JP2018511634A5 - - Google Patents

Download PDF

Info

Publication number
JP2018511634A5
JP2018511634A5 JP2017553956A JP2017553956A JP2018511634A5 JP 2018511634 A5 JP2018511634 A5 JP 2018511634A5 JP 2017553956 A JP2017553956 A JP 2017553956A JP 2017553956 A JP2017553956 A JP 2017553956A JP 2018511634 A5 JP2018511634 A5 JP 2018511634A5
Authority
JP
Japan
Prior art keywords
crystalline form
cancer
dihydro
solvent
salt
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.)
Granted
Application number
JP2017553956A
Other languages
English (en)
Japanese (ja)
Other versions
JP7320741B2 (ja
JP2018511634A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/CN2016/079251 external-priority patent/WO2016165626A1/en
Publication of JP2018511634A publication Critical patent/JP2018511634A/ja
Publication of JP2018511634A5 publication Critical patent/JP2018511634A5/ja
Priority to JP2021009106A priority Critical patent/JP7383652B2/ja
Application granted granted Critical
Publication of JP7320741B2 publication Critical patent/JP7320741B2/ja
Priority to JP2023190552A priority patent/JP2024012540A/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2017553956A 2015-04-15 2016-04-14 B-rafキナーゼのマレイン酸塩、結晶形、調整方法、及びその使用 Active JP7320741B2 (ja)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP2021009106A JP7383652B2 (ja) 2015-04-15 2021-01-22 B-rafキナーゼのマレイン酸塩、結晶形、調整方法、及びその使用
JP2023190552A JP2024012540A (ja) 2015-04-15 2023-11-08 B-rafキナーゼのマレイン酸塩、結晶形、調整方法、及びその使用

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CN2015076639 2015-04-15
CNPCT/CN2015/076639 2015-04-15
PCT/CN2016/079251 WO2016165626A1 (en) 2015-04-15 2016-04-14 Maleate salts of a b-raf kinase inhibitor, crystalline forms, methods of preparation, and uses therefore

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2021009106A Division JP7383652B2 (ja) 2015-04-15 2021-01-22 B-rafキナーゼのマレイン酸塩、結晶形、調整方法、及びその使用

Publications (3)

Publication Number Publication Date
JP2018511634A JP2018511634A (ja) 2018-04-26
JP2018511634A5 true JP2018511634A5 (enExample) 2019-05-23
JP7320741B2 JP7320741B2 (ja) 2023-08-04

Family

ID=57125563

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2017553956A Active JP7320741B2 (ja) 2015-04-15 2016-04-14 B-rafキナーゼのマレイン酸塩、結晶形、調整方法、及びその使用
JP2021009106A Active JP7383652B2 (ja) 2015-04-15 2021-01-22 B-rafキナーゼのマレイン酸塩、結晶形、調整方法、及びその使用
JP2023190552A Withdrawn JP2024012540A (ja) 2015-04-15 2023-11-08 B-rafキナーゼのマレイン酸塩、結晶形、調整方法、及びその使用

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP2021009106A Active JP7383652B2 (ja) 2015-04-15 2021-01-22 B-rafキナーゼのマレイン酸塩、結晶形、調整方法、及びその使用
JP2023190552A Withdrawn JP2024012540A (ja) 2015-04-15 2023-11-08 B-rafキナーゼのマレイン酸塩、結晶形、調整方法、及びその使用

Country Status (15)

Country Link
US (1) US10351559B2 (enExample)
EP (2) EP4119559A1 (enExample)
JP (3) JP7320741B2 (enExample)
KR (2) KR102643609B1 (enExample)
CN (2) CN113307805A (enExample)
AU (1) AU2016248376B2 (enExample)
CA (1) CA2981746C (enExample)
EA (1) EA035680B1 (enExample)
IL (2) IL255555B (enExample)
MX (1) MX381053B (enExample)
NZ (1) NZ735715A (enExample)
SG (1) SG11201707984TA (enExample)
TW (4) TWI792406B (enExample)
WO (1) WO2016165626A1 (enExample)
ZA (1) ZA201706392B (enExample)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BRPI0610308A8 (pt) 2005-05-26 2017-04-25 Neuron Systems Inc Composições e métodos para o tratamento de doença retinal
US9814701B2 (en) 2009-12-11 2017-11-14 Aldeyra Therapeutics, Inc. Compositions and methods for the treatment of macular degeneration
EP2797888B1 (en) 2011-12-31 2016-06-08 BeiGene, Ltd. Fused tricyclic compounds as raf kinase inhibitors
CN105120866B (zh) 2013-01-23 2020-02-14 奥尔德拉医疗公司 与毒性醛相关的疾病和治疗
JP7320741B2 (ja) * 2015-04-15 2023-08-04 ベイジーン リミテッド B-rafキナーゼのマレイン酸塩、結晶形、調整方法、及びその使用
WO2017035077A1 (en) 2015-08-21 2017-03-02 Aldeyra Therapeutics, Inc. Deuterated compounds and uses thereof
CN109475536B (zh) 2016-07-05 2022-05-27 百济神州有限公司 用于治疗癌症的PD-l拮抗剂和RAF抑制剂的组合
IL270224B1 (en) 2017-05-02 2024-04-01 Novartis Ag Combination therapy employing trametinib and a defined raf inhibitor
CN111356451A (zh) 2017-10-10 2020-06-30 奥尔德拉医疗公司 炎性病症的治疗
US12006298B2 (en) 2018-08-06 2024-06-11 Aldeyra Therapeutics, Inc. Polymorphic compounds and uses thereof
CA3117559C (en) * 2018-10-31 2023-09-26 Les Laboratoires Servier Hydrogen sulfate salt of a bcl-2 inhibitor, related crystalline form,method for preparing the same and pharmaceutical compositions containing the same
CN111484489B (zh) * 2019-01-25 2023-05-23 百济神州(北京)生物科技有限公司 无定形的b-raf激酶二聚体抑制剂
CN111484488A (zh) * 2019-01-25 2020-08-04 百济神州(北京)生物科技有限公司 一种b-raf激酶二聚体抑制剂的稳定结晶形式a
CN119684285A (zh) * 2019-03-15 2025-03-25 福马治疗股份有限公司 抑制环amp-应答元件结合蛋白(creb)
US12098132B2 (en) 2019-05-02 2024-09-24 Aldeyra Therapeutics, Inc. Process for preparation of aldehyde scavenger and intermediates
CA3137301A1 (en) 2019-05-02 2020-11-05 Aldeyra Therapeutics, Inc. Polymorphic compounds and uses thereof
EP4563150A3 (en) 2019-05-13 2025-07-23 Novartis AG New crystalline forms of n-(3-(2-(2-hydroxyethoxy)-6-morpholinopyridin-4-yl)-4-methvlphenyl)-2(trifluoromethyl) isonicotinamide as raf inhibitors for the treatment of cancer
CN111184693B (zh) * 2019-05-29 2023-07-21 百济神州(苏州)生物科技有限公司 一种raf激酶抑制剂制剂及其制备方法
AU2021246141A1 (en) * 2020-04-03 2022-12-01 Beigene, Ltd. Co-administration of mirdametinib and lifirafenib for use in treating cancers
EP4149470A4 (en) 2020-05-13 2024-04-24 Aldeyra Therapeutics, Inc. Pharmaceutical formulations and uses thereof
JP2025519981A (ja) * 2022-06-08 2025-06-30 マップキュア,エルエルシー B-raf阻害剤によるがんの治療方法

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1828186A1 (en) 2004-12-13 2007-09-05 Sunesis Pharmaceuticals, Inc. Pyrido pyrimidinones, dihydro pyrimido pyrimidinones and pteridinones useful as raf kinase inhibitors
TW200639163A (en) 2005-02-04 2006-11-16 Genentech Inc RAF inhibitor compounds and methods
KR20080074220A (ko) 2005-12-08 2008-08-12 밀레니엄 파머슈티컬스 인코퍼레이티드 키나아제 억제 활성을 갖는 비시클릭 화합물
ATE552245T1 (de) 2006-05-15 2012-04-15 Merck Sharp & Dohme Antidiabetische bicyclische verbindungen
KR20090052884A (ko) 2006-08-23 2009-05-26 화이자 프로덕츠 인크. Gsk-3 억제제로서의 피리미돈 화합물
US20080064729A1 (en) 2006-09-07 2008-03-13 Millennium Pharmaceuticals, Inc. Phenethylamide derivatives with kinase inhibitory activity
WO2008137770A1 (en) 2007-05-04 2008-11-13 Irm Llc Compounds and compositions as c-kit and pdgfr kinase inhibitors
US20100197924A1 (en) 2008-12-22 2010-08-05 Millennium Pharmaceuticals, Inc. Preparation of aminotetralin compounds
US9012464B2 (en) * 2010-11-25 2015-04-21 Ratiopharm Gmbh Salts and polymorphic forms of Afatinib
EP2797888B1 (en) * 2011-12-31 2016-06-08 BeiGene, Ltd. Fused tricyclic compounds as raf kinase inhibitors
JP7320741B2 (ja) 2015-04-15 2023-08-04 ベイジーン リミテッド B-rafキナーゼのマレイン酸塩、結晶形、調整方法、及びその使用

Similar Documents

Publication Publication Date Title
JP2018511634A5 (enExample)
JP2018528199A5 (enExample)
JP2020033359A5 (enExample)
AU2016260279B2 (en) Crystals of azabicyclic compound
TWI826373B (zh) (s)-2-((2-((s)-4-(二氟甲基)-2-氧代唑烷-3-基)-5,6-二氫苯并[f]咪唑并[1,2-d][1,4]氧氮呯-9-基)胺基)丙醯胺之多晶型及固體形式及製造方法
JP2013518041A5 (enExample)
CN107531682A (zh) B‑raf激酶抑制剂的马来酸盐、其结晶形式、制备方法和用途
JP2020517611A5 (enExample)
JP2019515024A (ja) ボルチオキセチンのパモ酸塩及びその結晶形
KR102666017B1 (ko) 엔잘루타미드 결정형의 제조 방법
CA3009713A1 (en) Crystalline forms of ponesimod and preparation method thereof
CA3142088A1 (en) Compound used as kinase inhibitor and application thereof
JP7124035B2 (ja) アクリジニウム臭化物の製造方法
AU2018372180B2 (en) Polymorphs and solid forms of a pyrimidinylamino-pyrazole compound, and methods of production
JP2013541589A5 (enExample)
JP6676626B2 (ja) アシルチオウレア化合物のメシル酸塩の結晶及びその製造方法
WO2016187028A1 (en) Heteroaryl compounds, synthesis thereof, and intermediates thereto
ES2727667T3 (es) Polimorfos de lenalidomida
JP2020530497A (ja) 3−(5−フルオロベンゾフラン−3−イル)−4−(5−メチル−5H−[1,3]ジオキソロ[4,5−f]インドール−7−イル)ピロール−2,5−ジオンの固体形態
CN111315748B (zh) 3-(5-氟苯并呋喃-3-基)-4-(5-甲基-5H-[1,3]间二氧杂环戊烯并[4,5-f]吲哚-7-基)吡咯-2,5-二酮晶体
JP2015521635A5 (enExample)
JP6165335B2 (ja) ゲフィチニブの新規な結晶形およびその製造方法
CA2561635C (en) New crystalline form of 8-cyano-1-cyclopropyl-7-(1s,6s-2,8-diazabicyclo[4.3.0]nonan-8-yl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
JPWO2011152411A1 (ja) チエノピリミジン誘導体の結晶
JP2010229098A (ja) イソインドリン誘導体のa型の結晶形の製造方法及びイソインドリン誘導体のa型の結晶形