JP2013512956A5 - - Google Patents

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JP2013512956A5
JP2013512956A5 JP2012543183A JP2012543183A JP2013512956A5 JP 2013512956 A5 JP2013512956 A5 JP 2013512956A5 JP 2012543183 A JP2012543183 A JP 2012543183A JP 2012543183 A JP2012543183 A JP 2012543183A JP 2013512956 A5 JP2013512956 A5 JP 2013512956A5
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diffraction pattern
ray powder
powder diffraction
crystalline
peaks
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JP2012543183A
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JP5714024B2 (ja
JP2013512956A (ja
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Priority claimed from PCT/US2010/059108 external-priority patent/WO2011071821A1/en
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JP2012543183A 2009-12-07 2010-12-06 3−(2,6−ジクロロ−3,5−ジメトキシ−フェニル)−1−{6−[4−(4−エチル−ピペラジン−1−イル)−フェニルアミノ]−ピリミジン−4−イル}−1−メチル−尿素の結晶形態およびその塩 Active JP5714024B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US26715509P 2009-12-07 2009-12-07
US61/267,155 2009-12-07
PCT/US2010/059108 WO2011071821A1 (en) 2009-12-07 2010-12-06 Crystalline forms of 3-(2,6-dichloro-3,5-dimethoxy-phenyl)-1-{6-[4-(4-ethyl-piperazin-1-yl)-phenylamino]-pyrimidin-4-yl}-1-methyl-urea and salts thereof.

Related Child Applications (1)

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JP2015008550A Division JP6019142B2 (ja) 2009-12-07 2015-01-20 3−(2,6−ジクロロ−3,5−ジメトキシ−フェニル)−1−{6−[4−(4−エチル−ピペラジン−1−イル)−フェニルアミノ]−ピリミジン−4−イル}−1−メチル−尿素の結晶形態およびその塩

Publications (3)

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JP2013512956A JP2013512956A (ja) 2013-04-18
JP2013512956A5 true JP2013512956A5 (enExample) 2014-01-16
JP5714024B2 JP5714024B2 (ja) 2015-05-07

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JP2012543183A Active JP5714024B2 (ja) 2009-12-07 2010-12-06 3−(2,6−ジクロロ−3,5−ジメトキシ−フェニル)−1−{6−[4−(4−エチル−ピペラジン−1−イル)−フェニルアミノ]−ピリミジン−4−イル}−1−メチル−尿素の結晶形態およびその塩
JP2015008550A Active JP6019142B2 (ja) 2009-12-07 2015-01-20 3−(2,6−ジクロロ−3,5−ジメトキシ−フェニル)−1−{6−[4−(4−エチル−ピペラジン−1−イル)−フェニルアミノ]−ピリミジン−4−イル}−1−メチル−尿素の結晶形態およびその塩

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JP2015008550A Active JP6019142B2 (ja) 2009-12-07 2015-01-20 3−(2,6−ジクロロ−3,5−ジメトキシ−フェニル)−1−{6−[4−(4−エチル−ピペラジン−1−イル)−フェニルアミノ]−ピリミジン−4−イル}−1−メチル−尿素の結晶形態およびその塩

Country Status (32)

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US (1) US9067896B2 (enExample)
EP (1) EP2509963B1 (enExample)
JP (2) JP5714024B2 (enExample)
KR (1) KR101787784B1 (enExample)
CN (5) CN111100078A (enExample)
AR (2) AR079257A1 (enExample)
AU (1) AU2010328391B2 (enExample)
BR (1) BR112012013784B1 (enExample)
CA (1) CA2781431C (enExample)
CL (1) CL2012001480A1 (enExample)
DK (1) DK2509963T3 (enExample)
EC (1) ECSP12012026A (enExample)
ES (1) ES2562462T3 (enExample)
GT (1) GT201200181A (enExample)
HR (1) HRP20160126T1 (enExample)
HU (1) HUE026983T2 (enExample)
IL (1) IL220012B (enExample)
JO (1) JO3061B1 (enExample)
MA (1) MA33849B1 (enExample)
MX (1) MX2012006562A (enExample)
MY (1) MY158333A (enExample)
NZ (3) NZ700778A (enExample)
PE (1) PE20121499A1 (enExample)
PH (2) PH12012501146A1 (enExample)
PL (1) PL2509963T3 (enExample)
RU (1) RU2572848C2 (enExample)
SG (1) SG10201408063SA (enExample)
SI (1) SI2509963T1 (enExample)
TN (1) TN2012000263A1 (enExample)
TW (1) TWI526440B (enExample)
WO (1) WO2011071821A1 (enExample)
ZA (1) ZA201203612B (enExample)

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EA038045B1 (ru) 2015-02-20 2021-06-28 Инсайт Корпорейшн Бициклические гетероциклы в качестве ингибиторов fgfr
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CN104803925B (zh) * 2015-04-16 2018-01-12 温州医科大学 一类以fgfr为靶点的2,4,5‑三取代嘧啶类化合物及其制备方法和用途
WO2016189472A1 (en) 2015-05-28 2016-12-01 Novartis Ag Fgfr inhibitor for use in the treatment of the phosphaturic mesenchymal tumor
WO2017104739A1 (ja) 2015-12-17 2017-06-22 エーザイ・アール・アンド・ディー・マネジメント株式会社 乳がん治療剤
US11357769B2 (en) 2016-05-10 2022-06-14 Eisai R&D Management Co., Ltd. Drug combinations for reducing cell viability and/or cell proliferation
WO2017198221A1 (zh) * 2016-05-20 2017-11-23 浙江海正药业股份有限公司 嘧啶类衍生物、其制备方法和其在医药上的用途
RU2769251C2 (ru) * 2016-08-23 2022-03-29 Эйсай Ар Энд Ди Менеджмент Ко., Лтд. Комбинированная терапия для лечения гепатоцеллюлярной карциномы
AR111960A1 (es) 2017-05-26 2019-09-04 Incyte Corp Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
CN107176954B (zh) * 2017-06-02 2019-01-11 无锡双良生物科技有限公司 一种egfr抑制剂的药用盐及其晶型、制备方法和应用
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US11174257B2 (en) 2018-05-04 2021-11-16 Incyte Corporation Salts of an FGFR inhibitor
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WO2020185532A1 (en) 2019-03-08 2020-09-17 Incyte Corporation Methods of treating cancer with an fgfr inhibitor
WO2021007269A1 (en) 2019-07-09 2021-01-14 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
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AU2020367905A1 (en) * 2019-10-14 2022-04-21 Hutchison Medipharma Limited The salts of a compound and the crystalline forms thereof
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US11566028B2 (en) 2019-10-16 2023-01-31 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
EP4069696A1 (en) 2019-12-04 2022-10-12 Incyte Corporation Tricyclic heterocycles as fgfr inhibitors
AU2020395185A1 (en) 2019-12-04 2022-06-02 Incyte Corporation Derivatives of an FGFR inhibitor
US12012409B2 (en) 2020-01-15 2024-06-18 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
JP2024513575A (ja) 2021-04-12 2024-03-26 インサイト・コーポレイション Fgfr阻害剤及びネクチン-4標的化剤を含む併用療法
WO2022261160A1 (en) 2021-06-09 2022-12-15 Incyte Corporation Tricyclic heterocycles as fgfr inhibitors
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CN115785001B (zh) * 2022-11-23 2023-09-15 斯坦德药典标准物质研发(湖北)有限公司 一种英菲格拉替尼的制备方法
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