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
JP2018511634A (ja
JP7320741B2 (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 (cg-RX-API-DMAC7.html) 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 (cg-RX-API-DMAC7.html)
EP (2) EP3283486B1 (cg-RX-API-DMAC7.html)
JP (3) JP7320741B2 (cg-RX-API-DMAC7.html)
KR (2) KR20240049684A (cg-RX-API-DMAC7.html)
CN (2) CN107531682B (cg-RX-API-DMAC7.html)
AU (1) AU2016248376B2 (cg-RX-API-DMAC7.html)
CA (1) CA2981746C (cg-RX-API-DMAC7.html)
EA (1) EA035680B1 (cg-RX-API-DMAC7.html)
IL (2) IL255555B (cg-RX-API-DMAC7.html)
MX (1) MX381053B (cg-RX-API-DMAC7.html)
NZ (1) NZ735715A (cg-RX-API-DMAC7.html)
SG (1) SG11201707984TA (cg-RX-API-DMAC7.html)
TW (4) TWI792406B (cg-RX-API-DMAC7.html)
WO (1) WO2016165626A1 (cg-RX-API-DMAC7.html)
ZA (1) ZA201706392B (cg-RX-API-DMAC7.html)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2609659C (en) 2005-05-26 2014-01-28 Neuron Systems, Inc. Azanaphthalenes, compositions and methods for treating retinal disease
CA2782015C (en) 2009-12-11 2020-08-25 Neuron Systems, Inc. Topical ophthalmic compositions and methods for the treatment of macular degeneration
CN103596926B (zh) 2011-12-31 2015-11-25 百济神州有限公司 作为raf激酶抑制剂的稠合三环化合物
AU2014209387B2 (en) 2013-01-23 2018-11-01 Aldeyra Therapeutics, Inc. Toxic aldehyde related diseases and treatment
EP3283486B1 (en) 2015-04-15 2022-07-27 BeiGene, Ltd. Maleate salts of a b-raf kinase inhibitor, crystalline forms, methods of preparation, and uses therefore
EP4400106A1 (en) 2015-08-21 2024-07-17 Aldeyra Therapeutics, Inc. Deuterated compounds and uses thereof
AU2017293423B2 (en) 2016-07-05 2023-05-25 Beone Medicines I Gmbh Combination of a PD-1 antagonist and a RAF inhibitor for treating cancer
DK3618875T3 (da) 2017-05-02 2023-07-10 Novartis Ag Kombinationsterapi omfattende en raf-inhibitor og trametinib
WO2019075136A1 (en) 2017-10-10 2019-04-18 Aldeyra Therapeutics, Inc. TREATMENT OF INFLAMMATORY DISORDERS
US12006298B2 (en) 2018-08-06 2024-06-11 Aldeyra Therapeutics, Inc. Polymorphic compounds and uses thereof
MY202547A (en) * 2018-10-31 2024-05-07 Servier Lab Novel salt of a bcl-2 inhibitor, related crystalline form, method for preparing the same and pharmaceutical compositions containing the same
CN116715662A (zh) * 2019-01-25 2023-09-08 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
MX2021010829A (es) * 2019-03-15 2021-12-10 Forma Therapeutics Inc Inhibición de la proteína de unión al elemento de respuesta a adenosín monofosfato (amp) cíclica (creb).
US12098132B2 (en) 2019-05-02 2024-09-24 Aldeyra Therapeutics, Inc. Process for preparation of aldehyde scavenger and intermediates
CN113784954A (zh) 2019-05-02 2021-12-10 奥尔德拉医疗公司 多晶型化合物和其用途
KR102881316B1 (ko) 2019-05-13 2025-11-05 노파르티스 아게 암 치료를 위한 raf 억제제로서의 n-(3-(2-(2-하이드록시에톡시)-6-모르폴리노피리딘-4-일)-4-메틸페닐)-2 (트리플루오로메틸)이소니코틴아미드의 새로운 결정질 형태
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
PE20231211A1 (es) * 2020-04-03 2023-08-17 Springworks Therapeutics Inc Administracion conjunta de mirdametinib y lifirafenib para uso en el tratamiento de canceres
CA3175856A1 (en) 2020-05-13 2021-11-18 Todd Brady 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
WO2006065703A1 (en) 2004-12-13 2006-06-22 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
CN101365682A (zh) * 2005-12-08 2009-02-11 千禧药品公司 具有激酶抑制活性的双环化合物
EP2021327B1 (en) 2006-05-15 2012-04-04 Merck Sharp & Dohme Corp. Antidiabetic bicyclic compounds
WO2008023239A1 (en) 2006-08-23 2008-02-28 Pfizer Products Inc. Pyrimidone compounds as gsk-3 inhibitors
WO2008030448A1 (en) 2006-09-07 2008-03-13 Millennium Pharmaceuticals, Inc. Phenethylamide derivatives with kinase inhibitory activity
AU2008247500A1 (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
JP5808818B2 (ja) * 2010-11-25 2015-11-10 ラツィオファーム・ゲーエムベーハー アファチニブの新規塩及び多形形態
CN103596926B (zh) 2011-12-31 2015-11-25 百济神州有限公司 作为raf激酶抑制剂的稠合三环化合物
EP3283486B1 (en) 2015-04-15 2022-07-27 BeiGene, Ltd. Maleate salts of a b-raf kinase inhibitor, crystalline forms, methods of preparation, and uses therefore

Similar Documents

Publication Publication Date Title
JP2018511634A5 (cg-RX-API-DMAC7.html)
JP2018528199A5 (cg-RX-API-DMAC7.html)
JP2020033359A5 (cg-RX-API-DMAC7.html)
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 (cg-RX-API-DMAC7.html)
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 (cg-RX-API-DMAC7.html)
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
JP6816036B2 (ja) ヒストン脱アセチル化阻害剤の結晶形態
JP2013541589A5 (cg-RX-API-DMAC7.html)
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 (cg-RX-API-DMAC7.html)
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