HK1034906A1 - Method and composition of an oral preparation of itraconazole. - Google Patents
Method and composition of an oral preparation of itraconazole.Info
- Publication number
- HK1034906A1 HK1034906A1 HK01105615A HK01105615A HK1034906A1 HK 1034906 A1 HK1034906 A1 HK 1034906A1 HK 01105615 A HK01105615 A HK 01105615A HK 01105615 A HK01105615 A HK 01105615A HK 1034906 A1 HK1034906 A1 HK 1034906A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- itraconazole
- composition
- oral preparation
- oral
- preparation
- Prior art date
Links
- VHVPQPYKVGDNFY-DFMJLFEVSA-N 2-[(2r)-butan-2-yl]-4-[4-[4-[4-[[(2r,4s)-2-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]piperazin-1-yl]phenyl]-1,2,4-triazol-3-one Chemical compound O=C1N([C@H](C)CC)N=CN1C1=CC=C(N2CCN(CC2)C=2C=CC(OC[C@@H]3O[C@](CN4N=CN=C4)(OC3)C=3C(=CC(Cl)=CC=3)Cl)=CC=2)C=C1 VHVPQPYKVGDNFY-DFMJLFEVSA-N 0.000 title 1
- 229960004130 itraconazole Drugs 0.000 title 1
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
- A61K31/33—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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
- A61K9/146—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
-
- 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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1635—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
-
- 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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1652—Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
-
- 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
- A61P31/10—Antimycotics
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Communicable Diseases (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR19970081947 | 1997-12-31 | ||
| KR1019980027730A KR100288890B1 (ko) | 1997-12-31 | 1998-07-10 | 이트라코나졸 경구용 제제 및 그의 제조방법 |
| PCT/KR1998/000436 WO1999033467A1 (en) | 1997-12-31 | 1998-12-17 | Method and composition of an oral preparation of itraconazole |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HK1034906A1 true HK1034906A1 (en) | 2001-11-09 |
Family
ID=26633347
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HK01105615A HK1034906A1 (en) | 1997-12-31 | 2001-08-13 | Method and composition of an oral preparation of itraconazole. |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US6485743B1 (pt) |
| EP (1) | EP1039909B1 (pt) |
| JP (1) | JP3696087B2 (pt) |
| CN (1) | CN1153570C (pt) |
| AU (1) | AU1511399A (pt) |
| BR (1) | BR9814729A (pt) |
| CA (1) | CA2317106C (pt) |
| DE (1) | DE69808670T2 (pt) |
| ES (1) | ES2185238T3 (pt) |
| HK (1) | HK1034906A1 (pt) |
| PL (1) | PL191181B1 (pt) |
| PT (1) | PT1039909E (pt) |
| TR (1) | TR200001880T2 (pt) |
| WO (1) | WO1999033467A1 (pt) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100694667B1 (ko) * | 1999-12-08 | 2007-03-14 | 동아제약주식회사 | 생체내이용률 향상과 개인간 및 개인내 흡수 편차를감소시킨 이트라코나졸 함유 항진균성 제제 |
| AU2331801A (en) * | 1999-12-23 | 2001-07-09 | F.H. Faulding & Co. Limited | Improved pharmaceutical compositions for poorly soluble drugs |
| FR2803748A1 (fr) * | 2000-01-14 | 2001-07-20 | Ethypharm Lab Prod Ethiques | Composition d'itraconazole et procede de preparation |
| KR20010097244A (ko) * | 2000-04-21 | 2001-11-08 | 유충식 | 위산도 비의존성 고용해도를 갖는 이트라코나졸 함유약학적 조성물 및 그 제조방법 |
| US8067032B2 (en) | 2000-12-22 | 2011-11-29 | Baxter International Inc. | Method for preparing submicron particles of antineoplastic agents |
| US9700866B2 (en) | 2000-12-22 | 2017-07-11 | Baxter International Inc. | Surfactant systems for delivery of organic compounds |
| IL156310A0 (en) * | 2000-12-22 | 2004-01-04 | Baxter Int | Method for preparing submicron particle suspensions |
| WO2002100407A1 (en) * | 2001-06-12 | 2002-12-19 | Smartrix Technologies Inc. | Itraconazole granulations: pharmaceutical formulations for oral administration and method of preparing same |
| KR100425755B1 (ko) * | 2001-08-27 | 2004-04-03 | 주식회사 원진신약 | 이트라코나졸을 함유하는 조성물 및 그 제조방법 |
| US20060003012A9 (en) | 2001-09-26 | 2006-01-05 | Sean Brynjelsen | Preparation of submicron solid particle suspensions by sonication of multiphase systems |
| BR0212833A (pt) | 2001-09-26 | 2004-10-13 | Baxter Int | Preparação de nanopartìculas de tamanho submìcron através de dispersão e de remoção de solvente ou de fase lìquida |
| FR2841138B1 (fr) * | 2002-06-25 | 2005-02-25 | Cll Pharma | Composition pharmaceutique solide contenant un principe actif lipophile, son procede de preparation |
| EP1521571A1 (en) * | 2002-07-04 | 2005-04-13 | Janssen Pharmaceutica N.V. | Solid dispersion comprising two different polymer matrixes |
| US20040086567A1 (en) * | 2002-10-30 | 2004-05-06 | Pawan Seth | Bioequivalent composition of itraconazole and a hydrophilic polymer |
| DK1438961T4 (da) * | 2003-01-14 | 2014-11-17 | Acino Pharma Ag | Bioækvivalent sammensætning af itraconazol dispergeret i en hydrofil polymer |
| JP4342426B2 (ja) * | 2004-11-24 | 2009-10-14 | 科研製薬株式会社 | イトラコナゾール経口投与用製剤 |
| ES2403006T3 (es) | 2005-08-22 | 2013-05-13 | The Johns Hopkins University | Antagonistas de la vía Hedgehog para tratar enfermedades |
| GB0607105D0 (en) * | 2006-04-10 | 2006-05-17 | Leuven K U Res & Dev | Enhancing solubility and dissolution rate of poorly soluble drugs |
| WO2008135828A2 (en) | 2007-05-03 | 2008-11-13 | Pfizer Products Inc. | Nanoparticles comprising a drug, ethylcellulose, and a bile salt |
| US8703204B2 (en) | 2007-05-03 | 2014-04-22 | Bend Research, Inc. | Nanoparticles comprising a cholesteryl ester transfer protein inhibitor and anon-ionizable polymer |
| WO2008149230A2 (en) | 2007-06-04 | 2008-12-11 | Pfizer Products Inc. | Nanoparticles comprising drug, a non-ionizable cellulosic polymer and tocopheryl polyethylene glycol succinate |
| WO2008149192A2 (en) | 2007-06-04 | 2008-12-11 | Pfizer Products Inc. | Nanoparticles comprising a non-ionizable cellulosic polymer and an amphiphilic non-ionizable block copolymer |
| US9724362B2 (en) | 2007-12-06 | 2017-08-08 | Bend Research, Inc. | Pharmaceutical compositions comprising nanoparticles and a resuspending material |
| US9233078B2 (en) | 2007-12-06 | 2016-01-12 | Bend Research, Inc. | Nanoparticles comprising a non-ionizable polymer and an Amine-functionalized methacrylate copolymer |
| CN104105472A (zh) | 2011-12-20 | 2014-10-15 | 维奥姆生物科学有限公司 | 用于治疗真菌感染的局部油组合物 |
| US9296753B2 (en) | 2012-06-04 | 2016-03-29 | Pharmacyclics Llc | Crystalline forms of a Bruton's tyrosine kinase inhibitor |
| CN104507480A (zh) | 2012-06-21 | 2015-04-08 | 梅恩医药国际有限公司 | 伊曲康唑组合物和剂型及其使用方法 |
| WO2014167554A2 (en) * | 2013-04-12 | 2014-10-16 | Vyome Biosciences Pvt. Ltd. | Composition and formulation of antimicrobial agents, processes thereof and methods for treating microbial infections |
| CN105491886B (zh) * | 2013-08-27 | 2019-01-29 | V·沃道里斯 | 苯达莫司汀医药组合物 |
| US10016500B2 (en) * | 2014-03-05 | 2018-07-10 | Professional Compounding Centers Of America | Poloxamer-based pharmaceutical compositions for treating wounds |
| WO2016022942A1 (en) * | 2014-08-07 | 2016-02-11 | Pharmacyclics Llc | Novel formulations of a bruton's tyrosine kinase inhibitor |
| CN104688536B (zh) * | 2015-02-03 | 2016-06-08 | 常州制药厂有限公司 | 一种伊曲康唑制剂的制备方法 |
| SG11201707122QA (en) | 2015-03-03 | 2017-09-28 | Pharmacyclics Llc | Pharmaceutical formulations of bruton's tyrosine kinase inhibtor |
| CN106511265A (zh) * | 2016-11-16 | 2017-03-22 | 北京万全德众医药生物技术有限公司 | 一种含有伊曲康唑的口服溶液及其制备工艺 |
| WO2019043427A1 (en) | 2017-09-01 | 2019-03-07 | Jordan Sweden Medical And Sterilization Company | FAST SELF-DISPERSION DOSAGE FORMS OF DEFERASIROX |
| CN109172532A (zh) * | 2018-10-24 | 2019-01-11 | 北京哈三联科技有限责任公司 | 一种伊曲康唑分散片及其制备方法和应用 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4218458A (en) | 1978-06-23 | 1980-08-19 | Janssen Pharmaceutica, N.V. | Heterocyclic derivatives of (4-aryloxy-methyl-1,3-dioxolan-2-yl)methyl-1H-imidazoles and 1H-1,2,4-triazoles |
| JPS57171428A (en) | 1981-04-13 | 1982-10-22 | Sankyo Co Ltd | Preparation of coated solid preparation |
| DE3346123A1 (de) | 1983-12-21 | 1985-06-27 | Janssen Pharmaceutica, N.V., Beerse | Pharmazeutische praeparate von in wasser schwerloeslichen oder instabilen arzneistoffen und verfahren zu ihrer herstellung |
| GB8506792D0 (en) | 1985-03-15 | 1985-04-17 | Janssen Pharmaceutica Nv | Derivatives of y-cyclodextrin |
| JPS63188621A (ja) * | 1987-01-30 | 1988-08-04 | Taisho Pharmaceut Co Ltd | 矯味経口製剤 |
| JPH0774151B2 (ja) * | 1987-10-12 | 1995-08-09 | 三井東圧化学株式会社 | 薬物の好ましくない官能的性質を隠蔽した散剤の製造方法 |
| GB8908250D0 (en) | 1989-04-12 | 1989-05-24 | Fisons Plc | Formulations |
| JP3034592B2 (ja) * | 1990-11-20 | 2000-04-17 | わかもと製薬株式会社 | 経口用固形製剤及びその製造法 |
| ATE138561T1 (de) | 1992-02-12 | 1996-06-15 | Janssen Cilag S P A | Liposomale itraconazol formulierungen |
| PH30929A (en) * | 1992-09-03 | 1997-12-23 | Janssen Pharmaceutica Nv | Beads having a core coated with an antifungal and a polymer. |
| TW438601B (en) | 1994-05-18 | 2001-06-07 | Janssen Pharmaceutica Nv | New mucoadhesive emulsion compositions and a process for the preparation thereof |
| FR2722984B1 (fr) | 1994-07-26 | 1996-10-18 | Effik Lab | Procede de preparation de formes pharmaceutiques seches et les compositions pharmaceutiques ainsi realisees |
| US5750147A (en) * | 1995-06-07 | 1998-05-12 | Emisphere Technologies, Inc. | Method of solubilizing and encapsulating itraconazole |
| KR19990044257A (ko) * | 1996-05-20 | 1999-06-25 | 디르크 반테 | 생체이용율이 개선된 항진균성 조성물 |
-
1998
- 1998-12-17 ES ES98959284T patent/ES2185238T3/es not_active Expired - Lifetime
- 1998-12-17 BR BR9814729-3A patent/BR9814729A/pt not_active Application Discontinuation
- 1998-12-17 DE DE69808670T patent/DE69808670T2/de not_active Expired - Lifetime
- 1998-12-17 TR TR2000/01880T patent/TR200001880T2/xx unknown
- 1998-12-17 EP EP98959284A patent/EP1039909B1/en not_active Expired - Lifetime
- 1998-12-17 WO PCT/KR1998/000436 patent/WO1999033467A1/en active IP Right Grant
- 1998-12-17 PT PT98959284T patent/PT1039909E/pt unknown
- 1998-12-17 PL PL341566A patent/PL191181B1/pl not_active IP Right Cessation
- 1998-12-17 CA CA002317106A patent/CA2317106C/en not_active Expired - Fee Related
- 1998-12-17 JP JP2000526224A patent/JP3696087B2/ja not_active Expired - Fee Related
- 1998-12-17 AU AU15113/99A patent/AU1511399A/en not_active Abandoned
- 1998-12-17 CN CNB988128144A patent/CN1153570C/zh not_active Expired - Fee Related
- 1998-12-17 US US09/582,536 patent/US6485743B1/en not_active Expired - Fee Related
-
2001
- 2001-08-13 HK HK01105615A patent/HK1034906A1/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| TR200001880T2 (tr) | 2000-11-21 |
| CA2317106A1 (en) | 1999-07-08 |
| EP1039909A1 (en) | 2000-10-04 |
| WO1999033467A1 (en) | 1999-07-08 |
| PL191181B1 (pl) | 2006-03-31 |
| PL341566A1 (en) | 2001-04-23 |
| PT1039909E (pt) | 2003-02-28 |
| DE69808670D1 (de) | 2002-11-14 |
| JP2001527044A (ja) | 2001-12-25 |
| EP1039909B1 (en) | 2002-10-09 |
| JP3696087B2 (ja) | 2005-09-14 |
| BR9814729A (pt) | 2002-01-08 |
| ES2185238T3 (es) | 2003-04-16 |
| DE69808670T2 (de) | 2003-07-03 |
| CA2317106C (en) | 2004-11-23 |
| CN1153570C (zh) | 2004-06-16 |
| AU1511399A (en) | 1999-07-19 |
| US6485743B1 (en) | 2002-11-26 |
| CN1285746A (zh) | 2001-02-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PC | Patent ceased (i.e. patent has lapsed due to the failure to pay the renewal fee) |
Effective date: 20101217 |