JP2015536986A5 - - Google Patents

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Publication number
JP2015536986A5
JP2015536986A5 JP2015541875A JP2015541875A JP2015536986A5 JP 2015536986 A5 JP2015536986 A5 JP 2015536986A5 JP 2015541875 A JP2015541875 A JP 2015541875A JP 2015541875 A JP2015541875 A JP 2015541875A JP 2015536986 A5 JP2015536986 A5 JP 2015536986A5
Authority
JP
Japan
Prior art keywords
pharmaceutically acceptable
independently
acceptable salt
phenyl
formula
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
JP2015541875A
Other languages
English (en)
Japanese (ja)
Other versions
JP2015536986A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2013/068691 external-priority patent/WO2014074580A1/en
Publication of JP2015536986A publication Critical patent/JP2015536986A/ja
Publication of JP2015536986A5 publication Critical patent/JP2015536986A5/ja
Pending legal-status Critical Current

Links

JP2015541875A 2012-11-07 2013-11-06 併用療法 Pending JP2015536986A (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201261723474P 2012-11-07 2012-11-07
US61/723,474 2012-11-07
US201361790796P 2013-03-15 2013-03-15
US61/790,796 2013-03-15
PCT/US2013/068691 WO2014074580A1 (en) 2012-11-07 2013-11-06 Combination therapy

Publications (2)

Publication Number Publication Date
JP2015536986A JP2015536986A (ja) 2015-12-24
JP2015536986A5 true JP2015536986A5 (enExample) 2016-12-22

Family

ID=49681127

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2015541875A Pending JP2015536986A (ja) 2012-11-07 2013-11-06 併用療法

Country Status (12)

Country Link
US (3) US20150290204A1 (enExample)
EP (1) EP2916841A1 (enExample)
JP (1) JP2015536986A (enExample)
KR (1) KR20150081344A (enExample)
CN (1) CN105120868A (enExample)
AU (2) AU2013341271A1 (enExample)
BR (1) BR112015010396A2 (enExample)
CA (1) CA2890699A1 (enExample)
IN (1) IN2015DN04175A (enExample)
MX (1) MX2015005798A (enExample)
RU (1) RU2015121424A (enExample)
WO (1) WO2014074580A1 (enExample)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9561228B2 (en) 2013-02-08 2017-02-07 Celgene Avilomics Research, Inc. ERK inhibitors and uses thereof
RU2016129953A (ru) * 2013-12-23 2018-01-30 Новартис Аг Фармацевтические комбинации
US10005760B2 (en) 2014-08-13 2018-06-26 Celgene Car Llc Forms and compositions of an ERK inhibitor
WO2016098042A1 (en) * 2014-12-19 2016-06-23 Novartis Ag Use of ceritinib (ldk-378) in the treatment of fes or fer mediated disorders, in particular proliferative disorders
WO2016130920A2 (en) * 2015-02-13 2016-08-18 Dana-Farber Cancer Institute, Inc. Lrrk2 inhibitors and methods of making and using the same
US11058977B2 (en) 2018-07-23 2021-07-13 Caterpillar Inc. 3D printed staged filtration media packs
US10981335B2 (en) 2019-02-06 2021-04-20 Caterpillar Inc. Filtration media packs produced using additive manufacturing
CN114302878A (zh) 2019-07-03 2022-04-08 大日本住友制药肿瘤公司 酪氨酸激酶非受体1(tnk1)抑制剂及其用途
GB201915618D0 (en) 2019-10-28 2019-12-11 Univ Oslo ALK inhibitors for treatment of ALK-negative cancer and antibody-mediated diseases
WO2021257857A1 (en) 2020-06-19 2021-12-23 Incyte Corporation Naphthyridinone compounds as jak2 v617f inhibitors
US11753413B2 (en) 2020-06-19 2023-09-12 Incyte Corporation Substituted pyrrolo[2,1-f][1,2,4]triazine compounds as JAK2 V617F inhibitors
US11767323B2 (en) 2020-07-02 2023-09-26 Incyte Corporation Tricyclic pyridone compounds as JAK2 V617F inhibitors
KR20230057341A (ko) 2020-07-02 2023-04-28 인사이트 코포레이션 Jak2 v617f 억제제로서 삼환계 우레아 화합물
WO2022046989A1 (en) 2020-08-27 2022-03-03 Incyte Corporation Tricyclic urea compounds as jak2 v617f inhibitors
WO2022140231A1 (en) 2020-12-21 2022-06-30 Incyte Corporation Deazaguaine compounds as jak2 v617f inhibitors
AR125273A1 (es) 2021-02-25 2023-07-05 Incyte Corp Lactamas espirocíclicas como inhibidores de jak2 v617f
PE20251706A1 (es) 2022-03-17 2025-07-02 Incyte Corp Compuestos de urea triciclica como inhibidores de v617f de jak2
CN116284001B (zh) * 2023-01-30 2025-06-06 中国药科大学 Dclk1抑制剂、制备方法、药物组合物和应用

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4261989A (en) 1979-02-19 1981-04-14 Kaken Chemical Co. Ltd. Geldanamycin derivatives and antitumor drug
CA2515726C (en) 2003-02-11 2012-07-10 Vernalis (Cambridge) Limited Isoxazole compounds
JO2783B1 (en) 2005-09-30 2014-03-15 نوفارتيس ايه جي Compounds 2-Amino-7, 8-dihydro-6H-Bayredo (3,4-D) Pyrimidine-5-Ones
ME00811B (me) * 2006-12-08 2012-03-20 Novartis Ag JEDINJENJA l KOMPOZICIJE KAO INHIBITORI PROTEIN KINAZE
JP2012528177A (ja) * 2009-05-27 2012-11-12 アボット・ラボラトリーズ キナーゼ活性のピリミジン阻害剤
WO2011060328A1 (en) * 2009-11-13 2011-05-19 Infinity Pharmaceuticals, Inc. Compositions, kits, and methods for identification, assessment, prevention, and therapy of cancer
US20130137709A1 (en) * 2010-05-05 2013-05-30 Nathanael S. Gray Compounds that modulate EGFR activity and methods for treating or preventing conditions therewith
BR112013019643B1 (pt) * 2011-02-02 2022-04-19 Novartis Ag Uso de inibidores de álcali
WO2013006864A2 (en) * 2011-07-07 2013-01-10 Synta Pharmaceuticals Corp. Treating cancer with hsp90 inhibitory compounds

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