JP2005503386A5 - - Google Patents

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Publication number
JP2005503386A5
JP2005503386A5 JP2003521228A JP2003521228A JP2005503386A5 JP 2005503386 A5 JP2005503386 A5 JP 2005503386A5 JP 2003521228 A JP2003521228 A JP 2003521228A JP 2003521228 A JP2003521228 A JP 2003521228A JP 2005503386 A5 JP2005503386 A5 JP 2005503386A5
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JP
Japan
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crystal
powder
crystals
ray diffraction
diethylamino
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JP2003521228A
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Japanese (ja)
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JP4159988B2 (ja
JP2005503386A (ja
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Priority claimed from PCT/US2002/025649 external-priority patent/WO2003016305A1/en
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Publication of JP2005503386A5 publication Critical patent/JP2005503386A5/ja
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JP2003521228A 2001-08-15 2002-08-13 N−[2−(ジエチルアミノ)エチル]−5−[(5−フルオロ−1,2−ジヒドロ−2−オキソ−3h−インドール−3−イリデン)メチル]−2,4−ジメチル−1h−ピロール−3−カルボキシアミドのリンゴ酸塩を含む結晶、その製法およびその組成物 Expired - Lifetime JP4159988B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US31235301P 2001-08-15 2001-08-15
PCT/US2002/025649 WO2003016305A1 (en) 2001-08-15 2002-08-13 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

Publications (3)

Publication Number Publication Date
JP2005503386A JP2005503386A (ja) 2005-02-03
JP2005503386A5 true JP2005503386A5 (https=) 2005-12-22
JP4159988B2 JP4159988B2 (ja) 2008-10-01

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JP2003521228A Expired - Lifetime JP4159988B2 (ja) 2001-08-15 2002-08-13 N−[2−(ジエチルアミノ)エチル]−5−[(5−フルオロ−1,2−ジヒドロ−2−オキソ−3h−インドール−3−イリデン)メチル]−2,4−ジメチル−1h−ピロール−3−カルボキシアミドのリンゴ酸塩を含む結晶、その製法およびその組成物

Country Status (42)

Country Link
US (2) US20030069298A1 (https=)
EP (3) EP2332934B1 (https=)
JP (1) JP4159988B2 (https=)
KR (1) KR100639281B1 (https=)
CN (2) CN100364991C (https=)
AP (1) AP1660A (https=)
AR (1) AR036261A1 (https=)
AU (1) AU2002324684B2 (https=)
BG (1) BG108553A (https=)
BR (1) BR0211612A (https=)
CA (1) CA2455050C (https=)
CO (1) CO5550431A2 (https=)
CU (1) CU23713B7 (https=)
CY (1) CY1121552T1 (https=)
CZ (1) CZ2004196A3 (https=)
DK (2) DK3168218T3 (https=)
EA (1) EA006445B9 (https=)
EC (1) ECSP044975A (https=)
ES (3) ES2705063T3 (https=)
GE (1) GEP20063777B (https=)
HR (1) HRP20040112B1 (https=)
HU (1) HU229206B1 (https=)
IL (1) IL160097A0 (https=)
IS (1) IS7147A (https=)
MA (1) MA27058A1 (https=)
ME (1) ME00414B (https=)
MX (1) MXPA04001452A (https=)
MY (1) MY139383A (https=)
NO (1) NO326508B1 (https=)
NZ (1) NZ531232A (https=)
OA (1) OA12650A (https=)
PL (1) PL216524B1 (https=)
PT (2) PT3168218T (https=)
RS (1) RS53251B (https=)
SI (2) SI3168218T1 (https=)
SK (1) SK902004A3 (https=)
TN (1) TNSN04028A1 (https=)
TR (1) TR201900509T4 (https=)
TW (1) TWI269796B (https=)
UA (1) UA76483C2 (https=)
WO (1) WO2003016305A1 (https=)
ZA (1) ZA200400706B (https=)

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WO2009150523A1 (en) * 2008-06-13 2009-12-17 Medichem, S.A. Process for preparing a 3-pyrrole substituted 2-indolinone malate salt
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CA2735084A1 (en) * 2008-08-25 2010-03-04 Generics [Uk] Limited Novel polymorphs of sunitinib and processes for their preparation
CN102197035A (zh) * 2008-08-25 2011-09-21 基因里克斯(英国)有限公司 舒尼替尼的结晶形式及其制备方法
EP2350056A1 (en) * 2008-10-10 2011-08-03 Medichem, S.A. Process for preparing a 3-pyrrole subsituted 2-indolinone malate salt
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EP2186809A1 (en) * 2008-11-13 2010-05-19 LEK Pharmaceuticals D.D. New crystal form of sunitinib malate
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EP2255792A1 (en) 2009-05-20 2010-12-01 Ratiopharm GmbH Pharmaceutical compositions for N-[2-(Diethylamino)ethyl]5-[(fluoro-1,2-dihydro-2-oxo-3H-indole-3-ylidene) methyl]-2,4-dimenthyl-1H-pyrrole-3-carboxamide
WO2011004200A1 (en) 2009-07-10 2011-01-13 Generics [Uk] Limited Novel pyrrole derivatives
CA2774634A1 (en) 2009-09-16 2011-03-24 Ranbaxy Laboratories Limited Salts of sunitinib
EP2499133A2 (en) * 2009-11-12 2012-09-19 Ranbaxy Laboratories Limited Process for the preparation of crystalline form i of l-malic acid salt of sunitinib
US8916716B2 (en) 2009-11-19 2014-12-23 Ranbaxy Laboratories Limited Process for the preparation of crystalline form II of L-malic acid salt of sunitinib
WO2011092664A1 (en) 2010-01-29 2011-08-04 Ranbaxy Laboratories Limited Crystalline forms of l-malic acid salt of sunitinib
WO2011100325A2 (en) 2010-02-09 2011-08-18 Sicor Inc. Polymorphs of sunitinib salts
WO2011104555A2 (en) 2010-02-25 2011-09-01 Generics [Uk] Limited Novel process
AU2011222470A1 (en) 2010-03-04 2012-09-27 Ranbaxy Laboratories Limited Process for the direct preparation of malic acid salt of sunitinib
US20160185760A1 (en) 2010-03-18 2016-06-30 Ranbaxy Laboratories Limited Process for the preparation of malic acid salt of sunitinib
WO2011128699A2 (en) 2010-04-16 2011-10-20 Generics [Uk] Limited Novel process
WO2012042421A1 (en) 2010-09-29 2012-04-05 Pfizer Inc. Method of treating abnormal cell growth
DK2699598T3 (en) 2011-04-19 2019-04-23 Pfizer COMBINATIONS OF ANTI-4-1BB ANTIBODIES AND ADCC-INducing ANTIBODIES FOR TREATMENT OF CANCER
ES2709110T3 (es) 2012-03-23 2019-04-15 Laurus Labs Ltd Un proceso mejorado para la preparación de sunitinib y sus sales de adición de ácido
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
AU2013255511B2 (en) 2012-05-04 2016-01-28 Pfizer Inc. Prostate-associated antigens and vaccine-based immunotherapy regimens
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CA2838587A1 (en) * 2013-10-18 2015-04-18 Hari Babu Matta Pure crystalline form ii of l-malic acid salt of sunitinib and processes for its preparation
JP2016535989A (ja) 2013-11-01 2016-11-24 ファイザー・インク 前立腺関連抗原を発現させるためのベクター
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
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