JP2021534129A5 - - Google Patents

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Publication number
JP2021534129A5
JP2021534129A5 JP2021506964A JP2021506964A JP2021534129A5 JP 2021534129 A5 JP2021534129 A5 JP 2021534129A5 JP 2021506964 A JP2021506964 A JP 2021506964A JP 2021506964 A JP2021506964 A JP 2021506964A JP 2021534129 A5 JP2021534129 A5 JP 2021534129A5
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JP
Japan
Prior art keywords
egfr
inhibitor
combination according
ret
patient
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
JP2021506964A
Other languages
English (en)
Japanese (ja)
Other versions
JP7490635B2 (ja
JP2021534129A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2019/045919 external-priority patent/WO2020033838A2/en
Publication of JP2021534129A publication Critical patent/JP2021534129A/ja
Publication of JP2021534129A5 publication Critical patent/JP2021534129A5/ja
Application granted granted Critical
Publication of JP7490635B2 publication Critical patent/JP7490635B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2021506964A 2018-08-10 2019-08-09 Egfr変異がんの処置 Active JP7490635B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201862717480P 2018-08-10 2018-08-10
US62/717,480 2018-08-10
US201862735730P 2018-09-24 2018-09-24
US62/735,730 2018-09-24
PCT/US2019/045919 WO2020033838A2 (en) 2018-08-10 2019-08-09 Treatment of egfr-mutant cancer

Publications (3)

Publication Number Publication Date
JP2021534129A JP2021534129A (ja) 2021-12-09
JP2021534129A5 true JP2021534129A5 (enExample) 2022-08-17
JP7490635B2 JP7490635B2 (ja) 2024-05-27

Family

ID=69415686

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2021506964A Active JP7490635B2 (ja) 2018-08-10 2019-08-09 Egfr変異がんの処置

Country Status (5)

Country Link
US (1) US20210308134A1 (enExample)
EP (1) EP3833372A4 (enExample)
JP (1) JP7490635B2 (enExample)
CN (1) CN112703014A (enExample)
WO (1) WO2020033838A2 (enExample)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016127074A1 (en) 2015-02-06 2016-08-11 Blueprint Medicines Corporation 2-(pyridin-3-yl)-pyrimidine derivatives as ret inhibitors
SI3371171T1 (sl) 2015-11-02 2024-03-29 Blueprint Medicines Corporation Inhibitorji ret
PE20210096A1 (es) 2018-04-03 2021-01-12 Blueprint Medicines Corp Inhibidor de ret para uso en tratar cancer que tiene una alteracion de ret
EP4157230A1 (en) * 2020-05-29 2023-04-05 Blueprint Medicines Corporation Pralsetinib pharmaceutical compositions
EP4157829A1 (en) * 2020-05-29 2023-04-05 Blueprint Medicines Corporation Solid forms of pralsetinib
WO2022046867A1 (en) * 2020-08-25 2022-03-03 Loxo Oncology, Inc. Osimertinib and selpercatinib combinations for the treatment of egfr- and ret-associated cancers
CN116867492A (zh) * 2020-11-20 2023-10-10 赫尔森保健股份公司 使用4-氨基-n-[4-(甲氧基甲基)苯基]-7-(1-甲基环丙基)-6-(3-吗啉代丙-1-炔-1-基)-7h-吡咯并[2,3-d]嘧啶-5-羧酰胺治疗肿瘤的方法
TW202309022A (zh) 2021-04-13 2023-03-01 美商努法倫特公司 用於治療具egfr突變之癌症之胺基取代雜環
CN113143931A (zh) * 2021-04-16 2021-07-23 南方医科大学 甲磺酸奥西替尼在制备寻常型银屑病治疗药物中的应用
CN116440136B (zh) * 2023-04-17 2024-02-09 浙江大学智能创新药物研究院 甲磺酸阿美替尼在制备治疗乐伐替尼心脏毒性药物中的应用

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CN1925855B (zh) 2003-12-19 2010-06-16 普莱希科公司 开发Ret调节剂的化合物和方法
WO2007087245A2 (en) 2006-01-24 2007-08-02 Merck & Co., Inc. Ret tyrosine kinase inhibition
WO2009003136A1 (en) 2007-06-26 2008-12-31 Rigel Pharmaceuticals, Inc. Substituted pyrimidine-2, 4 -diamines for treating cell proliferative disorders
WO2009100536A1 (en) 2008-02-15 2009-08-20 Methylgene Inc. Inhibitors of kinase activity with 1,2-di-cyclyl substituted alkyne structures
CN103764676A (zh) 2011-08-04 2014-04-30 日本国立癌症研究中心 Kif5b基因和ret基因的融合基因、以及以该融合基因为目标的判断癌症治疗有效性的方法
BR112014004213A2 (pt) 2011-08-23 2017-06-20 Found Medicine Inc novas moléculas de fusão kif5b-ret e usos das mesmas
CA2846496C (en) * 2011-09-02 2020-07-14 The Regents Of The University Of California Substituted pyrazolo[3,4-d]pyrimidines and uses thereof
JP2015109806A (ja) 2012-03-22 2015-06-18 アステラス製薬株式会社 新規ret融合体の検出法
EP2878672A4 (en) 2012-07-26 2016-02-17 Nat Cancer Ct FUSIONSGEN OF CEP55-GEN AND RET-GEN
CN105658814A (zh) 2013-08-20 2016-06-08 日本国立癌症研究中心 在肺癌中检测出的新型融合基因
WO2016127074A1 (en) 2015-02-06 2016-08-11 Blueprint Medicines Corporation 2-(pyridin-3-yl)-pyrimidine derivatives as ret inhibitors
BR112018000808A2 (pt) 2015-07-16 2018-09-04 Array Biopharma Inc compostos de pirazolo[1,5-a]piridina substituída como inibidores de ret cinase
CN105255927B (zh) 2015-09-30 2018-07-27 温州医科大学附属第一医院 一种kiaa1217-ret融合基因
SI3371171T1 (sl) 2015-11-02 2024-03-29 Blueprint Medicines Corporation Inhibitorji ret
MA43416A (fr) * 2015-12-11 2018-10-17 Regeneron Pharma Méthodes pour ralentir ou empêcher la croissance de tumeurs résistantes au blocage de l'egfr et/ou d'erbb3
US10183928B2 (en) 2016-03-17 2019-01-22 Blueprint Medicines Corporation Inhibitors of RET
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GB201705971D0 (en) 2017-04-13 2017-05-31 Cancer Res Tech Ltd Inhibitor compounds
US10934300B2 (en) 2017-06-23 2021-03-02 San Diego State University (Sdsu) Foundation Atropisomerism for enhanced kinase inhibitor selectivity
CN109180677A (zh) 2017-06-30 2019-01-11 厦门大学 取代芳基醚类化合物、其制备方法、药用组合物及其应用
WO2019008172A1 (en) 2017-07-07 2019-01-10 Nipd Genetics Public Company Limited ENRICHED MULTIPLEXED PARALLEL ANALYSIS IN TARGET FOR TUMOR BIOMARKER EVALUATION
LT3728271T (lt) 2017-12-19 2022-12-12 Turning Point Therapeutics, Inc. Makrocikliniai junginiai, skirti ligų gydymui
JP7060694B2 (ja) 2018-01-18 2022-04-26 アレイ バイオファーマ インコーポレイテッド Retキナーゼ阻害剤としての置換ピロロ[2,3-d]ピリミジン化合物
EP3740490A1 (en) 2018-01-18 2020-11-25 Array Biopharma, Inc. Substituted pyrazolo[3,4-d]pyrimidine compounds as ret kinase inhibitors
US11472802B2 (en) 2018-01-18 2022-10-18 Array Biopharma Inc. Substituted pyrazolyl[4,3-c]pyridine compounds as RET kinase inhibitors

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