WO2001041760A3 - Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect - Google Patents

Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect Download PDF

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Publication number
WO2001041760A3
WO2001041760A3 PCT/US2000/032434 US0032434W WO0141760A3 WO 2001041760 A3 WO2001041760 A3 WO 2001041760A3 US 0032434 W US0032434 W US 0032434W WO 0141760 A3 WO0141760 A3 WO 0141760A3
Authority
WO
WIPO (PCT)
Prior art keywords
cyclooxygenase
therapeutic effect
rapid onset
inhibitor compositions
compositions
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/US2000/032434
Other languages
French (fr)
Other versions
WO2001041760A8 (en
WO2001041760A9 (en
WO2001041760A2 (en
Inventor
Tugrul T Kararli
Mark J Kontny
Subhash Desai
Michael J Hageman
Royal J Haskell
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pharmacia LLC
Original Assignee
Pharmacia LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=46125549&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2001041760(A3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority to JP2001543105A priority Critical patent/JP2003523954A/en
Priority to EA200100870A priority patent/EA008242B1/en
Priority to EP04027798A priority patent/EP1525883A1/en
Priority to DK00980850T priority patent/DK1175214T3/en
Priority to EP00980850A priority patent/EP1175214B1/en
Priority to BR0008060-8A priority patent/BR0008060A/en
Priority to KR1020017010028A priority patent/KR100793668B1/en
Priority to AU18059/01A priority patent/AU784490B2/en
Priority to CA002362815A priority patent/CA2362815A1/en
Priority to CN00805974.8A priority patent/CN1433308A/en
Priority to PT00980850T priority patent/PT1175214E/en
Priority to CZ20013162A priority patent/CZ20013162A3/en
Priority to MXPA01008058A priority patent/MXPA01008058A/en
Priority to PE2000001301A priority patent/PE20010921A1/en
Priority to CO00093233A priority patent/CO5261556A1/en
Priority to AT00980850T priority patent/ATE283048T1/en
Application filed by Pharmacia LLC filed Critical Pharmacia LLC
Priority to PCT/US2000/032434 priority patent/WO2001041760A2/en
Priority to NZ513960A priority patent/NZ513960A/en
Priority to HU0201463A priority patent/HUP0201463A3/en
Priority to DE60016191T priority patent/DE60016191T2/en
Priority to PL00351944A priority patent/PL351944A1/en
Priority to ES00980850T priority patent/ES2236007T3/en
Priority to SK1267-2001A priority patent/SK12672001A3/en
Priority to US10/031,898 priority patent/US7172769B2/en
Priority to IL14476000A priority patent/IL144760A0/en
Priority to TW089125992A priority patent/TWI255180B/en
Priority to US09/874,504 priority patent/US20030064098A1/en
Publication of WO2001041760A2 publication Critical patent/WO2001041760A2/en
Priority to IL144760A priority patent/IL144760A/en
Priority to NO20013859A priority patent/NO20013859L/en
Priority to BG105808A priority patent/BG65239B1/en
Priority to ZA200107148A priority patent/ZA200107148B/en
Publication of WO2001041760A3 publication Critical patent/WO2001041760A3/en
Priority to US10/113,157 priority patent/US20020142045A1/en
Publication of WO2001041760A9 publication Critical patent/WO2001041760A9/en
Anticipated expiration legal-status Critical
Publication of WO2001041760A8 publication Critical patent/WO2001041760A8/en
Ceased legal-status Critical Current

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    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/60Heterocyclic 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 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
    • C07D213/61Halogen atoms or nitro radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic 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
    • C07D231/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D261/00Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/08Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more 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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    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic 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
    • C07D307/56Heterocyclic 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
    • C07D307/58One oxygen atom, e.g. butenolide
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    • C07DHETEROCYCLIC COMPOUNDS
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    • C07D311/02Heterocyclic 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
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/58Benzo[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

Pharmaceutical compositions are provided comprising one or more orally deliverable dose units, each comprising a selective cyclooxygenase-2 inhibitory drug of low water solubility in a therapeutically effective amount, wherein the drug is present in the form of solid particles, about 25 % to 100 % by weight of which are smaller than 1 νm. The compositions are useful in treatment or prophylaxis of cyclooxygenase-2 mediated conditions and disorders and have particular advantages where rapid onset of therapeutic effect is desired.
PCT/US2000/032434 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect Ceased WO2001041760A2 (en)

Priority Applications (32)

Application Number Priority Date Filing Date Title
IL14476000A IL144760A0 (en) 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect
NZ513960A NZ513960A (en) 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect
EP04027798A EP1525883A1 (en) 1999-12-08 2000-12-06 Ciclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect
DK00980850T DK1175214T3 (en) 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitor compositions with rapid onset of therapeutic effect
EP00980850A EP1175214B1 (en) 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect
BR0008060-8A BR0008060A (en) 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitory compositions having rapid onset of therapeutic efficacy
KR1020017010028A KR100793668B1 (en) 1999-12-08 2000-12-06 Celecoxib in solid form with enhanced bioavailability
AU18059/01A AU784490B2 (en) 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect
CA002362815A CA2362815A1 (en) 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect
CN00805974.8A CN1433308A (en) 2000-12-06 2000-12-06 Cyclooxygenase-2 inhibitor compositions having rapid on set therapeutic effect
PT00980850T PT1175214E (en) 1999-12-08 2000-12-06 COMPOSITIONS OF CYCLE-OXYGENASE-2 INHIBITOR WITH A QUICK START OF ITS THERAPEUTIC EFFECT
CZ20013162A CZ20013162A3 (en) 1999-12-08 2000-12-06 Preparations containing cyclooxygenase-2 inhibitor, exhibiting quick rise of therapeutic effect
MXPA01008058A MXPA01008058A (en) 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect.
PE2000001301A PE20010921A1 (en) 1999-12-08 2000-12-06 INHIBITING COMPOSITIONS OF CYCLOOXYGENASE-2 THAT HAVE A RAPID ONSET OF THERAPEUTIC EFFECT
CO00093233A CO5261556A1 (en) 1999-12-08 2000-12-06 CYCLLOXYGENASE-2 INHIBITING COMPOSITIONS THAT HAVE FAST THERAPEUTIC EFFECT ACCESS
AT00980850T ATE283048T1 (en) 1999-12-08 2000-12-06 COMPOSITIONS CONTAINING CYCLOOXYGENASE-2 INHIBITORS WITH A RAPID ONSET OF ACTION
EA200100870A EA008242B1 (en) 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect and methods for treating diseases
PCT/US2000/032434 WO2001041760A2 (en) 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect
HU0201463A HUP0201463A3 (en) 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect and their use
JP2001543105A JP2003523954A (en) 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitor composition with rapid onset of therapeutic effect
SK1267-2001A SK12672001A3 (en) 1999-12-08 2000-12-06 Compositions of cyclooxygenase-2 inhibitor having rapid onset of therapeutic effect
PL00351944A PL351944A1 (en) 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect
ES00980850T ES2236007T3 (en) 1999-12-08 2000-12-06 CYCLLOXYGENASA-2 EU INHIBITOR COMPOSITIONS HAS A FAST THERAPEUTIC EFFECT.
DE60016191T DE60016191T2 (en) 1999-12-08 2000-12-06 CYCLOOXYGENASE-2 INHIBITORY COMPOSITIONS WITH FAST ACTION INTRUSION
US10/031,898 US7172769B2 (en) 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect
TW089125992A TWI255180B (en) 1999-12-08 2001-05-31 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect
US09/874,504 US20030064098A1 (en) 1999-12-08 2001-06-05 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect
IL144760A IL144760A (en) 1999-12-08 2001-08-06 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect
NO20013859A NO20013859L (en) 1999-12-08 2001-08-08 Cyclooxygenase-2 inhibitory drugs with rapid onset of therapeutic effect
BG105808A BG65239B1 (en) 1999-12-08 2001-08-09 Polymorphic crystalline forms of celecoxib
ZA200107148A ZA200107148B (en) 1999-12-08 2001-08-29 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect.
US10/113,157 US20020142045A1 (en) 1999-12-08 2002-04-01 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US16985699P 1999-12-08 1999-12-08
US60/169,856 1999-12-08
PCT/US2000/032434 WO2001041760A2 (en) 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US10031898 A-371-Of-International 2000-12-06
US10/113,157 Continuation-In-Part US20020142045A1 (en) 1999-12-08 2002-04-01 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect

Publications (4)

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WO2001041760A2 WO2001041760A2 (en) 2001-06-14
WO2001041760A3 true WO2001041760A3 (en) 2001-11-08
WO2001041760A9 WO2001041760A9 (en) 2002-05-23
WO2001041760A8 WO2001041760A8 (en) 2002-10-17

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PCT/US2000/032434 Ceased WO2001041760A2 (en) 1999-12-08 2000-12-06 Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect

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US (3) US7172769B2 (en)
EP (2) EP1175214B1 (en)
JP (1) JP2003523954A (en)
KR (1) KR100793668B1 (en)
AT (1) ATE283048T1 (en)
AU (1) AU784490B2 (en)
BR (1) BR0008060A (en)
CA (1) CA2362815A1 (en)
CO (1) CO5261556A1 (en)
CZ (1) CZ20013162A3 (en)
DE (1) DE60016191T2 (en)
DK (1) DK1175214T3 (en)
EA (1) EA008242B1 (en)
ES (1) ES2236007T3 (en)
HU (1) HUP0201463A3 (en)
IL (2) IL144760A0 (en)
MX (1) MXPA01008058A (en)
NO (1) NO20013859L (en)
NZ (1) NZ513960A (en)
PE (1) PE20010921A1 (en)
PL (1) PL351944A1 (en)
PT (1) PT1175214E (en)
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7790905B2 (en) 2002-02-15 2010-09-07 Mcneil-Ppc, Inc. Pharmaceutical propylene glycol solvate compositions
US7927613B2 (en) 2002-02-15 2011-04-19 University Of South Florida Pharmaceutical co-crystal compositions
US8183290B2 (en) 2002-12-30 2012-05-22 Mcneil-Ppc, Inc. Pharmaceutically acceptable propylene glycol solvate of naproxen
US10633344B2 (en) 2002-03-01 2020-04-28 University Of South Florida Multiple-component solid phases containing at least one active pharmaceutical ingredient

Families Citing this family (60)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030040790A1 (en) * 1998-04-15 2003-02-27 Furst Joseph G. Stent coating
US20020099438A1 (en) 1998-04-15 2002-07-25 Furst Joseph G. Irradiated stent coating
US7967855B2 (en) * 1998-07-27 2011-06-28 Icon Interventional Systems, Inc. Coated medical device
US8070796B2 (en) 1998-07-27 2011-12-06 Icon Interventional Systems, Inc. Thrombosis inhibiting graft
US20040097549A1 (en) * 1999-03-10 2004-05-20 Pharmacia Corporation Method and composition for administering a cyclooxygenase-2 inhibitor
WO2001078724A1 (en) * 2000-04-18 2001-10-25 Pharmacia Corporation Rapid-onset formulation of a selective cyclooxigenase-2
US20040156872A1 (en) * 2000-05-18 2004-08-12 Elan Pharma International Ltd. Novel nimesulide compositions
UA80682C2 (en) * 2001-08-06 2007-10-25 Pharmacia Corp Orally deliverable stabilized oral suspension formulation and process for the incresaing physical stability of thixotropic pharmaceutical composition
AU2002334939A1 (en) * 2001-10-12 2003-04-22 Eugene R. Cooper Compositions having a combination of particles for immediate release and for controlled release
US8740973B2 (en) * 2001-10-26 2014-06-03 Icon Medical Corp. Polymer biodegradable medical device
JP2005512990A (en) * 2001-11-07 2005-05-12 ファルマシア・コーポレーション Orally disintegrating valdecoxib composition produced by fluidized bed granulation method
US20100311701A1 (en) * 2002-02-15 2010-12-09 Transform Pharmaceuticals, Inc Pharmaceutical Co-Crystal Compositions
WO2004026235A2 (en) * 2002-09-20 2004-04-01 Transform Pharmaceuticals, Inc. Pharmaceutical compositions with improved dissolution
WO2004000284A1 (en) * 2002-06-21 2003-12-31 Transform Pharmaceuticals, Inc. Pharmaceutical compositions with improved dissolution
GB0206200D0 (en) * 2002-03-15 2002-05-01 Glaxo Group Ltd Pharmaceutical compositions
US20040038303A1 (en) * 2002-04-08 2004-02-26 Unger Gretchen M. Biologic modulations with nanoparticles
GB0209257D0 (en) * 2002-04-23 2002-06-05 Novartis Ag Organic compounds
JP2006511499A (en) * 2002-05-13 2006-04-06 ファルマシア コーポレイション Stable amorphous celecoxib composite and its preparation
US8016881B2 (en) * 2002-07-31 2011-09-13 Icon Interventional Systems, Inc. Sutures and surgical staples for anastamoses, wound closures, and surgical closures
ATE325115T1 (en) 2002-08-19 2006-06-15 Glaxo Group Ltd PYRIMIDINE DERIVATIVES AS SELECTIVE COX-2 INHIBITORS
UY27939A1 (en) 2002-08-21 2004-03-31 Glaxo Group Ltd COMPOUNDS
GB0221443D0 (en) 2002-09-16 2002-10-23 Glaxo Group Ltd Pyridine derivates
GB0227443D0 (en) * 2002-11-25 2002-12-31 Glaxo Group Ltd Pyrimidine derivatives
US20040156894A1 (en) * 2003-02-07 2004-08-12 Grother Leon Paul Use of edible acids in fast-dispersing pharmaceutical solid dosage forms
WO2005016249A2 (en) * 2003-07-11 2005-02-24 Pharmacia Corporation Compositions of a chromene or phenyl acetic acid cyclooxygenase-2 selective inhibitor and an ace inhibitor for the treatment of central nervous system damage
US7282217B1 (en) 2003-08-29 2007-10-16 Kv Pharmaceutical Company Rapidly disintegrable tablets
TR200301552A1 (en) * 2003-09-18 2005-10-21 Nobel İlaç Sanayi̇ Ve Ti̇caret A. Ş. Novel oral pharmacological formulations of rofecoxib.
AU2003303744A1 (en) * 2003-10-31 2005-06-17 Elan Pharma International Ltd. Novel nimesulide compositions
US7211108B2 (en) * 2004-01-23 2007-05-01 Icon Medical Corp. Vascular grafts with amphiphilic block copolymer coatings
EP1814914A2 (en) * 2004-10-29 2007-08-08 The Regents of the University of Colorado Antibodies that bind urokinase-type plasminogen activator and epitopes therefor
US8323333B2 (en) * 2005-03-03 2012-12-04 Icon Medical Corp. Fragile structure protective coating
US9107899B2 (en) 2005-03-03 2015-08-18 Icon Medical Corporation Metal alloys for medical devices
US20060201601A1 (en) * 2005-03-03 2006-09-14 Icon Interventional Systems, Inc. Flexible markers
JP5335244B2 (en) * 2005-03-03 2013-11-06 アイコン メディカル コーポレーション Medical member using improved metal alloy
US20060264914A1 (en) * 2005-03-03 2006-11-23 Icon Medical Corp. Metal alloys for medical devices
WO2006110197A2 (en) * 2005-03-03 2006-10-19 Icon Medical Corp. Polymer biodegradable medical device
US7540995B2 (en) * 2005-03-03 2009-06-02 Icon Medical Corp. Process for forming an improved metal alloy stent
US8580954B2 (en) * 2006-03-28 2013-11-12 Hospira, Inc. Formulations of low dose diclofenac and beta-cyclodextrin
WO2008008291A2 (en) * 2006-07-13 2008-01-17 Icon Medical Corp. Stent
US7495024B2 (en) 2006-08-07 2009-02-24 Via Pharmaceuticals, Inc. Phenylalkyl N-hydroxyureas for combating atherosclerotic plaque
WO2008065502A1 (en) * 2006-11-29 2008-06-05 Pfizer Products Inc. Pharmaceutical compositions based on a) nanoparticles comprising enteric polymers and b) casein
WO2008135829A2 (en) * 2007-05-03 2008-11-13 Pfizer Products Inc. Nanoparticles comprising cox-2 inhibitors and a non-ionizable polymer
US9233078B2 (en) * 2007-12-06 2016-01-12 Bend Research, Inc. Nanoparticles comprising a non-ionizable polymer and an Amine-functionalized methacrylate copolymer
KR100922519B1 (en) 2008-11-12 2009-10-20 대원제약주식회사 Pharmaceutical preparations for oral administration with improved dissolution rate and stability containing felubiprofen
WO2010150144A2 (en) 2009-06-25 2010-12-29 Wockhardt Research Centre Low dose pharmaceutical compositions of celecoxib
US8398916B2 (en) 2010-03-04 2013-03-19 Icon Medical Corp. Method for forming a tubular medical device
KR101237646B1 (en) * 2010-12-09 2013-03-04 주식회사 드림파마 Solid dispersion comprising celecoxib with improved bioavailibity, pharmaceutical composition comprising the solid dispersion, and preparation method of the solid dispersion
CN102952117B (en) * 2011-08-25 2014-11-26 青岛欧博方医药科技有限公司 Preparation method of imidazole derivatives
KR20140100170A (en) * 2013-02-05 2014-08-14 에스케이케미칼주식회사 oral administrable celecoxib composition
RU2715714C2 (en) 2013-03-04 2020-03-03 Безен Хелткэа Люксембург Сарл Dry pharmaceutical compositions containing nanoparticles of active agent bound to carrier particles
US9517234B2 (en) 2013-03-15 2016-12-13 Cba Pharma, Inc. Tetrandrine family pharmaceutical formulations and method
KR101446601B1 (en) * 2014-01-29 2014-10-07 크리스탈지노믹스(주) Pharmaceutical composition and capsule formulation comprising 5-(4-(aminosulfonyl)phenyl)-2,2-dimethyl-4-(3-fluorophenyl)-3(2h)-furanone
WO2015199816A1 (en) 2014-06-24 2015-12-30 Icon Medical Corp. Improved metal alloys for medical devices
CA2959660A1 (en) 2014-09-03 2016-03-10 Genesegues, Inc. Therapeutic nanoparticles and related compositions, methods, and systems
AU2016267685A1 (en) * 2015-05-28 2017-12-07 Dr. Reddy's Laboratories Ltd. Oral composition of celecoxib for treatment of pain
HUP1500618A2 (en) 2015-12-16 2017-06-28 Druggability Tech Ip Holdco Ltd Complexes of celecoxib and its salts and derivatives, process for the preparation thereof and pharmaceutical composition containing them
WO2017151548A1 (en) 2016-03-04 2017-09-08 Mirus Llc Stent device for spinal fusion
CA3045128A1 (en) 2016-12-14 2018-06-21 Druggability Technologies Ip Holdco Limited Pharmaceutical composition containing celecoxib
CA3144079A1 (en) 2020-12-28 2022-06-28 Biodelivery Sciences International, Inc. Methods of treating pain
IT202400001236A1 (en) * 2024-01-23 2025-07-23 Regis S R L PROCEDURE FOR THE PRODUCTION OF REDISPERDABLE PIGMENT GRANULES AND RESPECTIVE REDISPERDABLE PIGMENT GRANULES

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996025405A1 (en) * 1995-02-13 1996-08-22 G.D. Searle & Co. Substituted isoxazoles for the treatment of inflammation
US5756529A (en) * 1995-09-29 1998-05-26 G.D. Searle & Co. Substituted pyrazolyl benzenesulfonamides for use in veterinary therapies
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
WO2000032189A1 (en) * 1998-11-30 2000-06-08 G. D. Searle & Co. Celecoxib compositions
WO2000053149A2 (en) * 1999-03-10 2000-09-14 G.D. Searle & Co. Method and composition for administering a cyclooxygenase-2 inhibitor

Family Cites Families (188)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4826689A (en) 1984-05-21 1989-05-02 University Of Rochester Method for making uniformly sized particles from water-insoluble organic compounds
FR2634376B1 (en) 1988-07-21 1992-04-17 Farmalyoc NOVEL SOLID AND POROUS UNIT FORM COMPRISING MICROPARTICLES AND / OR NANOPARTICLES, AS WELL AS ITS PREPARATION
IT1227626B (en) 1988-11-28 1991-04-23 Vectorpharma Int SUPPORTED DRUGS WITH INCREASED DISSOLUTION SPEED AND PROCEDURE FOR THEIR PREPARATION
US5298202A (en) * 1989-07-28 1994-03-29 W. R. Grace & Co.-Conn. Double bubble process for making strong, thin film
US5616458A (en) 1990-03-14 1997-04-01 Board Of Regents, University Of Tx System Tripterygium wilfordii hook F extracts and components, and uses thereof
IT1243390B (en) 1990-11-22 1994-06-10 Vectorpharma Int PHARMACEUTICAL COMPOSITIONS IN THE FORM OF PARTICLES SUITABLE FOR THE CONTROLLED RELEASE OF PHARMACOLOGICALLY ACTIVE SUBSTANCES AND PROCEDURE FOR THEIR PREPARATION.
US5145684A (en) 1991-01-25 1992-09-08 Sterling Drug Inc. Surface modified drug nanoparticles
US5552160A (en) * 1991-01-25 1996-09-03 Nanosystems L.L.C. Surface modified NSAID nanoparticles
WO1993025190A1 (en) 1992-06-10 1993-12-23 Eastman Kodak Company Surface modified nsaid nanoparticles
NZ248813A (en) 1992-11-25 1995-06-27 Eastman Kodak Co Polymeric grinding media used in grinding pharmaceutical substances
US5298262A (en) 1992-12-04 1994-03-29 Sterling Winthrop Inc. Use of ionic cloud point modifiers to prevent particle aggregation during sterilization
US5346702A (en) 1992-12-04 1994-09-13 Sterling Winthrop Inc. Use of non-ionic cloud point modifiers to minimize nanoparticle aggregation during sterilization
US5302401A (en) 1992-12-09 1994-04-12 Sterling Winthrop Inc. Method to reduce particle size growth during lyophilization
US5340564A (en) 1992-12-10 1994-08-23 Sterling Winthrop Inc. Formulations comprising olin 10-G to prevent particle aggregation and increase stability
US5336507A (en) 1992-12-11 1994-08-09 Sterling Winthrop Inc. Use of charged phospholipids to reduce nanoparticle aggregation
US5604260A (en) 1992-12-11 1997-02-18 Merck Frosst Canada Inc. 5-methanesulfonamido-1-indanones as an inhibitor of cyclooxygenase-2
US5429824A (en) 1992-12-15 1995-07-04 Eastman Kodak Company Use of tyloxapole as a nanoparticle stabilizer and dispersant
US5352459A (en) 1992-12-16 1994-10-04 Sterling Winthrop Inc. Use of purified surface modifiers to prevent particle aggregation during sterilization
US5543297A (en) 1992-12-22 1996-08-06 Merck Frosst Canada, Inc. Human cyclooxygenase-2 cDNA and assays for evaluating cyclooxygenase-2 activity
EP0764644A1 (en) 1993-01-15 1997-03-26 G.D. Searle & Co. Use of medicaments containing 3,4-diaryl furans and analogs thereof for treating a gastrointestinal condition
DE69421173T2 (en) 1993-03-15 2000-01-20 Mallinckrodt, Inc. NEW NITROGEN-SULFUR LIGANDS BASED ON A HETEROCYCLUS FOR USE IN MATERIALS FOR RADIOGRAPHIC IMAGING
US5380738A (en) 1993-05-21 1995-01-10 Monsanto Company 2-substituted oxazoles further substituted by 4-fluorophenyl and 4-methylsulfonylphenyl as antiinflammatory agents
US5436265A (en) 1993-11-12 1995-07-25 Merck Frosst Canada, Inc. 1-aroyl-3-indolyl alkanoic acids and derivatives thereof useful as anti-inflammatory agents
US5474995A (en) 1993-06-24 1995-12-12 Merck Frosst Canada, Inc. Phenyl heterocycles as cox-2 inhibitors
US5593992A (en) 1993-07-16 1997-01-14 Smithkline Beecham Corporation Compounds
US5353459A (en) * 1993-09-01 1994-10-11 Nike, Inc. Method for inflating a bladder
US5344991A (en) 1993-10-29 1994-09-06 G.D. Searle & Co. 1,2 diarylcyclopentenyl compounds for the treatment of inflammation
US5475018A (en) 1993-11-30 1995-12-12 G. D. Searle & Co. 1,5-diphenyl pyrazole compounds for treatment of inflammation
US5401765A (en) 1993-11-30 1995-03-28 G. D. Searle 1,4,5-triphenyl pyrazolyl compounds for the treatment of inflammation and inflammation-related disorders
ES2141916T3 (en) * 1993-11-30 2000-04-01 Searle & Co SUBSTITUTED PIRAZOLIL-BENZENOSULPHONAMIDES FOR THE TREATMENT OF INFLAMMATION.
US5434178A (en) 1993-11-30 1995-07-18 G.D. Searle & Co. 1,3,5 trisubstituted pyrazole compounds for treatment of inflammation
US5466823A (en) 1993-11-30 1995-11-14 G.D. Searle & Co. Substituted pyrazolyl benzenesulfonamides
US5393790A (en) 1994-02-10 1995-02-28 G.D. Searle & Co. Substituted spiro compounds for the treatment of inflammation
WO1995030652A1 (en) 1994-05-04 1995-11-16 G.D. Searle & Co. Substituted spirodienes for the treatment of inflammation
US5418254A (en) 1994-05-04 1995-05-23 G. D. Searle & Co. Substituted cyclopentadienyl compounds for the treatment of inflammation
US5587143A (en) 1994-06-28 1996-12-24 Nanosystems L.L.C. Butylene oxide-ethylene oxide block copolymer surfactants as stabilizer coatings for nanoparticle compositions
US5486534A (en) 1994-07-21 1996-01-23 G. D. Searle & Co. 3,4-substituted pyrazoles for the treatment of inflammation
EP0772606A1 (en) 1994-07-27 1997-05-14 G.D. SEARLE & CO. Substituted thiazoles for the treatment of inflammation
US5616601A (en) 1994-07-28 1997-04-01 Gd Searle & Co 1,2-aryl and heteroaryl substituted imidazolyl compounds for the treatment of inflammation
US5620999A (en) 1994-07-28 1997-04-15 Weier; Richard M. Benzenesulfonamide subtituted imidazolyl compounds for the treatment of inflammation
US5521213A (en) 1994-08-29 1996-05-28 Merck Frosst Canada, Inc. Diaryl bicyclic heterocycles as inhibitors of cyclooxygenase-2
US5420343A (en) 1994-08-31 1995-05-30 G. D. Searle & Co. Derivatives of aromatic cyclic alkylethers
US5585504A (en) 1994-09-16 1996-12-17 Merck & Co., Inc. Process of making cox-2 inhibitors having a lactone bridge
US5696143A (en) 1994-09-20 1997-12-09 Talley; John J. Benz G! indazolyl derivatives for the treatment of inflammation
US5547975A (en) 1994-09-20 1996-08-20 Talley; John J. Benzopyranopyrazolyl derivatives for the treatment of inflammation
JPH10507765A (en) 1994-10-27 1998-07-28 メルク フロスト カナダ インコーポレーテツド Stilbene derivatives useful as cyclooxygenase-2 inhibitors
US5739166A (en) 1994-11-29 1998-04-14 G.D. Searle & Co. Substituted terphenyl compounds for the treatment of inflammation
JP3181190B2 (en) 1994-12-20 2001-07-03 日本たばこ産業株式会社 Oxazole derivatives
JP2636819B2 (en) 1994-12-20 1997-07-30 日本たばこ産業株式会社 Oxazole-based heterocyclic aromatic compounds
DE69529690T2 (en) 1994-12-21 2003-11-13 Merck Frosst Canada & Co., Halifax DIARYL-2 (5H) -FUARANONE AS COX-2 INHIBITORS
US5585108A (en) 1994-12-30 1996-12-17 Nanosystems L.L.C. Formulations of oral gastrointestinal therapeutic agents in combination with pharmaceutically acceptable clays
US5560932A (en) 1995-01-10 1996-10-01 Nano Systems L.L.C. Microprecipitation of nanoparticulate pharmaceutical agents
US5662883A (en) 1995-01-10 1997-09-02 Nanosystems L.L.C. Microprecipitation of micro-nanoparticulate pharmaceutical agents
US5665331A (en) 1995-01-10 1997-09-09 Nanosystems L.L.C. Co-microprecipitation of nanoparticulate pharmaceutical agents with crystal growth modifiers
US5552422A (en) 1995-01-11 1996-09-03 Merck Frosst Canada, Inc. Aryl substituted 5,5 fused aromatic nitrogen compounds as anti-inflammatory agents
US5569448A (en) 1995-01-24 1996-10-29 Nano Systems L.L.C. Sulfated nonionic block copolymer surfactants as stabilizer coatings for nanoparticle compositions
AU4479096A (en) 1995-01-31 1996-08-21 Merck Frosst Canada Inc. 5-methanesulfonamido-3h-isobenzofuran-1-ones as inhibitors of cyclooxygenase-2
US5560931A (en) 1995-02-14 1996-10-01 Nawosystems L.L.C. Formulations of compounds as nanoparticulate dispersions in digestible oils or fatty acids
US5571536A (en) 1995-02-06 1996-11-05 Nano Systems L.L.C. Formulations of compounds as nanoparticulate dispersions in digestible oils or fatty acids
US5503723A (en) 1995-02-08 1996-04-02 Eastman Kodak Company Isolation of ultra small particles
US5518738A (en) * 1995-02-09 1996-05-21 Nanosystem L.L.C. Nanoparticulate nsaid compositions
US5534270A (en) 1995-02-09 1996-07-09 Nanosystems Llc Method of preparing stable drug nanoparticles
US5622938A (en) 1995-02-09 1997-04-22 Nano Systems L.L.C. Sugar base surfactant for nanocrystals
US5686470A (en) 1995-02-10 1997-11-11 Weier; Richard M. 2, 3-substituted pyridines for the treatment of inflammation
US5591456A (en) 1995-02-10 1997-01-07 Nanosystems L.L.C. Milled naproxen with hydroxypropyl cellulose as a dispersion stabilizer
US5596008A (en) 1995-02-10 1997-01-21 G. D. Searle & Co. 3,4-Diaryl substituted pyridines for the treatment of inflammation
US5633272A (en) 1995-02-13 1997-05-27 Talley; John J. Substituted isoxazoles for the treatment of inflammation
US5573783A (en) 1995-02-13 1996-11-12 Nano Systems L.L.C. Redispersible nanoparticulate film matrices with protective overcoats
US5510118A (en) 1995-02-14 1996-04-23 Nanosystems Llc Process for preparing therapeutic compositions containing nanoparticles
US5580579A (en) 1995-02-15 1996-12-03 Nano Systems L.L.C. Site-specific adhesion within the GI tract using nanoparticles stabilized by high molecular weight, linear poly (ethylene oxide) polymers
US5718919A (en) 1995-02-24 1998-02-17 Nanosystems L.L.C. Nanoparticles containing the R(-)enantiomer of ibuprofen
US5747001A (en) 1995-02-24 1998-05-05 Nanosystems, L.L.C. Aerosols containing beclomethazone nanoparticle dispersions
US5565188A (en) 1995-02-24 1996-10-15 Nanosystems L.L.C. Polyalkylene block copolymers as surface modifiers for nanoparticles
JP3802581B2 (en) 1995-03-01 2006-07-26 富山化学工業株式会社 Novel biphenyl derivatives or salts thereof and anti-inflammatory agents containing them
EA199700209A1 (en) 1995-04-04 1998-04-30 Глаксо Груп Лимитед IMIDAZO [1,2-a] PYRIDINE DERIVATIVES
US5691374A (en) 1995-05-18 1997-11-25 Merck Frosst Canada Inc. Diaryl-5-oxygenated-2-(5H) -furanones as COX-2 inhibitors
US5639780A (en) 1995-05-22 1997-06-17 Merck Frosst Canada, Inc. N-benzyl indol-3-yl butanoic acid derivatives as cyclooxygenase inhibitors
US5604253A (en) 1995-05-22 1997-02-18 Merck Frosst Canada, Inc. N-benzylindol-3-yl propanoic acid derivatives as cyclooxygenase inhibitors
US5510368A (en) 1995-05-22 1996-04-23 Merck Frosst Canada, Inc. N-benzyl-3-indoleacetic acids as antiinflammatory drugs
DK0828717T3 (en) 1995-05-25 2003-01-06 Searle & Co Process for the preparation of 3-haloalkyl-1H-pyrazole
CA2223154A1 (en) 1995-06-02 1996-12-05 G.D. Searle & Co. Heterocyclo substituted hydroxamic acid derivatives as cyclooxygenase-2 and 5-lipoxygenase inhibitors
US5643933A (en) 1995-06-02 1997-07-01 G. D. Searle & Co. Substituted sulfonylphenylheterocycles as cyclooxygenase-2 and 5-lipoxygenase inhibitors
US5739143A (en) 1995-06-07 1998-04-14 Smithkline Beecham Corporation Imidazole compounds and compositions
IL118544A (en) 1995-06-07 2001-08-08 Smithkline Beecham Corp Imidazole derivatives, process for their preparation and pharmaceutical compositions comprising them
GB9514518D0 (en) 1995-07-15 1995-09-13 Sod Conseils Rech Applic Guanidine salt inhibitors of NO synthase and cyclooxygenase
DE59605948D1 (en) 1995-07-21 2000-11-02 Nycomed Austria Gmbh Linz DERIVATIVES OF BENZOSULFONAMIDES AS AN INHIBITORS OF THE ENZYME CYCLOOXYGENASE II
JPH0977664A (en) 1995-09-13 1997-03-25 Yakult Honsha Co Ltd Cyclooxygenase-2 specific inhibitor and anti-inflammatory agent
JPH09176038A (en) 1995-09-18 1997-07-08 Hisamitsu Pharmaceut Co Inc Anti-inflammatory antisense drug
AU7284096A (en) 1995-10-09 1997-04-30 Dieter Binder Heterocyclically-substituted 1-indole carboxamides as cyclo-oxygenase-2 inhibitors
US5981576A (en) 1995-10-13 1999-11-09 Merck Frosst Canada, Inc. (Methylsulfonyl)phenyl-2-(5H)-furanones as COX-2 inhibitors
US6020343A (en) 1995-10-13 2000-02-01 Merck Frosst Canada, Inc. (Methylsulfonyl)phenyl-2-(5H)-furanones as COX-2 inhibitors
ATE386506T1 (en) 1995-10-17 2008-03-15 Jagotec Ag ADMINISTRATION OF INSOLUBLE DRUGS
US6057319A (en) 1995-10-30 2000-05-02 Merck Frosst Canada & Co. 3,4-Diaryl-2-hydroxy-2,5-dihydrofurans as prodrugs to cox-2 inhibitors
ZA97175B (en) 1996-01-11 1997-11-04 Smithkline Beecham Corp Novel substituted imidazole compounds.
AP9700912A0 (en) 1996-01-11 1997-01-31 Smithkline Beecham Corp Novel cycloalkyl substituted imidazoles
PL187516B1 (en) 1996-01-11 2004-07-30 Smithkline Beecham Corp Novel substituted derivatives of imidazole
US6046208A (en) 1996-01-11 2000-04-04 Smithkline Beecham Corporation Substituted imidazole compounds
US5789413A (en) 1996-02-01 1998-08-04 Merck Frosst Canada, Inc. Alkylated styrenes as prodrugs to COX-2 inhibitors
AU1671597A (en) 1996-02-13 1997-09-02 Chugai Seiyaku Kabushiki Kaisha Indole derivatives
ES2125161B1 (en) 1996-03-21 1999-11-16 Grupo Farmaceutico Almirall S NEW DERIVATIVES OF 2- (3H) -OXAZOLONA.
GB9607503D0 (en) 1996-04-11 1996-06-12 Merck Frosst Canada Inc Bisaryl cyclobutenes derivatives as cyclooxygenase inhibitors
US5807873A (en) 1996-04-04 1998-09-15 Laboratories Upsa Diarylmethylidenefuran derivatives and their uses in therapeutics
US5908858A (en) 1996-04-05 1999-06-01 Sankyo Company, Limited 1,2-diphenylpyrrole derivatives, their preparation and their therapeutic uses
SK285353B6 (en) 1996-04-12 2006-11-03 G. D. Searle & Co. Substituted benzensulfonamide derivatives as prodrugs of COX-2 inhibitors, pharmaceutical composition and method of their preparation and their use
US5922742A (en) 1996-04-23 1999-07-13 Merck Frosst Canada Pyridinyl-2-cyclopenten-1-ones as selective cyclooxygenase-2 inhibitors
DK0906279T3 (en) 1996-05-30 2003-02-03 Hoffmann La Roche pyrrole
US5883267A (en) 1996-05-31 1999-03-16 Merck & Co., Inc. Process for making phenyl heterocycles useful as cox-2 inhibitors
WO1997046532A1 (en) 1996-06-03 1997-12-11 Boehringer Ingelheim Pharmaceuticals, Inc. 2-benzyl-4-sulfonyl-4h-isoquinolin-1,3-diones and their use as anti-inflammatory agents
US5677318A (en) 1996-07-11 1997-10-14 Merck Frosst Canada, Inc. Diphenyl-1,2-3-thiadiazoles as anti-inflammatory agents
US5861419A (en) 1996-07-18 1999-01-19 Merck Frosst Canad, Inc. Substituted pyridines as selective cyclooxygenase-2 inhibitors
US5776967A (en) 1996-07-26 1998-07-07 American Home Products Corporation Pyranoindole inhibitors of COX--2
IL128031A0 (en) 1996-07-26 1999-11-30 American Home Prod Pyranoindole and carbazole inhibitors of cox-2
FR2751964B1 (en) 1996-08-01 1998-10-30 Union Pharma Scient Appl NOVEL CARBOCYCLIC DIARYLMETHYLENE DERIVATIVES, PROCESSES FOR THEIR PREPARATION, AND THERAPEUTIC USES
FR2751966B1 (en) 1996-08-01 1998-10-30 Union Pharma Scient Appl NOVEL 1,2-DIARYLINDOLES, DERIVATIVES THEREOF, AND THERAPEUTIC USES THEREOF
TR199900298T2 (en) 1996-08-14 1999-05-21 G.D. Searle &Co. The crystalline form of 4-(5-Methyl-3-phenylisoxazol-4-yl)BenzeneSulfonamide.
US5830911A (en) 1996-08-14 1998-11-03 American Home Products Corporation Pyranoindole and tetrahydrocarbazole inhibitors of COX-2
WO1998007425A1 (en) 1996-08-21 1998-02-26 Smithkline Beecham Corporation Imidazole compounds, compositions and use
US6005000A (en) 1996-08-22 1999-12-21 Oxis International, Inc. 5,5-Disubstituted-3, 4-dihydroxy-2(5H)-furanones and methods of use therefor
FR2753449B1 (en) 1996-09-13 1998-12-04 Union Pharma Scient Appl NOVEL 3,4-DIARYLOXAZOLONE DERIVATIVES, PROCESSES FOR THEIR PREPARATION, AND THERAPEUTIC USES
US5972950A (en) 1996-10-08 1999-10-26 Laboratories Upsa 1,2-diarylmethylene derivatives, their methods of preparation and their uses in therapeutics
DK1007067T3 (en) 1996-10-21 2002-05-06 Eurovita As Pharmaceutical preparations containing Parthenium integrifolium or parts thereof or an extract thereof, the use of such plant material for the manufacture of ...
US5681842A (en) 1996-11-08 1997-10-28 Abbott Laboratories Prostaglandin synthase-2 inhibitors
US5869524A (en) 1996-11-12 1999-02-09 American Home Products Corporation Indene inhibitors of COX-2
CN1237162A (en) 1996-11-12 1999-12-01 美国家用产品公司 Indene inhibitors of COX-2
DE69728688T2 (en) 1996-11-19 2004-08-19 Amgen Inc., Thousand Oaks ARYL AND HETEROARYL SUBSTITUTED CONDENSED PYRROLE AS AN ANTI-FLAMMING AGENT
US6096753A (en) 1996-12-05 2000-08-01 Amgen Inc. Substituted pyrimidinone and pyridone compounds and methods of use
EP0846689B1 (en) 1996-12-09 2004-01-14 Pfizer Inc. Benzimidazole compounds
US5935990A (en) 1996-12-10 1999-08-10 G.D. Searle & Co. Substituted pyrrolyl compounds for the treatment of inflammation
US5973191A (en) 1996-12-30 1999-10-26 Vanderbilt University Selective inhibitors of prostaglandin endoperoxide synthase-2
US5929076A (en) 1997-01-10 1999-07-27 Smithkline Beecham Corporation Cycloalkyl substituted imidazoles
PA8444901A1 (en) 1997-01-28 2000-05-24 Hoffmann La Roche DERIVATIVES OF 5-AROILNAPHTHALENE AS ANTI-INFLAMMATORY AGENTS
WO1998035666A1 (en) 1997-02-13 1998-08-20 Nanosystems Llc Formulations of nanoparticle naproxen tablets
US5783597A (en) 1997-03-04 1998-07-21 Ortho Pharmaceutical Corporation 2,5-disubstituted thiophenes: inhibitors of 5-lipoxygenase and inducible cyclooxygenase (COX-2) enzymes, composition and use
CA2283100A1 (en) 1997-03-14 1998-09-24 Merck Frosst Canada & Co. (methylsulfonyl)phenyl-2-(5h)-furanones with oxygen link as cox-2 inhibitors
US6071954A (en) 1997-03-14 2000-06-06 Merk Frosst Canada, Inc. (methylsulfonyl)phenyl-2-(5H)-furanones with oxygen link as COX-2 inhibitors
US6004960A (en) 1997-03-14 1999-12-21 Merck Frosst Canada, Inc. Pyridazinones as inhibitors of cyclooxygenase-2
AU6818298A (en) 1997-04-02 1998-10-22 Merck Frosst Canada & Co. Alpha-methylene gamma lactones as selective cyclooxygenase-2 inhibitors
SE9701304D0 (en) 1997-04-09 1997-04-09 Astra Pharma Prod Compounds
TW492959B (en) 1997-04-18 2002-07-01 Merck & Co Inc Process for making 2-aryl-3-aryl-5-halo pyridines useful as cox-2 inhibitors
US6034256A (en) 1997-04-21 2000-03-07 G.D. Searle & Co. Substituted benzopyran derivatives for the treatment of inflammation
SE9702534D0 (en) 1997-07-01 1997-07-01 Astra Pharma Prod Compounds
AR016294A1 (en) 1997-07-02 2001-07-04 Smithkline Beecham Corp IMIDAZOL SUBSTITUTE COMPOSITE, PHARMACEUTICAL COMPOSITION CONTAINING IT, ITS USE IN THE MANUFACTURE OF A MEDICINAL PRODUCT AND PROCEDURE FOR SUPREPARATION
WO1999001452A1 (en) 1997-07-02 1999-01-14 Smithkline Beecham Corporation Novel cycloalkyl substituted imidazoles
PT1005460E (en) 1997-08-22 2006-07-31 Abbott Lab BIOSSINTESE OF PROSTAGLANDINE-ENDOPEROXIDE H-SINTASE INHIBITORS
CA2299300C (en) 1997-08-22 2007-04-17 Abbott Laboratories Arylpyridazinones as prostaglandin endoperoxide h synthase bisoynthesis inhibitors
WO2000024719A1 (en) 1998-10-27 2000-05-04 Abbott Laboratories Prostaglandin endoperoxide h synthase biosynthesis inhibitors
CO4960662A1 (en) 1997-08-28 2000-09-25 Novartis Ag CERTAIN 5-ALKYL-2-ARYLAMINOPHENYLACETIC ACIDS AND THEIR DERIVATIVES
ES2256817T3 (en) 1997-09-05 2006-07-16 Glaxo Group Limited PHARMACEUTICAL COMPOSITIONS THAT INCLUDE DERIVATIVES OF 2,3-DIARIL-PIRAZOLO (1,5-B) PIRIDAZINE.
ES2131015B1 (en) 1997-09-12 2000-03-01 Almirall Prodesfarma Sa NEW DERIVATIVES OF 2- (3H) -OXAZOLONE, PROCEDURES FOR ITS PREPARATION AND USE IN PHARMACEUTICAL COMPOSITIONS.
EP1015431B1 (en) 1997-09-12 2005-04-20 Merck Frosst Canada & Co. 2-aminopyridines as inhibitors of cyclooxygenase-2
US6046217A (en) 1997-09-12 2000-04-04 Merck Frosst Canada & Co. 2,3,5-trisubstituted pyridines as inhibitors of cyclooxygenase-2
WO1999013755A1 (en) 1997-09-18 1999-03-25 Doppel Co., Ltd. Frame
AUPO941497A0 (en) 1997-09-24 1997-10-16 Fujisawa Pharmaceutical Co., Ltd. Novel compounds
US6040450A (en) 1997-09-25 2000-03-21 Merck & Co., Inc. Process for making diaryl pyridines useful as cox-2-inhibitors
FR2769311B1 (en) 1997-10-07 1999-12-24 Union Pharma Scient Appl NOVEL 3,4-DIARYLTHIAZOLIN-2-ONE OR -2-THIONE DERIVATIVES, PROCESSES FOR THEIR PREPARATION AND THERAPEUTIC USES
SE9703693D0 (en) 1997-10-10 1997-10-10 Astra Pharma Prod Novel combination
CA2307853A1 (en) 1997-10-30 1999-05-14 Merck Frosst Canada & Co. Diaryl-5-alkyl-5-methyl-2(5h)-furanones as selective cyclooxygenase-2 inhibitors
US6133292A (en) 1997-10-30 2000-10-17 Merck Frosst Canada & Co. Diaryl-5-alkyl-5-methyl-2-(5H)-furanones as selective cyclooxygenase-2-inhibitors
US6022884A (en) 1997-11-07 2000-02-08 Amgen Inc. Substituted pyridine compounds and methods of use
US6020347A (en) 1997-11-18 2000-02-01 Merck & Co., Inc. 4-substituted-4-piperidine carboxamide derivatives
AUPP042397A0 (en) 1997-11-18 1997-12-11 Fujisawa Pharmaceutical Co., Ltd. 5-arylpyrazole compounds
FR2771412B1 (en) 1997-11-26 2000-04-28 Adir NOVEL PYRROLE DERIVATIVES, THEIR PREPARATION PROCESS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
AP869A (en) 1998-01-05 2000-09-04 Pfizer 2,3-Substituted indole compounds as anti-inflammatory and analgesic agents.
HU227627B1 (en) 1998-04-24 2011-10-28 Merck Sharp & Dohme Process for synthesizing pyridine derivatives as cox-2 inhibitors and the intermediates
AU3993899A (en) * 1998-05-18 1999-12-06 Merck & Co., Inc. Method for treating or preventing chronic nonbacterial prostatitis and prostatodynia
ATE482945T1 (en) 1998-05-26 2010-10-15 Chugai Pharmaceutical Co Ltd HETEROCYCLIC INDOLE DERIVATIVES AND MONO- OR DIAZAINDOLE DERIVATIVES
AU3953899A (en) 1998-05-27 1999-12-13 Nippon Shinyaku Co. Ltd. Cyclooxygenase-2 inhibitors
ES2137138B1 (en) 1998-05-29 2000-09-16 Esteve Labor Dr DERIVATIVES OF PIRAZOLINES, THEIR PREPARATION AND THEIR APPLICATION AS MEDICINES.
TNSN99111A1 (en) 1998-06-11 2005-11-10 Pfizer NOVEL SULFONYLBENZENE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM.
CA2335472C (en) 1998-06-19 2008-10-28 Rtp Pharma Inc. Processes to generate submicron particles of water-insoluble compounds
JP2000016935A (en) 1998-07-01 2000-01-18 Dai Ichi Seiyaku Co Ltd Cyclooxygenase inhibitor
ES2140354B1 (en) 1998-08-03 2000-11-01 S A L V A T Lab Sa IMIDAZO (1,2A) AZINAS SUBSTITUTED AS SELECTIVE INHIBITORS OF COX-2.
KR100295206B1 (en) 1998-08-22 2001-07-12 서경배 Diarylbenzopyran derivatives and cyclooxygenase-2 inhibitor composition containing the same
ATE353010T1 (en) 1998-09-03 2007-02-15 Univ Loma Linda Med PHARMACEUTICAL COMPOSITION AND USE OF RNSAID FOR TREATING INFLAMMATION
US6277878B1 (en) 1998-09-07 2001-08-21 Pfizer Inc Substituted indole compounds as anti-inflammatory and analgesic agents
TW587079B (en) 1998-09-25 2004-05-11 Almirall Prodesfarma Ag 2-phenylpyran-4-one derivatives
WO2000018741A2 (en) 1998-09-30 2000-04-06 Fujisawa Pharmaceutical Co., Ltd. Pyrazole compounds as cox-2 inhibitors
WO2000018374A1 (en) 1998-10-01 2000-04-06 Elan Pharma International, Ltd. Controlled release nanoparticulate compositions
AR024222A1 (en) 1998-10-16 2002-09-25 Palau Pharma Sa IMIDAZOLES WITH ANTI-INFLAMMATORY ACTIVITY A PROCEDURE FOR THE PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING IT
US6077869A (en) 1998-10-29 2000-06-20 Ortho-Mcneil Pharmaceutical, Inc. Aryl phenylhydrazides as selective COX-2 inhibitors for treatment of inflammation
HUP0104204A3 (en) 1998-11-03 2002-06-28 Glaxo Group Ltd Pyrazolopyridine derivatives as cox-2 inhibitors, process for their preparation and pharmaceutical compositions thereof
US6180136B1 (en) 1998-11-10 2001-01-30 Idexx Laboratories, Inc. Phospholipid-coated microcrystals for the sustained release of pharmacologically active compounds and methods of their manufacture and use
US6143892A (en) 1998-11-20 2000-11-07 G. D. Searle & Co. Process for making 5-substituted pyrazoles
EP1133280A1 (en) 1998-11-20 2001-09-19 RTP Pharma Inc. Method of preparing stable suspensions of insoluble microparticles
ES2270634T3 (en) 1999-01-07 2007-04-01 Vanderbilt University CONVERSION OF COX-INHIBITION COMPOUNDS THAT ARE NOT SELECTIVE COH-2 INHIBITORS IN DERIVATIVES THAT ARE SELECTED COX-2 INHIBITORS.
US20010006686A1 (en) 1999-03-19 2001-07-05 David G. Corley Inflammatory mediation obtained from atractylodes lancea
US6077868A (en) 1999-07-20 2000-06-20 Wisconsin Alumni Research Foundation Selective inhibition of cyclooxygenase-2
US6083969A (en) 1999-10-20 2000-07-04 Ortho-Mcneil Pharaceutical, Inc. 1,3- and 2,3-diarylcycloalkano and cycloalkeno pyrazoles as selective inhibitors of cyclooxygenase-2 and antiinflammatory agents

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996025405A1 (en) * 1995-02-13 1996-08-22 G.D. Searle & Co. Substituted isoxazoles for the treatment of inflammation
US5756529A (en) * 1995-09-29 1998-05-26 G.D. Searle & Co. Substituted pyrazolyl benzenesulfonamides for use in veterinary therapies
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
WO2000032189A1 (en) * 1998-11-30 2000-06-08 G. D. Searle & Co. Celecoxib compositions
WO2000053149A2 (en) * 1999-03-10 2000-09-14 G.D. Searle & Co. Method and composition for administering a cyclooxygenase-2 inhibitor

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7790905B2 (en) 2002-02-15 2010-09-07 Mcneil-Ppc, Inc. Pharmaceutical propylene glycol solvate compositions
US7927613B2 (en) 2002-02-15 2011-04-19 University Of South Florida Pharmaceutical co-crystal compositions
US10633344B2 (en) 2002-03-01 2020-04-28 University Of South Florida Multiple-component solid phases containing at least one active pharmaceutical ingredient
US8183290B2 (en) 2002-12-30 2012-05-22 Mcneil-Ppc, Inc. Pharmaceutically acceptable propylene glycol solvate of naproxen

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ZA200107148B (en) 2002-11-29
SK12672001A3 (en) 2002-04-04
AU784490B2 (en) 2006-04-13
CO5261556A1 (en) 2003-03-31
EA200100870A1 (en) 2002-04-25
EP1525883A1 (en) 2005-04-27
ES2236007T3 (en) 2005-07-16
AU1805901A (en) 2001-06-18
US20020142045A1 (en) 2002-10-03
PE20010921A1 (en) 2001-09-10
HUP0201463A3 (en) 2004-06-28
EA008242B1 (en) 2007-04-27
KR100793668B1 (en) 2008-01-10
DK1175214T3 (en) 2006-07-17
HUP0201463A2 (en) 2004-05-28
PL351944A1 (en) 2003-07-14
NZ513960A (en) 2004-02-27
KR20020045582A (en) 2002-06-19
EP1175214B1 (en) 2004-11-24
US20040265382A1 (en) 2004-12-30
WO2001041760A2 (en) 2001-06-14
JP2003523954A (en) 2003-08-12
TWI255180B (en) 2006-05-21

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