AR030039A1 - Composicion farmaceutica que comprende una droga inhibidora selectiva de la ciclooxigenasa-2, su uso en la fabricacion de un medicamento para tratar o prevenir afecciones mediadas por la ciclooxigenasa-2 y metodo para hacer dicho medicamento - Google Patents
Composicion farmaceutica que comprende una droga inhibidora selectiva de la ciclooxigenasa-2, su uso en la fabricacion de un medicamento para tratar o prevenir afecciones mediadas por la ciclooxigenasa-2 y metodo para hacer dicho medicamentoInfo
- Publication number
- AR030039A1 AR030039A1 ARP000106475A ARP000106475A AR030039A1 AR 030039 A1 AR030039 A1 AR 030039A1 AR P000106475 A ARP000106475 A AR P000106475A AR P000106475 A ARP000106475 A AR P000106475A AR 030039 A1 AR030039 A1 AR 030039A1
- Authority
- AR
- Argentina
- Prior art keywords
- cyclooxygenase
- medicinal product
- drug
- manufacture
- pharmaceutical composition
- Prior art date
Links
- 239000003814 drug Substances 0.000 title abstract 7
- 229940079593 drug Drugs 0.000 title abstract 6
- 102000010907 Cyclooxygenase 2 Human genes 0.000 title abstract 3
- 108010037462 Cyclooxygenase 2 Proteins 0.000 title abstract 3
- 229940124639 Selective inhibitor Drugs 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 229940126601 medicinal product Drugs 0.000 title 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 239000002245 particle Substances 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 229940093444 Cyclooxygenase 2 inhibitor Drugs 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000003255 cyclooxygenase 2 inhibitor Substances 0.000 abstract 1
- 229910052736 halogen Chemical group 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 125000004970 halomethyl group Chemical group 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole 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
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- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/58—One oxygen atom, e.g. butenolide
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- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
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Abstract
Composicion farmacéutica que comprende una o más unidades de dosificacion de administracion oral, cada una de las cuales comprende una droga inhibidora selectiva de la ciclooxigenasa-2 de baja solubilidad en agua en una cantidad terapéuticamente efectiva, donde la droga está presente en partículas solidas que tienen un tamano promedio de partícula de 500 nm a 900 nm y donde la droga inhibidora selectiva de la ciclooxigenasa-2 es un compuesto de formula (1) donde: R3 es un grupo metilo o amino; R4 es hidrogeno o un grupo alquilo C1-4 o alcoxilo; X es N o CR5, donde R5 es hidrogeno o halogeno; e Y y Z son independientemente átomos de carbono o de nitrogeno que definen con los átomos adyacentes un anillo de 5 a 6 miembros que no está sustituido o que está sustituido en una o más posiciones con grupos oxo, halo, metilo o halometilo. El uso de dicha composicion en la fabricacion de un medicamento para tratar oralmente de una a seis veces por día mediante una o más unidades de dosificacion, una condicion o una afeccion médica en un sujeto para la cual está indicado el tratamiento con un inhibidor de la ciclooxigenasa-2 y el método para obtener dicho medicamento.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16985699P | 1999-12-08 | 1999-12-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR030039A1 true AR030039A1 (es) | 2003-08-13 |
Family
ID=22617480
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP000106473A AR027897A1 (es) | 1999-12-08 | 2000-12-05 | Forma de celecoxib en estado solido que exhiben biodisponibilidad aumentada |
| ARP000106475A AR030039A1 (es) | 1999-12-08 | 2000-12-06 | Composicion farmaceutica que comprende una droga inhibidora selectiva de la ciclooxigenasa-2, su uso en la fabricacion de un medicamento para tratar o prevenir afecciones mediadas por la ciclooxigenasa-2 y metodo para hacer dicho medicamento |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP000106473A AR027897A1 (es) | 1999-12-08 | 2000-12-05 | Forma de celecoxib en estado solido que exhiben biodisponibilidad aumentada |
Country Status (21)
| Country | Link |
|---|---|
| KR (1) | KR100717570B1 (es) |
| CN (1) | CN1216869C (es) |
| AR (2) | AR027897A1 (es) |
| AU (1) | AU2041201A (es) |
| BG (1) | BG65239B1 (es) |
| CO (1) | CO5251445A1 (es) |
| CZ (1) | CZ20012875A3 (es) |
| EA (1) | EA200401397A1 (es) |
| EC (1) | ECSP003807A (es) |
| ES (1) | ES2236011T3 (es) |
| HU (1) | HUP0200580A3 (es) |
| MY (2) | MY128366A (es) |
| NZ (1) | NZ529933A (es) |
| OA (1) | OA11831A (es) |
| PE (1) | PE20010911A1 (es) |
| PT (2) | PT1150960E (es) |
| SV (1) | SV2002000235A (es) |
| TW (1) | TWI276435B (es) |
| WO (1) | WO2001041536A2 (es) |
| YU (1) | YU57801A (es) |
| ZA (2) | ZA200107146B (es) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CZ302448B6 (cs) | 2000-07-20 | 2011-05-25 | Lauras As | Farmaceutický prostredek |
| PT1404300E (pt) | 2001-06-22 | 2009-11-09 | Bend Res Inc | Composições farmacêuticas de dispersões de fármacos e polímeros neutros |
| US7927613B2 (en) | 2002-02-15 | 2011-04-19 | University Of South Florida | Pharmaceutical co-crystal compositions |
| US7790905B2 (en) | 2002-02-15 | 2010-09-07 | Mcneil-Ppc, Inc. | Pharmaceutical propylene glycol solvate compositions |
| US7446107B2 (en) | 2002-02-15 | 2008-11-04 | Transform Pharmaceuticals, Inc. | Crystalline forms of conazoles and methods of making and using the same |
| WO2004061433A1 (en) * | 2002-12-30 | 2004-07-22 | Transform Pharmaceuticals, Inc. | Pharmaceutical compositions with improved dissolution |
| IL163846A0 (en) | 2002-03-01 | 2005-12-18 | Univ South Florida | Multiple-component solid phases containing at least one active pharmaceutical ingredient |
| BR0309913A (pt) * | 2002-05-13 | 2005-06-07 | Pharmacia Corp | Compósito estável de celecoxib amorfo e processo para fabricar o mesmo |
| AU2003243354A1 (en) | 2002-05-31 | 2003-12-19 | Transform Pharmaceuticals, Inc. | Novel conazole crystalline forms and related processes, pharmaceutical compositions and methods |
| CA2489984A1 (en) * | 2002-06-21 | 2003-12-31 | Transform Pharmaceuticals, Inc. | Pharmaceutical compositions with improved dissolution |
| US20060052432A1 (en) * | 2002-09-20 | 2006-03-09 | Julius Remenar | Pharmaceutical compositions with improved dissolution |
| JP5021934B2 (ja) * | 2002-12-30 | 2012-09-12 | トランスフォーム・ファーマシューティカルズ・インコーポレイテッド | 改善された溶解性を有する医薬組成物 |
| US8183290B2 (en) | 2002-12-30 | 2012-05-22 | Mcneil-Ppc, Inc. | Pharmaceutically acceptable propylene glycol solvate of naproxen |
| JP5438898B2 (ja) * | 2004-06-29 | 2014-03-12 | タケダ ファーマ アクティーゼルスカブ | 水不溶性薬剤の速放性医薬組成物の製造と、本発明の方法で得られた医薬組成物 |
| GB0423103D0 (en) * | 2004-10-19 | 2004-11-17 | Boots Healthcare Int Ltd | Therapeutic agents |
| AU2006224623A1 (en) * | 2005-03-14 | 2006-09-21 | Nycomed Gmbh | Method for preventing cardiovascular diseases |
| CN103462920A (zh) * | 2012-06-06 | 2013-12-25 | 南京亿华药业有限公司 | 一种口服环加氧酶-2抑制剂塞来昔布的组合物 |
| CN103524416B (zh) * | 2013-10-29 | 2016-08-17 | 湖北华世通生物医药科技有限公司 | 一种塞来昔布新晶型a及其制备方法 |
| CN103539739B (zh) * | 2013-10-30 | 2016-02-10 | 中美华世通生物医药科技(武汉)有限公司 | 一种塞来昔布新晶型b及其制备方法 |
| CN103508958A (zh) * | 2013-10-30 | 2014-01-15 | 中美华世通生物医药科技(武汉)有限公司 | 一种塞来昔布新晶型c及其制备方法 |
| KR101476096B1 (ko) * | 2014-03-28 | 2014-12-24 | 대원제약주식회사 | 용해도가 향상된 쎄레콕시브의 약제학적 조성물 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5474995A (en) * | 1993-06-24 | 1995-12-12 | Merck Frosst Canada, Inc. | Phenyl heterocycles as cox-2 inhibitors |
| CA2276946A1 (en) * | 1993-11-30 | 1995-06-08 | G.D. Searle & Co. | Substituted pyrazolyl benzenesulfonamides and pharmaceutical compositions containing the same |
| US5633272A (en) * | 1995-02-13 | 1997-05-27 | Talley; John J. | Substituted isoxazoles for the treatment of inflammation |
| BR9607035A (pt) * | 1995-02-13 | 1997-11-04 | Searle & Co | Isoxazois substituidos para o tratamento de inflamação |
| US5756529A (en) * | 1995-09-29 | 1998-05-26 | G.D. Searle & Co. | Substituted pyrazolyl benzenesulfonamides for use in veterinary therapies |
| US5981576A (en) * | 1995-10-13 | 1999-11-09 | Merck Frosst Canada, Inc. | (Methylsulfonyl)phenyl-2-(5H)-furanones as COX-2 inhibitors |
| EP0863134A1 (en) * | 1997-03-07 | 1998-09-09 | Merck Frosst Canada Inc. | 2-(3,5-difluorophenyl)-3-(4-(methyl-sulfonyl)phenyl)-2-cyclopenten-1-one useful as an inhibitor of cyclooxygenase-2 |
| CA2328992A1 (en) * | 1998-04-27 | 1999-11-04 | Northwest Hospital | Nr-cam gene, nucleic acids and nucleic acid products for therapeutic and diagnostic uses for tumors |
-
2000
- 2000-12-01 ES ES00983865T patent/ES2236011T3/es not_active Expired - Lifetime
- 2000-12-01 OA OA1200100210A patent/OA11831A/en unknown
- 2000-12-01 PT PT00983865T patent/PT1150960E/pt unknown
- 2000-12-01 NZ NZ529933A patent/NZ529933A/en unknown
- 2000-12-01 HU HU0200580A patent/HUP0200580A3/hu unknown
- 2000-12-01 CZ CZ20012875A patent/CZ20012875A3/cs unknown
- 2000-12-01 CN CN008060835A patent/CN1216869C/zh not_active Expired - Fee Related
- 2000-12-01 YU YU57801A patent/YU57801A/sh unknown
- 2000-12-04 AU AU20412/01A patent/AU2041201A/en not_active Withdrawn
- 2000-12-04 WO PCT/US2000/030180 patent/WO2001041536A2/en not_active Ceased
- 2000-12-04 EC EC2000003807A patent/ECSP003807A/es unknown
- 2000-12-05 AR ARP000106473A patent/AR027897A1/es unknown
- 2000-12-06 MY MYPI20005733A patent/MY128366A/en unknown
- 2000-12-06 KR KR1020017010017A patent/KR100717570B1/ko not_active Expired - Fee Related
- 2000-12-06 MY MYPI20005730A patent/MY128971A/en unknown
- 2000-12-06 AR ARP000106475A patent/AR030039A1/es unknown
- 2000-12-06 EA EA200401397A patent/EA200401397A1/ru unknown
- 2000-12-06 PT PT00982255T patent/PT1150959E/pt unknown
- 2000-12-06 PE PE2000001299A patent/PE20010911A1/es not_active Application Discontinuation
- 2000-12-08 SV SV2000000235A patent/SV2002000235A/es not_active Application Discontinuation
- 2000-12-11 CO CO00094077A patent/CO5251445A1/es not_active Application Discontinuation
-
2001
- 2001-05-18 TW TW089125991A patent/TWI276435B/zh not_active IP Right Cessation
- 2001-08-09 BG BG105808A patent/BG65239B1/bg unknown
- 2001-08-29 ZA ZA200107146A patent/ZA200107146B/xx unknown
- 2001-08-29 ZA ZA200107149A patent/ZA200107149B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MY128366A (en) | 2007-01-31 |
| BG65239B1 (bg) | 2007-09-28 |
| KR20020002386A (ko) | 2002-01-09 |
| CN1411447A (zh) | 2003-04-16 |
| AR027897A1 (es) | 2003-04-16 |
| CN1216869C (zh) | 2005-08-31 |
| CZ20012875A3 (cs) | 2002-02-13 |
| EA200401397A1 (ru) | 2005-08-25 |
| CO5251445A1 (es) | 2003-02-28 |
| BG105808A (en) | 2002-09-30 |
| ECSP003807A (es) | 2005-07-06 |
| ZA200107146B (en) | 2002-08-29 |
| PT1150960E (pt) | 2005-06-30 |
| HUP0200580A2 (hu) | 2002-11-28 |
| ZA200107149B (en) | 2003-02-28 |
| TWI276435B (en) | 2007-03-21 |
| OA11831A (en) | 2005-08-23 |
| ES2236011T3 (es) | 2005-07-16 |
| PT1150959E (pt) | 2008-04-21 |
| SV2002000235A (es) | 2002-06-13 |
| KR100717570B1 (ko) | 2007-05-15 |
| MY128971A (en) | 2007-03-30 |
| AU2041201A (en) | 2001-06-18 |
| NZ529933A (en) | 2005-06-24 |
| PE20010911A1 (es) | 2001-09-10 |
| HUP0200580A3 (en) | 2002-12-28 |
| WO2001041536A2 (en) | 2001-06-14 |
| YU57801A (sh) | 2005-07-19 |
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