited | Alpha, alpha-dialkylbenzyl derivatives |
US5130485A (en) | 1991-04-23 | 1992-07-14 | Eli Lilly And Company | N-hydroxy-N-(3-(2-substituted phenyl)prop-2-enyl)ureas and thioureas useful as 5-lipoxygenase inhibiting agents |
US5283361A (en) | 1991-04-23 | 1994-02-01 | Eli Lilly And Company | N-hydroxy-N-[3-[2-(halophenylthio)phenyl]prop-2-enyl]ureas as lipoxygenase inhibitors |
US5147893A (en) | 1991-05-09 | 1992-09-15 | G. D. Searle & Co. | Cyclic phenolic thioethers |
US5114958A (en) | 1991-05-09 | 1992-05-19 | Warner-Lambert Company | 1,2,4-oxadiazole and 1,2,4-thiadiazole derivatives of fenamates as antiinflammatory agents |
US5442111A (en) | 1991-05-24 | 1995-08-15 | Warner-Lambert Company | 3,5-di-tetriary-4-butyl-4-hydroxyphenyloxy- or tioalkylene N-hydroxyamides, N-hydroxythioamides, N-hydroxyureas, and N-hydroxythioureas as 5-lipoxygenase inhibitors |
SE9101642D0 (sv) | 1991-05-30 | 1991-05-30 | Kabi Pharmacia Ab | Phospholipids |
US5215630A (en) | 1991-06-04 | 1993-06-01 | Nippon Suisan Kaisha, Ltd. | Method of purifying eicosapentaenoic acid or the ester derivative thereof by fractional distillation |
DE4123613C1 (ru) | 1991-07-17 | 1993-02-04 | Gruenenthal Gmbh, 5100 Aachen, De | |
DE4124345A1 (de) | 1991-07-23 | 1993-01-28 | Gruenenthal Gmbh | Substituierte 3,4-dihydronaphthaline, diese verbindungen enthaltende arzneimittel und verfahren zur herstellung dieser verbindungen und arzneimittel |
AU2384292A (en) | 1991-07-30 | 1993-03-02 | North Carolina State University | Method and apparatus for measuring blood lipoprotein levels by nmr spectroscopy |
US5250547A (en) | 1991-08-29 | 1993-10-05 | Syntex (U.S.A.) Inc. | Benzopyran derivatives |
US5270319A (en) | 1991-09-09 | 1993-12-14 | Warner-Lambert Company | 5-hydroxy-2-pyrimidinylmethylene derivatives useful as antiinflammatory agents |
CA2076257A1 (en) | 1991-09-13 | 1993-03-14 | Jan Heeres | 4-¬4-¬4-(4-hydroxyphenyl)-1- piperazinyl|phenyl|-5-methyl-3h -1,2,4-triazol-3-one derivatives |
DE4133694C2 (de) | 1991-10-11 | 1993-10-07 | Fresenius Ag | Verwendung einer Emulsion mit mehrfach ungesättigten Fettsären zur i.v.-Verabreichung zur Behandlung von Hauterkrankungen |
JP3400466B2 (ja) | 1991-10-28 | 2003-04-28 | 日本水産株式会社 | 高純度エイコサペンタエン酸またはそのエステルの製造方法 |
US5476944A (en) | 1991-11-18 | 1995-12-19 | G. D. Searle & Co. | Derivatives of cyclic phenolic thioethers |
AU3128693A (en) | 1991-11-18 | 1993-06-15 | G.D. Searle & Co. | 2-(4-substituted)phenylmethylene derivatives and methods of use |
US5212189A (en) | 1991-12-17 | 1993-05-18 | Warner-Lambert Company | Thiadiazole or oxadiazole analogs of fenamic acids containing substituted hydroxamate side chains as antiinflammatory agents |
US5288896A (en) | 1992-01-15 | 1994-02-22 | Warner-Lambert Company | 3,5-di-t-butyl-4-hydroxylphenylmethylhydroxylamines and their derivatives, pharmaceutical compositions, and methods of use therefor |
DE4204686A1 (de) | 1992-02-17 | 1993-08-19 | Gruenenthal Gmbh | Imidazolylphenolderivate, diese enthaltende arzneimittel sowie ein verfahren zur herstellung dieser verbindungen und arzneimitteln |
US5220025A (en) | 1992-02-24 | 1993-06-15 | Warner-Lambert Company | 2-substituted amino-4, 6-di-tertiary-butyl-5-hydroxy-1, 3-pyrimidines as antiinflammatory agents |
US5196431A (en) | 1992-02-24 | 1993-03-23 | Warner-Lambert Company | 2-substituted amino-4, 6-di-tertiary-buthyl-5-hydroxy-1, 3-pyrimidines as antiinflammatory agents |
US5530141A (en) | 1992-03-04 | 1996-06-25 | Center For Innovative Technology | 2,4-diaryl-1,3-dithiolanes; 2,4-diaryl-1,3-dioxolanes; 2,4-diaryl-1,3-oxathiolanes; and 2,5-diaryl-1,3-oxathiolanes for the treatment of disorders mediated by platelet activating factor or products of 5-lipoxygenase |
US5639782A (en) | 1992-03-04 | 1997-06-17 | Center For Innovative Technology | Neolignan derivatives as platelet activating factor receptor antagonists and 5-lipoxygenase inhibitors |
US5187175A (en) | 1992-03-06 | 1993-02-16 | Warner-Lambert Company | 2-carbonyl substituted-5-hydroxy-1, 3-pyrimidines as antiinflammatory agents |
US5595872A (en) | 1992-03-06 | 1997-01-21 | Bristol-Myers Squibb Company | Nucleic acids encoding microsomal trigyceride transfer protein |
US5215986A (en) | 1992-06-01 | 1993-06-01 | Warner-Lambert Company | 5-hydroxy-2-pyrimidinylmethylene oxaza heterocycles |
US5208364A (en) | 1992-06-25 | 1993-05-04 | Bristol-Myers Squibb Co. | Antibiotic 5-lipoxygenase inhibitors |
US5314898A (en) | 1992-06-29 | 1994-05-24 | Merck & Co., Inc. | Aryl thiopyrano[4,3,2-cd]indoles as inhibitors of leukotriene biosynthesis |
ES2152952T3 (es) | 1992-07-13 | 2001-02-16 | Millennium Pharm Inc | 2,5-diaril tetrahidro-tiofenos, -furanos y analogos para el tratamiento de problemas inflamatorios e inmunes. |
US5358938A (en) | 1992-07-13 | 1994-10-25 | Cytomed, Inc. | Compounds and methods for the treatment of disorders mediated by platelet activating factor or products of 5-lipoxygenase |
US5463083A (en) | 1992-07-13 | 1995-10-31 | Cytomed, Inc. | Compounds and methods for the treatment of cardiovascular, inflammatory and immune disorders |
US5648486A (en) | 1992-07-13 | 1997-07-15 | Cytomed, Inc. | Compounds and methods for the treatment of inflammatory and immune disorders |
US5434151A (en) | 1992-08-24 | 1995-07-18 | Cytomed, Inc. | Compounds and methods for the treatment of disorders mediated by platelet activating factor or products of 5-lipoxygenase |
US5541218A (en) | 1992-07-23 | 1996-07-30 | Pfizer Inc. | Indolinyl N-hydroxyurea and N-hydroxamic acid derivatives as lipoxygenase inhibitors |
JPH0649479A (ja) | 1992-07-28 | 1994-02-22 | Maruha Corp | ω−3不飽和脂肪酸系化合物の安定化法 |
US5240929A (en) | 1992-08-03 | 1993-08-31 | Warner-Lambert Company | 2-heterocyclic-5-hydroxy-1,3-pyrimidines useful as antiinflammatory agents |
US5888541A (en) | 1992-08-21 | 1999-03-30 | Scotia Holdings Plc | Fatty acid treatment |
GB9217780D0 (en) | 1992-08-21 | 1992-10-07 | Efamol Holdings | Fatty acid treatment |
JPH0692847A (ja) | 1992-09-11 | 1994-04-05 | Mochida Pharmaceut Co Ltd | 骨粗鬆症治療剤 |
WO1994010125A1 (en) | 1992-10-27 | 1994-05-11 | Sandoz Ltd. | Glycerin derivatives and uses thereof |
US5288751A (en) | 1992-11-06 | 1994-02-22 | Abbott Laboratories | [(Substituted) phenyalkyl]furylalkynyl-and [substituted) phenyalkyl] thienylalkynyl-N-hydroxyurea inhibitors or leukotriene biosynthesis |
US5314900A (en) | 1992-11-19 | 1994-05-24 | Merck Frosst Canada, Inc. | Aryl thiopyrano[2,3,4-C,D]indoles as inhibitors of leukotriene biosynthesis |
US5292900A (en) | 1992-12-18 | 1994-03-08 | Abbott Laboratories | O-substituted N-hydroxyurea derivatives |
US5326907A (en) | 1992-12-18 | 1994-07-05 | G. D. Searle & Co. | 2-aminoethanesulfonic acid derivatives of 3,5-disubstituted-4-hydroxyphenolic thioethers |
GB9300125D0 (en) | 1993-01-06 | 1993-03-03 | Scotia Holdings Plc | Compositions containing esters of unsaturated fatty acids |
ES2062943B1 (es) | 1993-03-23 | 1995-11-16 | Uriach & Cia Sa J | Nuevos derivados de la (2-metil-3-piridil) cianometilpiperazinas. |
IL109311A0 (en) | 1993-04-16 | 1994-07-31 | Lilly Co Eli | 1H-indole-3-acetamide sPla2 inhibitors |
AP9400632A0 (en) | 1993-04-29 | 1995-10-07 | Zeneca Ltd | Ether derivatives. |
CA2161777A1 (en) | 1993-05-10 | 1994-11-24 | Nancy M. Gray | Methods and compositions using optically pure (+)-zileuton |
US6239170B1 (en) | 1993-05-28 | 2001-05-29 | Gurpreet S. Ahluwalia | Inhibition of hair growth |
WO1994028891A1 (en) | 1993-06-04 | 1994-12-22 | Martek Biosciences Corporation | Method of treating coronary vascular disease using docosahexaenoic acid |
JPH0738598A (ja) | 1993-06-29 | 1995-02-07 | Toshiba Corp | ネットワークアダプタ群管理装置 |
US5739135A (en) | 1993-09-03 | 1998-04-14 | Bristol-Myers Squibb Company | Inhibitors of microsomal triglyceride transfer protein and method |
GB9318611D0 (en) | 1993-09-08 | 1993-10-27 | Sandoz Nutrition Ltd | Improvements in or relating to organic compounds |
US5459154A (en) | 1993-11-08 | 1995-10-17 | American Home Products Corporation | N-hydroxyureas as 5-lipoxygenase inhibitors and inhibitors of oxidative modification of low density lipoprotein |
ES2087019B1 (es) | 1994-02-08 | 1997-03-16 | Bobel246 S L | Uso de derivados de fenoles 2,4-disubstituidos como inhibidores de la 5-lipoxigenasa. |
JP3325995B2 (ja) | 1994-02-28 | 2002-09-17 | ミサワホーム株式会社 | パネル接合構造 |
GB9403857D0 (en) | 1994-03-01 | 1994-04-20 | Scotia Holdings Plc | Fatty acid derivatives |
GB9404483D0 (en) | 1994-03-08 | 1994-04-20 | Norsk Hydro As | Refining marine oil compositions |
JPH09505081A (ja) | 1994-03-09 | 1997-05-20 | ファイザー・インコーポレーテッド | 5−リポキシゲナーゼ阻害物質としてのイソキサゾリン化合物 |
US6252084B1 (en) | 1994-03-15 | 2001-06-26 | Eli Lilly And Company | 1H-indole-3-acetamide sPLA2 inhibitors |
DE69503890T2 (de) | 1994-03-28 | 1998-12-10 | Pfizer | Benzisothiazol-derivate als inhibitoren der 5-lipoxygenase biosynthese |
MX9501608A (es) | 1994-04-01 | 1997-02-28 | Lilly Co Eli | 1h-indol-3-glioxilamidas inhibidoras de spla2. |
US5385929A (en) | 1994-05-04 | 1995-01-31 | Warner-Lambert Company | [(Hydroxyphenylamino) carbonyl] pyrroles |
US5534524A (en) | 1994-05-09 | 1996-07-09 | Board Of Regents, The University Of Texas System | Suppression of bone resorption by quinolines |
US5760081A (en) | 1994-05-10 | 1998-06-02 | The General Hospital Corporation | Omega 3 fatty acids in the prevention of ventricular fibrillation |
JP3179286B2 (ja) | 1994-05-19 | 2001-06-25 | ファイザー製薬株式会社 | N−ヒドロキシ尿素系抗炎症剤 |
JP3368100B2 (ja) | 1994-06-02 | 2003-01-20 | キヤノン株式会社 | 静電荷像現像用トナー |
US5703093A (en) | 1995-05-31 | 1997-12-30 | Cytomed, Inc. | Compounds and methods for the treatment of cardiovascular, inflammatory and immune disorders |
US5792776A (en) | 1994-06-27 | 1998-08-11 | Cytomed, Inc., | Compounds and methods for the treatment of cardiovascular, inflammatory and immune disorders |
US5750565A (en) | 1995-05-25 | 1998-05-12 | Cytomed, Inc. | Compounds and methods for the treatment of cardiovascular, inflammatory and immune disorders |
AU711482B2 (en) | 1994-06-28 | 1999-10-14 | Scotia Holdings Plc | Compositions for treatment of diabetic complications |
US6214876B1 (en) | 1994-07-21 | 2001-04-10 | Eli Lilly And Company | Indene-1-acetamide sPLA2 inhibitors |
US5641800A (en) | 1994-07-21 | 1997-06-24 | Eli Lilly And Company | 1H-indole-1-functional sPLA2 inhibitors |
JPH0850637A (ja) | 1994-08-04 | 1996-02-20 | Toshiba Corp | 帳票類取扱装置 |
IT1274734B (it) | 1994-08-25 | 1997-07-24 | Prospa Bv | Composizioni farmaceutiche contenenti acidi grassi poliinsaturi, loro esteri o sali, unitamente a vitamine o provitamine antiossidanti |
US5674488A (en) | 1994-10-07 | 1997-10-07 | Reich; John J. | Method for prevention and treatment of hyperchlolesterolemia by in vivo hydrogenation of cholesterol |
US5635514A (en) | 1994-10-25 | 1997-06-03 | G. D. Searle & Company | Heteroaralkyl and heteroarylthioalkyl thiophenolic compounds as 5-lipoxgenase inhibitors |
JPH08193074A (ja) | 1994-11-18 | 1996-07-30 | Nippon Bayeragrochem Kk | 除草性1−シクロプロピルテトラゾリノン類 |
JPH08165267A (ja) | 1994-12-14 | 1996-06-25 | Yakult Honsha Co Ltd | ジアリルヘプタノイド誘導体およびこれを含有する抗炎症剤 |
JP2780154B2 (ja) | 1995-02-17 | 1998-07-30 | 株式会社ヤクルト本社 | ヨーグルト |
US5514703A (en) | 1995-03-13 | 1996-05-07 | Eli Lilly And Company | Benzothiophene compounds useful for inhibiting lipoxygenase |
JPH0840981A (ja) | 1995-03-24 | 1996-02-13 | Nissui Pharm Co Ltd | エイコサペンタエノイルグリセライド |
US5516789A (en) | 1995-04-12 | 1996-05-14 | Abbott Laboratories | Lipoxygenase and cyclooxygenase inhibiting compounds |
MY118354A (en) | 1995-05-01 | 2004-10-30 | Scarista Ltd | 1,3-propane diol derivatives as bioactive compounds |
GB9509764D0 (en) | 1995-05-15 | 1995-07-05 | Tillotts Pharma Ag | Treatment of inflammatory bowel disease using oral dosage forms of omega-3 polyunsaturated acids |
AU5886296A (en) | 1995-06-02 | 1996-12-18 | G.D. Searle & Co. | Heterocyclo substituted hydroxamic acid derivatives as cyclo oxygenase-2 and 5-lipoxygenase inhibitors |
WO1996041626A1 (en) | 1995-06-12 | 1996-12-27 | G.D. Searle & Co. | Compositions comprising a cyclooxygenase-2 inhibitor and a 5-lipoxygenase inhibitor |
JPH0959206A (ja) | 1995-08-25 | 1997-03-04 | Nippon Oil & Fats Co Ltd | エイコサペンタエン酸およびエイコサペンタエン酸エステルの製造方法 |
GB9519661D0 (en) | 1995-09-27 | 1995-11-29 | Scotia Holdings Plc | Fatty acid treatment |
JP3552810B2 (ja) | 1995-09-27 | 2004-08-11 | 松下電器産業株式会社 | 部品供給部の部品一括交換方法と装置 |
ATE353957T1 (de) | 1995-11-09 | 2007-03-15 | Us Gov Health & Human Serv | Verwendung von lezithin-cholesterin- azetyltransferase für die behandlung von atherosklerose |
US5763496A (en) | 1995-11-27 | 1998-06-09 | The Research Foundation Of State University Of New York | Prevention of atherosclerosis using NADPH oxidase inhibitors |
US5762413A (en) | 1996-01-29 | 1998-06-09 | Alternate Realities Corporation | Tiltable hemispherical optical projection systems and methods having constant angular separation of projected pixels |
US6231189B1 (en) | 1996-01-29 | 2001-05-15 | Elumens Corporation | Dual polarization optical projection systems and methods |
ES2169351T3 (es) | 1996-02-13 | 2002-07-01 | Searle & Co | Combinaciones que tienen efectos inmunosupresores, que contienen inhibidores de ciclooxigenasa-2 y 5-lipoxigenasa. |
AU2738497A (en) | 1996-04-24 | 1997-11-12 | Brigham And Women's Hospital | Omega-3 fatty acids and omega-3 phosphatidylcholine in the treatment of bipolar disorder |
US6077828A (en) | 1996-04-25 | 2000-06-20 | Abbott Laboratories | Method for the prevention and treatment of cachexia and anorexia |
US6090547A (en) | 1997-04-25 | 2000-07-18 | Brigham & Women's Hospital | Identification of asthma patients who are candidates for effective treatment with 5-lipoxygenase inhibitors |
WO1997042347A2 (en) | 1996-05-06 | 1997-11-13 | Brigham And Women's Hospital | 5-lipoxygenase gene polymorphisms and their use in classifying patients |
US5885983A (en) | 1996-05-10 | 1999-03-23 | Bristol-Myers Squibb Company | Inhibitors of microsomal triglyceride transfer protein and method |
US5827875A (en) | 1996-05-10 | 1998-10-27 | Bristol-Myers Squibb Company | Inhibitors of microsomal triglyceride transfer protein and method |
US6248398B1 (en) | 1996-05-22 | 2001-06-19 | Applied Materials, Inc. | Coater having a controllable pressurized process chamber for semiconductor processing |
US6776986B1 (en) | 1996-06-06 | 2004-08-17 | Novartis Ag | Inhibition of HIV-1 replication by antisense RNA expression |
TW425285B (en) | 1996-06-10 | 2001-03-11 | Viva America Marketing Inc | Fish oil and garlic nutritive supplement |
US6063818A (en) | 1996-06-13 | 2000-05-16 | Cell Pathways Inc. | Substituted benzylidene indenyl formamides, acetamides and propionamides |
US5965619A (en) | 1996-06-13 | 1999-10-12 | Cell Pathways Inc. | Method for treating patients having precancerous lesions with substituted indene derivatives |
US6121321A (en) | 1996-06-13 | 2000-09-19 | Cell Pathways, Inc. | Substituted methoxy benzylidene indenyl acetic and propionic acids for treating patients with precancerous lesions |
US5998477A (en) | 1996-06-13 | 1999-12-07 | Cell Pathways Inc. | Substituted methoxy benzylidene indenyl-acetic and propionic acids for treating patients with precancerous lesions |
US5861399A (en) | 1996-07-17 | 1999-01-19 | Heart Care Partners | Methods and compositions for the rapid and enduring relief of inadequate myocardial function |
US6005000A (en) | 1996-08-22 | 1999-12-21 | Oxis International, Inc. | 5,5-Disubstituted-3, 4-dihydroxy-2(5H)-furanones and methods of use therefor |
DE19636150A1 (de) | 1996-09-06 | 1998-03-12 | Asta Medica Ag | N-substituierte Indol-3-glyoxylamide mit antiasthmatischer, antiallergischer und immunsuppressiver/immunmodulierender Wirkung |
US20020055539A1 (en) | 1996-10-02 | 2002-05-09 | Bockow Barry I. | Compositions and methods for treating cardiovascular conditions |
AU731692C (en) | 1996-10-11 | 2001-10-11 | Scarista Limited | Pharmaceutical preparation comprising eicosapentaenoic acid and/or stearidonic acid |
US6426335B1 (en) | 1997-10-17 | 2002-07-30 | Gilead Sciences, Inc. | Vascular endothelial growth factor (VEGF) nucleic acid ligand complexes |
US6713645B1 (en) | 1996-10-30 | 2004-03-30 | Eli Lilly And Company | Substituted tricyclics |
US6177440B1 (en) | 1996-10-30 | 2001-01-23 | Eli Lilly And Company | Substituted tricyclics |
US6569539B2 (en) | 1996-10-30 | 2003-05-27 | Tetra Level Holdings & Finance S.A. | Gas barrier packaging laminate method for production thereof and packaging containers |
JP4176166B2 (ja) * | 1996-11-15 | 2008-11-05 | 持田製薬株式会社 | 横紋筋融解症治療剤 |
ES2179156T3 (es) | 1996-11-20 | 2003-01-16 | Nutricia Nv | Composicion nutricional que incluye grasas para el tratamiento del sindrome metabolico. |
US5909734A (en) | 1996-12-03 | 1999-06-08 | Regents Of The University Of Michigan | Administration of products of the 5-lipoxygenase metabolic pathway to enhance antimicrobial defense |
US6353128B1 (en) | 1996-12-03 | 2002-03-05 | Eli Lilly And Company | Phenyl acetamides as sPLA2 inhibitors |
US5916922A (en) | 1996-12-03 | 1999-06-29 | Eli Lilly And Company | Phenyl glyoxamides as SPLA2 inhibitors |
ID18983A (id) | 1996-12-04 | 1998-05-28 | Lilly Co Eli | Pirazola sebagai inhibitor sekresi fosfolipase a2 non-pankreas pada manusia |
US6011049A (en) | 1997-02-19 | 2000-01-04 | Warner-Lambert Company | Combinations for diabetes |
CA2286108A1 (en) | 1997-04-18 | 1998-10-29 | John Anthony Ragan | Process and intermediates for the preparation of 4'-trifluoromethyl-biphenyl-2-carboxylic acid (1,2,3,4-tetrahydro-isoquinolin-6-yl)-amide |
US6177415B1 (en) | 1997-04-21 | 2001-01-23 | The United States Of America As Represented By The Secretary Of Agriculture | Bacteriohopanetetrol and related compounds useful for modulation of lipoxygenase activity and anti-inflammatory applications |
JP4231559B2 (ja) | 1997-04-23 | 2009-03-04 | オリザ油化株式会社 | リポキシゲナーゼ阻害剤 |
WO1998047507A1 (en) | 1997-04-24 | 1998-10-29 | Shionogi & Co., Ltd. | Method for the treatment of stroke using n-heterocyclic glyoxylamide compounds |
US20030008816A1 (en) | 1997-05-28 | 2003-01-09 | Pilon Aprile L. | Methods and compositions for the treatment of fibrotic conditions & impaired lung function & to enhance lymphocyte production |
US20060025348A1 (en) | 1997-05-28 | 2006-02-02 | Pilon Aprile L | Methods and compositions for the treatment of fibrotic conditions & impaired lung function & to enhance lymphocyte production |
US20020169108A1 (en) | 1997-05-28 | 2002-11-14 | Pilon Aprile L. | Methods and compositions for the treatment of fibrotic conditions & impaired lung function & to enhance lymphocyte production |
US20010006644A1 (en) | 1997-07-31 | 2001-07-05 | David J. Bova | Combinations of hmg-coa reductase inhibitors and nicotinic acid and methods for treating hyperlipidemia once a day at night |
US6767739B2 (en) | 2001-07-30 | 2004-07-27 | Isis Pharmaceuticals Inc. | Antisense modulation of microsomal triglyceride transfer protein expression |
WO1999009978A1 (en) | 1997-08-28 | 1999-03-04 | Eli Lilly And Company | Method for treatment of non-rheumatoid athritis |
IT1304595B1 (it) | 1997-08-29 | 2001-03-19 | Giorgio Endrici | Inibitore della 5-lipoossigenasi |
JPH1180083A (ja) | 1997-09-10 | 1999-03-23 | Nof Corp | エイコサペンタエン酸エステルの製造方法 |
US6218524B1 (en) | 1997-09-16 | 2001-04-17 | Eurona Medical Ab | Genetic polymorphisms in the microsomal triglyceride transfer protein promoter and uses thereof |
AU1200899A (en) | 1997-10-27 | 1999-05-17 | Eli Lilly And Company | Morpholino-n-ethyl ester prodrugs of indole spla2 inhibitors |
US6440961B1 (en) | 1997-10-27 | 2002-08-27 | Dr. Reddy's Research Foundation | Tricyclic compounds and their use in medicine: process for their preparation and pharmaceutical compositions containing them |
AU1279899A (en) | 1997-10-27 | 1999-05-17 | Eli Lilly And Company | N,n-diethylglycolamido ester prodrugs of indole spla2 inhibitors |
JP4309045B2 (ja) | 1997-10-30 | 2009-08-05 | 森下仁丹株式会社 | 不飽和脂肪酸またはその誘導体を内容物とするカプセル製剤およびその製造法 |
WO1999025339A1 (en) | 1997-11-14 | 1999-05-27 | Eli Lilly And Company | Treatment for alzheimer's disease |
AU1407399A (en) | 1997-11-14 | 1999-06-07 | Eli Lilly And Company | Treatment for alzheimer's disease |
TR200001522T2 (tr) | 1997-11-25 | 2000-12-21 | Warner-Lambert Company | Lipoprotein oksidasyonunun inhibisyonu. |
US6121323A (en) | 1997-12-03 | 2000-09-19 | 3M Innovative Properties Company | Bishydroxyureas |
EP1039893B1 (en) | 1997-12-10 | 2011-02-02 | Cyclosporine Therapeutics Limited | Pharmaceutical compositions containing an omega-3 fatty acid oil |
US5948779A (en) | 1997-12-12 | 1999-09-07 | Cell Pathways, Inc. | Substituted condensation products of n-benzyl-3-indenyl acetamides with heterocyclic aldehydes |
US6828344B1 (en) | 1998-02-25 | 2004-12-07 | Genetics Institute, Llc | Inhibitors of phospholipase enzymes |
US6916841B2 (en) | 1998-02-25 | 2005-07-12 | Genetics Institute, Llc | Inhibitors of phospholipase enzymes |
HUP0102812A3 (en) | 1998-03-03 | 2002-01-28 | Lilly Co Eli | Pharmaceutical compositions containing the phospholipase inhibitor sodium {[3-(2-amino-1,2-dioxoethyl)-2-ethyl-1-(phenylmethyl)-1h-indol-4-yl]oxy}acetate and process for pruducing them |
JP4412521B2 (ja) | 1998-03-31 | 2010-02-10 | 塩野義製薬株式会社 | sPLA2阻害作用を有するピロロ[1,2−a]ピラジン誘導体 |
HUP0101672A3 (en) | 1998-03-31 | 2002-05-28 | Inst For Pharm Discovery Inc | Substituted indolealkanoic acids |
US6028116A (en) | 1998-04-03 | 2000-02-22 | Cell Pathways, Inc. | Substituted condensation products of 1H-indenyl-hydroxyalkanes with aldehydes for neoplasia |
DZ2770A1 (fr) | 1998-04-17 | 2003-12-01 | Lilly Co Eli | Procédé de préparation de 1h-indol-3 glyoxamides substituées en position 4. |
US6407261B1 (en) | 1998-04-17 | 2002-06-18 | Eli Lilly And Company | Process for preparing 4-hdyroxy indole, indazole and carbazole compounds |
TR200003194T2 (tr) | 1998-05-01 | 2001-03-21 | Eli Lilly And Company | Hastalık tedavisine mahsus sPLA2 önleyici bileşikler |
CN1302300A (zh) | 1998-05-21 | 2001-07-04 | 盐野义制药株式会社 | 吡咯并[1,2-b]哒嗪sPLA2抑制剂 |
CA2319495A1 (en) | 1998-06-08 | 1999-12-16 | Advanced Medicine, Inc. | Multibinding inhibitors of microsomal triglyceride transferase protein |
US20020045271A1 (en) | 1998-06-10 | 2002-04-18 | Licata And Tyrrell P.C. | Compounds and methods for identifying compounds that interact with microsomal triglyceride transfer protein binding sites on apolipoprotein b and modulate lipid biosynthesis |
EP1091738B1 (en) | 1998-06-30 | 2006-12-06 | Eli Lilly And Company | BICYCLIC sPLA 2 INHIBITORS |
DE19830375A1 (de) | 1998-07-08 | 2000-01-13 | K D Pharma Bexbach Gmbh | Mikroverkapselte ungesättigte Fettsäure oder Fettsäureverbindung oder Mischung aus Fettsäuren und/oder Fettsäureverbindungen |
AU5331499A (en) | 1998-08-03 | 2000-02-28 | Eli Lilly And Company | Indole spla2 inhibitors |
WO2000007590A1 (en) | 1998-08-03 | 2000-02-17 | Eli Lilly And Company | INDOLE sPLA2 INHIBITORS |
US6576654B1 (en) | 1998-09-23 | 2003-06-10 | Eli Lilly And Company | Method for the treatment of cystic fibrosis |
US6221880B1 (en) | 1998-10-09 | 2001-04-24 | Schering Corporation | Composition and method for treating allergic diseases |
EP1157704B1 (en) | 1998-10-14 | 2006-06-14 | Shionogi & Co., Ltd. | Spla2 inhibitors for the treatment of ischaemic reperfusion injury |
US20030008914A1 (en) | 1998-10-16 | 2003-01-09 | C. Grace Yeh | Pharmaceutical formulations useful to treat inflammatory and immune disorders |
US6248553B1 (en) | 1998-10-22 | 2001-06-19 | Atairgin Technologies, Inc. | Enzyme method for detecting lysophospholipids and phospholipids and for detecting and correlating conditions associated with altered levels of lysophospholipids |
NZ500703A (en) | 1998-11-04 | 2001-06-29 | F | Preparation of food-grade marine edible oils by treatment with silica, vacuum steam deodorisation and addition of a herb extract |
TNSN99224A1 (fr) | 1998-12-01 | 2005-11-10 | Inst For Pharm Discovery Inc | Methodes de reduction des niveaux de glucose et triglyceride en serum et pour suppression de l'antigenese utilisant les acides la indolealkanoique |
US20020055529A1 (en) | 1998-12-02 | 2002-05-09 | Bisgaier Charles Larry | Method for treating alzheimer's disease |
CA2355900A1 (en) | 1998-12-17 | 2000-06-22 | Xenogen Corporation | Non-invasive evaluation of physiological response in a mammal |
EP1144305A4 (en) | 1998-12-22 | 2004-11-10 | Lilly Co Eli | NEW sPLA 2 INHIBITORS |
WO2000037472A2 (en) | 1998-12-22 | 2000-06-29 | Eli Lilly And Company | Substituted pirroloindoles |
US6194585B1 (en) | 1998-12-22 | 2001-02-27 | Pfizer Inc. | Process for preparing 5-lipoxygenase inhibitors |
IL143944A0 (en) | 1998-12-23 | 2002-04-21 | Searle Llc | Combinations for cardiovascular indications |
GB9901809D0 (en) | 1999-01-27 | 1999-03-17 | Scarista Limited | Highly purified ethgyl epa and other epa derivatives for psychiatric and neurological disorderes |
CA2260397A1 (en) | 1999-01-29 | 2000-07-29 | Atlantis Marine Inc. | Method of converting rendered triglyceride oil from marine sources into bland, stable food oil |
US20030104048A1 (en) | 1999-02-26 | 2003-06-05 | Lipocine, Inc. | Pharmaceutical dosage forms for highly hydrophilic materials |
US6193999B1 (en) | 1999-03-01 | 2001-02-27 | Banner Pharmacaps, Inc. | Gum acacia substituted soft gelatin capsules |
WO2000051576A2 (en) | 1999-03-03 | 2000-09-08 | Ida Royalty Aps | Novel pharmaceuticals, dietary supplements and cosmetic compositions, and the use of certain mixtures for preparing a medicament or a dietary supplement for the treatment or prevention of inflammation, hypersensitivity reactions or pain |
CA2362515C (en) | 1999-03-04 | 2008-07-15 | Suntory Limited | Utilization of material containing docosapentaenoic acid |
US20020110523A1 (en) | 1999-03-23 | 2002-08-15 | Cornelis Kluft | Methods for screening or monitoring the risk of cardiovascular disease relating to sex steroid compound or composition intake and methods for screening sex steroid compound |
US20020054871A1 (en) | 1999-04-12 | 2002-05-09 | Yadong Huang | Methods and compositions for use in the treatment of hyperlipidemia |
US6380397B1 (en) | 1999-04-15 | 2002-04-30 | Eli Lilly And Company | Process for preparing 4-substituted-1H-indole-3-glyoxamides |
US6274578B1 (en) | 1999-04-20 | 2001-08-14 | Eli Lilly And Company | sPLA2 inhibitor ester |
JP2001025519A (ja) | 1999-05-11 | 2001-01-30 | Mamiya Op Co Ltd | ゴルフクラブ用シャフト |
US6140327A (en) | 1999-05-12 | 2000-10-31 | Eli Lilly And Company | Morpholino-n-ethyl ester derivative of an indole sPLA2 inhibitor |
US7112609B2 (en) | 1999-06-01 | 2006-09-26 | Drugtech Corporation | Nutritional supplements |
US6207699B1 (en) | 1999-06-18 | 2001-03-27 | Richard Brian Rothman | Pharmaceutical combinations for treating obesity and food craving |
CA2311974A1 (en) | 1999-06-28 | 2000-12-28 | Nisshin Flour Milling Co., Ltd. | Processes of selectively separating and purifying eicosapentaenoic and docosahexaenoic acids or their esters |
GB9916536D0 (en) * | 1999-07-14 | 1999-09-15 | Scarista Limited | Nutritional or pharmaceutical compositions |
US6706752B1 (en) | 1999-07-19 | 2004-03-16 | Eli Lilly And Company | sPLA2 inhibitors |
US6703385B1 (en) | 1999-07-19 | 2004-03-09 | Shionogi & Co., Ltd. | Tricyclic compounds having sPLA2-inhibitory activities |
DE19933926A1 (de) | 1999-07-20 | 2001-01-25 | Boehringer Ingelheim Pharma | Biphenylderivate, ihre Herstellung und ihre Verwendung als Arzneimittel |
DK1072198T3 (da) | 1999-07-28 | 2008-09-22 | Swiss Caps Rechte & Lizenzen | Præparat til anvendelse som medikament og/eller ernæringstilskud |
WO2001009130A1 (fr) | 1999-08-02 | 2001-02-08 | Shionogi & Co., Ltd. | COMPOSES TRICYCLIQUES A ACTIVITES INHIBANT sPLA¿2? |
WO2001012600A1 (en) | 1999-08-12 | 2001-02-22 | Cor Therapeutics, Inc. | INHIBITORS OF FACTOR Xa |
JP4623483B2 (ja) | 1999-08-23 | 2011-02-02 | 塩野義製薬株式会社 | sPLA2阻害作用を有するピロロトリアジン誘導体 |
CA2382262C (en) | 1999-08-30 | 2004-12-07 | Ocean Nutrition Canada Ltd. | A nutritional supplement for lowering serum triglyceride and cholesterol levels |
US6344563B1 (en) | 1999-08-31 | 2002-02-05 | Timothy Norris | Process for making 5-lipoxygenase inhibitors having varied heterocyclic ring systems |
US6831095B1 (en) | 1999-09-20 | 2004-12-14 | Eli Lilly And Company | Hydroxyfunctional amide 1h-indole derivatives active as sPLA2 inhibitors |
CA2385406A1 (en) | 1999-09-21 | 2001-03-29 | Shionogi & Co., Ltd. | Gene encoding novel human secretory phospholipase a2 |
JP2003512349A (ja) | 1999-10-15 | 2003-04-02 | デュポン ファーマシューティカルズ カンパニー | ケモカイン受容体活性のモジュレーターとしてのベンジルシクロアルキルアミン |
US6261607B1 (en) | 1999-10-19 | 2001-07-17 | Thomas Newmark | Composition for promoting prostate health containing selenium and herbal extracts |
US6586438B2 (en) | 1999-11-03 | 2003-07-01 | Bristol-Myers Squibb Co. | Antidiabetic formulation and method |
CA2325358C (en) | 1999-11-10 | 2005-08-02 | Pfizer Products Inc. | 7-¬(4'-trifluoromethyl-biphenyl-2-carbonyl)amino|-quinoline-3-carboxylic acid amides, and methods of inhibiting the secretion of apolipoprotein b |
AU1304801A (en) | 1999-11-15 | 2001-05-30 | Shionogi & Co., Ltd. | Tricyclic azaindolizine derivatives having an SPLA2- inhibiting effect |
JP4170542B2 (ja) | 1999-11-18 | 2008-10-22 | 日油株式会社 | 高度不飽和脂肪酸誘導体の製造方法及び高純度エイコサペンタエン酸誘導体 |
DE19962300A1 (de) | 1999-12-23 | 2001-06-28 | Asta Medica Ag | Substituierte N-Benzyl-Indol-3-yl-glyoxylsäure-Derivate mit Antitumorwirkung |
US6878707B2 (en) | 2000-01-18 | 2005-04-12 | Novartis Ag | Carboxamides useful as inhibitors of microsomal triglyceride transfer protein and of apolipoprotein b secretion |
EP1125914A1 (en) | 2000-02-14 | 2001-08-22 | Nisshin Flour Milling Co., Ltd. | Process for separating and purifying eicosapentaenoic acid or its ester |
DE10007203A1 (de) | 2000-02-17 | 2001-08-23 | Asta Medica Ag | Neue Kombination nichtsedierender Antihistaminika mit Substanzen, die die Leukotrienwirkung beeinflussen, zur Behandlung der Rhinitis/Konjunktivitis |
SE0000754D0 (sv) | 2000-03-07 | 2000-03-07 | Amersham Pharm Biotech Ab | Mass spectral peak identification |
SK14922002A3 (sk) | 2000-03-17 | 2003-04-01 | Ajinomoto Co., Inc. | Farmaceutický prostriedok na prevenciu, zlepšenie a/alebo liečenie diabetickej komplikácie a použitie postprandiálnej látky na zníženie hladiny krvného cukru |
AU2001249348A1 (en) | 2000-03-22 | 2001-10-03 | Creighton University | Compositions derived from modiolus modiolus and methods for making and using same |
AU2001251665A1 (en) | 2000-04-17 | 2001-10-30 | Glaxo Group Limited | Medicine response assay in respiratory disease |
US6987105B2 (en) | 2000-04-28 | 2006-01-17 | Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College | Synthesis and use of thienotriazolodiazepines |
DE10022925A1 (de) | 2000-05-11 | 2001-11-15 | Basf Ag | Substituierte Indole als PARP-Inhibitoren |
ES2246769T3 (es) | 2000-05-22 | 2006-03-01 | Pro Aparts - Investimentos E Consultoria Lda | Composicion de acidos grasos que contiene al menos 80% en peso de epa y dha o sus derivados y su uso farmaceutico. |
GB0013378D0 (en) | 2000-06-01 | 2000-07-26 | Glaxo Group Ltd | Use of therapeutic benzamide derivatives |
DE10030375A1 (de) | 2000-06-21 | 2002-01-03 | Bayer Ag | Verwendung von MTP-Inhibitoren zur Senkung von ppTRL |
EP1299377A2 (en) | 2000-06-28 | 2003-04-09 | Eli Lilly And Company | Spla2 inhibitors |
GB0016045D0 (en) | 2000-06-29 | 2000-08-23 | Laxdale Limited | Therapeutic combinations of fatty acids |
AU2001267824A1 (en) | 2000-06-29 | 2002-01-08 | Shionogi And Co., Ltd. | Remedies for cancer |
US6967200B2 (en) | 2000-06-29 | 2005-11-22 | Shionogi & Co., Ltd. | Remedies for cirrhosis |
WO2002000621A1 (fr) | 2000-06-29 | 2002-01-03 | Shionogi & Co., Ltd. | Composes inhibiteurs de la spla2 de type x |
WO2002000257A1 (fr) | 2000-06-29 | 2002-01-03 | Shionogi & Co., Ltd. | Remedes a la maladie d'alzheimer |
GB0016452D0 (en) | 2000-07-04 | 2000-08-23 | Kilgowan Limited | Vitamin K and essential fatty acids |
US20020032238A1 (en) | 2000-07-08 | 2002-03-14 | Henning Priepke | Biphenylcarboxylic acid amides, the preparation thereof and the use thereof as medicaments |
CA2417127A1 (en) | 2000-07-24 | 2002-01-31 | The University Of Queensland | Compounds and inhibitors of phospholipases |
AU2001283085A1 (en) | 2000-08-04 | 2002-02-18 | R. Preston Mason | Synergistic effect of amlodipine and atorvastatin |
JP4391673B2 (ja) | 2000-08-08 | 2009-12-24 | 花王株式会社 | 油脂組成物 |
US6417367B1 (en) | 2000-08-11 | 2002-07-09 | Pfizer Inc. | Methods of making quinoline amides |
WO2002013818A1 (en) | 2000-08-15 | 2002-02-21 | South Alabama Medical Science Foundation | Treating sickle cell disease |
AU2001270937A1 (en) | 2000-08-15 | 2002-02-25 | Pfizer Products Inc. | Therapeutic combination |
US6383482B1 (en) | 2000-08-24 | 2002-05-07 | Vitacost.Com, Inc. | Weight loss composition containing green tea, hydroxycitric acid, 5-hydroxytryptophan, glucomannan, picolinate and lactobacillus |
US20120237626A9 (en) | 2000-12-05 | 2012-09-20 | Palu Afa Kehaati | Profiles of lipid proteins and inhibiting HMG-CoA reductase |
ATE354567T1 (de) | 2000-12-18 | 2007-03-15 | Lilly Co Eli | Benz(g)indole und deren verwendung als spla2 inhibitoren |
CA2431028A1 (en) | 2000-12-18 | 2002-06-27 | Ho-Shen Lin | Tetracyclic carbazole derivates and their use as spla2 inhibitors |
CA2431023A1 (en) | 2000-12-18 | 2002-06-27 | Eli Lilly And Company | Substituted benzoindoles as spla2 inhibitors |
JP2004518658A (ja) | 2000-12-18 | 2004-06-24 | イーライ・リリー・アンド・カンパニー | 新規なsPLA2インヒビター |
GB0101198D0 (en) | 2001-01-17 | 2001-02-28 | Scherer Technologies Inc R P | Ingestible compositions containing an odoriferous oil |
AU2002247004A1 (en) | 2001-01-19 | 2002-07-30 | Cambridge Scientific, Inc. | Methods of diagnosis and treatment of osteoporosis |
ITMI20010129A1 (it) | 2001-01-25 | 2002-07-25 | Pharmacia & Upjohn Spa | Acidi grassi essenziali nella terapia di insufficienza cardiaca e scompenso cardiaco |
WO2002062825A2 (en) | 2001-02-08 | 2002-08-15 | Millennium Pharmaceuticals, Inc. | Detection of polymorphisms in the human 5-lipoxygenase gene |
TWI314457B (ru) | 2001-03-19 | 2009-09-11 | Shionogi & Co | |
CA2441077A1 (en) | 2001-03-28 | 2002-10-10 | Eli Lilly And Company | Substituted carbazoles as inhibitors of spla2 |
US7524635B2 (en) | 2003-04-17 | 2009-04-28 | Biosite Incorporated | Methods and compositions for measuring natriuretic peptides and uses thereof |
GB0111282D0 (en) | 2001-05-09 | 2001-06-27 | Laxdale Ltd | Potentiation of therapeutic effects of fatty acids |
IL143379A (en) | 2001-05-24 | 2013-11-28 | Yissum Res Dev Co | Oligonucleotide against human ache isoform r and its uses |
PL364093A1 (en) | 2001-05-30 | 2004-12-13 | Laxdale Limited | Coenzyme q (ubiquinone) and eicosapentaenoic acid (epa) |
US7901713B2 (en) | 2001-06-20 | 2011-03-08 | Metaproteomics, Llc | Inhibition of COX-2 and/or 5-LOX activity by fractions isolated or derived from hops |
US6756399B2 (en) | 2001-06-29 | 2004-06-29 | The United States Of America As Represented By The Department Of Health And Human Services | Use of lipoxygenase inhibitors and PPAR ligands as anti-cancer therapeutic and intervention agents |
US6730694B1 (en) | 2001-07-20 | 2004-05-04 | Eli Lilly And Company | sPLA2 inhibitors |
US20120214771A1 (en) | 2001-07-27 | 2012-08-23 | Fontini Sampalis | Compositions for treatment of cardiometabolic disorders |
JP2005527464A (ja) | 2001-08-09 | 2005-09-15 | イーライ・リリー・アンド・カンパニー | sPLA2インヒビターとしてのシクロヘプタBインドール誘導体 |
US7109231B2 (en) | 2001-08-09 | 2006-09-19 | Eli Lilly And Company | Cyclohept[b]indole derivatives |
NZ531700A (en) | 2001-09-13 | 2006-10-27 | Synta Pharmaceuticals Corp | 1-Glyoxylamide indolizines for treating cancer |
CA2460347A1 (en) | 2001-09-13 | 2003-03-20 | Synta Pharmaceuticals Corp. | 3-glyoxlylamideindoles for treating cancer |
ITMI20012384A1 (it) | 2001-11-12 | 2003-05-12 | Quatex Nv | Uso di acidi grassi poliinsaturi per la prevenzione primaria di eventi cardiovascolari maggiori |
EP1450787A4 (en) | 2001-11-15 | 2006-01-25 | Galileo Pharmaceuticals Inc | FORMULATIONS AND METHODS FOR THE TREATMENT OR AMELIORATION OF INFLAMMATORY CONDITIONS |
US20040018248A1 (en) | 2001-11-29 | 2004-01-29 | Adrianne Bendich | Composition containing statins and calcium for improved cardiovascular health |
AU2002364900A1 (en) | 2001-11-30 | 2003-06-17 | Bristol-Myers Squibb Company | Polynucleotides encoding novel human mitochondrial and microsomal glycerol-3-phosphate acyl-transferases and variants thereof |
US7101875B2 (en) | 2001-12-03 | 2006-09-05 | Wyeth | Methods for treating arthritic disorders |
US6635771B2 (en) | 2001-12-03 | 2003-10-21 | Wyeth | N-benzhydryl indole compounds |
US6797708B2 (en) | 2001-12-03 | 2004-09-28 | Wyeth | Inhibitors of cytosolic phospholipase A2 |
US6984735B2 (en) | 2001-12-03 | 2006-01-10 | Wyeth | Process for making an aldehyde |
US6992100B2 (en) | 2001-12-06 | 2006-01-31 | Eli Lilly And Company | sPLA2 inhibitors |
TWI323658B (en) | 2001-12-06 | 2010-04-21 | Nat Health Research Institutes | Novel compounds of indol-3-yl-2-oxyacetylamide derivatives, pharmaceutical composition thereof, and method for manufacturing the same |
ITMI20020269A1 (it) | 2002-02-12 | 2003-08-12 | Victorix Assets Ltd | Uso di steri etilici di acidi poliinsaturi omega-3 in pazienti con insufficienza cardiaca |
JP2003306690A (ja) | 2002-02-18 | 2003-10-31 | Nooburu:Kk | 多価不飽和脂肪酸含有油脂組成物 |
HUP0200686A2 (hu) | 2002-02-22 | 2003-09-29 | EURO- "H" Beruházásszervezż és Ingatlanhasznosító Kft. | Elektronikus berendezés és eljárás számsorozat eltalálására irányuló játékokban való részvételre kommunikációs berendezésen keresztül |
US20030166614A1 (en) | 2002-03-01 | 2003-09-04 | Harrison Stanley F. | Method for reducing cholesterol and triglycerides |
US6900208B2 (en) | 2002-03-28 | 2005-05-31 | Bristol Myers Squibb Company | Pyrrolopyridazine compounds and methods of use thereof for the treatment of proliferative disorders |
EP2108370A1 (en) | 2002-04-30 | 2009-10-14 | Unigen Pharmaceuticals, Inc. | Formulation of a mixture of free-B-ring flavonoids and flavans as a therapeutic agent |
AU2003229993B2 (en) | 2002-05-03 | 2008-07-24 | Pronova Biopharma Norge As | Use of EPA and DHA in secondary prevention |
US8895059B2 (en) | 2002-06-05 | 2014-11-25 | Ivax Pharmaceuticals S.R.O. | Reduction of cross-linking gelatin in gelatin capsules |
US20030092767A1 (en) | 2002-06-07 | 2003-05-15 | Macias William Louis | Combination therapy for the treatment of inflammatory and respiratory diseases |
CA2390820A1 (en) | 2002-06-17 | 2003-12-17 | St. Vincent's Hospital Sydney Limited | Methods of diagnosis, prognosis and treatment of cardiovascular disease |
US6620813B1 (en) | 2002-06-21 | 2003-09-16 | Medinox, Inc. | Hydroxamate derivatives of non-steroidal anti-inflammatory drugs |
US20040077691A1 (en) | 2002-06-21 | 2004-04-22 | Medinox, Inc. | Hydroxamate derivatives of non-steroidal anti-inflammatory drugs |
US20040001874A1 (en) | 2002-06-24 | 2004-01-01 | Vital Living, Inc. | Safe and effective nutritional supplement formulations and associated regimens adapted to prevent and/or treat targeted diseases or medical or health conditions, and related methods |
US6653311B1 (en) | 2002-06-25 | 2003-11-25 | Board Of Supervisors Of Louisiana State University | 5-lipoxygenase inhibitors: (2-azinylamino) quinone derivatives |
EP1517667A2 (en) | 2002-07-02 | 2005-03-30 | Galileo Pharmaceuticals, Inc. | Compositions and methods for reduction of inflammatory symptoms and/or biomarkers in female subjects |
US20060211761A1 (en) | 2002-07-08 | 2006-09-21 | Yatendra Kumar | Hmg-coa-reductase inhibitors |
US20080200453A1 (en) | 2002-07-29 | 2008-08-21 | Cincotta Anthony H | Methods of treating metabolic syndrome using dopamine receptor agonists |
US20030087944A1 (en) | 2002-08-05 | 2003-05-08 | Macias William Louis | Method for the treatment of renal dysfunction with spla2 inhibitors |
JP4398862B2 (ja) | 2002-08-20 | 2010-01-13 | 興和株式会社 | 軟カプセル剤 |
DE20214847U1 (de) | 2002-09-24 | 2004-02-19 | Voss Automotive Gmbh | Anschlußvorrichtung für Rohrleitungen |
KR100539027B1 (ko) | 2002-10-18 | 2005-12-26 | 현대모비스 주식회사 | 차량의 조향각 검출 장치 |
US7511131B2 (en) | 2002-11-13 | 2009-03-31 | Genzyme Corporation | Antisense modulation of apolipoprotein B expression |
US8106019B2 (en) | 2002-11-15 | 2012-01-31 | Philadelphia Health & Education Corporation | CHEC-7 a novel sPLA2 inhibitor |
US7528112B2 (en) | 2002-11-15 | 2009-05-05 | Drexel University | Small survival-promoting/immunomodulatory peptide for treatment of brain damage, neurodegenerative disorders, and inflammatory disorders |
US8017651B2 (en) * | 2002-11-22 | 2011-09-13 | Bionexus, Ltd. | Compositions and methods for the treatment of HIV-associated fat maldistribution and hyperlipidemia |
AU2003284617A1 (en) | 2002-11-22 | 2004-06-18 | Nippon Suisan Kaisha, Ltd. | Composition containing organic substance having double bond with improved oxidation stability |
ITMI20022511A1 (it) * | 2002-11-26 | 2004-05-27 | Victorix Assets Ltd | Uso di composizioni farmaceutiche contenenti esteri etilici di acidi poliinsaturi omega-3 nella orevenzione della fibrillazione atriale. |
GB0228079D0 (en) | 2002-12-02 | 2003-01-08 | Laxdale Ltd | Huntington's Disease |
US8124582B2 (en) | 2002-12-06 | 2012-02-28 | Fibrogen, Inc. | Treatment of diabetes |
US20040198800A1 (en) | 2002-12-19 | 2004-10-07 | Geoffrey Allan | Lipoxygenase inhibitors as hypolipidemic and anti-hypertensive agents |
CA2505604A1 (en) | 2002-12-20 | 2004-07-08 | Pfizer Products Inc. | Microsomal triglyceride transfer protein inhibitors |
EP1581499A1 (en) | 2002-12-20 | 2005-10-05 | Pfizer Products Inc. | Microsomal triglyceride transfer protein inhibitors |
CA2512666A1 (en) | 2003-01-08 | 2004-07-29 | Flacco-Nesselroad Family Trust | Combination therapy for anticoagulation |
PT1581535E (pt) | 2003-01-09 | 2007-12-12 | Astellas Pharma Inc | Derivados de pirrolopiridazina |
GB0301701D0 (en) | 2003-01-24 | 2003-02-26 | Ensay Ltd | Psoriasis and Eicosapentaenoic acid |
MXPA05008216A (es) | 2003-01-31 | 2005-10-05 | Procter & Gamble | Medios para mejorar la apariencia del tejido queratinoso mamifero. |
EP1602372B1 (en) | 2003-02-07 | 2016-08-31 | Mochida Pharmaceutical Co., Ltd. | Drug for improving prognosis for subarachnoid hemorrhage |
WO2004073623A2 (en) | 2003-02-14 | 2004-09-02 | Children's Hospital & Research Center At Oakland | Treatment of conditions associated with decreased nitric oxide bioavailability, including elevated arginase conditions |
EP1595539A4 (en) | 2003-02-21 | 2007-04-11 | Mochida Pharm Co Ltd | DRUGS TO REDUCE THE SIDE EFFECTS OF RIBAVIRIN INTERFERON COMBINATION THERAPY |
BRPI0408006A (pt) | 2003-03-05 | 2006-02-14 | Solvay Pharm Gmbh | uso de ácidos graxos Èmega -3 no tratamento de pacientes diabéticos |
JP2006520335A (ja) | 2003-03-18 | 2006-09-07 | ノバルティス アクチエンゲゼルシャフト | 脂肪酸とアミノ酸を含有する組成物 |
US20050234073A1 (en) | 2003-03-24 | 2005-10-20 | Blumberg Richard S | Methods of inhibiting inflammation |
US20050090426A1 (en) | 2003-03-24 | 2005-04-28 | Blumberg Richard S. | Methods of inhibiting inflammation |
US7030112B2 (en) | 2003-03-25 | 2006-04-18 | Bristol-Myers Squibb Company | Pyrrolopyridazine compounds and methods of use thereof for the treatment of proliferative disorders |
US20070066577A1 (en) | 2003-04-03 | 2007-03-22 | Hea Young Park Choo | Benzoxazole derivative or analogue thereof for inhibiting 5-lipoxygenase and pharmaceutical composition containing same |
US7329682B2 (en) | 2003-04-03 | 2008-02-12 | Ewha University-Industry Collaboration Foundation | Method for inhibiting 5-lipoxygenase using a benzoxazole derivative |
US7598227B2 (en) | 2003-04-16 | 2009-10-06 | Isis Pharmaceuticals Inc. | Modulation of apolipoprotein C-III expression |
US7176281B2 (en) | 2003-04-30 | 2007-02-13 | National University Of Singapore | Phospholipase A2-inhibitory peptide with anti-arthritic and neuroprotective activities |
US7579433B2 (en) | 2003-04-30 | 2009-08-25 | National University Of Singapore | Methods and compositions for treatment of arthritis and cancer |
EP1479677A1 (en) | 2003-05-19 | 2004-11-24 | Aventis Pharma Deutschland GmbH | New indole derivatives as factor xa inhibitors |
US6846942B2 (en) | 2003-05-20 | 2005-01-25 | David Rubin | Method for preparing pure EPA and pure DHA |
US20040235807A1 (en) | 2003-05-21 | 2004-11-25 | Weinrich Karl P. | Formulations including a topical decongestant and a topical corticosteroid suitable for nasal administration and method for treating obstructive sleep apnea |
US7205329B2 (en) | 2003-05-30 | 2007-04-17 | Microbia, Inc. | Modulators of CRTH2 activity |
EP1637134A4 (en) | 2003-06-20 | 2010-01-27 | Mochida Pharm Co Ltd | COMPOSITION FOR THE PREVENTION AND TREATMENT OF VARICES |
WO2005020785A2 (en) | 2003-07-15 | 2005-03-10 | The Regents Of The University Of California | Discovery of the microorganism that causes the human autoimmune disease, primary biliary cirrhosis |
UA88767C2 (ru) | 2003-07-17 | 2009-11-25 | Плексікон, Інк. | Ppar активные соединения |
EP1558220B1 (en) | 2003-07-24 | 2010-02-10 | Wockhardt Limited | Oral compositions for treatment of diabetes |
ATE370955T1 (de) | 2003-07-31 | 2007-09-15 | Wyeth Corp | N-sulfonylheterocyclopyrrolylalkylamin verbindungen als 5-hydroxytryptamin-6 liganden. |
WO2005013907A2 (en) | 2003-08-07 | 2005-02-17 | Japan Tobacco Inc. | Pyrrolo[1,2-b]pyridazine derivatives |
WO2005018436A2 (en) | 2003-08-26 | 2005-03-03 | The Trustees Of Boston University | Methods for the diagnosis, prognosis and treatment of metabolic syndrome |
EP1664304A1 (en) | 2003-09-22 | 2006-06-07 | BioSpecific GmbH & Co.KG. | Method for neutralizing effects of secreted pla2 iia |
IL158600A (en) | 2003-10-26 | 2015-07-30 | Hermona Soreq | Dioxysoligonucleotide Antisense Against Acetylcholinesterase as an Anti-Inflammatory Agent |
CN101128475B (zh) | 2003-11-12 | 2012-06-20 | 纳幕尔杜邦公司 | 适用于改变产油植物及酵母中多不饱和脂肪酸水平的△15脂肪酸去饱和酶 |
ITMI20032247A1 (it) | 2003-11-19 | 2005-05-20 | Tiberio Bruzzese | Interazione di derivati polari di composti insaturi con substrati inorganici |
SE0303513D0 (sv) | 2003-12-19 | 2003-12-19 | Pronova Biocare As | Use of a fatty acid composition comprising at least one of epa and dha or any combinations thereof |
US20070105954A1 (en) | 2003-12-31 | 2007-05-10 | Ingennus Limited | Formulation containing a carboxylic acid or an ester thereof |
IL159729A0 (en) | 2004-01-06 | 2004-06-20 | Doron I Friedman | Non-aqueous composition for oral delivery of insoluble bioactive agents |
GB0403247D0 (en) | 2004-02-13 | 2004-03-17 | Tillotts Pharma Ag | A pharmaceutical composition |
US7022713B2 (en) * | 2004-02-19 | 2006-04-04 | Kowa Co., Ltd. | Hyperlipemia therapeutic agent |
EP1591114A1 (en) | 2004-03-12 | 2005-11-02 | Fournier Laboratories Ireland Limited | Use of metformin and orlistat for the treatment or prevention of obesity |
US20050215640A1 (en) | 2004-03-26 | 2005-09-29 | Baxter Jeffrey H | HMB compositions and uses thereof |
US7923043B2 (en) | 2004-03-30 | 2011-04-12 | Theta Biomedical Consulting & Development Co., Inc. | Method for protecting humans against superficial vasodilator flush syndrome |
US20050244367A1 (en) | 2004-05-03 | 2005-11-03 | Ilypsa, Inc. | Phospholipase inhibitors localized in the gastrointestinal lumen |
WO2005114190A2 (en) | 2004-05-19 | 2005-12-01 | Ppd Biomarker Discovery Sciences, Llc | Methods of identifying biomarkers |
US20050267145A1 (en) | 2004-05-28 | 2005-12-01 | Merrill Bryon A | Treatment for lung cancer |
TW200613009A (en) | 2004-06-11 | 2006-05-01 | Ono Pharmaceutical Co | Capsule having chewing stability |
GB0413729D0 (en) | 2004-06-18 | 2004-07-21 | Tillotts Pharma Ag | A pharmaceutical composition and its use |
GB0413730D0 (en) | 2004-06-18 | 2004-07-21 | Tillotts Pharma Ag | A pharmaceutical composition and its use |
EP2287328A3 (en) | 2004-07-16 | 2011-06-08 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Secretory phospholipase A2 (SPLA2) as prognostic and diagnostic marker for cardiovascular diseases |
JP2007284350A (ja) | 2004-07-27 | 2007-11-01 | Takeda Chem Ind Ltd | 糖尿病治療剤 |
MX2007001155A (es) | 2004-07-29 | 2007-08-14 | Creabilis Therapeutics Spa | Uso de inhibidores de k-252a y de quinasa para la prevencion o el tratamiento de patologias asociadas con hmgb1. |
US20070231345A1 (en) | 2004-08-02 | 2007-10-04 | Muhammed Majeed | Medicament containing natural leucotriene inhibitors singly or in combination with bioavailable organic selenium supplement for hyperproliferative dermatological conditions and therapeutic methods thereof |
ITRM20040395A1 (it) | 2004-08-03 | 2004-11-03 | Sigma Tau Ind Farmaceuti | Composizione comprendente statine e acidi grassi omega 3. |
WO2006017627A2 (en) | 2004-08-06 | 2006-02-16 | Barry Sears | Dietary compositions comprising docosahexaenoic acid and eicosapentaenoic acid and use thereof for treating insulin resistance |
RU2382642C2 (ru) * | 2004-08-06 | 2010-02-27 | Трансформ Фармасьютикалз, Инк. | Новые фармацевтические композиции статина и связанные с ними способы лечения |
US20090042979A1 (en) | 2004-08-06 | 2009-02-12 | Transform Pharmaceuticals Inc. | Novel Statin Pharmaceutical Compositions and Related Methods of Treatment |
WO2007130713A1 (en) | 2006-02-01 | 2007-11-15 | Transform Pharmaceuticals, Inc. | Novel fenofibrate formulations and related methods of treatment |
KR20070038553A (ko) | 2004-08-06 | 2007-04-10 | 트렌스폼 파마수티컬스 인코퍼레이티드 | 신규한 스타틴 약제학적 조성물 및 관련된 치료방법 |
WO2007130714A1 (en) | 2006-02-01 | 2007-11-15 | Transform Pharmaceuticals, Inc. | Novel statin pharmaceutical compositions and related methods of treatment |
EP1782807B1 (en) | 2004-08-18 | 2017-08-09 | Mochida Pharmaceutical Co., Ltd. | Jelly composition |
DK1781265T3 (da) | 2004-08-25 | 2010-08-02 | Essentialis Inc | Farmaceutiske formuleringer af kalium ATP-kanal-åbnere og anvendelser deraf |
MX2007002400A (es) | 2004-08-27 | 2007-05-04 | Senju Pharma Co | Liquido para lavado de ojos para terapia de ojos secos. |
KR100545304B1 (ko) | 2004-09-01 | 2006-05-08 | 주식회사 유니젠 | 아선약을 포함하는 운카리아 속 식물, 또는 이의 황금및/또는 녹차의 배합물을 포함하는 사이클로옥시게나제및/또는 5-리폭시게나제 억제용 조성물 |
WO2006027776A1 (en) | 2004-09-07 | 2006-03-16 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Agents, compositions and methods for treating pathologies in which regulating an ache-associated biological pathway is beneficial |
CN1759834B (zh) | 2004-09-17 | 2010-06-23 | 中国医学科学院医药生物技术研究所 | 黄连素或其与辛伐他汀联合在制备用于预防或治疗与血脂有关疾病或症状的产品中用途 |
WO2006035417A2 (en) * | 2004-09-27 | 2006-04-06 | Sigmoid Biotechnologies Limited | Dihydropyrimidine microcapsule - formulations |
WO2006044556A2 (en) | 2004-10-14 | 2006-04-27 | Galileo Pharmaceuticals, Inc. | Dual inhibitors of lipoxygenase for treating diabetes |
US20100021555A1 (en) | 2004-10-15 | 2010-01-28 | Karl Geiringer | Compositions containing high omega-3 and low saturated fatty acid levels |
ES2255426B1 (es) * | 2004-10-19 | 2007-08-16 | Gp Pharm, S.A. | Formulacion farmaceutica que comprende microcapsulas de estatinas suspendidas en ester alquilicos de acidos grasos poliinsaturados (pufa). |
KR101086037B1 (ko) | 2004-10-27 | 2011-11-22 | 에스케이케미칼주식회사 | 호흡기질환 예방 및 치료에 유용한 산두근 추출물 |
JP2008521829A (ja) | 2004-11-30 | 2008-06-26 | プレキシコン,インコーポレーテッド | Ppar活性化合物 |
FR2878747B1 (fr) * | 2004-12-03 | 2007-03-30 | Pierre Fabre Medicament Sa | Utilisation d'acide(s) gras omega-3 pour le traitement de l'hypercholesterolemie causee par un traitement anti-retroviral chez les patients infectes par le vih |
US20070191467A1 (en) | 2004-12-06 | 2007-08-16 | Reliant Pharmaceutical, Inc. | Statin and omega-3 fatty acids for lipid therapy |
WO2006062748A2 (en) | 2004-12-06 | 2006-06-15 | Reliant Pharmaceuticals, Inc. | Omega-3 fatty acids and dyslipidemic agent for lipid therapy |
US20090239927A1 (en) | 2004-12-06 | 2009-09-24 | George Bobotas | Statin and Omega-3 Fatty Acids For Lipid Therapy |
CN101098690A (zh) | 2004-12-06 | 2008-01-02 | 瑞莱恩特医药品有限公司 | 用于血脂治疗的ω-3脂肪酸和脂血异常剂 |
US20060135610A1 (en) | 2004-12-22 | 2006-06-22 | Bortz Jonathan D | Cardiovascular compositions |
GB2421909A (en) | 2004-12-23 | 2006-07-12 | Laxdale Ltd | Pharmaceutical compositions comprising EPA and methods of use |
US20080200707A1 (en) | 2005-01-04 | 2008-08-21 | Mochida-Pharmaceuticals Pharmaceutical Co., Ltd. | Lipotoxicity Relieving Agent |
WO2006073147A1 (ja) | 2005-01-04 | 2006-07-13 | Mochida Pharmaceutical Co., Ltd. | 脂肪毒性の改善剤 |
ATE528005T1 (de) | 2005-01-10 | 2011-10-15 | Cortendo Ab Publ | 2s,4r ketoconazol zur behandlung von diabetes, metabolischem syndrom und anderen erkrankungen |
US20060172012A1 (en) | 2005-01-28 | 2006-08-03 | Finley John W | Anti-inflammatory supplement compositions and regimens to reduce cardiovascular disease risks |
US20060189682A1 (en) | 2005-02-02 | 2006-08-24 | Payne Joseph E | Water soluble prodrugs of COX-2 inhibitors |
US20060235009A1 (en) | 2005-02-08 | 2006-10-19 | Richard Glickman | Treatment of vascular, autoimmune and inflammatory diseases using low dosages of IMPDH inhibitors |
AU2006214018A1 (en) | 2005-02-17 | 2006-08-24 | Merck Sharp & Dohme Corp. | Method of treating atherosclerosis, dyslipidemias and related conditions |
US20100254951A1 (en) | 2005-02-22 | 2010-10-07 | Mochida Pharmaceutical Co., Ltd. | Nerve Regeneration Promoting Agent |
BRPI0607569A2 (pt) | 2005-03-08 | 2009-09-15 | Reliant Pharmaceuticals Inc | composição farmacêutica compreendendo estatina e ácidos graxos Èmega-3, na forma de dosagem unitária |
US8980915B2 (en) | 2005-04-19 | 2015-03-17 | Surface Logix, Inc. | Inhibitors of microsomal triglyceride transfer protein and apo-B secretion |
JP2008540394A (ja) | 2005-05-04 | 2008-11-20 | プロノヴァ バイオファーマ ノルゲ アクティーゼルスカブ | 脂肪酸組成物、即ち、dha誘導体の医薬としての使用 |
WO2006129193A2 (en) | 2005-05-27 | 2006-12-07 | Pfizer Products Inc. | Combination of a cannabinoid-1- receptor-antagonist and a microsomal triglyceride transfer protein inhibitor for treating obesity or mainataining weight loss |
ATE552246T1 (de) | 2005-05-31 | 2012-04-15 | Pfizer | Substituierte aryloxy-n- bicyclomethylacetamidverbindungen als vr1- antagonisten |
JP5134916B2 (ja) | 2005-07-08 | 2013-01-30 | 持田製薬株式会社 | 心血管イベント発症予防用組成物 |
KR101465715B1 (ko) | 2005-07-08 | 2014-11-27 | 모치다 세이야쿠 가부시키가이샤 | 심혈관 이벤트 발병 예방용 조성물 |
MX2008000915A (es) | 2005-07-18 | 2008-04-04 | Reliant Pharmaceuticals Inc | Tratamiento con inhibidores de absorcion de colesterol basados en azetidinona y acidos grasos omega-3 y un producto de combinacion de los mismos. |
US7628027B2 (en) | 2005-07-19 | 2009-12-08 | Hussmann Corporation | Refrigeration system with mechanical subcooling |
EP1915160A2 (en) | 2005-07-22 | 2008-04-30 | Ranbaxy Laboratories Limited | Derivatives of monosaccharides for the treatment of copd and allergic rhinitis |
RU2290185C1 (ru) | 2005-07-26 | 2006-12-27 | Дмитрий Николаевич Мясников | Композиция для нормализации липидного обмена и снижения массы тела и способ её получения |
EA200800451A1 (ru) | 2005-07-28 | 2008-08-29 | Релайэнт Фармасьютикалз, Инк. | Лечение дигидропиридиновыми блокаторами кальциевых каналов и жирными кислотами омега-3 и их комбинированным продуктом |
ITMI20051560A1 (it) | 2005-08-10 | 2007-02-11 | Tiberio Bruzzese | Composizione di acidi grassi n-3 con elevata concentrazione di epa e-o dha e contenente acidi grassi n-6 |
AU2006279325B2 (en) | 2005-08-18 | 2013-06-27 | Accelalox, Inc. | Methods for bone treatment by modulating an arachidonic acid metabolic or signaling pathway |
KR100704009B1 (ko) | 2005-08-30 | 2007-04-04 | 한국화학연구원 | 염증억제 활성을 가지는6-알킬아미노-2-메틸-2'-(n-메틸치환술폰아미도)메틸-2h-1-벤조피란 유도체 |
RU2302248C2 (ru) | 2005-08-30 | 2007-07-10 | Федеральное государственное унитарное предприятие Тихоокеанский научно-исследовательский рыбохозяйственный центр | Средство, обладающее липидкорригирующими, гипокоагуляционными и антиоксидантными свойствами |
US7405302B2 (en) | 2005-10-11 | 2008-07-29 | Amira Pharmaceuticals, Inc. | 5-lipoxygenase-activating protein (FLAP) inhibitors |
EP1951220A2 (en) | 2005-10-18 | 2008-08-06 | Aegerion Pharmaceuticals | Compositions for lowering serum cholesterol and/or triglycerides |
US20070093524A1 (en) | 2005-10-25 | 2007-04-26 | Wyeth | 5-Lipoxygenase modulators |
EP1948168A4 (en) | 2005-10-28 | 2010-10-06 | Numerate Inc | COMPOSITIONS AND TREATMENTS FOR INHIBITING KINASE AND / OR HMG-COA REDUCTASE |
US20070244128A1 (en) | 2005-11-04 | 2007-10-18 | Amira Pharmaceuticals, Inc. | 5-lipoxygenase-activating protein (flap) inhibitors |
US20070219206A1 (en) | 2005-11-04 | 2007-09-20 | Amira Pharmaceuticals, Inc. | 5-lipoxygenase-activating protein (flap) inhibitors |
US20070105793A1 (en) | 2005-11-04 | 2007-05-10 | Curt Hendrix | Compositions and methods using nicotinic acid for treatment of hypercholesterolemia, hyperlipidemia nd cardiovascular disease |
US7977359B2 (en) | 2005-11-04 | 2011-07-12 | Amira Pharmaceuticals, Inc. | 5-lipdxygenase-activating protein (FLAP) inhibitors |
US20070225285A1 (en) | 2005-11-04 | 2007-09-27 | Amira Pharmaceuticals, Inc. | 5-lipoxygenase-activating protein (flap) inhibitors |
GB2431927B (en) | 2005-11-04 | 2010-03-17 | Amira Pharmaceuticals Inc | 5-Lipoxygenase-activating protein (FLAP) inhibitors |
US20070104779A1 (en) | 2005-11-07 | 2007-05-10 | Rongen Roelof M | Treatment with omega-3 fatty acids and products thereof |
BRPI0618455A2 (pt) | 2005-11-11 | 2011-08-30 | Mochida Pharm Co Ltd | composição de geléia |
CN101309669A (zh) | 2005-11-15 | 2008-11-19 | 巴克斯特国际公司 | 脂氧合酶抑制剂的组合物 |
WO2007058523A1 (en) | 2005-11-17 | 2007-05-24 | N.V. Nutricia | Composition with docosapentaenoic acid |
US20070116758A1 (en) | 2005-11-21 | 2007-05-24 | Dafna Dlugatch | Atorvastatin formulation |
US20070202206A1 (en) | 2005-11-29 | 2007-08-30 | Palu Afa K | Morinda Citrifolia Leaf Juice And Leaf Extract Based Formulations |
US7652068B2 (en) | 2005-12-20 | 2010-01-26 | Cenestra Llc | Omega 3 fatty acid formulations |
US20070237848A1 (en) | 2005-12-21 | 2007-10-11 | Brad Rawson | MORINDA CITRIFOLIA BASED COMPOSITIONS FOR TREATMENT OF ANTI-INFLAMMATORY DISEASES THROUGH INHIBITION OF COX-1, COX-2, INTERLEUKIN-1beta, INTERLEUKIN-6, TNF-alpha, HLE, AND iNOS |
ES2366034T3 (es) | 2005-12-23 | 2011-10-14 | N.V. Nutricia | Composición que comprende ácidos grasos poliinsaturados, proteínas, manganeso y/o molibdeno y nucleósidos/nucleótidos para el tratamiento de la demencia. |
WO2007081773A2 (en) | 2006-01-05 | 2007-07-19 | Reliant Pharmaceuticals, Inc | Treatment of fatty liver |
WO2007087250A2 (en) | 2006-01-23 | 2007-08-02 | Amira Pharmaceuticals, Inc. | Tricyclic inhibitors of 5-lipoxygenase |
US20070202159A1 (en) | 2006-02-02 | 2007-08-30 | Mathur Rajeev S | Pharmaceutical composition comprising stabilized statin particles |
ES2448424T3 (es) | 2006-02-07 | 2014-03-13 | Mochida Pharmaceutical Co., Ltd. | Composición para prevenir la recurrencia de accidente cerebrovascular |
JP5069448B2 (ja) | 2006-02-07 | 2012-11-07 | 持田製薬株式会社 | 脳卒中再発予防用組成物 |
JP4005104B2 (ja) | 2006-02-07 | 2007-11-07 | 持田製薬株式会社 | 脳卒中再発予防用組成物 |
WO2007095174A2 (en) | 2006-02-14 | 2007-08-23 | Intercept Pharmaceuticals, Inc. | Bile acid derivatives as fxr ligands for the prevention or treatment of fxr-mediated diseases or conditions |
WO2007098189A2 (en) | 2006-02-21 | 2007-08-30 | Critical Therapeutics, Inc. | New crystal forms and pharmaceutical compositions of (+) -r-zileuton |
JP2009529044A (ja) | 2006-03-03 | 2009-08-13 | モンサント テクノロジー エルエルシー | 心臓血管健康を改善するための手段 |
WO2007103557A2 (en) | 2006-03-09 | 2007-09-13 | Reliant Pharmaceuticals, Inc. | Coating capsules with active pharmaceutical ingredients |
US8784886B2 (en) | 2006-03-09 | 2014-07-22 | GlaxoSmithKline, LLC | Coating capsules with active pharmaceutical ingredients |
WO2007128801A1 (en) | 2006-05-08 | 2007-11-15 | Novartis Ag | Combination of organic compounds |
EP2777701A1 (en) | 2006-05-31 | 2014-09-17 | Mochida Pharmaceutical Co., Ltd. | Composition for preventing the occurrence of a cardiovascular event in multiple risk patient comprising the ethyl ester of all-cis-5,8,11,14,17-icosapentaenoic acid |
US20090042835A1 (en) | 2006-06-02 | 2009-02-12 | Davis Roger A | Compositions and methods for ameliorating hyperlipidemia |
AU2007254827A1 (en) | 2006-06-02 | 2007-12-13 | San Diego State University Research Foundation | Compositions and methods for ameliorating hyperlipidemia |
US20070292501A1 (en) | 2006-06-05 | 2007-12-20 | Udell Ronald G | Chewable soft gelatin capsules |
AU2007270135B9 (en) | 2006-07-05 | 2013-06-27 | Fermentalg | Production of ultrapure EPA and polar lipids from largely heterotrophic culture |
WO2008012329A2 (en) | 2006-07-28 | 2008-01-31 | V. Mane Fils | Seamless capsules containing high amounts of polyunsaturated fatty acids and a flavouring component |
JP5223177B2 (ja) | 2006-08-23 | 2013-06-26 | 地方独立行政法人北海道立総合研究機構 | アルミニウム回収用材料、同材料の製造方法及びアルミニウムの回収方法 |
CA2661404A1 (en) | 2006-09-05 | 2008-03-13 | Schering Corporation | Pharmaceutical combinations for lipid management and in the treatment of atherosclerosis and hepatic steatosis |
US20080085911A1 (en) | 2006-10-10 | 2008-04-10 | Reliant Pharmaceuticals, Inc. | Statin and omega-3 fatty acids for reduction of apo-b levels |
EA018734B1 (ru) | 2006-10-10 | 2013-10-30 | Релайэнт Фармасьютикалз, Инк. | СТАТИН И ОМЕГА-3 ЖИРНЫЕ КИСЛОТЫ ДЛЯ СНИЖЕНИЯ УРОВНЕЙ Apo-B |
EA200970374A1 (ru) * | 2006-10-13 | 2009-10-30 | Релайэнт Фармасьютикалз, Инк. | Лечение антиаритмическими средствами и омега-3 жирными кислотами и их комбинированным продуктом |
WO2008088415A1 (en) | 2006-10-18 | 2008-07-24 | Reliant Pharmaceuticals, Inc. | Omega-3 fatty acids for reduction of lp-pla2 levels |
US20080306154A1 (en) | 2006-11-03 | 2008-12-11 | My Svensson | Treatment and prevention of major adverse cardiovascular events or major coronary evens by administering Omega-3 fatty acids |
US20080125490A1 (en) | 2006-11-03 | 2008-05-29 | My Svensson | Treatment and prevention of cardiovascular disease in patients with chronic kidney disease by administering Omega-3 Fatty Acids |
US20080226758A1 (en) | 2006-11-28 | 2008-09-18 | Shixin Deng | Lipoxygenase and Cyclooxygenase Inhibition |
US20090042849A1 (en) | 2006-12-06 | 2009-02-12 | Yochai Birnbaum | Phosphorylation of 5-lipoxygenase at ser523 and uses thereof |
WO2008079398A1 (en) | 2006-12-21 | 2008-07-03 | Aegerion Pharmaceuticals, Inc. | Methods for treating obesity with a combination comprising a mtp inhibitor and a cholesterol absorption inhibitor |
EP2119443B1 (en) | 2007-01-17 | 2014-08-20 | Mochida Pharmaceutical Co., Ltd. | Composition for prevention or treatment of disease associated with thrombus or embolus |
CA2676485A1 (en) | 2007-01-23 | 2008-07-31 | Reddy Us Therapeutics, Inc. | Methods and compositions for the treatment of insulin resistance, diabetes, and diabetes-associated dyslipidemia |
US20080185198A1 (en) | 2007-02-02 | 2008-08-07 | Steven Mark Jones | Next generation hybrid III parallel/series hybrid system |
US20080249130A1 (en) | 2007-02-09 | 2008-10-09 | Sirtris Pharmaceuticals, Inc. | Gut microsomal triglyceride transport protein inhibitors |
DK2121576T3 (en) | 2007-02-15 | 2016-02-15 | Ct De Rech Sur Les Biotechnologies Marine | Polyunsaturated fatty acid monoglycerides, derivatives, and uses thereof |
CA2677036A1 (en) | 2007-03-06 | 2008-09-12 | Bioriginal Food & Science Corp. | Soft gelatin capsule shells containing oil soluble flavoring and methods of making the same |
WO2008115529A1 (en) | 2007-03-20 | 2008-09-25 | Reliant Pharmaceuticals, Inc. | Compositions comprising omega-3 fatty acids and cetp inhibitors |
US8048880B2 (en) | 2007-05-03 | 2011-11-01 | Anthera Pharmaceuticals, Inc. | Treatment of cardiovascular disease and dyslipidemia using secretory phospholipase A2 (SPLA2) inhibitors and SPLA2 inhibitor combination therapies |
WO2008145170A1 (de) | 2007-05-31 | 2008-12-04 | Siemens Aktiengesellschaft | Verfahren zum konfigurieren einer automatisierungsanlage |
US20080299187A1 (en) * | 2007-06-01 | 2008-12-04 | Joar Opheim | Substances for Reducing Occurence of Major Cardiac Events in Humans |
WO2008157740A2 (en) | 2007-06-20 | 2008-12-24 | Ironwood Pharmaceuticals, Inc. | Faah inhibitors |
EP2172225B1 (en) | 2007-06-29 | 2019-08-07 | Takeda Pharmaceutical Company Limited | Seamless capsule |
US20090092595A1 (en) | 2007-07-13 | 2009-04-09 | Regents Of The University Of California | Suppression of sPLA2-integrin binding for treating an inflammatory condition |
US20090062369A1 (en) | 2007-08-31 | 2009-03-05 | Joaquim Trias | Use of secretory phospholipase a2 (spla2) inhibitors to decrease spla2 levels |
US8969400B2 (en) | 2007-10-01 | 2015-03-03 | Duke University | Pharmaceutical compositions of 5-hydroxytryptophan and serotonin-enhancing compound |
US8361534B2 (en) | 2007-12-20 | 2013-01-29 | Abbott Laboratories | Stable nutritional powder |
BRPI0820584A2 (pt) | 2007-12-20 | 2015-07-14 | Abbott Lab | Pó nutricional estável |
EP2455071A1 (en) | 2008-01-10 | 2012-05-23 | Takeda Pharmaceutical Company Limited | Capsule Formulation |
US20090182049A1 (en) | 2008-01-16 | 2009-07-16 | Joar Arild Opheim | Pharmaceutical Composition and Method for Treating Hypertriglyceridemia and Hypercholesterolemia in Humans |
CN102099451B (zh) | 2008-05-15 | 2015-07-15 | 普罗诺瓦生物医药挪威公司 | 磷虾油提取方法 |
JPWO2009142242A1 (ja) | 2008-05-20 | 2011-09-29 | 持田製薬株式会社 | ハイリスク患者の心血管イベント予防用組成物 |
US20110082119A1 (en) | 2008-06-13 | 2011-04-07 | Takashi Yano | Prophylactic/ameliorating or therapeutic agent for non-alcoholic steatohepatitis |
US20110092592A1 (en) | 2008-06-13 | 2011-04-21 | Takashi Yano | Diagnosis and treatment of hepatic disorder |
JPWO2009154230A1 (ja) | 2008-06-17 | 2011-12-01 | 持田製薬株式会社 | 非アルコール性脂肪肝炎の予防/改善・治療薬 |
KR20110039249A (ko) | 2008-07-07 | 2011-04-15 | 모치다 세이야쿠 가부시키가이샤 | 지질 이상증의 개선 또는 치료약 |
PL2334295T3 (pl) | 2008-09-02 | 2017-12-29 | Amarin Pharmaceuticals Ltd | Kompozycja farmaceutyczna zawierająca kwas eikozapentaenowy i kwas nikotynowy oraz sposoby jej zastosowania |
EP2343066A4 (en) | 2008-09-30 | 2012-08-29 | Mochida Pharm Co Ltd | THERAPEUTIC AGENT FOR HEPATITIS C |
WO2010040012A1 (en) | 2008-10-01 | 2010-04-08 | Martek Biosciences Corporation | Compositions and methods for reducing triglyceride levels |
US20120035105A1 (en) | 2009-01-09 | 2012-02-09 | Sdg, Inc. | Insulin Therapies for the Treatment of Diabetes, Diabetes Related Ailments, and/or Diseases or Conditions Other Than Diabetes or Diabetes Related Ailments |
EP2405921A4 (en) | 2009-01-26 | 2013-05-22 | Protiva Biotherapeutics Inc | COMPOSITIONS AND METHODS FOR INACTIVATION OF APOLIPOPROTEIN C-III EXPRESSION |
SI3037089T1 (sl) | 2009-02-10 | 2020-03-31 | Amarin Pharmaceuticals Ireland Limited, | Etilester eikozapentaenojske kisline za zdravljenje hipertrigliceridemije |
US11395811B2 (en) | 2009-03-09 | 2022-07-26 | Pronova Biopharma Norge As | Compositions comprising a fatty acid oil mixture comprising EPA and DHA in free acid form and a surfactant, and methods and uses thereof |
US8241672B2 (en) | 2009-03-11 | 2012-08-14 | Stable Solutions Llc | Omega-3 enriched fish oil-in-water parenteral nutrition emulsions |
WO2010117951A1 (en) | 2009-04-06 | 2010-10-14 | The Regents Of The University Of California | Inhibitors of soluble epoxide hydrolase to inhibit or prevent niacin-induced flushing |
BRPI1014405A2 (pt) | 2009-04-29 | 2016-04-05 | Amarin Corp Plc | composições farmacêuticas compreendendo epa e um agente cardiovascular e métodos de seu uso |
EP3797591A1 (en) | 2009-04-29 | 2021-03-31 | Amarin Pharmaceuticals Ireland Limited | Stable pharmaceutical composition and methods of using same |
CA2762939C (en) | 2009-05-22 | 2017-07-18 | Mochida Phamaceutical Co., Ltd. | Self-emulsifying composition of .omega.3 fatty acid |
RU2402326C1 (ru) | 2009-06-22 | 2010-10-27 | Учреждение Российской академии медицинских наук Дальневосточный научный центр физиологии и патологии дыхания Сибирского отделения Российской академии медицинских наук (ДНЦ ФПД СО РАМН) | Способ коррекции инсулинорезистентности при метаболическом синдроме |
US8557275B2 (en) | 2009-07-23 | 2013-10-15 | U.S. Nutraceuticals, LLC | Composition and method to alleviate joint pain using a mixture of fish oil and fish oil derived, choline based, phospholipid bound fatty acid mixture including polyunsaturated EPA and DHA |
SG10201500431SA (en) | 2009-09-01 | 2015-03-30 | Catabasis Pharmaceuticals Inc | Fatty acid niacin conjugates and their uses |
SG10201405994UA (en) | 2009-09-23 | 2014-10-30 | Amarin Pharmaceuticals Ie Ltd | Pharmaceutical Composition Comprising Omega-3 Fatty Acid And Hydroxy-derivative Of A Statin And Methods Of Using Same |
EP2488022B1 (en) | 2009-10-16 | 2018-01-10 | Mochida Pharmaceutical Co., Ltd. | Compositions |
US9060981B2 (en) | 2009-10-16 | 2015-06-23 | Mochida Pharmaceutical Co., Ltd. | Marker associated with non-alcoholic steatohepatitis |
CN102821602B (zh) | 2010-01-08 | 2016-04-20 | 凯特贝希制药公司 | 脂肪酸富马酸酯衍生物及其用途 |
US20110178105A1 (en) | 2010-01-15 | 2011-07-21 | E.I. Du Pont De Nemours And Company | Clinical benefits of eicosapentaenoic acid in humans |
MX337315B (es) | 2010-03-04 | 2016-02-25 | Amarin Pharma Inc | Composiciones y metodos para tratar y/o prevenir enfermedad cardiovascular. |
US8846321B2 (en) | 2010-03-12 | 2014-09-30 | President And Fellows Of Harvard College | Association of levels of HDL-cholesterol apolipoprotein CIII with the risk of coronary heart disease and cardiovascular events |
US8663704B2 (en) | 2010-04-30 | 2014-03-04 | U.S. Nutraceuticals, LLC | Composition and method to improve blood lipid profiles and optionally reduce low density lipoprotein (LDL) per-oxidation in humans |
EP2566350B1 (en) | 2010-05-05 | 2016-05-04 | St. Giles Foods Limited | Edible compositions and methods of manufacturing edible compositions |
ES2710540T5 (es) | 2010-06-30 | 2022-08-26 | Mochida Pharm Co Ltd | Preparación de compuesto de ácido graso omega-3 |
WO2012032414A2 (en) | 2010-09-08 | 2012-03-15 | Pronova Biopharma Norge As | Compositions comprising a fatty acid oil mixture, a surfactant, and a statin |
US10557856B2 (en) | 2010-09-24 | 2020-02-11 | University Of Pittsburgh-Of The Commonwealth System Of Higher Education | Biomarkers of renal injury |
CA2815361A1 (en) | 2010-10-20 | 2012-04-26 | Glycomark, Inc. | Improved identification of pre-diabetes using a combination of mean glucose and 1,5-anhydroglucitol markers |
CN103338762B (zh) | 2010-11-09 | 2015-03-25 | 持田制药株式会社 | 血糖值上升抑制剂 |
US11712429B2 (en) | 2010-11-29 | 2023-08-01 | Amarin Pharmaceuticals Ireland Limited | Low eructation composition and methods for treating and/or preventing cardiovascular disease in a subject with fish allergy/hypersensitivity |
NZ712068A (en) | 2010-11-29 | 2017-03-31 | Amarin Pharmaceuticals Ie Ltd | Low eructation composition and methods for treating and/or preventing cardiovascular disease in a subject with fish allergy/hypersensitivity |
EP2471537A1 (en) | 2010-12-30 | 2012-07-04 | PregLem S.A. | Treatment of pain associated with dislocation of basal endometrium |
EP2502506A1 (en) | 2011-03-21 | 2012-09-26 | Abbott Laboratories | Methods for improving bone health in infants using long chain polyunsaturated fatty acids |
KR101310710B1 (ko) | 2011-03-23 | 2013-09-27 | 한미약품 주식회사 | 오메가-3 지방산 에스테르 및 HMG-CoA 환원효소 억제제를 포함하는 경구용 복합 조성물 |
US20120264824A1 (en) | 2011-04-15 | 2012-10-18 | Mochida Pharmaceutical Co., Ltd. | Compositions and methods for treating non-alcoholic steatohepatitis |
US8660662B2 (en) | 2011-04-22 | 2014-02-25 | Medtronic, Inc. | Low impedance, low modulus wire configurations for a medical device |
SG194671A1 (en) | 2011-04-27 | 2013-12-30 | Isis Pharmaceuticals Inc | Modulation of apolipoprotein ciii (apociii) expression |
EP2755646A4 (en) | 2011-09-15 | 2015-06-10 | Omthera Pharmaceuticals Inc | METHOD AND COMPOSITIONS FOR TREATING, REVERSING, INHIBITING OR PREVENTING RESISTANCE TO THROMBIA THERAPY |
EP2775837A4 (en) | 2011-11-07 | 2015-10-28 | Amarin Pharmaceuticals Ie Ltd | METHODS OF TREATING HYPERTRIGLYCERIDEMIA |
US11291643B2 (en) | 2011-11-07 | 2022-04-05 | Amarin Pharmaceuticals Ireland Limited | Methods of treating hypertriglyceridemia |
EP2792746A4 (en) | 2011-12-12 | 2015-09-16 | Nat Cerebral & Cardiovascular Ct | OLIGONUCLEOTIDE AND THERAPEUTIC FOR HYPERLIPIDEMIA WITH THIS AS AN ACTIVE SUBSTANCE |
ES2891473T3 (es) | 2012-01-06 | 2022-01-28 | Amarin Pharmaceuticals Ie Ltd | Composiciones y métodos para reducir los niveles de alta sensibilidad (hs-CRP) en un sujeto |
WO2013136277A1 (en) | 2012-03-13 | 2013-09-19 | Unimark Remedies Ltd. | Pharmaceutical compositions for treatment of cardiovascular diseases |
EP3072510B1 (en) | 2012-03-30 | 2019-05-08 | Micelle BioPharma, Inc. | Omega-3 fatty acid ester compositions |
KR20150028233A (ko) | 2012-05-07 | 2015-03-13 | 옴테라 파마슈티칼스, 인크. | 스타틴 및 오메가-3 지방산의 조성물 |
KR102125034B1 (ko) | 2012-05-15 | 2020-06-19 | 모치다 세이야쿠 가부시키가이샤 | 고혈중 고감도 c반응성 단백질 환자의 심혈관 질병 1차 예방제 |
EP2854951B1 (de) | 2012-05-30 | 2016-09-07 | Clariant International Ltd. | Zusammensetzung enthaltend aminosäuretenside, betaine und n-methyl-n-acylglucamine mit verbesserter schaumqualität und höherer viskosität |
US20140080850A1 (en) | 2012-06-05 | 2014-03-20 | Amarin Pharmaceuticals Ireland Limited | Pharmaceutical composition comprising an omega-3 fatty acid and a hydroxy-derivative of a statin and methods of using same |
US20130324607A1 (en) | 2012-06-05 | 2013-12-05 | Amarin Pharmaceuticals Ireland Limited | Methods of treating hypercholesterolemia |
CA2876139A1 (en) | 2012-06-07 | 2013-12-12 | President And Fellows Of Harvard College | Nanotherapeutics for drug targeting |
EP2861227A4 (en) | 2012-06-17 | 2016-01-27 | Matinas Biopharma Inc | OMEGA-3 PENTAIC ACID COMPOSITIONS AND METHODS OF USE |
HUE053111T2 (hu) | 2012-06-29 | 2021-06-28 | Amarin Pharmaceuticals Ie Ltd | Módszerek kardiovaszkuláris események veszélyének csökkentésére sztatin terápiával kezelt alanyban eikozapentaénsav-etilészter alkalmazásával |
CA2878267A1 (en) | 2012-06-29 | 2014-01-03 | Amarin Pharmaceuticals Ireland Limited | Methods of treating pediatric metabolic syndrome |
US20140004183A1 (en) | 2012-06-29 | 2014-01-02 | Amarin Pharmaceuticals Ireland Limited | Methods for treating cardiovascular disease in statin-tolerant subjects |
US20140005265A1 (en) | 2012-06-29 | 2014-01-02 | Amarin Pharmaceuticals Ireland Limited | Methods for treating hypertriglyceridemia |
US20150157593A1 (en) | 2012-06-29 | 2015-06-11 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing ldl-p |
CN104797249A (zh) | 2012-09-28 | 2015-07-22 | 持田制药株式会社 | 用于减少新发糖尿病的组合物 |
WO2014057522A1 (en) | 2012-10-12 | 2014-04-17 | Mochida Pharmaceutical Co., Ltd. | Compositions and methods for treating non-alcoholic steatohepatitis |
EP2719382A1 (en) | 2012-10-12 | 2014-04-16 | Mochida Pharmaceutical Co., Ltd. | Ethyl Eicosapentanoate and Pharmaceutical Compositions Comprising Ethyl Eicosapentanoate as an Active Ingredient for Use in the Treatment of Non-Alcoholic Steatohepatitis |
US20140142127A1 (en) | 2012-10-23 | 2014-05-22 | Almburg, Llc | Stable Compositions of HMG-COA Reductase Inhibitors and Omega-3 Oils |
WO2014074552A2 (en) | 2012-11-06 | 2014-05-15 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides without raising ldl-c levels in a subject on concomitant statin therapy |
US8703188B1 (en) * | 2012-11-19 | 2014-04-22 | Azanta A/S | Dispersible tablet |
US20140213648A1 (en) | 2012-12-31 | 2014-07-31 | Amarin Pharmaceuticals Ireland Limited | Methods of increasing epa blood levels |
US9814733B2 (en) | 2012-12-31 | 2017-11-14 | A,arin Pharmaceuticals Ireland Limited | Compositions comprising EPA and obeticholic acid and methods of use thereof |
US20140187633A1 (en) | 2012-12-31 | 2014-07-03 | Amarin Pharmaceuticals Ireland Limited | Methods of treating or preventing nonalcoholic steatohepatitis and/or primary biliary cirrhosis |
US9452151B2 (en) | 2013-02-06 | 2016-09-27 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing apolipoprotein C-III |
US20140221358A1 (en) | 2013-02-06 | 2014-08-07 | Amarin Pharmaceuticals Ireland Limited | Compositions comprising eicosapentaenoic acid and diazoxide and methods of use thereof |
US20140221452A1 (en) | 2013-02-06 | 2014-08-07 | Amarin Pharmaceuticals Ireland Limited | Compositions comprising eicosapentaenoic acid and 5-htp and methods of use thereof |
US20140221676A1 (en) | 2013-02-06 | 2014-08-07 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for treating and/or preventing cardiovascular disease |
US9624492B2 (en) | 2013-02-13 | 2017-04-18 | Amarin Pharmaceuticals Ireland Limited | Compositions comprising eicosapentaenoic acid and mipomersen and methods of use thereof |
US9662307B2 (en) | 2013-02-19 | 2017-05-30 | The Regents Of The University Of Colorado | Compositions comprising eicosapentaenoic acid and a hydroxyl compound and methods of use thereof |
US20140242216A1 (en) | 2013-02-24 | 2014-08-28 | Mead Johnson Nutrition Company | Amino Acid And Protein Hydrolysate Based Formulas With A Stable Emulsion System |
US20140249214A1 (en) | 2013-03-01 | 2014-09-04 | Amarin Pharmaceuticals Ireland Limited | Co-administration of warfarin and ethyl eicosapentaenoate |
US20140249225A1 (en) | 2013-03-01 | 2014-09-04 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing or preventing oxidative modification of membrane polyunsaturated fatty acids |
WO2014134466A1 (en) | 2013-03-01 | 2014-09-04 | Amarin Pharmaceuticals Ireland Limited. | Co-administration of atorvastatin and ethyl eicosapentaenoic acid or a derivative thereof |
US20140249220A1 (en) | 2013-03-01 | 2014-09-04 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for reducing a fatty acid desaturation index in a subject in need thereof |
US20140255537A1 (en) | 2013-03-11 | 2014-09-11 | Mead Johnson Nutrition Company | Nutritional Compositions Containing an Enriched Lipid Fraction and Uses Thereof |
US9661874B2 (en) | 2013-03-11 | 2017-05-30 | Mead Johnson Nutrition Company | Nutritional compositions containing structured fat globules and uses thereof |
US9283201B2 (en) | 2013-03-14 | 2016-03-15 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for treating or preventing obesity in a subject in need thereof |
US20140275252A1 (en) | 2013-03-14 | 2014-09-18 | Amarin Pharmaceuticals Ireland Limited | Methods of treating traumatic brain injury |
US20140271907A1 (en) | 2013-03-14 | 2014-09-18 | Amarin Pharmaceuticals Ireland Limited | Compositions comprising eicosapentaenoic acid and krill oil and methods of use thereof |
US20140271841A1 (en) | 2013-03-15 | 2014-09-18 | Amarin Pharmaceuticals Ireland Limited | Pharmaceutical composition comprising eicosapentaenoic acid and derivatives thereof and a statin |
US10441560B2 (en) | 2013-03-15 | 2019-10-15 | Mochida Pharmaceutical Co., Ltd. | Compositions and methods for treating non-alcoholic steatohepatitis |
EP2968245B1 (en) | 2013-03-15 | 2021-05-05 | Mochida Pharmaceutical Co., Ltd. | Compositions and methods for treating non-alcoholic steatohepatitis |
WO2014179325A1 (en) | 2013-04-29 | 2014-11-06 | Matinas Biopharma, Inc. | Omega-3 fatty acid formulations for use as pharmaceutical treatment |
KR102240429B1 (ko) | 2013-05-06 | 2021-04-15 | 한미약품 주식회사 | 로수바스타틴 또는 이의 약학적으로 허용되는 염이 함유된 필름 코팅층을 포함하는 복합 제형 |
US20140357717A1 (en) | 2013-06-04 | 2014-12-04 | Amarin Pharmaceuticals Ireland Limited | Methods of treating hypertriglyceridemia |
US10966968B2 (en) | 2013-06-06 | 2021-04-06 | Amarin Pharmaceuticals Ireland Limited | Co-administration of rosiglitazone and eicosapentaenoic acid or a derivative thereof |
US9663499B2 (en) | 2013-06-07 | 2017-05-30 | The California Institute For Biomedical Research | Small molecule inhibitors of fibrosis |
US20160135702A1 (en) | 2013-06-21 | 2016-05-19 | The Board Of Trustees Of The Leland Stanford Junior University | Techniques for Predicting Cardiac Arrhythmias Based on Signals from Leads of Electrocardiography |
ES2817527T3 (es) | 2013-07-18 | 2021-04-07 | Mochida Pharm Co Ltd | Composición autoemulsionante de ácidos grasos omega-3 |
ES2841344T3 (es) | 2013-07-18 | 2021-07-08 | Mochida Pharm Co Ltd | Composición autoemulsionante de ácidos grasos omega-3 |
US20150045431A1 (en) | 2013-08-06 | 2015-02-12 | Amarin Pharmaceuticals Ireland Limited | Methods of treating a cardiovascular disorder in a subject on apo-c3 modulating therapy |
US20150051282A1 (en) | 2013-08-14 | 2015-02-19 | Amarin Pharmaceuticals Ireland Limited | Methods of treating a cardiovascular disorder and/or joint pain in a subject on glucosamine therapy |
US20150065572A1 (en) | 2013-09-04 | 2015-03-05 | Amarin Pharmaceuticals Ireland Limited | Methods of treating or preventing prostate cancer |
US20150073050A1 (en) | 2013-09-09 | 2015-03-12 | Amarin Pharmaceuticals Ireland Limited | Co-administration of omeprazole and eicosapentaenoic acid or a derivative thereof |
WO2015053379A1 (en) | 2013-10-07 | 2015-04-16 | Mochida Pharmaceutical Co., Ltd. | Compositions and methods for treating non-alcoholic steatohepatitis |
US9585859B2 (en) | 2013-10-10 | 2017-03-07 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides without raising LDL-C levels in a subject on concomitant statin therapy |
WO2015066512A1 (en) | 2013-10-31 | 2015-05-07 | Amarin Pharmaceuticals Ireland Limited | Methods of treating hypertriglyceridemia |
DK3129018T3 (da) | 2014-04-11 | 2020-01-20 | Cymabay Therapeutics Inc | Behandling af NAFLD og NASH |
US10561631B2 (en) | 2014-06-11 | 2020-02-18 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing RLP-C |
WO2015195662A1 (en) | 2014-06-16 | 2015-12-23 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing or preventing oxidation of small dense ldl or membrane polyunsaturated fatty acids |
WO2016019223A1 (en) | 2014-08-01 | 2016-02-04 | Western Michigan University Research Foundation | Self-supported electronic devices |
JP6514720B2 (ja) | 2015-01-21 | 2019-05-15 | 持田製薬株式会社 | ω3脂肪酸の自己乳化組成物 |
WO2016117621A1 (ja) | 2015-01-21 | 2016-07-28 | 持田製薬株式会社 | ω3脂肪酸の自己乳化組成物 |
WO2016140949A1 (en) | 2015-03-02 | 2016-09-09 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing or preventing oxidative modification of membrane polyunsaturated fatty acids |
US20170151202A1 (en) | 2015-09-09 | 2017-06-01 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing or preventing oxidation of small dense ldl or membrane polyunsaturated fatty acids |
US10406130B2 (en) | 2016-03-15 | 2019-09-10 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing or preventing oxidation of small dense LDL or membrane polyunsaturated fatty acids |
PT3275438T (pt) | 2016-07-29 | 2021-01-25 | Kowa Co | Métodos de prevenção de eventos cardiovasculares em populações dislipidémicas de risco residual |
US11197870B2 (en) | 2016-11-10 | 2021-12-14 | Galmed Research And Development Ltd | Treatment for hepatic fibrosis |
WO2018213663A1 (en) | 2017-05-19 | 2018-11-22 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides in a subject having reduced kidney function |
US20190054058A1 (en) | 2017-08-15 | 2019-02-21 | Amarin Pharmaceuticals Ireland Limited | Methods of Treating or Preventing Bone Loss |
US20190054054A1 (en) | 2017-08-15 | 2019-02-21 | Amarin Pharmaceuticals Ireland Limited | Methods reducing or preventing oxidation of high density lipoprotein (HDL) |
US20190209506A1 (en) | 2018-01-09 | 2019-07-11 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing or preventing oxidation of ldl or lipid membranes in a subject in need thereof |
US11058661B2 (en) | 2018-03-02 | 2021-07-13 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides in a subject on concomitant statin therapy and having hsCRP levels of at least about 2 mg/L |
US20190275057A1 (en) | 2018-03-06 | 2019-09-12 | Amarin Pharmaceuticals Ireland Limited | Compositions and Methods for Lowering Triglycerides in a Subject with Reduced Kidney Function and Diabetes Mellitus |
BR112021002884A2 (pt) | 2018-08-17 | 2021-05-11 | Amarin Pharmaceuticals Ireland Limited | métodos para reduzir a necessidade de revascularização arterial periférica em um sujeito tratado com estatina |
PT4056176T (pt) * | 2018-09-24 | 2024-05-27 | Amarin Pharmaceuticals Ie Ltd | Métodos de redução do risco de eventos cardiovasculares num indivíduo |
CN113164426A (zh) | 2018-09-26 | 2021-07-23 | 阿马里纳药物爱尔兰有限公司 | 用于治疗或预防由暴露于空气污染引起的疾病和/或病症的组合物和方法 |
CA3126718A1 (en) | 2019-02-15 | 2020-08-20 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a statin-treated subject by increasing serum and plasma epa and dpa levels |
CN114144192A (zh) | 2019-08-01 | 2022-03-04 | 赢创运营有限公司 | 包含ω-3脂肪酸盐和来自乳香属物种的胶树脂提取物的制剂 |
EP4058141A4 (en) | 2019-11-12 | 2023-11-22 | Amarin Pharmaceuticals Ireland Limited | METHODS FOR REDUCING THE RISK OF CARDIOVASCULAR EVENTS IN A SUBJECT SUFFERING FROM ATRIAL FIBRILLATION AND/OR ATRIAL FLUTTER |
-
2010
- 2010-04-29 BR BRPI1014405A patent/BRPI1014405A2/pt not_active Application Discontinuation
- 2010-04-29 NZ NZ734905A patent/NZ734905A/en unknown
- 2010-04-29 EP EP20175804.2A patent/EP3791880A1/en active Pending
- 2010-04-29 NZ NZ720946A patent/NZ720946A/en unknown
- 2010-04-29 NZ NZ789295A patent/NZ789295A/en unknown
- 2010-04-29 CA CA2759176A patent/CA2759176C/en active Active
- 2010-04-29 US US13/124,628 patent/US20120093922A1/en not_active Abandoned
- 2010-04-29 MY MYPI2011005155A patent/MY173994A/en unknown
- 2010-04-29 NZ NZ624963A patent/NZ624963A/en unknown
- 2010-04-29 EP EP19156780.9A patent/EP3563842A1/en not_active Withdrawn
- 2010-04-29 KR KR1020117026224A patent/KR101357438B1/ko active IP Right Grant
- 2010-04-29 WO PCT/US2010/032948 patent/WO2010127099A2/en active Application Filing
- 2010-04-29 CN CN2010800192980A patent/CN102413825A/zh active Pending
- 2010-04-29 EP EP10770320.9A patent/EP2424521A4/en not_active Withdrawn
- 2010-04-29 RU RU2013106526A patent/RU2624506C2/ru active
- 2010-04-29 MY MYPI2016001750A patent/MY198422A/en unknown
- 2010-04-29 CN CN201610682334.0A patent/CN106822080A/zh active Pending
- 2010-04-29 AU AU2010241567A patent/AU2010241567B2/en active Active
- 2010-04-29 CN CN201710273241.7A patent/CN107233337A/zh active Pending
- 2010-04-29 US US13/266,085 patent/US11033523B2/en active Active
- 2010-04-29 RU RU2011148363/15A patent/RU2489145C1/ru active
- 2010-04-29 SG SG2011079415A patent/SG175390A1/en unknown
- 2010-04-29 MX MX2011011517A patent/MX2011011517A/es active IP Right Grant
- 2010-04-29 EP EP22152979.5A patent/EP4008327A1/en active Pending
- 2010-04-29 NZ NZ595789A patent/NZ595789A/en unknown
- 2010-04-29 CN CN201410136828.XA patent/CN104042617A/zh active Pending
- 2010-04-29 NZ NZ771180A patent/NZ771180A/en unknown
-
2011
- 2011-10-18 ZA ZA2011/07623A patent/ZA201107623B/en unknown
- 2011-10-28 MX MX2022009942A patent/MX2022009942A/es unknown
- 2011-10-28 MX MX2020004099A patent/MX2020004099A/es unknown
- 2011-11-29 CO CO11163910A patent/CO6470839A2/es not_active Application Discontinuation
-
2012
- 2012-03-12 US US13/417,899 patent/US8563608B2/en active Active
- 2012-03-13 US US13/418,591 patent/US20120172432A1/en not_active Abandoned
- 2012-07-02 US US13/540,319 patent/US8618166B2/en active Active
-
2013
- 2013-02-04 US US13/758,332 patent/US20130195972A1/en not_active Abandoned
- 2013-04-12 RU RU2013116807A patent/RU2648826C2/ru active
- 2013-05-20 US US13/898,447 patent/US8691871B2/en active Active
- 2013-05-20 US US13/898,457 patent/US8680144B2/en active Active
-
2014
- 2014-02-07 US US14/175,602 patent/US9056088B2/en active Active
- 2014-02-07 US US14/175,515 patent/US20140155455A1/en not_active Abandoned
- 2014-11-07 US US14/536,161 patent/US10888537B2/en active Active
-
2015
- 2015-03-17 HK HK15102705.5A patent/HK1202795A1/xx unknown
- 2015-05-05 US US14/704,329 patent/US9855237B2/en active Active
-
2016
- 2016-09-22 US US15/273,430 patent/US10220013B2/en active Active
-
2017
- 2017-06-19 RU RU2017121277A patent/RU2746945C2/ru active
- 2017-10-05 US US15/725,617 patent/US10265287B2/en active Active
- 2017-12-22 RU RU2022100434A patent/RU2022100434A/ru unknown
-
2018
- 2018-11-02 US US16/179,763 patent/US10940131B2/en active Active
-
2019
- 2019-02-25 US US16/284,543 patent/US10624870B2/en active Active
- 2019-04-19 US US16/389,317 patent/US10792267B2/en active Active
- 2019-12-10 US US16/709,492 patent/US10987331B2/en active Active
-
2020
- 2020-09-21 US US17/027,069 patent/US11154526B2/en active Active
- 2020-12-18 US US17/127,652 patent/US20210113509A1/en active Pending
- 2020-12-18 US US17/127,398 patent/US20210100765A1/en active Pending
- 2020-12-18 US US17/127,354 patent/US20210100764A1/en active Pending
-
2021
- 2021-03-22 US US17/208,091 patent/US20210212974A1/en active Pending
- 2021-08-03 US US17/393,213 patent/US20210379002A1/en not_active Abandoned
- 2021-12-01 US US17/457,160 patent/US11400069B2/en active Active
- 2021-12-01 US US17/457,126 patent/US11690820B2/en active Active
-
2022
- 2022-04-20 US US17/725,357 patent/US20220241234A1/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6620821B2 (en) * | 2000-06-15 | 2003-09-16 | Bristol-Myers Squibb Company | HMG-CoA reductase inhibitors and method |
US8410086B2 (en) * | 2009-06-15 | 2013-04-02 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides |
US8455472B2 (en) * | 2009-06-15 | 2013-06-04 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides without raising LDL-C levels in a subject on concomitant statin therapy |
Non-Patent Citations (6)
Title |
---|
Calabresi (Atherosclerosis (2000) 148:387-396). * |
Davidson (Clinical Therapeutics (2007) 29:1354-1367). * |
Hayashi et. al. (Current Therapeutic research (1995) 56:24-31). * |
Mori et. al. (Am. J. Clin. Nutr. (2000) 71:1085-1094). * |
Okumura et. al. (The American Journal of medical Sciences (2002) 324:247-253). * |
Saito et. al. (Atherosclerosis (2008) 135-140). * |
Cited By (196)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10314803B2 (en) | 2008-09-02 | 2019-06-11 | Amarin Pharmaceuticals Ireland Limited | Pharmaceutical composition comprising eicosapentaenoic acid and nicotinic acid and methods of using same |
US10624870B2 (en) | 2009-04-29 | 2020-04-21 | Amarin Pharmaceuticals Ireland Limited | Methods of treating mixed dyslipidemia |
US9056088B2 (en) | 2009-04-29 | 2015-06-16 | Amarin Pharmaceuticals Ireland Limited | Pharmaceutical compositions comprising fatty acids |
US9585856B2 (en) | 2009-04-29 | 2017-03-07 | Amarin Pharmaceuticals Ireland Limited | Stable pharmaceutical composition and methods of using same |
US10987331B2 (en) | 2009-04-29 | 2021-04-27 | Amarin Pharmaceuticals Ireland Limited | Methods of treating mixed dyslipidemia |
US9855237B2 (en) | 2009-04-29 | 2018-01-02 | Amarin Pharmaceuticals Ireland Limited | Methods of treating mixed dyslipidemia |
US10940131B2 (en) | 2009-04-29 | 2021-03-09 | Amarin Pharmaceuticals Ireland Limited | Methods of treating mixed dyslipidemia |
US10010517B2 (en) | 2009-04-29 | 2018-07-03 | Amarin Pharmaceuticals Ireland Limited | Stable pharmaceutical composition and methods of using same |
US10220013B2 (en) | 2009-04-29 | 2019-03-05 | Amarin Pharmaceuticals Ireland Limited | Methods of treating mixed dyslipidemia |
US11400069B2 (en) | 2009-04-29 | 2022-08-02 | Amarin Pharmaceuticals Ireland Limited | Methods of treating mixed dyslipidemia |
US9060982B2 (en) | 2009-04-29 | 2015-06-23 | Amarin Pharmaceuticals Ireland Limited | Stable pharmaceutical composition and methods of using same |
US9060983B2 (en) | 2009-04-29 | 2015-06-23 | Amarin Pharmaceuticals Ireland Limited | Stable pharmaceutical composition and methods of using same |
US9072715B2 (en) | 2009-04-29 | 2015-07-07 | Amarin Pharmaceuticals Ireland Limited | Stable pharmaceutical composition and methods of using same |
US10265287B2 (en) | 2009-04-29 | 2019-04-23 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing triglycerides and LDL-C |
US11213504B2 (en) | 2009-04-29 | 2022-01-04 | Amarin Pharmaceuticals Ireland Limited | Stable pharmaceutical composition and methods of using same |
US11154526B2 (en) | 2009-04-29 | 2021-10-26 | Amarin Pharmaceuticals Ireland Limited | Methods of treating mixed dyslipidemia |
US9138415B2 (en) | 2009-04-29 | 2015-09-22 | Amarin Pharmaceuticals Ireland Limited | Stable pharmaceutical composition and methods of using same |
US11147787B2 (en) | 2009-04-29 | 2021-10-19 | Amarin Pharmaceuticals Ireland Limited | Stable pharmaceutical composition and methods of using same |
US11103477B2 (en) | 2009-04-29 | 2021-08-31 | Amarin Pharmaceuticals Ireland Limited | Stable pharmaceutical composition and methods of using same |
US11033523B2 (en) | 2009-04-29 | 2021-06-15 | Amarin Pharmaceuticals Ireland Limited | Pharmaceutical compositions comprising EPA and a cardiovascular agent and methods of using the same |
US10449172B2 (en) | 2009-04-29 | 2019-10-22 | Amarin Pharmaceuticals Ireland Limited | Stable pharmaceutical composition and methods of using same |
US11690820B2 (en) | 2009-04-29 | 2023-07-04 | Amarin Pharmaceuticals Ireland Limited | Methods of treating mixed dyslipidemia |
US10792267B2 (en) | 2009-04-29 | 2020-10-06 | Amarin Pharmaceuticals Ireland Limited | Methods of treating mixed dyslipidemia |
US10842766B2 (en) | 2009-04-29 | 2020-11-24 | Amarin Pharmaceuticals Ireland Limited | Stable pharmaceutical composition and methods of using same |
US10888537B2 (en) | 2009-04-29 | 2021-01-12 | Amarin Pharmaceuticals Ireland Limited | Pharmaceutical compositions comprising omega-3 fatty acids |
US10881632B2 (en) | 2009-04-29 | 2021-01-05 | Amarin Pharmaceuticals Ireland Limited | Stable pharmaceutical composition and methods of using same |
US11439618B2 (en) | 2009-06-15 | 2022-09-13 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides |
US11464757B2 (en) | 2009-06-15 | 2022-10-11 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides |
US10842768B2 (en) | 2009-06-15 | 2020-11-24 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides |
US11007173B2 (en) | 2009-09-23 | 2021-05-18 | Amarin Pharmaceuticals Ireland Limited | Pharmaceutical composition comprising omega-3 fatty acid and hydroxy-derivative of a statin and methods of using same |
US10493058B2 (en) | 2009-09-23 | 2019-12-03 | Amarin Pharmaceuticals Ireland Limited | Pharmaceutical composition comprising omega-3 fatty acid and hydroxy-derivative of a statin and methods of using same |
US11712428B2 (en) | 2010-11-29 | 2023-08-01 | Amarin Pharmaceuticals Ireland Limited | Low eructation composition and methods for treating and/or preventing cardiovascular disease in a subject with fish allergy/hypersensitivity |
US11712429B2 (en) | 2010-11-29 | 2023-08-01 | Amarin Pharmaceuticals Ireland Limited | Low eructation composition and methods for treating and/or preventing cardiovascular disease in a subject with fish allergy/hypersensitivity |
US8952000B2 (en) * | 2011-02-16 | 2015-02-10 | Pivotal Therapeutics Inc. | Cholesterol absorption inhibitor and omega 3 fatty acids for the reduction of cholesterol and for the prevention or reduction of cardiovascular, cardiac and vascular events |
US20130040927A1 (en) * | 2011-02-16 | 2013-02-14 | Pivotal Therapeutics Inc. | Cholesterol absorption inhibitor and omega 3 fatty acids for the reduction of cholesterol and for the prevention or reduction of cardiovascular, cardiac and vascular events |
US20120302639A1 (en) * | 2011-02-16 | 2012-11-29 | Pivotal Therapeutics Inc. | Omega 3 formulations for treatment of risk factors for cardiovascular disease and protection against sudden death |
US9303038B2 (en) | 2011-09-06 | 2016-04-05 | Cellix Bio Private Limited | Compositions and methods for the treatment of epilepsy and neurological diseases |
US10632094B2 (en) | 2011-11-07 | 2020-04-28 | Amarin Pharmaceuticals Ireland Limited | Methods of treating hypertriglyceridemia |
US11291643B2 (en) | 2011-11-07 | 2022-04-05 | Amarin Pharmaceuticals Ireland Limited | Methods of treating hypertriglyceridemia |
US10537544B2 (en) | 2011-11-07 | 2020-01-21 | Amarin Pharmaceuticals Ireland Limited | Methods of treating hypertriglyceridemia |
US10973796B2 (en) | 2012-01-06 | 2021-04-13 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering levels of high-sensitivity C-reactive protein (hs-CRP) in a subject |
US9827219B2 (en) | 2012-01-06 | 2017-11-28 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering levels of high-sensitivity C-reactive protein (HS-CRP) in a subject |
US9375490B2 (en) | 2012-03-30 | 2016-06-28 | Sancilio & Company, Inc. | Stable micelles of fatty acid esters for the treatment of disease states |
US9480651B2 (en) | 2012-03-30 | 2016-11-01 | Sancilio & Company, Inc. | Omega-3 fatty acid ester compositions unitary pharmaceutical dosage forms |
US9364562B2 (en) | 2012-03-30 | 2016-06-14 | Sancilio & Company, Inc. | Functional foods and kits containing stable micelles of fatty acid esters |
US9364560B2 (en) | 2012-03-30 | 2016-06-14 | Sancilio & Company, Inc. | Stable micelles of fatty acid esters for the treatment of non-alcoholic fatty liver diseases |
US9364561B2 (en) | 2012-03-30 | 2016-06-14 | Sancilio & Company, Inc | Stable micelles of fatty acid esters for the treatment of macular degeneration and primary sclerosing cholangitis |
US9364559B2 (en) | 2012-03-30 | 2016-06-14 | Sancilio & Company, Inc. | Stable micelles of fatty acid esters |
US9370585B2 (en) | 2012-03-30 | 2016-06-21 | Sancilio & Company, Inc. | Stable micelles of mixed fatty acids |
US10898458B2 (en) | 2012-03-30 | 2021-01-26 | Micelle Biopharma, Inc. | Self-micellizing fatty acids and fatty acid ester compositions and their use in the treatment of disease states |
US9364558B2 (en) | 2012-03-30 | 2016-06-14 | Sancilio & Company, Inc. | Stable micelles of fatty acid esters for the treatment of cardiovascular disease |
US10287528B2 (en) | 2012-03-30 | 2019-05-14 | Micelle Biopharma, Inc. | Omega-3 fatty acid ester compositions |
US9302016B2 (en) | 2012-03-30 | 2016-04-05 | Sancilio & Company, Inc. | Omega-3 fatty acid ester compositions |
US10894027B2 (en) | 2012-03-30 | 2021-01-19 | Micelle Biopharma, Inc. | Sickle cell disease treatment utilizing omega-3 fatty acids |
US9302017B2 (en) | 2012-03-30 | 2016-04-05 | Sancilio & Company, Inc. | Omega-3 fatty acid ester compositions |
US9399634B2 (en) | 2012-05-07 | 2016-07-26 | Cellix Bio Private Limited | Compositions and methods for the treatment of depression |
US9738631B2 (en) | 2012-05-07 | 2017-08-22 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurological disorders |
US9642915B2 (en) | 2012-05-07 | 2017-05-09 | Cellix Bio Private Limited | Compositions and methods for the treatment of neuromuscular disorders and neurodegenerative diseases |
US10259885B2 (en) | 2012-05-08 | 2019-04-16 | Alderbio Holdings Llc | Anti-PCSK9 antibodies and use thereof |
US9309233B2 (en) | 2012-05-08 | 2016-04-12 | Cellix Bio Private Limited | Compositions and methods for the treatment of blood clotting disorders |
US9434704B2 (en) | 2012-05-08 | 2016-09-06 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurological degenerative disorders |
US9403826B2 (en) | 2012-05-08 | 2016-08-02 | Cellix Bio Private Limited | Compositions and methods for the treatment of inflammatory disorders |
US9255154B2 (en) | 2012-05-08 | 2016-02-09 | Alderbio Holdings, Llc | Anti-PCSK9 antibodies and use thereof |
US9266823B2 (en) | 2012-05-08 | 2016-02-23 | Cellix Bio Private Limited | Compositions and methods for the treatment of parkinson's disease |
US9522884B2 (en) | 2012-05-08 | 2016-12-20 | Cellix Bio Private Limited | Compositions and methods for the treatment of metabolic disorders |
US9499526B2 (en) | 2012-05-10 | 2016-11-22 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurologic diseases |
US9403857B2 (en) | 2012-05-10 | 2016-08-02 | Cellix Bio Private Limited | Compositions and methods for the treatment of metabolic syndrome |
US9339484B2 (en) | 2012-05-10 | 2016-05-17 | Cellix Bio Private Limited | Compositions and methods for the treatment of restless leg syndrome and fibromyalgia |
US9321775B2 (en) | 2012-05-10 | 2016-04-26 | Cellix Bio Private Limited | Compositions and methods for the treatment of moderate to severe pain |
US9315461B2 (en) | 2012-05-10 | 2016-04-19 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurologic diseases |
US9394288B2 (en) | 2012-05-10 | 2016-07-19 | Cellix Bio Private Limited | Compositions and methods for the treatment of asthma and allergy |
US9242939B2 (en) | 2012-05-10 | 2016-01-26 | Cellix Bio Private Limited | Compositions and methods for the treatment of respiratory disorders |
US9315478B2 (en) | 2012-05-10 | 2016-04-19 | Cellix Bio Private Limited | Compositions and methods for the treatment of metabolic syndrome |
US9573927B2 (en) | 2012-05-10 | 2017-02-21 | Cellix Bio Private Limited | Compositions and methods for the treatment of severe pain |
US9499527B2 (en) | 2012-05-10 | 2016-11-22 | Cellix Bio Private Limited | Compositions and methods for the treatment of familial amyloid polyneuropathy |
US9346742B2 (en) | 2012-05-10 | 2016-05-24 | Cellix Bio Private Limited | Compositions and methods for the treatment of fibromyalgia pain |
US9233161B2 (en) | 2012-05-10 | 2016-01-12 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurological conditions |
US9273061B2 (en) | 2012-05-10 | 2016-03-01 | Cellix Bio Private Limited | Compositions and methods for the treatment of chronic pain |
US9580383B2 (en) | 2012-05-23 | 2017-02-28 | Cellix Bio Private Limited | Compositions and methods for the treatment of multiple sclerosis |
US9765020B2 (en) | 2012-05-23 | 2017-09-19 | Cellix Bio Private Limited | Dichlorophenyl-imino compounds and compositions, and methods for the treatment of mucositis |
US9227974B2 (en) | 2012-05-23 | 2016-01-05 | Cellex Bio Private Limited | Compositions and methods for the treatment of respiratory disorders |
US9498461B2 (en) | 2012-05-23 | 2016-11-22 | Cellix Bio Private Limited | Compositions and methods for the treatment of inflammatory bowel disease |
US9492409B2 (en) | 2012-05-23 | 2016-11-15 | Cellix Bio Private Limited | Compositions and methods for the treatment of local pain |
US9434729B2 (en) | 2012-05-23 | 2016-09-06 | Cellix Bio Private Limited | Compositions and methods for the treatment of periodontitis and rheumatoid arthritis |
US10058521B2 (en) | 2012-06-17 | 2018-08-28 | Matinas Biopharma Inc. | Omega-3 pentaenoic acid compositions and methods of use |
US8906964B2 (en) | 2012-06-17 | 2014-12-09 | Matinas Biopharma, Inc. | Methods of administering compositions comprising docosapentaenoic acid |
WO2013192109A1 (en) * | 2012-06-17 | 2013-12-27 | Matinas Biopharma, Inc. | Omega-3 pentaenoic acid compositions and methods of use |
US9693986B2 (en) | 2012-06-29 | 2017-07-04 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject on statin therapy |
US10278935B2 (en) | 2012-06-29 | 2019-05-07 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject on statin therapy |
US9918955B2 (en) | 2012-06-29 | 2018-03-20 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject on statin therapy |
US9918954B2 (en) | 2012-06-29 | 2018-03-20 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject on statin therapy |
US9603826B2 (en) | 2012-06-29 | 2017-03-28 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject on statin therapy |
US10278936B2 (en) | 2012-06-29 | 2019-05-07 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject on statin therapy |
US10383840B2 (en) | 2012-06-29 | 2019-08-20 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject at risk for cardiovascular disease |
US10016386B2 (en) | 2012-06-29 | 2018-07-10 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject on statin therapy |
US9693985B2 (en) | 2012-06-29 | 2017-07-04 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject on statin therapy |
US10792270B2 (en) | 2012-06-29 | 2020-10-06 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject at risk for cardiovascular disease |
US9693984B2 (en) | 2012-06-29 | 2017-07-04 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject on statin therapy |
US10576054B1 (en) | 2012-06-29 | 2020-03-03 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject at risk for cardiovascular disease |
US10278937B2 (en) | 2012-06-29 | 2019-05-07 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject on statin therapy |
US10568861B1 (en) | 2012-06-29 | 2020-02-25 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject at risk for cardiovascular disease |
US10555924B2 (en) | 2012-06-29 | 2020-02-11 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject at risk for cardiovascular disease |
US10278939B2 (en) | 2012-06-29 | 2019-05-07 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject on statin therapy |
US9623001B2 (en) | 2012-06-29 | 2017-04-18 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject on statin therapy |
US10555925B1 (en) | 2012-06-29 | 2020-02-11 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject at risk for cardiovascular disease |
US10894028B2 (en) | 2012-06-29 | 2021-01-19 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject at risk for cardiovascular disease |
US10278938B2 (en) | 2012-06-29 | 2019-05-07 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject on statin therapy |
US9610272B2 (en) | 2012-06-29 | 2017-04-04 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of a cardiovascular event in a subject on statin therapy |
US9403793B2 (en) | 2012-07-03 | 2016-08-02 | Cellix Bio Private Limited | Compositions and methods for the treatment of moderate to severe pain |
US9187427B2 (en) | 2012-08-03 | 2015-11-17 | Cellix Bio Private Limited | N-substituted nicotinamide compounds and compositions for the treatment migraine and neurologic diseases |
US9624168B2 (en) | 2012-09-06 | 2017-04-18 | Cellix Bio Private Limited | Compositions and methods for the treatment inflammation and lipid disorders |
US9670153B2 (en) | 2012-09-08 | 2017-06-06 | Cellix Bio Private Limited | Compositions and methods for the treatment of inflammation and lipid disorders |
US11229618B2 (en) | 2012-11-06 | 2022-01-25 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides without raising LDL-C levels in a subject on concomitant statin therapy |
US11179362B2 (en) | 2012-11-06 | 2021-11-23 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides without raising LDL-C levels in a subject on concomitant statin therapy |
WO2014084433A1 (ko) * | 2012-11-30 | 2014-06-05 | 경상대학교 산학협력단 | 퍼옥시좀 증식인자 활성화 수용체 델타 작용물질을 유효성분으로 함유하는 심근경색후 심근상처치유 촉진용 조성물 |
US11141399B2 (en) | 2012-12-31 | 2021-10-12 | Amarin Pharmaceuticals Ireland Limited | Methods of treating or preventing nonalcoholic steatohepatitis and/or primary biliary cirrhosis |
US9814733B2 (en) | 2012-12-31 | 2017-11-14 | A,arin Pharmaceuticals Ireland Limited | Compositions comprising EPA and obeticholic acid and methods of use thereof |
US10265290B2 (en) | 2013-02-06 | 2019-04-23 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing apolipoprotein C-III |
US10166209B2 (en) | 2013-02-06 | 2019-01-01 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing apolipoprotein C-III |
US9452151B2 (en) | 2013-02-06 | 2016-09-27 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing apolipoprotein C-III |
US11185525B2 (en) | 2013-02-06 | 2021-11-30 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing apolipoprotein C-III |
US10675263B2 (en) | 2013-02-06 | 2020-06-09 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing apolipoprotein C-III |
US10610508B2 (en) | 2013-02-06 | 2020-04-07 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing apolipoprotein C-III |
US10973797B2 (en) | 2013-02-06 | 2021-04-13 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing apolipoprotein c-III |
US10167467B2 (en) | 2013-02-13 | 2019-01-01 | Amarin Pharmaceuticals Ireland Limited | Compositions comprising eicosapentaenoic acid and mipomersen and methods of use thereof |
US10851374B2 (en) | 2013-02-13 | 2020-12-01 | Amarin Pharmaceuticals Ireland Limited | Compositions comprising eicosapentaenoic acid and mipomersen and methods of use thereof |
US9624492B2 (en) | 2013-02-13 | 2017-04-18 | Amarin Pharmaceuticals Ireland Limited | Compositions comprising eicosapentaenoic acid and mipomersen and methods of use thereof |
US9662307B2 (en) | 2013-02-19 | 2017-05-30 | The Regents Of The University Of Colorado | Compositions comprising eicosapentaenoic acid and a hydroxyl compound and methods of use thereof |
US9855240B2 (en) | 2013-02-19 | 2018-01-02 | Amarin Pharmaceuticals Ireland Limited | Compositions comprising eicosapentaenoic acid and a hydroxyl compound and methods of use thereof |
WO2014158256A1 (en) * | 2013-03-13 | 2014-10-02 | Matinas Biopharma Inc. | Omega-3 pentaenoic acid compositions and methods of use |
WO2014143272A1 (en) * | 2013-03-13 | 2014-09-18 | Matinas Biopharma Inc. | Omega-3 pentaenoic acid compositions and methods of use |
US10206898B2 (en) | 2013-03-14 | 2019-02-19 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for treating or preventing obesity in a subject in need thereof |
US9283201B2 (en) | 2013-03-14 | 2016-03-15 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for treating or preventing obesity in a subject in need thereof |
US11547710B2 (en) | 2013-03-15 | 2023-01-10 | Amarin Pharmaceuticals Ireland Limited | Pharmaceutical composition comprising eicosapentaenoic acid and derivatives thereof and a statin |
US11549142B2 (en) | 2013-03-27 | 2023-01-10 | Hoffmann-La Roche Inc. | CETP inhibitors for therapeutic use |
US10711303B2 (en) | 2013-03-27 | 2020-07-14 | Hoffman-La Roche Inc. | CETP inhibitors for therapeutic use |
US9909178B2 (en) | 2013-03-27 | 2018-03-06 | Hoffmann-La Roche Inc. | Dalcetrapib for therapeutic use |
US9333187B1 (en) | 2013-05-15 | 2016-05-10 | Cellix Bio Private Limited | Compositions and methods for the treatment of inflammatory bowel disease |
US9174931B2 (en) | 2013-06-04 | 2015-11-03 | Cellix Bio Private Limited | Compositions for the treatment of diabetes and pre-diabetes |
US10966968B2 (en) | 2013-06-06 | 2021-04-06 | Amarin Pharmaceuticals Ireland Limited | Co-administration of rosiglitazone and eicosapentaenoic acid or a derivative thereof |
US10888539B2 (en) | 2013-09-04 | 2021-01-12 | Amarin Pharmaceuticals Ireland Limited | Methods of treating or preventing prostate cancer |
US10722485B2 (en) * | 2013-10-10 | 2020-07-28 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides without raising LDL-C levels in a subject on concomitant statin therapy |
US10292959B2 (en) * | 2013-10-10 | 2019-05-21 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides without raising LDL-C levels in a subject on concomitant statin therapy |
US20220323394A1 (en) * | 2013-10-10 | 2022-10-13 | Amarin Pharmaceuticals Ireland Limited | Compositions and Methods for Lowering Triglycerides Without Raising LDL-C Levels in a Subject on Concomitant Statin Therapy |
US11285127B2 (en) | 2013-10-10 | 2022-03-29 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides without raising LDL-C levels in a subject on concomitant statin therapy |
US9585859B2 (en) * | 2013-10-10 | 2017-03-07 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides without raising LDL-C levels in a subject on concomitant statin therapy |
US20150164850A1 (en) * | 2013-10-10 | 2015-06-18 | Amarin Pharmaceuticals Ireland Limited | Compositions and Methods for Lowering Triglycerides Without Raising LDL-C Levels in a Subject on Concomitant Statin Therapy |
US20190282533A1 (en) * | 2013-10-10 | 2019-09-19 | Amarin Pharmaceuticals Ireland Limited | Compositions and Methods for Lowering Triglycerides Without Raising LDL-C Levels in a Subject on Concomitant Statin Therapy |
US9840472B2 (en) | 2013-12-07 | 2017-12-12 | Cellix Bio Private Limited | Compositions and methods for the treatment of mucositis |
US11052063B2 (en) | 2014-06-11 | 2021-07-06 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing RLP-C |
US10561631B2 (en) | 2014-06-11 | 2020-02-18 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing RLP-C |
US11446269B2 (en) | 2014-06-16 | 2022-09-20 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing or preventing oxidation of small dense LDL or membrane polyunsaturated fatty acids |
US10172818B2 (en) | 2014-06-16 | 2019-01-08 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing or preventing oxidation of small dense LDL or membrane polyunsaturated fatty acids |
US11401554B2 (en) | 2014-07-30 | 2022-08-02 | Hoffman-La Roche Inc. | Genetic markers for predicting responsiveness to therapy with HDL-raising or HDL mimicking agent |
US10584385B2 (en) | 2014-07-30 | 2020-03-10 | Hoffmann-La Roche Inc. | Genetic markers for predicting responsiveness to therapy with HDL-raising or HDL mimicking agent |
US9771355B2 (en) | 2014-09-26 | 2017-09-26 | Cellix Bio Private Limited | Compositions and methods for the treatment of epilepsy and neurological disorders |
US9988340B2 (en) | 2014-09-29 | 2018-06-05 | Cellix Bio Private Limited | Compositions and methods for the treatment of multiple sclerosis |
US9102649B1 (en) | 2014-09-29 | 2015-08-11 | Mahesh Kandula | Compositions and methods for the treatment of multiple sclerosis |
US9725404B2 (en) | 2014-10-27 | 2017-08-08 | Cellix Bio Private Limited | Compositions and methods for the treatment of multiple sclerosis |
US9321716B1 (en) | 2014-11-05 | 2016-04-26 | Cellix Bio Private Limited | Compositions and methods for the treatment of metabolic syndrome |
US9290486B1 (en) | 2014-11-05 | 2016-03-22 | Cellix Bio Private Limited | Compositions and methods for the treatment of epilepsy |
US9173877B1 (en) | 2014-11-05 | 2015-11-03 | Cellix Bio Private Limited | Compositions and methods for the treatment of local pain |
US10208014B2 (en) | 2014-11-05 | 2019-02-19 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurological disorders |
US9284287B1 (en) | 2014-11-05 | 2016-03-15 | Cellix Bio Private Limited | Compositions and methods for the suppression of carbonic anhydrase activity |
US9175008B1 (en) | 2014-11-05 | 2015-11-03 | Cellix Bio Private Limited | Prodrugs of anti-platelet agents |
US9108942B1 (en) | 2014-11-05 | 2015-08-18 | Mahesh Kandula | Compositions and methods for the treatment of moderate to severe pain |
US9150557B1 (en) | 2014-11-05 | 2015-10-06 | Cellix Bio Private Limited | Compositions and methods for the treatment of hyperglycemia |
US9932294B2 (en) | 2014-12-01 | 2018-04-03 | Cellix Bio Private Limited | Compositions and methods for the treatment of multiple sclerosis |
US9206111B1 (en) | 2014-12-17 | 2015-12-08 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurological diseases |
US9096537B1 (en) | 2014-12-31 | 2015-08-04 | Mahesh Kandula | Compositions and methods for the treatment of mucositis |
US10227301B2 (en) | 2015-01-06 | 2019-03-12 | Cellix Bio Private Limited | Compositions and methods for the treatment of inflammation and pain |
US10343994B2 (en) | 2015-01-06 | 2019-07-09 | Mahesh Kandula | Compositions and methods for the treatment of inflammation and pain |
US10406130B2 (en) | 2016-03-15 | 2019-09-10 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing or preventing oxidation of small dense LDL or membrane polyunsaturated fatty acids |
US10842765B2 (en) | 2016-03-15 | 2020-11-24 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing or preventing oxidation of small dense ldl or membrane polyunsaturated fatty acids |
US10858422B2 (en) | 2016-05-31 | 2020-12-08 | Abcentra, Llc | Methods for treating systemic lupus erythematosus with an anti-apolipoprotein B antibody |
US10434141B2 (en) | 2016-05-31 | 2019-10-08 | Abcentra, Llc | Methods for treating systemic lupus erythematosus with an anti-apolipoprotein B antibody |
US10966951B2 (en) | 2017-05-19 | 2021-04-06 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides in a subject having reduced kidney function |
WO2019008101A1 (en) | 2017-07-06 | 2019-01-10 | Evonik Technochemie Gmbh | ENTERICALLY COATED SOLID DOSAGE FORM COMPRISING AMINO ACIDS SALTS OF OMEGA-3 FATTY ACIDS |
WO2019034698A1 (en) | 2017-08-15 | 2019-02-21 | Evonik Technochemie Gmbh | TABLET WITH HIGH ACTIVE INGREDIENT CONTENT OF OMEGA-3 FATTY ACID AMINO ACID SALTS |
CN111712240A (zh) * | 2017-12-06 | 2020-09-25 | 巴斯夫股份公司 | 用于治疗非酒精性脂肪性肝炎的脂肪酸衍生物 |
US11058661B2 (en) | 2018-03-02 | 2021-07-13 | Amarin Pharmaceuticals Ireland Limited | Compositions and methods for lowering triglycerides in a subject on concomitant statin therapy and having hsCRP levels of at least about 2 mg/L |
US11369582B2 (en) | 2018-09-24 | 2022-06-28 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of cardiovascular events in a subject |
US11717504B2 (en) | 2018-09-24 | 2023-08-08 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of cardiovascular events in a subject |
US10786478B2 (en) | 2018-09-24 | 2020-09-29 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of cardiovascular events in a subject |
US10668042B2 (en) | 2018-09-24 | 2020-06-02 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of cardiovascular events in a subject |
US11298333B1 (en) | 2018-09-24 | 2022-04-12 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of cardiovascular events in a subject |
US11000499B2 (en) | 2018-09-24 | 2021-05-11 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of cardiovascular events in a subject |
US11116742B2 (en) | 2018-09-24 | 2021-09-14 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of cardiovascular events in a subject |
US11116743B2 (en) | 2018-09-24 | 2021-09-14 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of cardiovascular events in a subject |
WO2021023849A1 (en) | 2019-08-08 | 2021-02-11 | Evonik Operations Gmbh | Down streaming process for the production of polyunsaturated fatty acid salts |
WO2021023857A1 (en) | 2019-08-08 | 2021-02-11 | Evonik Operations Gmbh | Solubility enhancement of poorly soluble actives |
US20220016025A1 (en) * | 2020-07-08 | 2022-01-20 | Vinayak Dinesh DENDUKURI | Formulations of nebivolol |
US20230390194A1 (en) * | 2020-07-08 | 2023-12-07 | Novick Bio Sciences Pvt Ltd | Formulations of nebivolol |
WO2022032077A3 (en) * | 2020-08-06 | 2022-03-10 | Redux Therapeutics, Llc | Compositions and methods for treating metabolic dysregulation |
US11986452B2 (en) | 2021-04-21 | 2024-05-21 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of heart failure |
WO2024102429A1 (en) * | 2022-11-10 | 2024-05-16 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing risks of cardiovascular events in subjects with low baseline epa:aa ratio |
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US11690820B2 (en) | Methods of treating mixed dyslipidemia | |
AU2020202913A1 (en) | Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same | |
NZ752610B2 (en) | Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: AMARIN CORPORATION PLC., IRELAND Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:MANKU, MEHAR;ROWE, JONATHAN;SIGNING DATES FROM 20091007 TO 20100105;REEL/FRAME:028291/0129 |
|
AS | Assignment |
Owner name: AMARIN PHARMACEUTICALS IRELAND LIMITED, IRELAND Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:AMARIN CORPORATION PLC;REEL/FRAME:028295/0289 Effective date: 20120313 |
|
AS | Assignment |
Owner name: BIOPHARMA SECURED DEBT FUND II HOLDINGS CAYMAN LP, Free format text: SECURITY AGREEMENT;ASSIGNOR:AMARIN PHARMACEUTICALS IRELAND LIMITED;REEL/FRAME:029499/0087 Effective date: 20121219 Owner name: BIOPHARMA SECURED DEBT FUND II HOLDINGS CAYMAN LP, CAYMAN ISLANDS Free format text: SECURITY AGREEMENT;ASSIGNOR:AMARIN PHARMACEUTICALS IRELAND LIMITED;REEL/FRAME:029499/0087 Effective date: 20121219 |
|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |
|
AS | Assignment |
Owner name: CPPIB CREDIT EUROPE S.A R.L., LUXEMBOURG Free format text: PATENT SECURITY ASSIGNMENT AND ASSUMPTION AGREEMENT;ASSIGNOR:BIOPHARMA SECURED DEBT FUND II HOLDINGS CAYMAN LP;REEL/FRAME:044956/0395 Effective date: 20171220 |
|
AS | Assignment |
Owner name: CPPIB CREDIT EUROPE S.A R.L., LUXEMBOURG Free format text: SECURITY INTEREST;ASSIGNOR:AMARIN PHARMACEUTICALS IRELAND LIMITED;REEL/FRAME:044938/0257 Effective date: 20171220 |
|
AS | Assignment |
Owner name: AMARIN PHARMACEUTICALS IRELAND LIMITED, IRELAND Free format text: RELEASE BY SECURED PARTY;ASSIGNOR:CPPIB CREDIT EUROPE S.A R.L.;REEL/FRAME:054484/0552 Effective date: 20201119 |