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Withdrawn legal-status Critical Current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がんの治療または予防のための(a)サイクリン依存性キナーゼ4/6(cdk4/6)阻害剤のlee011(=リボシクリブ)および(b)上皮成長因子受容体(egfr)阻害剤のエルロチニブを含む医薬組み合わせ物 Withdrawn JP2018526376A (ja)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JP2018511135A Withdrawn JP2018526376A (ja) 2015-08-28 2016-08-24 がんの治療または予防のための(a)サイクリン依存性キナーゼ4/6(cdk4/6)阻害剤のlee011(=リボシクリブ)および(b)上皮成長因子受容体(egfr)阻害剤のエルロチニブを含む医薬組み合わせ物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 (23)

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Publication number Priority date Publication date Assignee Title
EP2937345B1 (en) 2009-12-29 2018-03-21 Dana-Farber Cancer Institute, Inc. Type ii raf kinase inhibitors
JP6106685B2 (ja) 2011-11-17 2017-04-05 ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド C−jun−n−末端キナーゼ(jnk)の阻害剤
EP2909194A1 (en) 2012-10-18 2015-08-26 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
USRE48175E1 (en) 2012-10-19 2020-08-25 Dana-Farber Cancer Institute, Inc. Hydrophobically tagged small molecules as inducers of protein degradation
AU2014337044A1 (en) 2013-10-18 2016-05-05 Dana-Farber Cancer Institute, Inc. Polycyclic inhibitors of cyclin-dependent kinase 7 (CDK7)
WO2015058126A1 (en) 2013-10-18 2015-04-23 Syros Pharmaceuticals, Inc. Heteroaromatic compounds useful for the treatment of prolferative diseases
US10870651B2 (en) 2014-12-23 2020-12-22 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (CDK7)
CN107427521B (zh) 2015-03-27 2021-08-03 达纳-法伯癌症研究所股份有限公司 细胞周期蛋白依赖性激酶的抑制剂
CA2986441A1 (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
US11395821B2 (en) 2017-01-30 2022-07-26 G1 Therapeutics, Inc. Treatment of EGFR-driven cancer with fewer side effects
EP3585389A4 (en) 2017-02-22 2020-12-23 G1 Therapeutics, Inc. EGFR-CAUSED CANCER TREATMENT WITH LESS SIDE EFFECTS
WO2018218633A1 (en) * 2017-06-02 2018-12-06 Beijing Percans Oncology Co. Ltd. Combination therapies for treating cancers
EP3661519A1 (en) * 2017-08-03 2020-06-10 Novartis AG Therapeutic combination of a third generation egfr tyrosine kinase inhibitor and a cyclin d kinase inhibitor
WO2019136451A1 (en) 2018-01-08 2019-07-11 G1 Therapeutics, Inc. G1t38 superior dosage regimes
WO2019195959A1 (en) 2018-04-08 2019-10-17 Cothera Biosciences, Inc. Combination therapy for cancers with braf mutation
TWI762784B (zh) * 2018-05-23 2022-05-01 大陸商江蘇恒瑞醫藥股份有限公司 Cdk4/6抑制劑與egfr抑制劑聯合在製備治療腫瘤疾病的藥物中的用途
EP3810132A4 (en) 2018-06-25 2022-06-22 Dana-Farber Cancer Institute, Inc. TAIRE FAMILY KINASE INHIBITORS AND RELATED USES
WO2020036852A1 (en) 2018-08-13 2020-02-20 Beijing Percans Oncology Co. Ltd. Biomarkers for cancer therapy
US20220047546A1 (en) * 2018-09-12 2022-02-17 The Board Of Regents Of The University Of Oklahoma Combination cancer therapies
CN113164477A (zh) 2018-12-14 2021-07-23 达纳-法伯癌症研究所股份有限公司 C-jun-n-末端激酶的吡唑并吡啶抑制剂及其用途
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
ATE446955T1 (de) 1995-03-30 2009-11-15 Pfizer Prod Inc Chinazolinone derivate
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
AU2009284098B2 (en) * 2008-08-22 2012-03-29 Astex Therapeutics Ltd. Pyrrolopyrimidine compounds as CDK inhibitors
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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