[go: up one dir, main page]

MA27058A1 - Cristaux comprenant un sel d'acide malique de n-[2-(diethylamino) ethyl]-5-[(5-fluoro-1,2-dihydro-2-oxo-3h-indole-3-ylidene) methyl]-2,4-dimethyl-1h-pyrrole-3-carboxamide, procedes pour leur preparation et compositions les contenant - Google Patents

Cristaux comprenant un sel d'acide malique de n-[2-(diethylamino) ethyl]-5-[(5-fluoro-1,2-dihydro-2-oxo-3h-indole-3-ylidene) methyl]-2,4-dimethyl-1h-pyrrole-3-carboxamide, procedes pour leur preparation et compositions les contenant

Info

Publication number
MA27058A1
MA27058A1 MA27522A MA27522A MA27058A1 MA 27058 A1 MA27058 A1 MA 27058A1 MA 27522 A MA27522 A MA 27522A MA 27522 A MA27522 A MA 27522A MA 27058 A1 MA27058 A1 MA 27058A1
Authority
MA
Morocco
Prior art keywords
ylidene
carboxamide
diethylamino
pyrrole
dihydro
Prior art date
Application number
MA27522A
Other languages
English (en)
Inventor
Michael Hawley
Thomas J Fleck
Stephen P Prescott
Mark T Maloney
Original Assignee
Upjohn Co
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=23211067&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA27058(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Upjohn Co filed Critical Upjohn Co
Publication of MA27058A1 publication Critical patent/MA27058A1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Oncology (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyrrole Compounds (AREA)

Abstract

Deposantsociété dite: pharmacia & upjohn companyrevendication de prioritesus 15 août 2001 60/312,353voir en annexe le titre de l'invention et le texte de l'abrégécristaux comprenant un sel d'acide malique den-[2-(diéthylamino)éthyl]-5-[(5-fluoro-1,2-dihydro-2-oxo-3h-indole-3-ylidène)méthyl]-2,4-diméthyl-lh-pyrrole-3-carboxamide, procédés pour leur préparation et compositions les contenantla présente invention propose des cristaux et des compositions les contenant, dans lesquelles les cristaux comprennent un sel d'acide malique de n-[2-(diéthylamino) éthyl]-5-[(5-fluoro-1,2-dihydro-2-oxo-3 h-indole-3-ylidène) méthyl]-2,4-diméthyl-1h-pyrrole-3-carboxamide. Des procédés pour la préparation de ces cristaux sont également décrits.
MA27522A 2001-08-15 2004-02-11 Cristaux comprenant un sel d'acide malique de n-[2-(diethylamino) ethyl]-5-[(5-fluoro-1,2-dihydro-2-oxo-3h-indole-3-ylidene) methyl]-2,4-dimethyl-1h-pyrrole-3-carboxamide, procedes pour leur preparation et compositions les contenant MA27058A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US31235301P 2001-08-15 2001-08-15
PCT/US2002/025649 WO2003016305A1 (fr) 2001-08-15 2002-08-13 Cristaux comprenant un sel d'acide malique de n-[2-(diethylamino)ethyl]-5-[(5-fluoro-1,2-dihydro-2-oxo-3h-indol-3-ylidene)methyl]-2,4-dimethyl-1h-pyrrole-3-carboxamide, procedes de preparation associes et compositions correspondantes

Publications (1)

Publication Number Publication Date
MA27058A1 true MA27058A1 (fr) 2004-12-20

Family

ID=23211067

Family Applications (1)

Application Number Title Priority Date Filing Date
MA27522A MA27058A1 (fr) 2001-08-15 2004-02-11 Cristaux comprenant un sel d'acide malique de n-[2-(diethylamino) ethyl]-5-[(5-fluoro-1,2-dihydro-2-oxo-3h-indole-3-ylidene) methyl]-2,4-dimethyl-1h-pyrrole-3-carboxamide, procedes pour leur preparation et compositions les contenant

Country Status (42)

Country Link
US (2) US20030069298A1 (fr)
EP (3) EP1419151B1 (fr)
JP (1) JP4159988B2 (fr)
KR (1) KR100639281B1 (fr)
CN (2) CN100364991C (fr)
AP (1) AP1660A (fr)
AR (1) AR036261A1 (fr)
AU (1) AU2002324684B2 (fr)
BG (1) BG108553A (fr)
BR (1) BR0211612A (fr)
CA (1) CA2455050C (fr)
CO (1) CO5550431A2 (fr)
CU (1) CU23713B7 (fr)
CY (1) CY1121552T1 (fr)
CZ (1) CZ2004196A3 (fr)
DK (2) DK3168218T3 (fr)
EA (1) EA006445B9 (fr)
EC (1) ECSP044975A (fr)
ES (3) ES2453164T3 (fr)
GE (1) GEP20063777B (fr)
HR (1) HRP20040112B1 (fr)
HU (1) HU229206B1 (fr)
IL (1) IL160097A0 (fr)
IS (1) IS7147A (fr)
MA (1) MA27058A1 (fr)
ME (1) ME00414B (fr)
MX (1) MXPA04001452A (fr)
MY (1) MY139383A (fr)
NO (1) NO326508B1 (fr)
NZ (1) NZ531232A (fr)
OA (1) OA12650A (fr)
PL (1) PL216524B1 (fr)
PT (2) PT1419151E (fr)
RS (1) RS53251B (fr)
SI (2) SI3168218T1 (fr)
SK (1) SK902004A3 (fr)
TN (1) TNSN04028A1 (fr)
TR (1) TR201900509T4 (fr)
TW (1) TWI269796B (fr)
UA (1) UA76483C2 (fr)
WO (1) WO2003016305A1 (fr)
ZA (1) ZA200400706B (fr)

Families Citing this family (59)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HRP20040112B1 (en) 2001-08-15 2012-03-31 Pharmacia & Upjohn Company Crystals including a malic acid salt of n-[2-(diethylamino)ethyl]-5-[(5-fluoro-2-oxo-3h-indole-3-ylidene)methyl]-2,4-dimethyl-1h-pyrrole-3-carboxamide, processes for its preparation and compositions thereof
HN2003000272A (es) * 2002-09-10 2008-07-29 Pharmacia Italia Spa Formulaciones que comprenden un compuesto de indolinona
BRPI0415022A (pt) * 2003-10-02 2006-11-28 Pharmacia & Upjohn Co Llc sais e polimorfos de um composto de indolinona substituìda com pirrol
US20060009510A1 (en) * 2004-07-09 2006-01-12 Pharmacia & Upjohn Company Llc Method of synthesizing indolinone compounds
WO2006019835A1 (fr) * 2004-07-22 2006-02-23 Eli Lilly And Company Hydrate variable cristallin de sel (s)-6-(4-(2-((3-(9h-carbazol-4-yloxy)-2-hydroxypropyl)amino)-2-methylpropyl)phenoxy)-3-pyridinicarbox amide hemisuccinate
CA2603445A1 (fr) * 2005-05-12 2006-11-16 Pfizer Inc. Polytherapie anticancereuse faisant intervenir du malate de sunitinib
ES2328407T3 (es) * 2005-09-19 2009-11-12 Pfizer Products Incorporated Formas salinas solidas de una 2-indolinona sustituida con pirrol.
US20090004213A1 (en) 2007-03-26 2009-01-01 Immatics Biotechnologies Gmbh Combination therapy using active immunotherapy
EP2220072A2 (fr) 2007-11-21 2010-08-25 Teva Pharmaceutical Industries Ltd. Polymorphes de base de sunitinib et procédés pour les préparer
US20100256392A1 (en) * 2007-11-21 2010-10-07 Teva Pharmaceutical Industries Ltd. Polymorphs of sunitinib base and processes for preparation thereof
EP2229380A1 (fr) * 2007-12-12 2010-09-22 Medichem, S.A. Formes polymorphes d'une 2-indolinone substituée par 3-pyrrole
EP2113248A1 (fr) 2008-04-29 2009-11-04 Ratiopharm GmbH Composition pharmaceutique comportant du N-[2-(diethylamino)ethyl]-5-[5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2-dimethyl-1H-pyrrole-3-carboxamide
EP2090306A1 (fr) 2008-02-13 2009-08-19 Ratiopharm GmbH Compositions pharmaceutiques comportant du N-[2-(diethylamino)ethyl]-5-[5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide
CN101983195A (zh) * 2008-02-21 2011-03-02 基因里克斯(英国)有限公司 新型多晶型物及其制备方法
EP2098521A1 (fr) * 2008-03-06 2009-09-09 Ratiopharm GmbH Formules cristallines de N-[2-(diéthylamino)éthyl]-5-[5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidène)méthyl]-2,4-diméthyl-1H-pyrrole-3-carboxamide
JP2011516488A (ja) * 2008-03-31 2011-05-26 テバ ファーマシューティカル インダストリーズ リミティド スニチニブ及びその塩の調製方法
CA2720943A1 (fr) * 2008-04-16 2009-10-22 Natco Pharma Limited Nouvelles formes polymorphes du sunitinib base
RU2468022C2 (ru) * 2008-05-23 2012-11-27 Шанхай Инститьют Оф Фармасьютикал Индастри Производные дигидроиндолона
AR072117A1 (es) * 2008-06-13 2010-08-04 Medichem Sa Procedimiento para preparar una sal de malato 3-pirrol sustituido 2-indolinona, intermediario de sintesis y una composicion farmaceutica que la comprende.
EP2138167A1 (fr) 2008-06-24 2009-12-30 ratiopharm GmbH Compositions pharmaceutiques comportant du N-[2-(diethylamino)ethyl]-5-[5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide
WO2009156837A2 (fr) * 2008-06-26 2009-12-30 Medichem, S.A. Forme amorphe d'un sel de malate de 2-indolinone à substitution 3-pyrrole
US20110257237A1 (en) * 2008-07-10 2011-10-20 Generics [Uk] Limited Process for the preparation of crystalline forms of sunitinib malate
CN102164913A (zh) * 2008-07-24 2011-08-24 麦迪凯姆股份公司 一种3-吡咯替代的2-吲哚酮苹果酸盐的结晶体形式
WO2010011834A2 (fr) * 2008-07-24 2010-01-28 Teva Pharmaceutical Industries Ltd. Sunitinib et ses sels et leurs polymorphes
CN102197034A (zh) * 2008-08-25 2011-09-21 基因里克斯(英国)有限公司 舒尼替尼的新型多晶型物及其制备方法
CA2734965A1 (fr) * 2008-08-25 2010-03-04 Generics [Uk] Limited Nouvelle forme cristalline et ses procedes de preparation
AR073807A1 (es) * 2008-10-10 2010-12-01 Medichem Sa Proceso para preparar el malato de sunitinib, sal de un acido mas debil que el malato como compuesto intermediario, y proceso para preparar dicha sal intermediaria.
EP2181991A1 (fr) * 2008-10-28 2010-05-05 LEK Pharmaceuticals D.D. Nouveaux sels de sunitinib
EP2186809A1 (fr) * 2008-11-13 2010-05-19 LEK Pharmaceuticals D.D. Nouvelle forme cristalline du malate de sunitinib
EP2373643A4 (fr) * 2009-01-02 2013-08-07 Hetero Research Foundation Nouveaux polymorphes de malate de sunitinib
KR101733773B1 (ko) 2009-01-16 2017-05-10 엑셀리시스, 인코포레이티드 N-(4-{〔6,7-비스(메틸옥시)퀴놀린-4-일〕옥시}페닐)-n'-(4-플루오로페닐)사이클로프로판-1,1-디카르복사미드의 말산염 및 그 결정형
EP2255792A1 (fr) 2009-05-20 2010-12-01 Ratiopharm GmbH Composition pharmaceutique pour n-[2-(diethylamino)ethyl]5-[(fluoro-1,2-dihydro-2-oxo-3H-indole-3-ylidene) methyl]-2,4-dimenthyl-1h-pyrrole-3-carboxamide
WO2011004200A1 (fr) 2009-07-10 2011-01-13 Generics [Uk] Limited Nouveaux dérivés de pyrrole
CA2774634A1 (fr) 2009-09-16 2011-03-24 Ranbaxy Laboratories Limited Sels de sunitinib
WO2011058521A2 (fr) 2009-11-12 2011-05-19 Ranbaxy Laboratories Limited Procédé de préparation de la forme cristalline i du sel d'acide l-malique de sunitinib
EP2501694A1 (fr) 2009-11-19 2012-09-26 Ranbaxy Laboratories Limited Procédé de préparation de la forme cristalline ii du sel d'acide malique l du sunitinib
EP2528913A1 (fr) 2010-01-29 2012-12-05 Ranbaxy Laboratories Limited Formes cristallines du sel d'acide l-malique du sunitinib
WO2011100325A2 (fr) 2010-02-09 2011-08-18 Sicor Inc. Polymorphes de sels de sunitinib
WO2011104555A2 (fr) 2010-02-25 2011-09-01 Generics [Uk] Limited Nouveau procédé
EP2542550A1 (fr) 2010-03-04 2013-01-09 Ranbaxy Laboratories Limited Procédé de préparation directe de sel d'acide malique de sunitinib
WO2011114246A1 (fr) 2010-03-18 2011-09-22 Ranbaxy Laboratories Limited Procédé pour la préparation du sel de l'acide maléique du sunitinib
WO2011128699A2 (fr) 2010-04-16 2011-10-20 Generics [Uk] Limited Procédés inédits
WO2012042421A1 (fr) 2010-09-29 2012-04-05 Pfizer Inc. Procédé de traitement de la croissance cellulaire anormale
US20140178368A1 (en) 2011-04-19 2014-06-26 Leslie Lynne SHARP Combinations of anti-4-1bb antibodies and adcc-inducing antibodies for the treatment of cancer
WO2013140232A1 (fr) 2012-03-23 2013-09-26 Laurus Labs Private Limited Procédé perfectionné pour la préparation de sunitinib et de ses sels d'addition avec un acide
PL399027A1 (pl) 2012-04-27 2013-10-28 Instytut Farmaceutyczny Sposób otrzymywania N-[2-(dietylamino)etylo]-5-formylo-2,4-dimetylo-1H-pirolo-3-karboksyamidu o wysokiej czystosci i jego zastosowanie do wytwarzania sunitynibu
SG11201406592QA (en) 2012-05-04 2014-11-27 Pfizer Prostate-associated antigens and vaccine-based immunotherapy regimens
US9604968B2 (en) 2013-10-18 2017-03-28 Sun Pharmaceutical Industries Limited Pure crystalline Form II of L-malic acid salt of sunitinib and processes for its preparation
CA2838585A1 (fr) 2013-10-18 2015-04-18 Hari Babu Matta Sel de sunitinib d'acide ascorbique
WO2015063647A1 (fr) 2013-11-01 2015-05-07 Pfizer Inc. Vecteurs d'expression d'antigènes associés à la prostate
CN104693187A (zh) * 2013-12-10 2015-06-10 安杰世纪生物科技(北京)有限公司 一种舒尼替尼L-苹果酸盐晶型λ及其制备方法
CN104744442B (zh) * 2013-12-25 2019-05-28 江苏豪森药业集团有限公司 苹果酸舒尼替尼的制备方法
RU2567535C1 (ru) * 2014-10-01 2015-11-10 Олег Ростиславович Михайлов КРИСТАЛЛИЧЕСКАЯ ε-МОДИФИКАЦИЯ N-[2-(ДИЭТИЛАМИНО)ЭТИЛ]-5-[(Z)-(5-ФТОР-1,2-ДИГИДРО-2-ОКСО-3Н-ИНДОЛ-3-ИЛИДЕН)МЕТИЛ]-2,4-ДИМЕТИЛ-1Н-ПИРРОЛ-3-КАРБОКСАМИД МАЛАТА, СПОСОБ ЕЕ ПОЛУЧЕНИЯ И ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ НА ЕЕ ОСНОВЕ
CN105712979A (zh) * 2014-12-05 2016-06-29 广州白云山医药集团股份有限公司白云山制药总厂 一种苹果酸舒尼替尼晶型ⅰ的制备方法
EP3539536A1 (fr) 2018-03-15 2019-09-18 MH10 Spolka z ograniczona odpowiedzialnoscia Composition pharmaceutique de sunitinib ou de son sel dans sa forme polymorphe i
JP2022529290A (ja) * 2019-04-18 2022-06-20 メーター ヘルス インコーポレイテッド 呼吸性不整脈を処置するための方法および組成物
EP3958845A1 (fr) 2019-04-25 2022-03-02 Synthon B.V. Composition pharmaceutique comprenant du sunitinib amorphe
JP7633786B2 (ja) * 2020-09-18 2025-02-20 日本化薬株式会社 スニチニブリンゴ酸塩を有効成分とする医薬錠剤
KR20240025990A (ko) 2022-08-19 2024-02-27 주식회사 스카이테라퓨틱스 무정형 수니티닙, 그 제조방법 및 이를 포함한 의약 조성물

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR0179053B1 (ko) 1990-10-15 1999-03-20 알렌 제이.스피겔 인돌 유도체
IL100091A (en) * 1990-12-12 1998-08-16 Zeneca Ltd Pharmaceutical compositions containing a physical form of n-[4-[5-(cyclopentyloxycarbonyl)amino-1-methyl indol-3-yl-methyl]-2-methylbenzenesulpho-namide and process for their preparation
CZ282060B6 (cs) 1992-06-05 1997-05-14 Merck Sharp And Dohme Limited Sulfátová sůl substituovaného triazolu, způsob její výroby, farmaceutický prostředek s jejím obsahem a způsob jeho výroby
AU694419B2 (en) 1993-03-12 1998-07-23 Zoetis P&U Llc Crystalline ceftiofur free acid
US6329364B1 (en) 1994-08-31 2001-12-11 Eli Lilly And Company Crystalline form of dihydro-2,3-benzodiazepine derivative
DE19503966C2 (de) 1995-02-07 1998-07-02 Mack Chem Pharm Kristallmodifikation von 2,4-Diamino-6-hydroxymethylpteridin-Hydrobromid, Verfahren zu dessen Herstellung und dessen Verwendung
US5597663A (en) * 1995-05-30 1997-01-28 Motorola, Inc. Low temperature molten lithium salt electrolytes for electrochemical cells
US5880141A (en) * 1995-06-07 1999-03-09 Sugen, Inc. Benzylidene-Z-indoline compounds for the treatment of disease
US5673451A (en) * 1995-07-06 1997-10-07 Moore; James R. Instructional toothbrush
US20020038021A1 (en) 1995-12-11 2002-03-28 Barton Kathleen P. Eplerenone crystalline form exhibiting enhanced dissolution rate
US20020045746A1 (en) 1995-12-11 2002-04-18 Barton Kathleen P. Eplerenone crystalline form
US6066647A (en) 1996-07-29 2000-05-23 Pfizer Inc. Zwitterionic forms of trovafloxacin
DE69717281T2 (de) 1996-08-14 2003-09-04 G.D. Searle & Co., Chicago Kristalline form von 4-[5-methyl-3-phenylisoxazol-4-yl]benzolsulfonamid
KR100530601B1 (ko) 1996-12-25 2005-11-23 니폰 가야꾸 가부시끼가이샤 시스플라틴 미분말 및 그의 제조방법
US5777185A (en) * 1997-09-09 1998-07-07 Laroche Industries Inc. Production of organic fluorine compounds
US6133305A (en) * 1997-09-26 2000-10-17 Sugen, Inc. 3-(substituted)-2-indolinones compounds and use thereof as inhibitors of protein kinase activity
US6012678A (en) * 1998-01-26 2000-01-11 The Boeing Company Galley vacuum waste disposal system
EP1956015B2 (fr) 1998-06-19 2018-11-14 Teijin Limited Polymorphe d'acide 2-(3-cyano-4-isobutyloxyphenyl)-4-methyl-5-thiazolecarboxylique et son procédé de production
ATE234830T1 (de) * 1998-12-17 2003-04-15 Hoffmann La Roche 4-alkenyl (und alkinyl)oxoindole als inhibitoren cyclinabhängiger kinasen, insbesondere cdk2
US6239141B1 (en) 1999-06-04 2001-05-29 Pfizer Inc. Trovafloxacin oral suspensions
PT1233943E (pt) * 1999-11-24 2011-09-01 Sugen Inc Formulações para agentes farmacêuticos ionizáveis como ácidos livres ou bases livres
ATE369359T1 (de) * 2000-02-15 2007-08-15 Sugen Inc Pyrrol substituierte indolin-2-on protein kinase inhibitoren
US6316672B1 (en) 2001-01-31 2001-11-13 Grayson Walker Stowell Form a of fluoxetine hydrochloride
HRP20040112B1 (en) 2001-08-15 2012-03-31 Pharmacia & Upjohn Company Crystals including a malic acid salt of n-[2-(diethylamino)ethyl]-5-[(5-fluoro-2-oxo-3h-indole-3-ylidene)methyl]-2,4-dimethyl-1h-pyrrole-3-carboxamide, processes for its preparation and compositions thereof
CN101983195A (zh) 2008-02-21 2011-03-02 基因里克斯(英国)有限公司 新型多晶型物及其制备方法
WO2009156837A2 (fr) 2008-06-26 2009-12-30 Medichem, S.A. Forme amorphe d'un sel de malate de 2-indolinone à substitution 3-pyrrole

Also Published As

Publication number Publication date
MY139383A (en) 2009-09-30
EA006445B1 (ru) 2005-12-29
SI1419151T1 (sl) 2014-04-30
MXPA04001452A (es) 2004-05-20
ME00414B (me) 2011-10-10
NO20041054L (no) 2004-03-12
EA006445B9 (ru) 2017-02-28
US20070191458A1 (en) 2007-08-16
CN1789264A (zh) 2006-06-21
HRP20040112A2 (en) 2004-06-30
EP3168218A1 (fr) 2017-05-17
CU20040029A7 (es) 2008-03-14
RS53251B (sr) 2014-08-29
TNSN04028A1 (fr) 2006-06-01
EA200400183A1 (ru) 2004-08-26
SI3168218T1 (sl) 2019-05-31
PT1419151E (pt) 2014-03-27
TWI269796B (en) 2007-01-01
AR036261A1 (es) 2004-08-25
TR201900509T4 (tr) 2019-02-21
ES2453164T3 (es) 2014-04-04
HRP20040112B1 (en) 2012-03-31
EP2332934A1 (fr) 2011-06-15
CA2455050C (fr) 2007-02-20
BR0211612A (pt) 2004-08-24
NZ531232A (en) 2004-11-26
AP2004002976A0 (en) 2004-03-31
OA12650A (en) 2006-06-19
NO326508B1 (no) 2008-12-15
ES2623094T3 (es) 2017-07-10
US7435832B2 (en) 2008-10-14
WO2003016305A1 (fr) 2003-02-27
RS10304A (sr) 2007-02-05
ECSP044975A (es) 2004-03-23
HUP0700036A2 (en) 2008-10-28
JP4159988B2 (ja) 2008-10-01
IS7147A (is) 2004-02-10
DK3168218T3 (en) 2019-01-14
DK1419151T3 (da) 2014-03-31
PL216524B1 (pl) 2014-04-30
CO5550431A2 (es) 2005-08-31
CN1543462A (zh) 2004-11-03
KR100639281B1 (ko) 2006-10-31
CN100364991C (zh) 2008-01-30
UA76483C2 (en) 2006-08-15
CN100439360C (zh) 2008-12-03
IL160097A0 (en) 2004-06-20
EP1419151B1 (fr) 2014-02-26
PL368317A1 (en) 2005-03-21
ES2705063T3 (es) 2019-03-21
CY1121552T1 (el) 2020-05-29
CU23713B7 (es) 2011-10-05
HK1066542A1 (en) 2005-03-24
US20030069298A1 (en) 2003-04-10
GEP20063777B (en) 2006-03-27
CZ2004196A3 (cs) 2005-01-12
AP1660A (en) 2006-09-09
AU2002324684B2 (en) 2006-10-05
KR20040030074A (ko) 2004-04-08
SK902004A3 (sk) 2005-03-04
PT3168218T (pt) 2019-01-11
EP2332934B1 (fr) 2017-03-01
EP1419151A1 (fr) 2004-05-19
HK1088008A1 (zh) 2006-10-27
EP3168218B1 (fr) 2018-11-14
JP2005503386A (ja) 2005-02-03
HU229206B1 (en) 2013-09-30
ZA200400706B (en) 2005-05-25
BG108553A (bg) 2005-04-30
CA2455050A1 (fr) 2003-02-27

Similar Documents

Publication Publication Date Title
MA27058A1 (fr) Cristaux comprenant un sel d'acide malique de n-[2-(diethylamino) ethyl]-5-[(5-fluoro-1,2-dihydro-2-oxo-3h-indole-3-ylidene) methyl]-2,4-dimethyl-1h-pyrrole-3-carboxamide, procedes pour leur preparation et compositions les contenant
MA27347A1 (fr) Inhibiteurs de protease du vih, compositions les contenant, leurs utilisations pharmaceutiques et matieres pour leur synthese
TNSN04159A1 (fr) Synthese controlee de ziprasidone et compositions en contenant
EP1502603A4 (fr) MEDICAMENT CONTENANT UNE COMPOSITION D'ANTICORPS APPROPRIEE AU PATIENT SOUFFRANT DE POLYMORPHISME FC gammma RIIIA
MA26555A1 (fr) Composes inhibant la map kinase p38, compositions pharmaceutiques les contenant, leur utilisation, procede pour la preparation de ces composes et produits intermediaires utiles dans ce procede.
EP1049459A4 (fr) Compositions liquides orales
DE60037726D1 (de) Carbonsäurederivate die die bindung von integrinen an ihre rezeptoren hemmen
IL160545A0 (en) (-)-1-(3,4-dichlorophenyl) -3- azabicyclo [3.1.0] hexane, compositions thereof and uses as a dopamine-reuptake inhibitor
CA2530006A1 (fr) Inhibiteurs de la beta-secretase de phenylcarboxylate destines au traitement de la maladie d'alzheimer
MA28007A1 (fr) Composes organiques
DE69719755D1 (de) Polymorphe verbindungen
MA27774A1 (fr) Inhibiteurs de phosphatidylinositol 3-kinase
MA31169B1 (fr) Preparation solide comprenant de l'alogliptine et de la pioglitazone
MA27135A1 (fr) Agents antidiabetiques oraux
TNSN98013A1 (fr) Derives de 5 - aroylnaphtalene a action anti-inflammatoire et analgesique, compositions pharmaceutiques les contenant, et procedes pour les utiliser et les preparer.
CA2247526A1 (fr) Cristaux de maltitol de formes particulieres, compositions cristallines les contenant et procedes pour leur preparation
TNSN99146A1 (fr) Derives de 1-heteroaryl-pyrrolidine, -piperidine et - homopiperidine nouveaux, procede pour leur preparation et compositions pharmaceutiques les contenant
UA83870C2 (ru) Замещенные бицикло[3.1.1]гептаном производные бензимидазолона и хиназолинона как агонисты человеческих рецепторов orl1
MA25072A1 (fr) PROCEDES PERFECTIONNéS POUR LA PREPARATION SECRETAGOGUES D'HORMONES DE CROISSANCE
DZ3047A1 (fr) Sel mutuel d'amlopidine et d'atorvastatine, procédé pour sa préparation et compositions pharmaceutiques les contenant.
MXPA02012015A (es) Ligandos de receptores para integrinas.
FR2869539A1 (fr) Compositions pharmaceutiques pour la prevention et le traitement de l'atherosclerose
EP1706123A4 (fr) Compositions derivees de portulaca oleracea l. et procede d'utilisation de ces dernieres pour moduler les niveaux de glucose sanguin
TR200202110T2 (tr) "5-[{6-(2-Flüore benzil) oksi-2-naftil}metil]-2,4-tiyazolidin dion kristalleri"
MA26626A1 (fr) Derives de 2"-desoxy-hygromycine a nouveaux, procede pour leur preparation et compositions pharmaceutiques les contenant