PL1830869T3 - Sposób leczenia lub profilaktyki - Google Patents
Sposób leczenia lub profilaktykiInfo
- Publication number
- PL1830869T3 PL1830869T3 PL05821524T PL05821524T PL1830869T3 PL 1830869 T3 PL1830869 T3 PL 1830869T3 PL 05821524 T PL05821524 T PL 05821524T PL 05821524 T PL05821524 T PL 05821524T PL 1830869 T3 PL1830869 T3 PL 1830869T3
- Authority
- PL
- Poland
- Prior art keywords
- prophylaxis
- treatment
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/08—Peptides having 5 to 11 amino acids
-
- 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
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- A61P25/06—Antimigraine agents
-
- 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
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/88—Oxygen atoms
- C07D239/90—Oxygen atoms with acyclic radicals attached in position 2 or 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/74—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving hormones or other non-cytokine intercellular protein regulatory factors such as growth factors, including receptors to hormones and growth factors
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2500/00—Screening for compounds of potential therapeutic value
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2004907332A AU2004907332A0 (en) | 2004-12-24 | Method of Treatment or Prophylaxis | |
EP20050821524 EP1830869B1 (en) | 2004-12-24 | 2005-12-23 | Method of treatment or prophylaxis |
PCT/AU2005/001975 WO2006066361A1 (en) | 2004-12-24 | 2005-12-23 | Method of treatment or prophylaxis |
Publications (1)
Publication Number | Publication Date |
---|---|
PL1830869T3 true PL1830869T3 (pl) | 2013-11-29 |
Family
ID=36601295
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL05821524T PL1830869T3 (pl) | 2004-12-24 | 2005-12-23 | Sposób leczenia lub profilaktyki |
Country Status (17)
Country | Link |
---|---|
US (5) | US7795275B2 (pl) |
EP (3) | EP2650011A1 (pl) |
JP (1) | JP4966202B2 (pl) |
CN (3) | CN101087619B (pl) |
CY (1) | CY1114424T1 (pl) |
DK (1) | DK1830869T3 (pl) |
ES (1) | ES2425567T3 (pl) |
HK (1) | HK1103364A1 (pl) |
HR (1) | HRP20130738T1 (pl) |
ME (1) | ME01597B (pl) |
NZ (1) | NZ555334A (pl) |
PL (1) | PL1830869T3 (pl) |
PT (1) | PT1830869E (pl) |
RS (1) | RS52927B (pl) |
SI (1) | SI1830869T1 (pl) |
WO (1) | WO2006066361A1 (pl) |
ZA (3) | ZA200704909B (pl) |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2650011A1 (en) * | 2004-12-24 | 2013-10-16 | Spinifex Pharmaceuticals Pty Ltd | Method of treatment or prophylaxis |
US8551950B2 (en) | 2006-03-20 | 2013-10-08 | Spinifex Pharmaceuticals Pty Ltd | Method of treatment or prophylaxis of inflammatory pain |
CN101522676A (zh) * | 2006-10-05 | 2009-09-02 | Cv医药有限公司 | 用作硬脂酰-CoA脱氢酶抑制剂的双环含氮杂环化合物 |
US20080255161A1 (en) * | 2007-04-11 | 2008-10-16 | Dmitry Koltun | 3-HYDROQUINAZOLIN-4-ONE DERIVATIVES FOR USE AS STEAROYL CoA DESATURASE INHIBITORS |
US20090105283A1 (en) * | 2007-04-11 | 2009-04-23 | Dmitry Koltun | 3-HYDROQUINAZOLIN-4-ONE DERIVATIVES FOR USE AS STEAROYL CoA DESATURASE INHIBITORS |
US7828840B2 (en) | 2007-11-15 | 2010-11-09 | Med Institute, Inc. | Medical devices and methods for local delivery of angiotensin II type 2 receptor antagonists |
WO2010056230A1 (en) * | 2008-10-15 | 2010-05-20 | Cv Therapeutics, Inc. | 3-hydroquinazolin-4-one derivatives for use as stearoyl coa desaturase inhibitors |
WO2010045374A1 (en) * | 2008-10-15 | 2010-04-22 | Gilead Palo Alto, Inc. | 3-hydroquinazolin-4-one derivatives for use as stearoyl coa desaturase inhibitors |
AU2011207104C1 (en) * | 2010-01-19 | 2015-10-08 | Novartis Ag | Methods and compositions for improved nerve conduction velocity |
DE102010013075A1 (de) | 2010-03-26 | 2011-09-29 | B. Braun Melsungen Ag | Antimikrobielle Wundauflage |
GB201007286D0 (en) | 2010-04-30 | 2010-06-16 | Astex Therapeutics Ltd | New compounds |
NZ708529A (en) * | 2010-07-21 | 2016-11-25 | Novartis Ag | Salt and solvates of a tetrahydroisoquinoline derivative |
GB201020179D0 (en) | 2010-11-29 | 2011-01-12 | Astex Therapeutics Ltd | New compounds |
EP2748166B1 (en) | 2011-08-23 | 2018-07-11 | Asana BioSciences, LLC | Pyrimido-pyridazinone compounds and use thereof |
GB201118654D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
GB201118652D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
GB201118675D0 (en) | 2011-10-28 | 2011-12-14 | Astex Therapeutics Ltd | New compounds |
GB201118656D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
CN107011229B (zh) | 2012-01-06 | 2019-11-05 | 诺华股份有限公司 | 杂环化合物和它们的使用方法 |
ES2798289T3 (es) | 2012-01-25 | 2020-12-10 | Novartis Ag | Compuestos heterocíclicos y métodos para su uso |
AU2013202978B2 (en) | 2012-01-25 | 2016-05-19 | Novartis Ag | Heterocyclic compounds and methods for their use |
GB201209613D0 (en) | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
GB201209609D0 (en) | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
GB201307577D0 (en) | 2013-04-26 | 2013-06-12 | Astex Therapeutics Ltd | New compounds |
WO2015003223A1 (en) | 2013-07-08 | 2015-01-15 | Spinifex Pharmaceuticals Pty Ltd | Heterocyclic compounds and methods of their use |
KR102361200B1 (ko) * | 2013-09-30 | 2022-02-09 | 에프엠씨 코포레이션 | 발포 제형 및 전달 장치 |
WO2015109210A1 (en) | 2014-01-17 | 2015-07-23 | Cardioxyl Pharmaceuticals, Inc. | N-hydroxymethanesulfonamide nitroxyl donors |
JO3512B1 (ar) | 2014-03-26 | 2020-07-05 | Astex Therapeutics Ltd | مشتقات كينوكسالين مفيدة كمعدلات لإنزيم fgfr كيناز |
JP6980385B2 (ja) | 2014-03-26 | 2021-12-15 | アステックス、セラピューティックス、リミテッドAstex Therapeutics Limited | Fgfr阻害剤とigf1r阻害剤の組合せ |
HUE053654T2 (hu) | 2014-03-26 | 2021-07-28 | Astex Therapeutics Ltd | FGFR- és CMET-inhibitorok kombinációi a rák kezelésére |
AR100936A1 (es) | 2014-06-24 | 2016-11-09 | Fmc Corp | Formulaciones de espumas y concentrados emulsionables |
JP6667551B2 (ja) | 2015-01-13 | 2020-03-18 | ノバルティス アーゲー | アンジオテンシンii2型拮抗薬としてのピロリジン誘導体 |
JOP20200201A1 (ar) | 2015-02-10 | 2017-06-16 | Astex Therapeutics Ltd | تركيبات صيدلانية تشتمل على n-(3.5- ثنائي ميثوكسي فينيل)-n'-(1-ميثيل إيثيل)-n-[3-(ميثيل-1h-بيرازول-4-يل) كينوكسالين-6-يل]إيثان-1.2-ثنائي الأمين |
WO2016142867A1 (en) | 2015-03-12 | 2016-09-15 | Novartis Ag | Heterocyclic compounds and methods for their use |
US10478494B2 (en) | 2015-04-03 | 2019-11-19 | Astex Therapeutics Ltd | FGFR/PD-1 combination therapy for the treatment of cancer |
CN106478502B (zh) * | 2015-08-29 | 2021-04-27 | 上海翰森生物医药科技有限公司 | 1,2,3,4-四氢异喹啉衍生物、其制备方法和应用 |
KR20180052631A (ko) | 2015-09-23 | 2018-05-18 | 얀센 파마슈티카 엔.브이. | 비-헤테로아릴 치환된 1,4-벤조디아제핀 및 암의 치료를 위한 이의 용도 |
BR112018005637B1 (pt) | 2015-09-23 | 2023-11-28 | Janssen Pharmaceutica Nv | Compostos derivados de quinoxalina, quinolina e quinazolinona,composições farmacêuticas que os compreende, e uso dos referidos compostos |
MA44111A (fr) | 2015-12-23 | 2018-10-31 | Fmc Corp | Traitement in situ de semences dans un sillon |
US20190152918A1 (en) | 2016-06-27 | 2019-05-23 | Ratiopharm Gmbh | Crystalline calcium salt of (s)-2-(diphenylacetyl)-1,2,3,4-tetrahydro-6-methoxy-5-(phenylmethoxy)-3-isoquinoline carboxylic acid |
JP2019514862A (ja) | 2017-03-23 | 2019-06-06 | ノバルティス アーゲー | (s)−2−(ジフェニルアセチル)−1,2,3,4−テトラヒドロ−6−メトキシ−5−(フェニルメトキシ)−3−イソキノリンカルボン酸ナトリウムの無水結晶形 |
CN110914243B (zh) * | 2017-06-09 | 2023-02-28 | 山东丹红制药有限公司 | 作为at2r受体拮抗剂的羧酸衍生物 |
GB201710906D0 (en) * | 2017-07-06 | 2017-08-23 | Vicore Pharma Ab | Compounds and methods for treating peripheral neuropathy |
CA3091300A1 (en) * | 2018-02-23 | 2019-08-29 | Beijing Tide Pharmaceutical Co., Ltd. | Receptor inhibitors, pharmaceutical compositions comprising the same, and usage thereof |
US11453690B2 (en) | 2018-03-23 | 2022-09-27 | Beijing Tide Pharmaceutical Co., Ltd. | Receptor inhibitor, pharmaceutical composition comprising same, and use thereof |
WO2019238962A1 (en) * | 2018-06-14 | 2019-12-19 | University College Cork - National University Of Ireland, Cork | Peptide for disease treatment |
WO2020012266A1 (en) | 2018-07-12 | 2020-01-16 | Novartis Ag | Biocatalytic synthesis of olodanrigan (ema401) from 3-(2-(benzyloxy)-3-methoxyphenyl)propenoic acid with phenylalanine ammonia lyase |
WO2023006893A1 (en) | 2021-07-30 | 2023-02-02 | Confo Therapeutics N.V. | Compounds for the treatment of pain, in particular neuropathic pain, and/or other diseases or disorders that are associated with at2r and/or at2r mediated signaling |
US20230373919A1 (en) | 2022-05-17 | 2023-11-23 | Eli Lilly And Company | At2r antagonists and uses thereof |
Family Cites Families (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3531485A (en) | 1967-08-14 | 1970-09-29 | American Home Prod | Aryl-substituted diazabicycloalkanes |
US3957795A (en) | 1974-01-28 | 1976-05-18 | Delmar Chemicals Limited | Novel cyclopentene and cyclopentane derivatives |
US3975795A (en) | 1975-01-20 | 1976-08-24 | Union Carbide Corporation | Product stuffing apparatus and method |
US4812462A (en) | 1986-04-01 | 1989-03-14 | Warner-Lambert Company | 4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylic acid analogs having antihypertensive activity |
US5091390A (en) | 1990-09-20 | 1992-02-25 | E. I. Du Pont De Nemours And Company | Treatment of CNS disorders with 4,5,6,7-tetrahydro-1H-imidazo (4,5-)-pyridines and analogs |
EP0551432A1 (en) | 1990-10-02 | 1993-07-21 | Warner-Lambert Company | 4,5,6,7-tetrahydro-1h-imidazo 4,5-c]pyridine derivatives and analogues as angiotensin ii receptor antagonists |
US5385894A (en) * | 1991-03-06 | 1995-01-31 | Merck & Co., Inc. | Disubstituted 6-aminoquinazolinones |
US5238942A (en) | 1991-05-10 | 1993-08-24 | Merck & Co., Inc. | Substituted quinazolinones bearing acidic functional groups as angiotensin ii antagonists |
US5292726A (en) | 1991-05-22 | 1994-03-08 | Merck & Co., Inc. | N,N-diacylpiperazines |
US5204354A (en) * | 1992-02-14 | 1993-04-20 | Merck & Co., Inc. | Substituted quinazolinones as neurotensin antagonists useful in the treatment of CNS disorders |
GB9208116D0 (en) | 1992-04-13 | 1992-05-27 | Ici Plc | Therapeutic agents |
WO1993020816A1 (en) | 1992-04-13 | 1993-10-28 | Zeneca Limited | Angiotensin ii antagonists against disorders associated with impaired neuronal conduction velocity, especially diabetic neuropathy |
US5246943A (en) * | 1992-05-19 | 1993-09-21 | Warner-Lambert Company | Substituted 1,2,3,4-tetahydroisoquinolines with angiotensin II receptor antagonist properties |
US5236934A (en) | 1992-08-26 | 1993-08-17 | E. I. Du Pont De Nemours And Company | 1,2,3,4-tetrahydroisoquinolines useful in the treatment of CNS disorders |
US5344830A (en) | 1992-12-10 | 1994-09-06 | Merck & Co., Inc. | N,N-diacylpiperazine tachykinin antagonists |
US5683997A (en) | 1992-12-11 | 1997-11-04 | Ciba-Geigy Corporation | Substituted benzazepinones |
US5395844A (en) | 1993-06-10 | 1995-03-07 | The Du Pont Merck Pharmaceutical Company | Imidazole 5-position substituted angiotensin II antagonists |
US5348955A (en) | 1993-06-22 | 1994-09-20 | Merck & Co., Inc. | N,N-diacylpiperazines |
US5338740A (en) | 1993-07-13 | 1994-08-16 | Pfizer Inc. | Angiotensin II receptor antagonists |
AP9400651A0 (en) | 1993-07-15 | 1995-12-30 | Pfizer | Azacyclic-heterocyclic compounds as angiotensin II receptor antagonists. |
US5409926A (en) | 1993-07-19 | 1995-04-25 | Merck & Co., Inc. | AT-2 antagonist inhibition of vascular restenosis |
US5610165A (en) | 1994-02-17 | 1997-03-11 | Merck & Co., Inc. | N-acylpiperidine tachykinin antagonists |
FR2739625B1 (fr) | 1995-10-09 | 1997-12-05 | Atochem Elf Sa | Copolymeres hydrosolubles associatifs triblocs |
GB2323783A (en) | 1997-04-02 | 1998-10-07 | Ferring Bv Group Holdings | Inhibitors of farnesyl protein transferase |
WO1999007413A1 (en) | 1997-08-11 | 1999-02-18 | Algos Pharmaceutical Corporation | Substance p inhibitors in combination with nmda-blockers for treating pain |
US6277839B1 (en) | 1998-10-07 | 2001-08-21 | Merck Frosst Canada & Co. | Biphenylene lactams as prostaglandin receptor ligands |
WO2000038676A1 (en) * | 1998-12-23 | 2000-07-06 | Novartis Ag | Use of at-1 receptor antagonist or at-2 receptor modulator for treating diseases associated with an increase of at-1 or at-2 receptors |
AU2092601A (en) * | 1999-12-15 | 2001-06-25 | Bristol-Myers Squibb Company | Biphenyl sulfonamides as dual angiotensin endothelin receptor antagonists |
AU1793101A (en) | 1999-12-16 | 2001-06-25 | University Of Southern California | Methods for treating and preventing damage to mucosal tissue |
US6653332B2 (en) | 2000-05-03 | 2003-11-25 | Tularik Inc. | Combination therapeutic compositions and method of use |
WO2002005799A2 (en) | 2000-07-13 | 2002-01-24 | Pharmacia Corporation | Combination of a cox-2 inhibitor and a vasomodulator for treating pain and headache pain |
WO2002040008A2 (en) | 2000-11-17 | 2002-05-23 | Warner-Lambert Company Llc | Treatment of sexual dysfunction with non peptide bombesin receptor antagonists |
EG23054A (en) | 2001-01-22 | 2004-02-29 | Sankyo Co | Pyrrole derivatives their preparation and their therapeutic uses |
AU2002245340A1 (en) | 2001-01-29 | 2002-08-12 | Cognetix, Inc. | B-superfamily conotoxins |
CA2436361C (en) | 2001-01-29 | 2010-11-02 | Takeda Chemical Industries, Ltd. | Angiotensin ii antagonistic compound for use as analgesic and antiinflammatory agent |
PL374384A1 (pl) | 2001-12-14 | 2005-10-17 | Targacept, Inc. | Sposoby i kompozycje do leczenia schorzeń centralnego układu nerwowego |
WO2003064414A1 (en) | 2002-01-29 | 2003-08-07 | Vicore Pharma Ab. | Tricyclic compounds useful as angiotensin ii agonists |
AR038377A1 (es) | 2002-02-08 | 2005-01-12 | Merck & Co Inc | Derivados de n-bifenil-aminocicloalcancarboxamida (con sustitucion con metilo) |
US20030199424A1 (en) | 2002-03-20 | 2003-10-23 | Smith Maree Therese | Method of treatment and/or prophylaxis |
US7348348B2 (en) | 2002-04-30 | 2008-03-25 | Merck & Co. Inc. | Aryl-link-aryl substituted thiazolidine-dione and oxazolidine-dione as sodium channel blockers |
WO2003097024A1 (en) | 2002-05-17 | 2003-11-27 | Faust Pharmaceuticals | Methods for the prevention and/or the treatment of neurological disorders |
AU2003237224A1 (en) | 2002-05-29 | 2003-12-19 | Merck And Co., Inc. | 1,2 diamido cycloalkyl sodium channel blockers |
GB0212412D0 (en) | 2002-05-29 | 2002-07-10 | Novartis Ag | Combination of organic compounds |
EP1551457A1 (en) | 2002-07-16 | 2005-07-13 | Elan Pharma International Limited | Liquid dosage compositions of stable nanoparticulate active agents |
JO2397B1 (en) | 2002-12-20 | 2007-06-17 | ميرك شارب اند دوم كوربوريشن | Terazol derivatives as beta-hydroxy steroid dihydrogenase-1 inhibitors |
DE10300973A1 (de) | 2003-01-14 | 2004-07-22 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Carbonsäuren und deren Ester, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
PA8597401A1 (es) | 2003-03-14 | 2005-05-24 | Pfizer | Derivados del acido 3-(1-[3-(1,3-benzotiazol-6-il) propilcarbamoil] cicloalquil) propanoico como inhibidores de nep |
WO2004099248A2 (en) | 2003-05-05 | 2004-11-18 | Bayer Healthcare Ag | Diagnostics and therapeutics for diseases associated with g-protein-coupled receptor agtr2 (agtr2) |
US7157584B2 (en) | 2004-02-25 | 2007-01-02 | Takeda Pharmaceutical Company Limited | Benzimidazole derivative and use thereof |
EP2650011A1 (en) | 2004-12-24 | 2013-10-16 | Spinifex Pharmaceuticals Pty Ltd | Method of treatment or prophylaxis |
EP2377531A2 (en) | 2006-05-09 | 2011-10-19 | Braincells, Inc. | Neurogenesis by modulating angiotensin |
-
2005
- 2005-12-23 EP EP20130162570 patent/EP2650011A1/en not_active Withdrawn
- 2005-12-23 PL PL05821524T patent/PL1830869T3/pl unknown
- 2005-12-23 ES ES05821524T patent/ES2425567T3/es active Active
- 2005-12-23 PT PT58215245T patent/PT1830869E/pt unknown
- 2005-12-23 CN CN2005800441997A patent/CN101087619B/zh not_active Expired - Fee Related
- 2005-12-23 NZ NZ555334A patent/NZ555334A/en not_active IP Right Cessation
- 2005-12-23 WO PCT/AU2005/001975 patent/WO2006066361A1/en active Application Filing
- 2005-12-23 CN CN201210208621.XA patent/CN102861019B/zh not_active Expired - Fee Related
- 2005-12-23 DK DK05821524T patent/DK1830869T3/da active
- 2005-12-23 EP EP20050821524 patent/EP1830869B1/en active Active
- 2005-12-23 RS RSP20130354 patent/RS52927B/en unknown
- 2005-12-23 ME MEP-2013-88A patent/ME01597B/me unknown
- 2005-12-23 JP JP2007547106A patent/JP4966202B2/ja active Active
- 2005-12-23 SI SI200531764T patent/SI1830869T1/sl unknown
- 2005-12-23 CN CN2010105444424A patent/CN102049048B/zh not_active Expired - Fee Related
- 2005-12-23 EP EP20130162564 patent/EP2650010A1/en not_active Withdrawn
- 2005-12-23 US US11/315,354 patent/US7795275B2/en not_active Expired - Fee Related
-
2007
- 2007-06-20 ZA ZA2007/04909A patent/ZA200704909B/en unknown
- 2007-11-05 HK HK07111990A patent/HK1103364A1/xx not_active IP Right Cessation
-
2010
- 2010-08-03 US US12/849,727 patent/US8492382B2/en not_active Expired - Fee Related
-
2011
- 2011-06-24 US US13/167,980 patent/US8404686B2/en not_active Expired - Fee Related
-
2012
- 2012-10-01 ZA ZA2012/07323A patent/ZA201207323B/en unknown
- 2012-10-01 ZA ZA2012/07322A patent/ZA201207322B/en unknown
-
2013
- 2013-06-20 US US13/923,085 patent/US8722675B2/en not_active Expired - Fee Related
- 2013-08-06 HR HRP20130738TT patent/HRP20130738T1/hr unknown
- 2013-08-13 CY CY20131100691T patent/CY1114424T1/el unknown
-
2014
- 2014-03-28 US US14/229,746 patent/US9018207B2/en not_active Expired - Fee Related
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ZA200704909B (en) | Method of treatment or prophylaxis | |
PL2302097T3 (pl) | Metoda obróbki powierzchni | |
EP2032131A4 (en) | Methods of Treatment | |
EP1838714A4 (en) | METHODS OF TREATING PAIN | |
IL178996A0 (en) | Thienopyridinone compounds and methods of treatment | |
IL182436A0 (en) | Thienopyridinone compounds and methods of treatment | |
ZA200808183B (en) | Method of treatment or prophylaxis of inflammatory pain | |
EP1799258A4 (en) | METHODS FOR TREATMENT OF ANGIOGENESIS | |
GB0610746D0 (en) | Method of treatment | |
ZA200709024B (en) | Method of well treatment and construction | |
EP1809276A4 (en) | PROCESSING PROCESS | |
EP1737445A4 (en) | METHOD FOR TREATING DOWN SYNDROME | |
EP2083848A4 (en) | PROCEDURE FOR TREATMENT AND PROPHYLAXIS | |
GB0306309D0 (en) | Method of treatment | |
GB0302572D0 (en) | Method of treatment | |
GB0402578D0 (en) | Methods of treatment of atherosclerosis | |
GB0426196D0 (en) | Methods of treatment | |
GB0419175D0 (en) | Method of treatment and compositions | |
GB0327975D0 (en) | Methods of treatment | |
AU2004907332A0 (en) | Method of Treatment or Prophylaxis | |
EP1793831A4 (en) | PROCESS FOR TREATMENT OR PROTECTION AGAINST LYMPHODIES | |
GB0421176D0 (en) | Treatment of atherosclerosis | |
GB0522330D0 (en) | Method of treatment | |
GB0422012D0 (en) | Methods of treatment | |
HU0400952D0 (en) | Treatment of anus-cancer |