IL111991A - Liquid pharmaceutical composition of HIV protease inhibitors in organic solvent - Google Patents
Liquid pharmaceutical composition of HIV protease inhibitors in organic solventInfo
- Publication number
- IL111991A IL111991A IL11199194A IL11199194A IL111991A IL 111991 A IL111991 A IL 111991A IL 11199194 A IL11199194 A IL 11199194A IL 11199194 A IL11199194 A IL 11199194A IL 111991 A IL111991 A IL 111991A
- Authority
- IL
- Israel
- Prior art keywords
- pharmaceutical composition
- organic solvent
- hiv protease
- protease inhibitors
- liquid pharmaceutical
- Prior art date
Links
Classifications
-
- 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
- A61K9/0087—Galenical forms not covered by A61K9/02 - A61K9/7023
- A61K9/0095—Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
-
- 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
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
-
- 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
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/14—Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
-
- 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
- A61K47/44—Oils, fats or waxes according to two or more groups of A61K47/02-A61K47/42; Natural or modified natural oils, fats or waxes, e.g. castor oil, polyethoxylated castor oil, montan wax, lignite, shellac, rosin, beeswax or lanolin
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/28—Radicals substituted by nitrogen atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US18902194A | 1994-01-28 | 1994-01-28 | |
US28323994A | 1994-07-29 | 1994-07-29 |
Publications (2)
Publication Number | Publication Date |
---|---|
IL111991A0 IL111991A0 (en) | 1995-03-15 |
IL111991A true IL111991A (en) | 2000-07-26 |
Family
ID=26884695
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IL11199194A IL111991A (en) | 1994-01-28 | 1994-12-15 | Liquid pharmaceutical composition of HIV protease inhibitors in organic solvent |
Country Status (14)
Country | Link |
---|---|
US (1) | US5484801A (xx) |
EP (1) | EP0732923B1 (xx) |
JP (1) | JP4353542B2 (xx) |
KR (1) | KR100360963B1 (xx) |
AT (1) | ATE210441T1 (xx) |
AU (1) | AU700942B2 (xx) |
CA (1) | CA2178632C (xx) |
DE (1) | DE69524567T2 (xx) |
DK (1) | DK0732923T3 (xx) |
ES (1) | ES2169121T3 (xx) |
HK (1) | HK1011609A1 (xx) |
IL (1) | IL111991A (xx) |
PT (1) | PT732923E (xx) |
WO (1) | WO1995020384A1 (xx) |
Families Citing this family (94)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE230402T1 (de) * | 1992-12-29 | 2003-01-15 | Abbott Lab | Hemmer der retroviralen protease |
IL110752A (en) * | 1993-09-13 | 2000-07-26 | Abbott Lab | Liquid semi-solid or solid pharmaceutical composition for an HIV protease inhibitor |
EP0769936A1 (en) * | 1994-07-22 | 1997-05-02 | G.D. Searle & Co. | Self-emulsifying drug delivery system |
US5705524A (en) * | 1994-11-04 | 1998-01-06 | Gilead Sciences, Inc. | Thiepane compounds |
US6034118A (en) * | 1994-11-04 | 2000-03-07 | Gilead Sciences, Inc. | Thiepane compounds |
US6037157A (en) | 1995-06-29 | 2000-03-14 | Abbott Laboratories | Method for improving pharmacokinetics |
DK0861085T3 (da) | 1995-11-13 | 2005-11-21 | Vitaleech Bioscience N V | Antivirale isolater opnået fra igler |
US5914332A (en) | 1995-12-13 | 1999-06-22 | Abbott Laboratories | Retroviral protease inhibiting compounds |
US6730679B1 (en) | 1996-03-22 | 2004-05-04 | Smithkline Beecham Corporation | Pharmaceutical formulations |
AU3146997A (en) * | 1996-06-03 | 1998-01-05 | Merck & Co., Inc. | Pediatric formulation for hiv protease inhibitors |
ES2169880T3 (es) | 1996-10-18 | 2002-07-16 | Vertex Pharma | Inhibidores de proteasas de serina, particularmente de la proteasa ns3 del virus de la hepatitis c. |
US6232333B1 (en) | 1996-11-21 | 2001-05-15 | Abbott Laboratories | Pharmaceutical composition |
ZA9710071B (en) * | 1996-11-21 | 1998-05-25 | Abbott Lab | Pharmaceutical composition. |
US6894171B1 (en) * | 1998-07-20 | 2005-05-17 | Abbott Laboratories | Polymorph of a pharmaceutical |
CO5090830A1 (es) | 1998-07-20 | 2001-10-30 | Abbott Lab | Poliformo de un agente farmaceutico |
WO2000028994A1 (en) * | 1998-11-18 | 2000-05-25 | Supratek Pharma Inc. | Copolymer compositions for treating viral infections |
MXPA01005884A (es) | 1998-12-11 | 2002-04-24 | Pharmasolutions Inc | Composiciones auto-emulsionantes para medicamentos escasamente solubles en agua. |
BE1012622A3 (fr) * | 1999-04-21 | 2001-01-09 | Solvay | Procede pour la separation d'enantiomeres et reactif enantiopur. |
US6057289A (en) * | 1999-04-30 | 2000-05-02 | Pharmasolutions, Inc. | Pharmaceutical composition comprising cyclosporin in association with a carrier in a self-emulsifying drug delivery system |
KR100815412B1 (ko) † | 1999-06-04 | 2008-03-20 | 아보트 러보러터리즈 | 개선된 약제학적 제형 |
US7141593B1 (en) * | 1999-06-04 | 2006-11-28 | Abbott Laboratories | Pharmaceutical formulations |
US6589962B1 (en) | 1999-07-20 | 2003-07-08 | Merck & Co., Inc. | Alpha-hydroxy-gamma-[[(carbocyclic-or heterocyclic-substituted)amino]carbonyl]alkanamide derivatives and uses thereof |
EP1202626A4 (en) * | 1999-07-20 | 2002-10-30 | Merck & Co Inc | ALPHA HYDROXY GAMMA (CARBOZYCLIC OR HETEROCYCLICALLY SUBSTITUTED) AMINOCARBONYLALKANAMIDE DERIVATIVES AND THEIR USE |
ATE329579T1 (de) | 1999-11-12 | 2006-07-15 | Abbott Lab | Feste dispersion mit ritonavir, fenofibrat oder griseofulvin |
AU777824B2 (en) | 1999-11-24 | 2004-11-04 | Merck Sharp & Dohme Corp. | Gamma-hydroxy-2-(fluoroalkylaminocarbonyl)-1- piperazinepentanamides as HIV protease inhibitors |
GB0000313D0 (en) | 2000-01-10 | 2000-03-01 | Astrazeneca Uk Ltd | Formulation |
PT1248600E (pt) | 2000-01-19 | 2008-08-25 | Abbott Lab | Formulações farmacêuticas melhoradas de inibidores da protease do vih |
US7138538B2 (en) * | 2000-04-14 | 2006-11-21 | Solvay (Societe Anonyme) | Process for the separation of enantiomers and enantiopure reagent |
SV2003000617A (es) | 2000-08-31 | 2003-01-13 | Lilly Co Eli | Inhibidores de la proteasa peptidomimetica ref. x-14912m |
US6911214B2 (en) | 2000-09-05 | 2005-06-28 | Abbott Laboratories | Flavoring systems for pharmaceutical compositions and methods of making such compositions |
MXPA03001952A (es) * | 2000-09-05 | 2003-09-10 | Abbott Lab | Sistemas saborizantes para composiciones farmaceuticas y metodos para hacer dichas composiciones. |
KR100847679B1 (ko) * | 2000-10-31 | 2008-07-23 | 베링거 인겔하임 파마슈티칼즈, 인코포레이티드 | 피라논 프로테아제 억제제의 경구 투여 자가-유화 제형 |
WO2002051414A1 (fr) * | 2000-12-22 | 2002-07-04 | Takeda Chemical Industries, Ltd. | Compositions médicinales s'administrant par voie orale |
EP1374855A1 (en) * | 2001-03-30 | 2004-01-02 | Takeda Chemical Industries, Ltd. | Medicinal solutions |
US20030138483A1 (en) * | 2001-05-25 | 2003-07-24 | Sergio Petriconi | Soft elastic capsules and compositions thereof |
US20030191121A1 (en) * | 2001-08-09 | 2003-10-09 | Miller Ross A. | Piperazine carboxamide intermediates of HIV protease inhibitors and processes for their preparation |
US20040067216A1 (en) * | 2002-02-22 | 2004-04-08 | Karki Shyam B. | Hiv protease inhibitors supported on cation exchange resins for oral administration |
IL163666A0 (en) | 2002-02-22 | 2005-12-18 | New River Pharmaceuticals Inc | Active agent delivery systems and methods for protecting and administering active agents |
AU2002350719A1 (en) * | 2002-11-29 | 2004-06-23 | Janssen Pharmaceutica N.V. | Pharmaceutical compositions comprising a basic respectively acidic drug compound, a surfactant and a physiologically tolerable water-soluble acid respectively base |
EP1575595A1 (en) * | 2002-12-16 | 2005-09-21 | Boehringer Ingelheim International GmbH | Use of a combination containing a non-nucleoside reverse transcriptase inhibitor (nnrti) with an inhibitor of cytochrome p450, such as protease inhibitors |
US8377952B2 (en) | 2003-08-28 | 2013-02-19 | Abbott Laboratories | Solid pharmaceutical dosage formulation |
US8025899B2 (en) | 2003-08-28 | 2011-09-27 | Abbott Laboratories | Solid pharmaceutical dosage form |
TWI359147B (en) | 2003-09-05 | 2012-03-01 | Vertex Pharma | Inhibitors of serine proteases, particularly hcv n |
NZ545871A (en) * | 2003-09-12 | 2010-04-30 | Vertex Pharma | Animal model for protease activity and liver damage |
TW200528472A (en) | 2003-10-10 | 2005-09-01 | Vertex Pharma | Inhibitors of serine proteases, particularly HCV ns3-ns4a protease |
EP1944042A1 (en) | 2003-10-27 | 2008-07-16 | Vertex Pharmceuticals Incorporated | Combinations for HCV treatment |
US7494660B2 (en) * | 2003-10-27 | 2009-02-24 | Vertex Pharmaceuticals Incorporated | HCV NS3-NS4A protease resistance mutants |
AU2005212257A1 (en) | 2004-02-04 | 2005-08-25 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly HCV NS3-NS4A protease |
EP1804821A4 (en) | 2004-10-01 | 2009-07-15 | Vertex Pharma | INHIBITION OF HCV NS3-NS4A PROTEASE |
MY141025A (en) | 2004-10-29 | 2010-02-25 | Vertex Pharma | Dose forms |
WO2006090270A1 (en) * | 2005-02-28 | 2006-08-31 | Ranbaxy Laboratories Limited | Acid addition salt of 2-isopropyl-4-(((n-methyl)amino)methyl)thiazole and its?use in the preparation of ritonavir |
BRPI0614620A2 (pt) * | 2005-07-29 | 2011-04-12 | Tibotec Pharm Ltd | compostos inibidores macrocìclicos do vìrus da hepatite c, uso dos mesmos, processo para preparar os referidos compostos, combinação e composição farmacêutica |
JO2768B1 (en) | 2005-07-29 | 2014-03-15 | تيبوتيك فارماسيوتيكالز ليمتد | Large cyclic inhibitors of hepatitis C virus |
RU2436787C2 (ru) | 2005-07-29 | 2011-12-20 | Тиботек Фармасьютикалз Лтд. | Макроциклические ингибиторы вируса гепатита с |
MY144607A (en) * | 2005-07-29 | 2011-10-14 | Tibotec Pharm Ltd | Macrocylic inhibitors of hepatitis c virus |
ME01318B (me) * | 2005-07-29 | 2013-12-20 | Tibotec Pharm Ltd | Makrociklički inhibitori virusa hepatitisa C |
PE20070211A1 (es) | 2005-07-29 | 2007-05-12 | Medivir Ab | Compuestos macrociclicos como inhibidores del virus de hepatitis c |
PE20070210A1 (es) | 2005-07-29 | 2007-04-16 | Tibotec Pharm Ltd | Compuestos macrociclicos como inhibidores del virus de hepatitis c |
MY144895A (en) * | 2005-07-29 | 2011-11-30 | Tibotec Pharm Ltd | Macrocylic inhibitors of hepatitis c virus |
JP2009505966A (ja) | 2005-08-02 | 2009-02-12 | バーテックス ファーマシューティカルズ インコーポレイテッド | セリンプロテアーゼのインヒビター |
AR055395A1 (es) * | 2005-08-26 | 2007-08-22 | Vertex Pharma | Compuestos inhibidores de la actividad de la serina proteasa ns3-ns4a del virus de la hepatitis c |
US7964624B1 (en) * | 2005-08-26 | 2011-06-21 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases |
US7705138B2 (en) | 2005-11-11 | 2010-04-27 | Vertex Pharmaceuticals Incorporated | Hepatitis C virus variants |
EP2392588A3 (en) | 2005-11-11 | 2012-03-07 | Vertex Pharmaceuticals Incorporated | Hepatitis C virus variants |
JP5436864B2 (ja) | 2006-02-27 | 2014-03-05 | バーテックス ファーマシューティカルズ インコーポレイテッド | Vx−950を含む共結晶体およびそれを含む医薬組成物 |
CA2646229A1 (en) * | 2006-03-16 | 2007-09-27 | Vertex Pharmaceuticals Incorporated | Deuterated hepatitis c protease inhibitors |
EP2097402B1 (en) | 2006-11-17 | 2014-04-09 | Janssen R&D Ireland | Macrocyclic inhibitors of hepatitis c virus |
AU2008212758B2 (en) * | 2007-02-08 | 2014-01-30 | Medivir Ab | Pyrimidine substituted macrocyclic HCV inhibitors |
JP2010519330A (ja) * | 2007-02-27 | 2010-06-03 | バーテックス ファーマシューティカルズ インコーポレイテッド | 共結晶体およびそれを含む医薬組成物 |
JP2010519329A (ja) * | 2007-02-27 | 2010-06-03 | バーテックス ファーマシューティカルズ インコーポレイテッド | セリンプロテアーゼ阻害剤 |
ATE548044T1 (de) | 2007-05-04 | 2012-03-15 | Vertex Pharma | Kombinationstherapie zur behandlung von hiv- infektionen |
NZ583699A (en) * | 2007-08-30 | 2012-04-27 | Vertex Pharma | Co-crystals of vx-950 (telaprevir) other components and pharmaceutical compositions comprising the same |
AU2008305678A1 (en) * | 2007-09-25 | 2009-04-02 | Merck Sharp & Dohme Corp. | HIV protease inhibitors |
AP3010A (en) * | 2007-10-29 | 2014-10-31 | Cipla Ltd | Novel antiretroviral combination |
PA8809601A1 (es) | 2007-12-24 | 2009-07-23 | Cipla Ltd | Combinación anti-retroviral |
UY31950A (es) | 2008-07-01 | 2010-01-29 | Medivir Ab | Inhibidores de ciclopropil-polimerasa |
WO2010093843A2 (en) | 2009-02-12 | 2010-08-19 | Vertex Pharmaceuticals Incorporated | Hcv combination therapies |
UA103801C2 (ru) | 2009-04-25 | 2013-11-25 | Ф. Хоффманн-Ля Рош Аг | Способ повышения биодоступности ингибитора протеазы ns3/4a вируса гепатита с |
JP2012528160A (ja) | 2009-05-27 | 2012-11-12 | メルク・シャープ・エンド・ドーム・コーポレイション | Hivプロテアーゼ阻害薬 |
KR20120139699A (ko) | 2010-01-29 | 2012-12-27 | 버텍스 파마슈티칼스 인코포레이티드 | C형 간염 바이러스 감염의 치료 요법 |
WO2012010942A2 (en) | 2010-07-22 | 2012-01-26 | Lupin Limited | Novel pharmaceutical composition(s) of hiv protease inhibitor(s) |
WO2012055031A1 (en) | 2010-10-28 | 2012-05-03 | Merck Canada Inc. | Hiv protease inhibitors |
WO2012109646A1 (en) | 2011-02-11 | 2012-08-16 | Vertex Pharmaceuticals Incorporated | Treatment of hcv in hiv infection patients |
CA2837266A1 (en) | 2011-05-27 | 2012-12-06 | Hetero Research Foundation | Amorphous ritonavir co-precipitated |
WO2013059928A1 (en) | 2011-10-26 | 2013-05-02 | Merck Canada Inc. | Hiv protease inhibitors |
JP2015527403A (ja) | 2012-09-11 | 2015-09-17 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | Hivプロテアーゼ阻害剤 |
WO2015013835A1 (en) | 2013-07-31 | 2015-02-05 | Merck Sharp & Dohme Corp. | Piperazine derivatives as hiv protease inhibitors |
UA117375C2 (uk) | 2013-09-04 | 2018-07-25 | Медівір Аб | Інгібітори полімерази hcv |
EP3057976A1 (en) | 2013-10-17 | 2016-08-24 | Medivir Ab | Hcv polymerase inhibitors |
WO2015095265A1 (en) | 2013-12-19 | 2015-06-25 | Merck Sharp & Dohme Corp. | Hiv protease inhibitors |
US9834526B2 (en) | 2013-12-19 | 2017-12-05 | Merck Sharp & Dohme Corp. | HIV protease inhibitors |
WO2015134366A1 (en) | 2014-03-06 | 2015-09-11 | Merck Sharp & Dohme Corp. | Hiv protease inhibitors |
US10138255B2 (en) | 2014-03-10 | 2018-11-27 | Merck Sharp & Dohme Corp. | Piperazine derivatives as HIV protease inhibitors |
WO2016069955A1 (en) | 2014-10-29 | 2016-05-06 | Wisconsin Alumni Research Foundation | Boronic acid inhibitors of hiv protease |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5086165A (en) * | 1989-03-08 | 1992-02-04 | Washington University | Inhibitors of retroviral protease with a ketomethylene isosteric replaced amide bond |
US5342922A (en) * | 1989-03-08 | 1994-08-30 | Washington University | Inhibitors of retroviral protease |
US5354866A (en) * | 1989-05-23 | 1994-10-11 | Abbott Laboratories | Retroviral protease inhibiting compounds |
US5256677A (en) * | 1989-05-23 | 1993-10-26 | Abbott Laboratories | Retroviral protease inhibiting compounds |
US5164300A (en) * | 1989-12-28 | 1992-11-17 | Washington University | Method for determining activity of retroviral protease |
JPH05508855A (ja) * | 1990-07-06 | 1993-12-09 | スミスクライン・ビーチャム・コーポレイション | レトロウイルスプロテアーゼ阻害剤 |
US5171662A (en) * | 1990-09-13 | 1992-12-15 | The Upjohn Company | Method of detecting HIV protease activity |
US5183826A (en) * | 1990-09-25 | 1993-02-02 | Merck & Co., Inc. | Antiviral agent |
IE20010533A1 (en) * | 1990-11-20 | 2003-03-05 | Abbott Lab | Intermediates for preparing retroviral protease inhibiting compounds |
EP0575500A4 (en) * | 1991-03-08 | 1994-06-01 | Smithkline Beecham Corp | Hiv protease inhibitors |
EP0532466A3 (en) * | 1991-09-12 | 1993-06-16 | Ciba-Geigy Ag | Derivatives of 5-amino-4-hydroxy-hexanoic acid and their therapeutical use |
US5250563A (en) * | 1991-09-25 | 1993-10-05 | Merck & Co., Inc. | Inhibitors of HIV protease |
US5296604A (en) * | 1992-05-15 | 1994-03-22 | Miles Inc. | Proline derivatives and compositions for their use as inhibitors of HIV protease |
ATE230402T1 (de) * | 1992-12-29 | 2003-01-15 | Abbott Lab | Hemmer der retroviralen protease |
-
1994
- 1994-12-15 IL IL11199194A patent/IL111991A/xx not_active IP Right Cessation
-
1995
- 1995-01-03 JP JP52005995A patent/JP4353542B2/ja not_active Expired - Lifetime
- 1995-01-03 PT PT95906790T patent/PT732923E/pt unknown
- 1995-01-03 AT AT95906790T patent/ATE210441T1/de active
- 1995-01-03 AU AU15248/95A patent/AU700942B2/en not_active Expired
- 1995-01-03 DE DE69524567T patent/DE69524567T2/de not_active Expired - Lifetime
- 1995-01-03 WO PCT/US1995/000232 patent/WO1995020384A1/en active IP Right Grant
- 1995-01-03 EP EP95906790A patent/EP0732923B1/en not_active Expired - Lifetime
- 1995-01-03 ES ES95906790T patent/ES2169121T3/es not_active Expired - Lifetime
- 1995-01-03 DK DK95906790T patent/DK0732923T3/da active
- 1995-01-03 KR KR1019960704162A patent/KR100360963B1/ko not_active IP Right Cessation
- 1995-01-03 CA CA002178632A patent/CA2178632C/en not_active Expired - Lifetime
- 1995-05-12 US US08/440,277 patent/US5484801A/en not_active Expired - Lifetime
-
1998
- 1998-11-30 HK HK98112594A patent/HK1011609A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
AU700942B2 (en) | 1999-01-14 |
WO1995020384A1 (en) | 1995-08-03 |
ES2169121T3 (es) | 2002-07-01 |
IL111991A0 (en) | 1995-03-15 |
PT732923E (pt) | 2002-05-31 |
US5484801A (en) | 1996-01-16 |
EP0732923A1 (en) | 1996-09-25 |
ATE210441T1 (de) | 2001-12-15 |
DE69524567T2 (de) | 2002-09-05 |
JP4353542B2 (ja) | 2009-10-28 |
KR100360963B1 (ko) | 2003-02-11 |
HK1011609A1 (en) | 1999-07-16 |
AU1524895A (en) | 1995-08-15 |
DK0732923T3 (da) | 2002-04-08 |
CA2178632A1 (en) | 1995-08-03 |
CA2178632C (en) | 2006-04-11 |
EP0732923B1 (en) | 2001-12-12 |
DE69524567D1 (de) | 2002-01-24 |
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