AR027896A1 - Composiciones valdecoxib - Google Patents
Composiciones valdecoxibInfo
- Publication number
- AR027896A1 AR027896A1 ARP000106472A ARP000106472A AR027896A1 AR 027896 A1 AR027896 A1 AR 027896A1 AR P000106472 A ARP000106472 A AR P000106472A AR P000106472 A ARP000106472 A AR P000106472A AR 027896 A1 AR027896 A1 AR 027896A1
- Authority
- AR
- Argentina
- Prior art keywords
- valdecoxib compositions
- valdecoxib
- compositions
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title 1
- LNPDTQAFDNKSHK-UHFFFAOYSA-N valdecoxib Chemical compound CC=1ON=C(C=2C=CC=CC=2)C=1C1=CC=C(S(N)(=O)=O)C=C1 LNPDTQAFDNKSHK-UHFFFAOYSA-N 0.000 title 1
- 229960002004 valdecoxib Drugs 0.000 title 1
Classifications
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- 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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- A—HUMAN NECESSITIES
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- 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
- A61K31/415—1,2-Diazoles
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- 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
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- A61K9/5021—Organic macromolecular compounds
- A61K9/5026—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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- C07D307/58—One oxygen atom, e.g. butenolide
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- 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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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Diabetes (AREA)
- Dermatology (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Emergency Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Molecular Biology (AREA)
- Urology & Nephrology (AREA)
- Biophysics (AREA)
- Immunology (AREA)
- Neurology (AREA)
- Endocrinology (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Toxicology (AREA)
- Cardiology (AREA)
- Reproductive Health (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Gastroenterology & Hepatology (AREA)
- Neurosurgery (AREA)
- Vascular Medicine (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16985699P | 1999-12-08 | 1999-12-08 | |
| US18163500P | 2000-02-10 | 2000-02-10 | |
| US20226900P | 2000-05-05 | 2000-05-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR027896A1 true AR027896A1 (es) | 2003-04-16 |
Family
ID=27389729
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP000106472A AR027896A1 (es) | 1999-12-08 | 2000-12-06 | Composiciones valdecoxib |
Country Status (29)
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| EP (1) | EP1165072A2 (enExample) |
| JP (1) | JP2003516353A (enExample) |
| KR (2) | KR100645866B1 (enExample) |
| CN (2) | CN1203852C (enExample) |
| AR (1) | AR027896A1 (enExample) |
| AU (3) | AU1930301A (enExample) |
| BG (1) | BG105873A (enExample) |
| BR (1) | BR0008059A (enExample) |
| CA (1) | CA2362816C (enExample) |
| CO (1) | CO5261582A1 (enExample) |
| CR (1) | CR6458A (enExample) |
| CZ (1) | CZ20013163A3 (enExample) |
| EA (1) | EA003639B1 (enExample) |
| EE (1) | EE200100414A (enExample) |
| HK (1) | HK1041637A1 (enExample) |
| HR (1) | HRP20010582A2 (enExample) |
| HU (1) | HUP0200409A3 (enExample) |
| IL (2) | IL144763A0 (enExample) |
| IS (1) | IS6040A (enExample) |
| MY (1) | MY138227A (enExample) |
| NO (1) | NO20013858L (enExample) |
| NZ (1) | NZ513963A (enExample) |
| PE (1) | PE20010940A1 (enExample) |
| PL (1) | PL351069A1 (enExample) |
| SK (1) | SK12692001A3 (enExample) |
| TR (1) | TR200102297T1 (enExample) |
| TW (1) | TWI265808B (enExample) |
| WO (2) | WO2001041761A2 (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2251361T3 (es) | 1998-10-30 | 2006-05-01 | Rj Innovation | Un metodo de prevencion de hipocalcemia puerperal en animales y composiciones utilizadas en el mismo. |
| CZ20022047A3 (cs) | 1999-12-23 | 2003-09-17 | Pfizer Products Inc. | Farmaceutické kompozice poskytující zvýšenou koncentraci léčiva |
| CN1638739A (zh) * | 2000-08-18 | 2005-07-13 | 法玛西雅厄普约翰美国公司 | 治疗成瘾性障碍的化合物 |
| AU2002303577B2 (en) * | 2001-05-04 | 2006-06-08 | Merck & Co., Inc. | Method and compositions for treating migraines |
| JP2005506987A (ja) * | 2001-09-26 | 2005-03-10 | ファルマシア・コーポレーション | 感覚的に許容される口内崩壊性組成物 |
| CZ2004456A3 (cs) * | 2001-10-10 | 2005-03-16 | Pharmacia Corporation | Kompozice na bázi valdekoxibu připravená rozprašovacím sušením, která se rozpadá v ústech |
| GB0124459D0 (en) * | 2001-10-11 | 2001-12-05 | Novartis Ag | Organic compounds |
| BR0213973A (pt) * | 2001-11-07 | 2004-08-31 | Pharmacia Corp | Composições de valdecoxib que se desintegram intra-oralmente preparadas pelo processo de granulação em leito fluidizado |
| RU2004114552A (ru) * | 2001-11-13 | 2005-02-20 | Фармация Корпорейшн (Us) | Пероральная дозированная форма сульфонамидного пролекарства |
| JP2006502083A (ja) * | 2002-01-07 | 2006-01-19 | ファルマシア コーポレイション | 高められた溶解速度を有する薬物混合物 |
| GB0201520D0 (en) * | 2002-01-23 | 2002-03-13 | Novartis Ag | Pharmaceutical uses |
| US20050025791A1 (en) * | 2002-06-21 | 2005-02-03 | Julius Remenar | Pharmaceutical compositions with improved dissolution |
| US7790905B2 (en) * | 2002-02-15 | 2010-09-07 | Mcneil-Ppc, Inc. | Pharmaceutical propylene glycol solvate compositions |
| WO2004026235A2 (en) * | 2002-09-20 | 2004-04-01 | Transform Pharmaceuticals, Inc. | Pharmaceutical compositions with improved dissolution |
| US7927613B2 (en) * | 2002-02-15 | 2011-04-19 | University Of South Florida | Pharmaceutical co-crystal compositions |
| EP1480639A1 (en) * | 2002-02-22 | 2004-12-01 | Warner-Lambert Company LLC | Combinations of an alpha-2-delta ligand with a selective inhibitor of cyclooxygenase-2 |
| JP4906233B2 (ja) * | 2002-03-01 | 2012-03-28 | ユニバーシティー オブ サウス フロリダ | 少なくとも1種の有効薬剤成分を含有する多構成要素固相 |
| GB0209265D0 (en) * | 2002-04-23 | 2002-06-05 | Novartis Ag | Organic compounds |
| GB0209257D0 (en) * | 2002-04-23 | 2002-06-05 | Novartis Ag | Organic compounds |
| AU2003247793A1 (en) * | 2002-06-26 | 2004-01-19 | Pharmacia Corporation | Stable liquid parenteral parecoxib formulation |
| JP2006514687A (ja) * | 2002-08-30 | 2006-05-11 | ファルマシア コーポレイション | 再現性のある医薬放出特性を示す医薬固形投与形態 |
| JP4494712B2 (ja) * | 2002-11-12 | 2010-06-30 | 大日本住友製薬株式会社 | マルチプルユニット型徐放性製剤 |
| DE50309605D1 (de) | 2002-11-22 | 2008-05-21 | Gruenenthal Gmbh | Verwendung von (1RS,3RS,6RS)-6-dimethylaminomethyl-1-(3-methoxy-phenyl)-cyclohexan-1,3-diol zur Behandlung von Entzündungsschmerz |
| US8183290B2 (en) | 2002-12-30 | 2012-05-22 | Mcneil-Ppc, Inc. | Pharmaceutically acceptable propylene glycol solvate of naproxen |
| US20050070524A1 (en) * | 2003-06-06 | 2005-03-31 | Pharmacia Corporation | Compositions of a cyclooxygenase-2 selective inhibitor and an anticonvulsant agent for the treatment of central nervous system disorders |
| US20050004224A1 (en) * | 2003-06-10 | 2005-01-06 | Pharmacia Corporation | Treatment of Alzheimer's disease with the R(-) isomer of a 2-arylpropionic acid non-steroidal anti-inflammatory drug alone or in combination with a cyclooxygenase-2 selective inhibitor |
| US20050080083A1 (en) * | 2003-07-10 | 2005-04-14 | Pharmacia Corporation | Compositions of a cyclooxygenase-2 selective inhibitor and an angiotensin II receptor antagonist for the treatment of central nervous system damage |
| CA2542277A1 (en) * | 2003-10-21 | 2005-05-12 | Pharmacia Corporation | Method for the treatment or prevention of respiratory inflammation with a cyclooxygenase-2 inhibitor in combination with a phosphodiesterase 4 inhibitor and compositions therewith |
| UA85750C2 (uk) | 2004-09-01 | 2009-02-25 | Евро-Селтик С.А. | Комбінація дозованих форм з контрольованим вивільненням опіоїдів |
| EP1868567A4 (en) * | 2005-03-29 | 2010-09-29 | Mcneil Ppc Inc | COMPOSITIONS WITH HYDROPHILIC DRUGS IN A HYDROPHOBIC MEDIUM |
| PT1885339E (pt) * | 2005-05-05 | 2015-10-12 | Bristol Myers Squibb Holdings Ireland | Formulações de um inibidor src/abl |
| US7942818B2 (en) * | 2006-02-01 | 2011-05-17 | University Of Florida Research Foundation, Inc. | Obstetric analgesia system |
| WO2007109244A2 (en) * | 2006-03-21 | 2007-09-27 | Morehouse School Of Medicine | Novel nanoparticles for delivery of active agents |
| EP1923053A1 (en) * | 2006-09-27 | 2008-05-21 | Novartis AG | Pharmaceutical compositions comprising nilotinib or its salt |
| JP5284967B2 (ja) | 2007-02-01 | 2013-09-11 | 武田薬品工業株式会社 | 打錠障害を生じない錠剤製剤 |
| FR2963889B1 (fr) * | 2010-08-20 | 2013-04-12 | Debregeas Et Associes Pharma | Formulations a base de nalbuphine et leurs utilisations |
| WO2019036503A1 (en) | 2017-08-14 | 2019-02-21 | Spruce Biosciences, Inc. | CORTICOTROPIN RELEASE FACTOR RECEPTOR ANTAGONISTS |
| CA3064445A1 (en) * | 2017-08-14 | 2019-02-21 | Spruce Biosciences, Inc. | Corticotropin releasing factor receptor antagonists |
| CN108644512B (zh) * | 2018-07-09 | 2023-06-30 | 南京氟源化工管道设备有限公司 | 一种钢衬聚四氟乙烯三通及其模压工艺 |
| EP3904356A4 (en) * | 2018-12-24 | 2022-09-21 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | TREATMENT USE OF PYRROLOPYRIMIDINE COMPOUND AND SOLID PHARMACEUTICAL COMPOSITION OF PYRROLOPYRIMIDINE COMPOUND |
| EP4175572A4 (en) | 2020-08-12 | 2024-03-27 | Spruce Biosciences, Inc. | Methods and compositions for treating polycystic ovary syndrome |
| US11273128B1 (en) * | 2021-04-15 | 2022-03-15 | Sandoz Ag | Elagolix formulation |
| US11708372B2 (en) | 2021-11-19 | 2023-07-25 | Spruce Biosciences, Inc. | Crystalline composition of tildacerfont and methods of use and preparation thereof |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0809636B1 (en) * | 1995-02-13 | 2002-09-04 | G.D. Searle & Co. | Substituted isoxazoles for the treatment of inflammation |
| 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 |
| SA99191255B1 (ar) * | 1998-11-30 | 2006-11-25 | جي دي سيرل اند كو | مركبات سيليكوكسيب celecoxib |
| CA2363590A1 (en) * | 1999-03-10 | 2000-09-14 | G.D. Searle & Co. | Method and composition for administering a cyclooxygenase-2 inhibitor |
-
2000
- 2000-12-04 BR BR0008059-4A patent/BR0008059A/pt not_active Application Discontinuation
- 2000-12-04 HR HR20010582A patent/HRP20010582A2/hr not_active Application Discontinuation
- 2000-12-04 CN CNB008059063A patent/CN1203852C/zh not_active Expired - Fee Related
- 2000-12-04 TR TR2001/02297T patent/TR200102297T1/xx unknown
- 2000-12-04 KR KR1020067002453A patent/KR100645866B1/ko not_active Expired - Fee Related
- 2000-12-04 PL PL00351069A patent/PL351069A1/xx not_active Application Discontinuation
- 2000-12-04 CN CNA200510065059XA patent/CN1679556A/zh active Pending
- 2000-12-04 WO PCT/US2000/032417 patent/WO2001041761A2/en not_active Ceased
- 2000-12-04 AU AU19303/01A patent/AU1930301A/en not_active Abandoned
- 2000-12-04 JP JP2001543106A patent/JP2003516353A/ja active Pending
- 2000-12-04 CA CA002362816A patent/CA2362816C/en not_active Expired - Fee Related
- 2000-12-04 EE EEP200100414A patent/EE200100414A/xx unknown
- 2000-12-04 KR KR1020017010031A patent/KR100664479B1/ko not_active Expired - Fee Related
- 2000-12-04 IL IL14476300A patent/IL144763A0/xx active IP Right Grant
- 2000-12-06 NZ NZ513963A patent/NZ513963A/en unknown
- 2000-12-06 HU HU0200409A patent/HUP0200409A3/hu unknown
- 2000-12-06 AU AU19310/01A patent/AU777402B2/en not_active Ceased
- 2000-12-06 AR ARP000106472A patent/AR027896A1/es unknown
- 2000-12-06 PE PE2000001298A patent/PE20010940A1/es not_active Application Discontinuation
- 2000-12-06 US US09/731,349 patent/US20020013357A1/en not_active Abandoned
- 2000-12-06 WO PCT/US2000/032433 patent/WO2001041762A2/en not_active Ceased
- 2000-12-06 TW TW089125989A patent/TWI265808B/zh not_active IP Right Cessation
- 2000-12-06 EP EP00982254A patent/EP1165072A2/en not_active Ceased
- 2000-12-06 SK SK1269-2001A patent/SK12692001A3/sk unknown
- 2000-12-06 CZ CZ20013163A patent/CZ20013163A3/cs unknown
- 2000-12-06 MY MYPI20005731A patent/MY138227A/en unknown
- 2000-12-06 HK HK02102619.5A patent/HK1041637A1/zh unknown
- 2000-12-06 EA EA200100872A patent/EA003639B1/ru not_active IP Right Cessation
- 2000-12-11 CO CO00094074A patent/CO5261582A1/es unknown
-
2001
- 2001-08-06 IL IL144763A patent/IL144763A/en not_active IP Right Cessation
- 2001-08-07 IS IS6040A patent/IS6040A/is unknown
- 2001-08-08 NO NO20013858A patent/NO20013858L/no not_active Application Discontinuation
- 2001-09-04 BG BG105873A patent/BG105873A/bg unknown
- 2001-09-11 CR CR6458A patent/CR6458A/es not_active Application Discontinuation
-
2005
- 2005-01-04 AU AU2005200015A patent/AU2005200015A1/en not_active Abandoned
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