JP2015523397A5 - - Google Patents

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Publication number
JP2015523397A5
JP2015523397A5 JP2015524444A JP2015524444A JP2015523397A5 JP 2015523397 A5 JP2015523397 A5 JP 2015523397A5 JP 2015524444 A JP2015524444 A JP 2015524444A JP 2015524444 A JP2015524444 A JP 2015524444A JP 2015523397 A5 JP2015523397 A5 JP 2015523397A5
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JP
Japan
Prior art keywords
cancer
combination
proliferative
inhibitor
treatment
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JP2015524444A
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English (en)
Japanese (ja)
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JP2015523397A (ja
JP6320379B2 (ja
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Priority claimed from PCT/US2013/051990 external-priority patent/WO2014018725A1/en
Publication of JP2015523397A publication Critical patent/JP2015523397A/ja
Publication of JP2015523397A5 publication Critical patent/JP2015523397A5/ja
Application granted granted Critical
Publication of JP6320379B2 publication Critical patent/JP6320379B2/ja
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JP2015524444A 2012-07-26 2013-07-25 Cdk4/6阻害剤およびb−raf阻害剤の組合せ医薬 Active JP6320379B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201261676134P 2012-07-26 2012-07-26
US61/676,134 2012-07-26
US201361830911P 2013-06-04 2013-06-04
US61/830,911 2013-06-04
PCT/US2013/051990 WO2014018725A1 (en) 2012-07-26 2013-07-25 Pharmaceutical combinations of a cdk4/6 inhibitor and a b-raf inhibitor

Publications (3)

Publication Number Publication Date
JP2015523397A JP2015523397A (ja) 2015-08-13
JP2015523397A5 true JP2015523397A5 (US20070167479A1-20070719-C00034.png) 2016-08-25
JP6320379B2 JP6320379B2 (ja) 2018-05-09

Family

ID=48917729

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2015524444A Active JP6320379B2 (ja) 2012-07-26 2013-07-25 Cdk4/6阻害剤およびb−raf阻害剤の組合せ医薬

Country Status (16)

Country Link
US (1) US9700557B2 (US20070167479A1-20070719-C00034.png)
EP (1) EP2877174B1 (US20070167479A1-20070719-C00034.png)
JP (1) JP6320379B2 (US20070167479A1-20070719-C00034.png)
KR (1) KR102113363B1 (US20070167479A1-20070719-C00034.png)
CN (1) CN104507474B (US20070167479A1-20070719-C00034.png)
AR (1) AR091876A1 (US20070167479A1-20070719-C00034.png)
AU (1) AU2013295771B2 (US20070167479A1-20070719-C00034.png)
CA (1) CA2874860C (US20070167479A1-20070719-C00034.png)
ES (1) ES2778059T3 (US20070167479A1-20070719-C00034.png)
HK (1) HK1210721A1 (US20070167479A1-20070719-C00034.png)
IN (1) IN2015DN00376A (US20070167479A1-20070719-C00034.png)
JO (1) JO3776B1 (US20070167479A1-20070719-C00034.png)
MX (1) MX360045B (US20070167479A1-20070719-C00034.png)
RU (1) RU2685250C2 (US20070167479A1-20070719-C00034.png)
TW (1) TWI599357B (US20070167479A1-20070719-C00034.png)
WO (1) WO2014018725A1 (US20070167479A1-20070719-C00034.png)

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EP2934515B1 (en) * 2012-12-20 2018-04-04 Novartis AG A pharmaceutical combination comprising binimetinib
ES2798899T3 (es) * 2013-02-25 2020-12-14 Novartis Ag Mutación novedosa del receptor de andrógenos
CN105209073A (zh) * 2013-03-21 2015-12-30 诺华股份有限公司 包含B-Raf抑制剂和第二抑制剂的组合疗法
CA2972076A1 (en) * 2014-12-23 2016-06-30 Millennium Pharmaceuticals, Inc. Combination of raf inhibitors and aurora kinase inhibitors
CN105753869B (zh) * 2015-04-01 2018-09-25 苏州晶云药物科技有限公司 一种cdk抑制剂和mek抑制剂的共晶及其制备方法
US10323035B2 (en) * 2015-04-01 2019-06-18 Crystal Pharmatech Co., Ltd. Co-crystal of a CDK inhibitor and an MEK inhibitor and process of preparation thereof
JP2018526377A (ja) * 2015-08-28 2018-09-13 ノバルティス アーゲー がんを治療するための、任意にpi3k阻害剤のbyl719を更に含む、cdk4/6阻害剤のlee011とmek1/2阻害剤トラメチニブの組み合わせ物
CN105732642B (zh) * 2015-11-18 2018-09-25 苏州晶云药物科技有限公司 一种cdk抑制剂和mek抑制剂的共晶及其制备方法
SG11201810793XA (en) * 2016-06-03 2018-12-28 Giordano Caponigro Pharmaceutical combinations
IL264950B2 (en) * 2016-08-23 2024-01-01 Eisai R&D Man Co Ltd Combined treatments for the treatment of malignant liver cell carcinoma
CN109715163B (zh) * 2016-09-19 2022-11-22 诺华股份有限公司 包含raf抑制剂和erk抑制剂的治疗组合
WO2018081211A1 (en) * 2016-10-26 2018-05-03 Li George Y Deuterated 7-cyclopentyl-n, n-dimethyl-2-((5-(piperazin-1-yl)pyridin-2-yl)amino)-7h-pyrrolo[2,3-d]pyrimdine-6-carboxamide
US11395821B2 (en) 2017-01-30 2022-07-26 G1 Therapeutics, Inc. Treatment of EGFR-driven cancer with fewer side effects
MX2019012884A (es) * 2017-05-02 2020-01-14 Novartis Ag Terapia de combinacion.
JP2021509680A (ja) 2018-01-08 2021-04-01 ジー1、セラピューティクス、インコーポレイテッドG1 Therapeutics, Inc. G1t38の優れた投与レジメン
US11174252B2 (en) 2018-02-15 2021-11-16 Nuvation Bio Inc. Heterocyclic compounds as kinase inhibitors
WO2019195959A1 (en) * 2018-04-08 2019-10-17 Cothera Biosciences, Inc. Combination therapy for cancers with braf mutation
US11633401B2 (en) 2018-07-06 2023-04-25 Memorial Sloan Kettering Cancer Center Combination therapy with MEK inhibitor and CDK4/6 inhibitor to treat pancreatic cancer
BR112021011699A2 (pt) * 2018-12-20 2021-09-08 Novartis Ag Terapia de combinação com um inibidor de raf e um inibidor de cdk4/6 para uso no tratamento contra câncer
TW202114667A (zh) * 2019-09-11 2021-04-16 大陸商江蘇恒瑞醫藥股份有限公司 Mek抑制劑與cdk4/6抑制劑聯合在製備治療腫瘤的藥物中的用途
WO2021229439A1 (en) * 2020-05-12 2021-11-18 Novartis Ag Therapeutic combinations comprising a craf inhibitor
WO2023230554A1 (en) 2022-05-25 2023-11-30 Pfizer Inc. Combination of a braf inhibitor, an egfr inhibitor, and a pd-1 antagonist for the treatment of braf v600e-mutant, msi-h/dmmr colorectal cancer

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2549159T3 (es) * 2002-03-13 2015-10-23 Array Biopharma, Inc. Derivados de bencimidazol N3-alquilados como inhibidores de MEK
US7235537B2 (en) * 2002-03-13 2007-06-26 Array Biopharma, Inc. N3 alkylated benzimidazole derivatives as MEK inhibitors
WO2005094830A1 (en) * 2004-03-30 2005-10-13 Pfizer Products Inc. Combinations of signal transduction inhibitors
CA2729914A1 (en) * 2008-07-11 2010-01-14 Novartis Ag Combination of (a) a phosphoinositide 3-kinase inhibitor and (b) a modulator of ras/raf/mek pathway
CA2734802C (en) * 2008-08-22 2016-05-31 Novartis Ag Pyrrolopyrimidine compounds as cdk inhibitors
JO3002B1 (ar) * 2009-08-28 2016-09-05 Irm Llc مركبات و تركيبات كمثبطات كيناز بروتين
AU2011240735B2 (en) 2010-04-13 2015-01-29 Novartis Ag Combination comprising a cyclin dependent kinase 4 or cyclin dependent kinase (CDK4/6) inhibitor and an mTOR inhibitor for treating cancer

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