AR006345A1 - A PHARMACEUTICAL COMPOSITION FOR ORAL ADMINISTRATION INCLUDING AN HIV PROTEASE INHIBITOR AND A WATER-SOLUBLE TOCOFEROL DERIVATIVE, AND A METHOD FOR PREPARING SUCH COMPOSITION. - Google Patents
A PHARMACEUTICAL COMPOSITION FOR ORAL ADMINISTRATION INCLUDING AN HIV PROTEASE INHIBITOR AND A WATER-SOLUBLE TOCOFEROL DERIVATIVE, AND A METHOD FOR PREPARING SUCH COMPOSITION.Info
- Publication number
- AR006345A1 AR006345A1 ARP970101146A ARP970101146A AR006345A1 AR 006345 A1 AR006345 A1 AR 006345A1 AR P970101146 A ARP970101146 A AR P970101146A AR P970101146 A ARP970101146 A AR P970101146A AR 006345 A1 AR006345 A1 AR 006345A1
- Authority
- AR
- Argentina
- Prior art keywords
- composition
- hiv protease
- water
- protease inhibitor
- derivative
- Prior art date
Links
- 239000004030 hiv protease inhibitor Substances 0.000 title abstract 3
- 229940122440 HIV protease inhibitor Drugs 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 abstract 2
- 229960001295 tocopherol Drugs 0.000 abstract 2
- 229930003799 tocopherol Natural products 0.000 abstract 2
- 235000010384 tocopherol Nutrition 0.000 abstract 2
- 239000011732 tocopherol Substances 0.000 abstract 2
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 1
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 abstract 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 abstract 1
- 238000013160 medical therapy Methods 0.000 abstract 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 1
- -1 tetrahydro-3-furanyl Chemical group 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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
- 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
- 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
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
-
- 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
- A61K31/63—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide
- A61K31/635—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide having a heterocyclic ring, e.g. sulfadiazine
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Virology (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Se refiere a composiciones farmacéutica que contienen los inhibidores de proteasa del VIH, que incluyen específicamente el éster tetrahidro-3-furanílicodel ácido 3S-[3R*(1R*,2S*)]-3-[[(4-aminofenil)sulfonil](2-metilpropil)-amino] -2-hidroxi-]-fenilmetil)-propil]carbámico (conocido alternativamente comoVX 478 o 141W94), y un tocoferol, y a su uso en terapia médica. Las composiciones pueden ser preparadas disolviendo un inhibidor de proteasa delVIH en un derivado del tocoferolsol uble en agua.Refers to pharmaceutical compositions containing HIV protease inhibitors, specifically including 3S- [3R * (1R *, 2S *)] - 3 - [[(4-aminophenyl) sulfonyl] acid tetrahydro-3-furanyl). (2-methylpropyl) -amino] -2-hydroxy -] - phenylmethyl) -propyl] carbamic (alternatively known as VX 478 or 141W94), and a tocopherol, and its use in medical therapy. Compositions can be prepared by dissolving an HIV protease inhibitor in a tocopherol soluble derivative in water.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1389396P | 1996-03-22 | 1996-03-22 | |
| GBGB9606372.2A GB9606372D0 (en) | 1996-03-26 | 1996-03-26 | Pharmaceutical formulations |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR006345A1 true AR006345A1 (en) | 1999-08-25 |
Family
ID=26308992
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP970101146A AR006345A1 (en) | 1996-03-22 | 1997-03-21 | A PHARMACEUTICAL COMPOSITION FOR ORAL ADMINISTRATION INCLUDING AN HIV PROTEASE INHIBITOR AND A WATER-SOLUBLE TOCOFEROL DERIVATIVE, AND A METHOD FOR PREPARING SUCH COMPOSITION. |
Country Status (12)
| Country | Link |
|---|---|
| JP (1) | JP3117726B2 (en) |
| AR (1) | AR006345A1 (en) |
| BG (1) | BG64457B1 (en) |
| CO (1) | CO4790151A1 (en) |
| HU (1) | HU228026B1 (en) |
| ID (1) | ID16781A (en) |
| IL (1) | IL126185A (en) |
| MY (1) | MY126358A (en) |
| OA (1) | OA10880A (en) |
| PL (1) | PL187919B1 (en) |
| TW (1) | TW455491B (en) |
| WO (1) | WO1997035587A1 (en) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1017366A4 (en) * | 1996-09-01 | 2006-03-22 | Pharmos Corp | Solid coprecipitates for enhanced bioavailability of lipophilic substances |
| WO1998057648A1 (en) * | 1997-06-16 | 1998-12-23 | Vertex Pharmaceuticals Incorporated | Methods of increasing the bioavailability of stable crystal polymorphs of a compound |
| US5891845A (en) * | 1997-11-21 | 1999-04-06 | Fuisz Technologies Ltd. | Drug delivery systems utilizing liquid crystal structures |
| ES2140329B1 (en) * | 1997-12-04 | 2000-10-16 | Univ Granada | USE OF MASLINIC ACID AS A PROTEASE INHIBITOR FOR THE TREATMENT OF DISEASE CAUSED BY THE VIRUSES OF ACQUIRED IMMUNODEFICIENCY. |
| GB9812189D0 (en) * | 1998-06-05 | 1998-08-05 | Glaxo Group Ltd | Methods and compositions for increasing penetration of HIV protease inhibitors |
| EP1354587A1 (en) * | 2000-12-22 | 2003-10-22 | Takeda Chemical Industries, Ltd. | Medicinal compositions for oral use |
| WO2004050068A1 (en) | 2002-11-29 | 2004-06-17 | Janssen Pharmaceutica N.V. | Pharmaceutical compositions comprising a basic respectively acidic drug compound, a surfactant and a physiologically tolerable water-soluble acid respectively base |
| JP2006518380A (en) | 2003-01-31 | 2006-08-10 | スミスクライン・ビーチャム・コーポレイション | Solid dispersion composition |
| US20060068007A1 (en) * | 2004-09-24 | 2006-03-30 | Boehringer Ingelheim Pharmaceuticals, Inc. | Class of surfactant-like materials |
| CN101031284A (en) * | 2004-09-30 | 2007-09-05 | 伊斯曼化学公司 | Pharmaceutical formulations containing vitamin e tpgs molecules that solubilize lipophilic drugs without significant efflux inhibition, and use of such formulations |
| EP1880715A1 (en) * | 2006-07-19 | 2008-01-23 | Abbott GmbH & Co. KG | Pharmaceutically acceptable solubilizing composition and pharmaceutical dosage form containing same |
| SA109300195B1 (en) | 2008-03-28 | 2013-04-20 | Astrazeneca Ab | A Novel Anti-Cancer Pharmaceutical Composition |
| ITRM20120331A1 (en) | 2012-07-12 | 2014-01-13 | Guidotti & C Spa Labor | LIQUID ORAL PEDIATRIC COMPOSITIONS CONTAINING NEPADUTANT. |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU1677092A (en) * | 1991-03-20 | 1992-10-21 | Vertex Pharmaceuticals Incorporated | Tetrahydroxyalkane derivatives as inhibitors of hiv aspartyl protease |
| ES2112880T3 (en) * | 1991-11-08 | 1998-04-16 | Merck & Co Inc | HIV PROTEASE INHIBITORS USEFUL FOR AIDS TREATMENT. |
| IS2334B (en) * | 1992-09-08 | 2008-02-15 | Vertex Pharmaceuticals Inc., (A Massachusetts Corporation) | Aspartyl protease inhibitor of a new class of sulfonamides |
| WO1994013629A1 (en) * | 1992-12-11 | 1994-06-23 | Vertex Pharmaceuticals Incorporated | Mannitol derivatives and their use as inhibitors of aspartyl protease |
| US5484926A (en) * | 1993-10-07 | 1996-01-16 | Agouron Pharmaceuticals, Inc. | HIV protease inhibitors |
| ES2189721T3 (en) * | 1992-12-29 | 2003-07-16 | Abbott Lab | RETROVIRAL PROTEASA INHIBITORS. |
| US5714518A (en) * | 1993-01-15 | 1998-02-03 | Agouron Pharmaceuticals | HIV protease inhibitors and methods of making the same |
| AU1046895A (en) * | 1993-11-05 | 1995-05-23 | Merck & Co., Inc. | New quinazolines as inhibitors of hiv reverse transcriptase |
| IL111584A0 (en) * | 1993-11-18 | 1995-01-24 | Merck & Co Inc | Prodrugs of an inhibitor of hiv protease and pharmaceutical compositions containing them |
| CA2178760C (en) * | 1993-12-15 | 2000-08-01 | Joel R. Huff | Hiv protease inhibitors |
| WO1995024385A1 (en) * | 1994-03-07 | 1995-09-14 | Vertex Pharmaceuticals Incorporated | Sulphonamide derivatives as aspartyl protease inhibitors |
| GB9409778D0 (en) * | 1994-05-16 | 1994-07-06 | Dumex Ltd As | Compositions |
| US5527829A (en) * | 1994-05-23 | 1996-06-18 | Agouron Pharmaceuticals, Inc. | HIV protease inhibitors |
| EP0825849A1 (en) * | 1995-05-19 | 1998-03-04 | Abbott Laboratories | Self-emulsifying formulations of lipophilic drugs |
-
1997
- 1997-03-20 MY MYPI97001186A patent/MY126358A/en unknown
- 1997-03-21 AR ARP970101146A patent/AR006345A1/en active IP Right Grant
- 1997-03-21 JP JP09534017A patent/JP3117726B2/en not_active Expired - Lifetime
- 1997-03-21 HU HU9901887A patent/HU228026B1/en unknown
- 1997-03-21 ID IDP970927A patent/ID16781A/en unknown
- 1997-03-21 IL IL12618597A patent/IL126185A/en not_active IP Right Cessation
- 1997-03-21 WO PCT/EP1997/001438 patent/WO1997035587A1/en not_active Ceased
- 1997-03-21 CO CO97015457A patent/CO4790151A1/en unknown
- 1997-03-21 PL PL32891697A patent/PL187919B1/en unknown
- 1997-03-21 TW TW086103607A patent/TW455491B/en not_active IP Right Cessation
-
1998
- 1998-09-18 OA OA9800171A patent/OA10880A/en unknown
- 1998-10-12 BG BG102838A patent/BG64457B1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BG102838A (en) | 1999-09-30 |
| JP3117726B2 (en) | 2000-12-18 |
| JP2000500504A (en) | 2000-01-18 |
| HU228026B1 (en) | 2012-08-28 |
| BG64457B1 (en) | 2005-03-31 |
| PL328916A1 (en) | 1999-03-01 |
| HUP9901887A3 (en) | 2000-02-28 |
| TW455491B (en) | 2001-09-21 |
| IL126185A (en) | 2003-05-29 |
| ID16781A (en) | 1997-11-13 |
| CO4790151A1 (en) | 1999-05-31 |
| MY126358A (en) | 2006-09-29 |
| PL187919B1 (en) | 2004-11-30 |
| IL126185A0 (en) | 1999-05-09 |
| HUP9901887A2 (en) | 1999-12-28 |
| WO1997035587A1 (en) | 1997-10-02 |
| OA10880A (en) | 2001-10-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant, registration |