OA12650A - Crystals including a malic acid salt of N-Ä2-(diethylamino)ethylÜ-5-Ä(5-fluoro-2-oxo-3H-indole-3-ylidene)methylÜ-2,4-dimethyl-1H-pyrrole-3-carboxamide, processes for its preparation and compositions thereof. - Google Patents

Crystals including a malic acid salt of N-Ä2-(diethylamino)ethylÜ-5-Ä(5-fluoro-2-oxo-3H-indole-3-ylidene)methylÜ-2,4-dimethyl-1H-pyrrole-3-carboxamide, processes for its preparation and compositions thereof. Download PDF

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Publication number
OA12650A
OA12650A OA1200400044A OA1200400044A OA12650A OA 12650 A OA12650 A OA 12650A OA 1200400044 A OA1200400044 A OA 1200400044A OA 1200400044 A OA1200400044 A OA 1200400044A OA 12650 A OA12650 A OA 12650A
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OA
OAPI
Prior art keywords
crystal
malic acid
diethylamino
oxo
dimethyl
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OA1200400044A
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English (en)
Inventor
Thomas J Fleck
Michael Hawley
Mark T Maloney
Stephen P Prescott
Original Assignee
Upjohn Co
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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=OA12650(A) "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 OA12650A publication Critical patent/OA12650A/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic 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
    • C07D403/06—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/06—Antipsoriatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

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  • 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)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Oncology (AREA)
  • Obesity (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)
OA1200400044A 2001-08-15 2002-08-13 Crystals including a malic acid salt of N-Ä2-(diethylamino)ethylÜ-5-Ä(5-fluoro-2-oxo-3H-indole-3-ylidene)methylÜ-2,4-dimethyl-1H-pyrrole-3-carboxamide, processes for its preparation and compositions thereof. OA12650A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US31235301P 2001-08-15 2001-08-15

Publications (1)

Publication Number Publication Date
OA12650A true OA12650A (en) 2006-06-19

Family

ID=23211067

Family Applications (1)

Application Number Title Priority Date Filing Date
OA1200400044A OA12650A (en) 2001-08-15 2002-08-13 Crystals including a malic acid salt of N-Ä2-(diethylamino)ethylÜ-5-Ä(5-fluoro-2-oxo-3H-indole-3-ylidene)methylÜ-2,4-dimethyl-1H-pyrrole-3-carboxamide, processes for its preparation and compositions thereof.

Country Status (43)

Country Link
US (2) US20030069298A1 (fr)
EP (3) EP3168218B1 (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) DK1419151T3 (fr)
EA (1) EA006445B9 (fr)
EC (1) ECSP044975A (fr)
ES (3) ES2705063T3 (fr)
GE (1) GEP20063777B (fr)
HK (2) HK1066542A1 (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 (58)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3168218B1 (fr) 2001-08-15 2018-11-14 Pharmacia & Upjohn Company LLC Un cristal 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 pour utilisation comme un médicament
TW200418836A (en) * 2002-09-10 2004-10-01 Pharmacia Italia Spa Formulations comprising an indolinone compound
RU2319702C2 (ru) * 2003-10-02 2008-03-20 Фармация Энд Апджон Компани Ллс Негигроскопическая кристаллическая малеатная соль 5-[(z)-(5-фтор-2-оксо-1,2-дигидро-3h-индол-3-илиден)метил]-n-[(2s)-2-гидрокси-3-морфолин-4-илпропил]-2,4-диметил-1h-пиррол-3-карбоксамида, фармацевтическая композиция и способ лечения рака
US20060009510A1 (en) * 2004-07-09 2006-01-12 Pharmacia & Upjohn Company Llc Method of synthesizing indolinone compounds
US7834187B2 (en) * 2004-07-22 2010-11-16 Eli Lilly And Company Crystalline variable hydrate of (S)-6-(4-(2-((3-9H-carbazol-4-yloxy)-2-hydroxypropyl)amino)-2-methylpropyl)phenoxy)-3-pyridinecarbox amide hemisuccinate salt
US20080193448A1 (en) * 2005-05-12 2008-08-14 Pfizer Inc. Combinations and Methods of Using an Indolinone Compound
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
US20100256392A1 (en) * 2007-11-21 2010-10-07 Teva Pharmaceutical Industries Ltd. Polymorphs of sunitinib base and processes for preparation thereof
WO2009067686A2 (fr) * 2007-11-21 2009-05-28 Teva Pharmaceutical Industries Ltd. Hémi-l-malate de sunitinib, polymorphes et leur préparation, polymorphes de malate de sunitinib racémique, compositions contenant une base de sunitinib et de l'acide malique et leur préparation
WO2009074862A1 (fr) * 2007-12-12 2009-06-18 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
WO2009104021A2 (fr) * 2008-02-21 2009-08-27 Generics [Uk] Limited Nouveaux polymorphes et procédés de préparation
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
WO2009124037A1 (fr) * 2008-03-31 2009-10-08 Teva Pharmaceutical Industries Ltd. Procédés de préparation de sunitinib et de sels de ce dernier
EP2280960A1 (fr) * 2008-04-16 2011-02-09 Natco Pharma Limited Nouvelles formes polymorphes du sunitinib base
CA2725001C (fr) * 2008-05-23 2014-05-13 Jiangsu Chiatai Tianqing Pharmaceutical Co., Ltd. Derives de dihydroindolinone
EP2313371B1 (fr) * 2008-06-13 2012-08-15 Medichem, S.A. Procédé de préparation d un sel 2-indolinone malate à substitution 3 pyrrole
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
AU2009269768A1 (en) * 2008-07-10 2010-01-14 Generics [Uk] Limited Processes for the preparation of crystalline forms of sunitinib malate
KR20110036588A (ko) * 2008-07-24 2011-04-07 테바 파마슈티컬 인더스트리즈 리미티드 수니티닙 아세테이트 및 이의 다형을 통한 수니티닙 말레이트의 제조 방법
EP2342195B1 (fr) 2008-07-24 2014-09-10 Medichem, S.A. Formes cristallines d un sel de malate de 2-indolinone à substitution 3-pyrrole
AU2009286520A1 (en) * 2008-08-25 2010-03-04 Generics [Uk] Limited Crystalline form of sunitinib and processes for its preparation
JP2012500838A (ja) * 2008-08-25 2012-01-12 ジェネリクス・（ユーケー）・リミテッド スニチニブの新規な多形およびその調製方法
CN102177155A (zh) * 2008-10-10 2011-09-07 麦迪凯姆股份公司 一种3-吡咯取代的2-吲哚酮苹果酸盐的制备工艺
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
US8329740B2 (en) 2009-01-02 2012-12-11 Hetero Research Foundation Polymorphs of sunitinib malate
TWI447108B (zh) 2009-01-16 2014-08-01 Exelixis Inc Ｎ－（４－｛〔６，７雙（甲氧基）喹啉－４－基〕氧基｝苯基）－ｎ’－（４－氟苯基）環丙烷－１，１－二甲醯胺之蘋果酸鹽及其結晶型
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
EP2477978A1 (fr) 2009-09-16 2012-07-25 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
WO2011061613A1 (fr) 2009-11-19 2011-05-26 Ranbaxy Laboratories Limited Procédé de préparation de la forme cristalline ii du sel d'acide malique l du sunitinib
CA2788709A1 (fr) 2010-01-29 2011-08-04 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
CA2792039A1 (fr) 2010-03-04 2011-09-09 Ranbaxy Laboratories Limited Procede de preparation directe de sel d'acide malique de sunitinib
AU2011228765A1 (en) 2010-03-18 2012-10-11 Ranbaxy Laboratories Limited Process for the preparation of malic acid salt of 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
EP3536708A1 (fr) 2011-04-19 2019-09-11 Pfizer Inc Combinaisons d'anticorps anti-4-1bb et d'anticorps induisant une cytotoxicité à médiation cellulaire dépendante d'un anticorps (adcc) pour le traitement du 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
MX359257B (es) 2012-05-04 2018-09-19 Pfizer Antígenos asociados a próstata y regímenes de inmunoterapia basados en vacuna.
CA2838587A1 (fr) * 2013-10-18 2015-04-18 Hari Babu Matta Forme cristalline pure ii de sel d'acide l-malique de sunitinib et procede pour sa preparation
US9278955B2 (en) 2013-10-18 2016-03-08 Sun Pharmaceutical Industries Limited Ascorbic acid salt of sunitinib
KR102006527B1 (ko) 2013-11-01 2019-08-02 화이자 인코포레이티드 전립선-연관 항원의 발현을 위한 벡터
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
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
RO111767B1 (ro) 1990-10-15 1997-01-30 Pfizer Derivati de indol, procedee si intermediari pentru prepararea acestora, compozitii farmaceutice si metoda pentru tratarea unor afectiuni
IL100091A (en) * 1990-12-12 1998-08-16 Zeneca Ltd Pharmaceutical preparations containing the physical form of [4] 5) Cyclopentyloxycarbyl (amino 1 methyl indole 3 methyl methyl [3 methoxybenzoyl [2 methylbenzole)
AU659311B2 (en) 1992-06-05 1995-05-11 Merck Sharp & Dohme Limited The sulphate salt of a substituted triazole, pharmaceutical compositions thereof, and their use in therapy
SK283674B6 (sk) 1993-03-12 2003-11-04 Pharmacia & Upjohn Company Kryštalická voľná kyselina ceftiofuru a spôsob jej prípravy a farmaceutická kompozícia, ktorá ju obsahuje
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
BR9711151A (pt) * 1996-08-14 1999-08-17 Searle & Co Forma cristalina de 4-¬5-metil-3-fenilsoxazol-4-il¾benzenossulfonamida
US6251355B1 (en) * 1996-12-25 2001-06-26 Nippon Kayaku Kabushiki Kaisha Fine cisplatin powder and process for the production thereof
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
TR200000458T1 (tr) * 1998-06-19 2000-10-23 Teijin Limited 2-(3-siyano-4-izobütiloksifenil)-4-Metil-5-tiazolkarboksilik asit ve bunun üretilmesi için yöntem.
ES2192877T3 (es) * 1998-12-17 2003-10-16 Hoffmann La Roche 4-alquenil (y alquinil) oxindoles como inhibidores de kinasas ciclina-dependientes, en particular cdk2.
US6239141B1 (en) * 1999-06-04 2001-05-29 Pfizer Inc. Trovafloxacin oral suspensions
AU1928501A (en) * 1999-11-24 2001-06-04 Sugen, Inc. Formulations for pharmaceutical agents ionizable as free acids or free bases
ME00415B (me) * 2000-02-15 2011-10-10 Pharmacia & Upjohn Co Llc Pirol supstituisani 2-indol protein kinazni inhibitori
US6316672B1 (en) * 2001-01-31 2001-11-13 Grayson Walker Stowell Form a of fluoxetine hydrochloride
EP3168218B1 (fr) 2001-08-15 2018-11-14 Pharmacia & Upjohn Company LLC Un cristal 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 pour utilisation comme un médicament
WO2009104021A2 (fr) 2008-02-21 2009-08-27 Generics [Uk] Limited Nouveaux polymorphes et procédés de préparation
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

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IL160097A0 (en) 2004-06-20
HRP20040112B1 (en) 2012-03-31
DK1419151T3 (da) 2014-03-31
JP4159988B2 (ja) 2008-10-01
ES2623094T3 (es) 2017-07-10
JP2005503386A (ja) 2005-02-03
EA200400183A1 (ru) 2004-08-26
EP3168218A1 (fr) 2017-05-17
PL368317A1 (en) 2005-03-21
NO326508B1 (no) 2008-12-15
IS7147A (is) 2004-02-10
RS53251B (sr) 2014-08-29
KR100639281B1 (ko) 2006-10-31
SI3168218T1 (sl) 2019-05-31
HRP20040112A2 (en) 2004-06-30
KR20040030074A (ko) 2004-04-08
MY139383A (en) 2009-09-30
HK1066542A1 (en) 2005-03-24
US7435832B2 (en) 2008-10-14
CU20040029A7 (es) 2008-03-14
ES2453164T3 (es) 2014-04-04
EP3168218B1 (fr) 2018-11-14
AR036261A1 (es) 2004-08-25
AP2004002976A0 (en) 2004-03-31
UA76483C2 (en) 2006-08-15
TWI269796B (en) 2007-01-01
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