JP2018090566A5 - - Google Patents

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Publication number
JP2018090566A5
JP2018090566A5 JP2017219019A JP2017219019A JP2018090566A5 JP 2018090566 A5 JP2018090566 A5 JP 2018090566A5 JP 2017219019 A JP2017219019 A JP 2017219019A JP 2017219019 A JP2017219019 A JP 2017219019A JP 2018090566 A5 JP2018090566 A5 JP 2018090566A5
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JP
Japan
Prior art keywords
pharmaceutical composition
pharmaceutically acceptable
acceptable salt
lung cancer
small cell
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.)
Pending
Application number
JP2017219019A
Other languages
English (en)
Japanese (ja)
Other versions
JP2018090566A (ja
Filing date
Publication date
Application filed filed Critical
Publication of JP2018090566A publication Critical patent/JP2018090566A/ja
Publication of JP2018090566A5 publication Critical patent/JP2018090566A5/ja
Pending legal-status Critical Current

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JP2017219019A 2016-11-16 2017-11-14 非小細胞肺癌の治療のためのegfr t790m阻害剤およびcdk阻害剤の組合せ Pending JP2018090566A (ja)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201662423146P 2016-11-16 2016-11-16
US62/423146 2016-11-16
US201762571114P 2017-10-11 2017-10-11
US62/571114 2017-10-11

Publications (2)

Publication Number Publication Date
JP2018090566A JP2018090566A (ja) 2018-06-14
JP2018090566A5 true JP2018090566A5 (enExample) 2020-12-24

Family

ID=60543611

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2017219019A Pending JP2018090566A (ja) 2016-11-16 2017-11-14 非小細胞肺癌の治療のためのegfr t790m阻害剤およびcdk阻害剤の組合せ

Country Status (6)

Country Link
US (1) US20190275049A1 (enExample)
EP (1) EP3541389A1 (enExample)
JP (1) JP2018090566A (enExample)
CA (1) CA3043681A1 (enExample)
TW (1) TW201822769A (enExample)
WO (1) WO2018091999A1 (enExample)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2019006523A (es) 2016-12-05 2019-10-15 G1 Therapeutics Inc Conservacion de respuesta inmunitaria durante regimenes de quimioterapia.
US11395821B2 (en) 2017-01-30 2022-07-26 G1 Therapeutics, Inc. Treatment of EGFR-driven cancer with fewer side effects
WO2019136451A1 (en) 2018-01-08 2019-07-11 G1 Therapeutics, Inc. G1t38 superior dosage regimes
JP7698418B2 (ja) * 2018-03-13 2025-06-25 ボード オブ リージェンツ,ザ ユニバーシティ オブ テキサス システム Egfr活性化変異を有するがんを治療するための方法
KR20220009446A (ko) * 2019-05-15 2022-01-24 더 보드 오브 리젠츠 오브 더 유니버시티 오브 텍사스 시스템 비-소세포 폐암의 치료를 위한 방법 및 조성물
US12390464B2 (en) 2019-09-23 2025-08-19 Beta Pharma, Inc. Treatment of EGFR mutant-related cancers using a combination of EGFR and CDK4/6 inhibitors
EP3797776B1 (en) * 2019-09-30 2025-07-23 Universitätsmedizin Mainz Cdk4/6 inhibitors for the treatment of psoriasis
CN111557943A (zh) * 2020-04-30 2020-08-21 天津医科大学总医院 Pd0332991联合奥希替尼在制备治疗nsclc药物中的应用
US10988479B1 (en) 2020-06-15 2021-04-27 G1 Therapeutics, Inc. Morphic forms of trilaciclib and methods of manufacture thereof
WO2022253222A1 (zh) * 2021-06-04 2022-12-08 洪明奇 医药组合物治疗肺癌的用途

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE60303009T2 (de) 2002-01-22 2006-07-13 Warner-Lambert Co. Llc 2-(pyridin-2-ylamino)-pyrido[2,3-d]pyrimidin-7-one
JP4053073B2 (ja) 2003-07-11 2008-02-27 ワーナー−ランバート カンパニー リミテッド ライアビリティー カンパニー 選択的cdk4阻害剤のイセチオン酸塩
RU2009108006A (ru) 2006-09-08 2010-10-20 Пфайзер Продактс Инк. (Us) Синтез 2-(пиридин-2-иламино)-пиридо[2, 3-d]пиримидин-7-онов
PL2958916T3 (pl) 2013-02-21 2019-01-31 Pfizer Inc. Stałe postacie selektywnego inhibitora CDK4/6
UA115388C2 (uk) 2013-11-21 2017-10-25 Пфайзер Інк. 2,6-заміщені пуринові похідні та їх застосування в лікуванні проліферативних захворювань
WO2016015598A1 (en) * 2014-07-26 2016-02-04 Sunshine Lake Pharma Co., Ltd. 2-amino-pyrido[2,3-d]pyrimidin-7(8h)-one derivatives as cdk inhibitors and uses thereof
AR104068A1 (es) * 2015-03-26 2017-06-21 Hoffmann La Roche Combinaciones de un compuesto inhibidor de fosfoinosítido 3-cinasa y un compuesto inhibidor de cdk4/6 para el tratamiento del cáncer

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