JP2018526376A5 - - Google Patents

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Publication number
JP2018526376A5
JP2018526376A5 JP2018511135A JP2018511135A JP2018526376A5 JP 2018526376 A5 JP2018526376 A5 JP 2018526376A5 JP 2018511135 A JP2018511135 A JP 2018511135A JP 2018511135 A JP2018511135 A JP 2018511135A JP 2018526376 A5 JP2018526376 A5 JP 2018526376A5
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JP
Japan
Prior art keywords
cancer
pharmaceutical combination
combination according
compound
formula
Prior art date
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Application number
JP2018511135A
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English (en)
Japanese (ja)
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JP2018526376A (ja
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Publication date
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Priority claimed from PCT/IB2016/055044 external-priority patent/WO2017037576A1/en
Publication of JP2018526376A publication Critical patent/JP2018526376A/ja
Publication of JP2018526376A5 publication Critical patent/JP2018526376A5/ja
Withdrawn legal-status Critical Current

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JP2018511135A 2015-08-28 2016-08-24 がんの治療または予防のための(a)サイクリン依存性キナーゼ4/6(cdk4/6)阻害剤のlee011(=リボシクリブ)および(b)上皮成長因子受容体(egfr)阻害剤のエルロチニブを含む医薬組み合わせ物 Withdrawn JP2018526376A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201562211031P 2015-08-28 2015-08-28
US62/211,031 2015-08-28
PCT/IB2016/055044 WO2017037576A1 (en) 2015-08-28 2016-08-24 Pharmaceutical combinations comprising (a) the cyclin dependent kinase 4/6 (cdk4/6) inhibitor lee011 (=ribociclib), and (b) the epidermal growth factor receptor (egfr) inhibitor erlotinib, for the treatment or prevention of cancer

Publications (2)

Publication Number Publication Date
JP2018526376A JP2018526376A (ja) 2018-09-13
JP2018526376A5 true JP2018526376A5 (enExample) 2019-10-03

Family

ID=56896739

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2018511135A Withdrawn JP2018526376A (ja) 2015-08-28 2016-08-24 がんの治療または予防のための(a)サイクリン依存性キナーゼ4/6(cdk4/6)阻害剤のlee011(=リボシクリブ)および(b)上皮成長因子受容体(egfr)阻害剤のエルロチニブを含む医薬組み合わせ物

Country Status (6)

Country Link
US (1) US20180243304A1 (enExample)
EP (1) EP3340990B1 (enExample)
JP (1) JP2018526376A (enExample)
CN (1) CN108348522A (enExample)
ES (1) ES2761885T3 (enExample)
WO (1) WO2017037576A1 (enExample)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9180127B2 (en) 2009-12-29 2015-11-10 Dana-Farber Cancer Institute, Inc. Type II Raf kinase inhibitors
US9382239B2 (en) 2011-11-17 2016-07-05 Dana-Farber Cancer Institute, Inc. Inhibitors of c-Jun-N-terminal kinase (JNK)
US10112927B2 (en) 2012-10-18 2018-10-30 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (CDK7)
US9758522B2 (en) 2012-10-19 2017-09-12 Dana-Farber Cancer Institute, Inc. Hydrophobically tagged small molecules as inducers of protein degradation
CN105849099B (zh) 2013-10-18 2020-01-17 达纳-法伯癌症研究所股份有限公司 周期蛋白依赖性激酶7(cdk7)的多环抑制剂
EP3057955B1 (en) 2013-10-18 2018-04-11 Syros Pharmaceuticals, Inc. Heteroaromatic compounds useful for the treatment of prolferative diseases
WO2016105528A2 (en) 2014-12-23 2016-06-30 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
CA2978518C (en) 2015-03-27 2023-11-21 Nathanael S. Gray Inhibitors of cyclin-dependent kinases
WO2016201370A1 (en) * 2015-06-12 2016-12-15 Dana-Farber Cancer Institute, Inc. Combination therapy of transcription inhibitors and kinase inhibitors
WO2017044858A2 (en) 2015-09-09 2017-03-16 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinases
WO2017160568A1 (en) * 2016-03-16 2017-09-21 Eli Lilly And Company Combination therapy comprising the cdk4/6 inhibitor necitumumab and the egfr inhibitor abemaciclib for use in treating cancer
WO2018156812A1 (en) 2017-02-22 2018-08-30 G1 Therapeutics, Inc. Treatment of egfr-driven cancer with fewer side effects
US11395821B2 (en) 2017-01-30 2022-07-26 G1 Therapeutics, Inc. Treatment of EGFR-driven cancer with fewer side effects
WO2018218633A1 (en) * 2017-06-02 2018-12-06 Beijing Percans Oncology Co. Ltd. Combination therapies for treating cancers
RU2020108191A (ru) * 2017-08-03 2021-09-03 Новартис Аг Терапевтическая комбинация ингибитора тирозинкиназы egfr третьего поколения и ингибиторa циклин-d-киназы
KR20200108867A (ko) 2018-01-08 2020-09-21 쥐원 쎄라퓨틱스, 인크. G1t38 우수한 투여 요법
WO2019195959A1 (en) 2018-04-08 2019-10-17 Cothera Biosciences, Inc. Combination therapy for cancers with braf mutation
MX2020012540A (es) * 2018-05-23 2021-02-16 Jiangsu Hengrui Medicine Co Uso de inhibidor de cdk4/6 en combinacion con inhibidor del egfr en la preparacion de medicamento para tratar enfermedades tumorales.
CN112367991A (zh) 2018-06-25 2021-02-12 达纳-法伯癌症研究所股份有限公司 Taire家族激酶抑制剂及其用途
JP7507145B2 (ja) 2018-08-13 2024-06-27 ベイジン パーカンズ オンコロジー カンパニー リミテッド 癌治療のためのバイオマーカー
EP3849310A4 (en) * 2018-09-12 2022-07-06 The Board of Regents of the University of Oklahoma COMBINATION CANCER THERAPIES
EP4626890A1 (en) 2022-12-01 2025-10-08 KRKA, d.d., Novo mesto Ribociclib salts and formulations thereof

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2161290T3 (es) 1995-03-30 2001-12-01 Pfizer Derivados de quinazolina.
US6706721B1 (en) * 1998-04-29 2004-03-16 Osi Pharmaceuticals, Inc. N-(3-ethynylphenylamino)-6,7-bis(2-methoxyethoxy)-4-quinazolinamine mesylate anhydrate and monohydrate
SI2331547T1 (sl) * 2008-08-22 2014-11-28 Novartis Ag Pirolopirimidinske spojine kot CDK inhibitorji
AR083797A1 (es) * 2010-11-10 2013-03-20 Novartis Ag Succinato de dimetil-amida del acido 7-ciclopentil-2-(5-piperazin-1-il-piridin-2-il-amino)-7h-pirrolo-[2,3-d]pirimidin-6-carboxilico, proceso para prepararla, intermediarios de dicha sintesis y proceso de preparacion de los mismos

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