JPWO2020247643A5 - - Google Patents

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Publication number
JPWO2020247643A5
JPWO2020247643A5 JP2021571896A JP2021571896A JPWO2020247643A5 JP WO2020247643 A5 JPWO2020247643 A5 JP WO2020247643A5 JP 2021571896 A JP2021571896 A JP 2021571896A JP 2021571896 A JP2021571896 A JP 2021571896A JP WO2020247643 A5 JPWO2020247643 A5 JP WO2020247643A5
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JP
Japan
Prior art keywords
pharmaceutically acceptable
crystalline form
acceptable salt
compound
ray powder
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
JP2021571896A
Other languages
English (en)
Japanese (ja)
Other versions
JP2022534788A (ja
Publication date
Application filed filed Critical
Priority claimed from PCT/US2020/036137 external-priority patent/WO2020247643A1/en
Publication of JP2022534788A publication Critical patent/JP2022534788A/ja
Publication of JPWO2020247643A5 publication Critical patent/JPWO2020247643A5/ja
Pending legal-status Critical Current

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JP2021571896A 2019-06-07 2020-06-04 Shp2阻害物質である{6-[(2-アミノ-3-クロロピリジン-4-イル)スルファニル]-3-[(3s,4s)-4-アミノ-3-メチル-2-オキサ-8-アザスピロ[4.5]デカン-8-イル]-5-メチルピラジン-2-イル}メタノールの固体形態 Pending JP2022534788A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201962858837P 2019-06-07 2019-06-07
US62/858,837 2019-06-07
PCT/US2020/036137 WO2020247643A1 (en) 2019-06-07 2020-06-04 Solid forms of {6-[(2-amino-3-chloropyridin-4-yl)sulfanyl]-3-[(3s,4s)-4-amino-3-methyl-2-oxa-8-azaspiro[4.5]decan-8-yl]-5-methylpyrazin-2-yl}methanol, an shp2 inhibitor

Publications (2)

Publication Number Publication Date
JP2022534788A JP2022534788A (ja) 2022-08-03
JPWO2020247643A5 true JPWO2020247643A5 (ko) 2023-06-07

Family

ID=71787182

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2021571896A Pending JP2022534788A (ja) 2019-06-07 2020-06-04 Shp2阻害物質である{6-[(2-アミノ-3-クロロピリジン-4-イル)スルファニル]-3-[(3s,4s)-4-アミノ-3-メチル-2-オキサ-8-アザスピロ[4.5]デカン-8-イル]-5-メチルピラジン-2-イル}メタノールの固体形態

Country Status (14)

Country Link
US (2) US11220501B2 (ko)
EP (1) EP3980128A1 (ko)
JP (1) JP2022534788A (ko)
KR (1) KR20220019017A (ko)
CN (2) CN115141205A (ko)
AU (1) AU2020288631A1 (ko)
BR (1) BR112021022635A2 (ko)
CA (1) CA3142430A1 (ko)
IL (1) IL288568A (ko)
MA (1) MA56113A (ko)
MX (1) MX2021014855A (ko)
SG (1) SG11202112461QA (ko)
TW (1) TW202112785A (ko)
WO (1) WO2020247643A1 (ko)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2018328273A1 (en) 2017-09-07 2020-03-12 Revolution Medicines, Inc. SHP2 inhibitor compositions and methods for treating cancer
EP3980128A1 (en) 2019-06-07 2022-04-13 Revolution Medicines, Inc. Solid forms of {6-[(2-amino-3-chloropyridin-4-yl)sulfanyl]-3-[(3s,4s)-4-amino-3-methyl-2-oxa-8-azaspiro[4.5]decan-8-yl]-5-methylpyrazin-2-yl}methanol, an shp2 inhibitor
TW202313041A (zh) 2021-06-09 2023-04-01 瑞士商諾華公司 包含達拉菲尼、曲美替尼和shp2抑制劑之三重藥物組合
TW202317100A (zh) 2021-06-23 2023-05-01 瑞士商諾華公司 包含kras g12c抑制劑的藥物組合及其用於治療癌症之用途
WO2023031781A1 (en) 2021-09-01 2023-03-09 Novartis Ag Pharmaceutical combinations comprising a tead inhibitor and uses thereof for the treatment of cancers

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5262564A (en) 1992-10-30 1993-11-16 Octamer, Inc. Sulfinic acid adducts of organo nitroso compounds useful as retroviral inactivating agents anti-retroviral agents and anti-tumor agents
CN109983001B (zh) * 2016-07-12 2023-04-04 锐新医药公司 作为变构shp2抑制剂的2,5-双取代型3-甲基吡嗪及2,5,6-三取代型3-甲基吡嗪
AU2018328273A1 (en) 2017-09-07 2020-03-12 Revolution Medicines, Inc. SHP2 inhibitor compositions and methods for treating cancer
SG11202009793TA (en) 2018-04-10 2020-10-29 Revolution Medicines Inc Shp2 inhibitor compositions, methods for treating cancer and methods for identifying a subject with shp2 mutations
EP3980128A1 (en) 2019-06-07 2022-04-13 Revolution Medicines, Inc. Solid forms of {6-[(2-amino-3-chloropyridin-4-yl)sulfanyl]-3-[(3s,4s)-4-amino-3-methyl-2-oxa-8-azaspiro[4.5]decan-8-yl]-5-methylpyrazin-2-yl}methanol, an shp2 inhibitor

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