JP2014507412A5 - - Google Patents

Download PDF

Info

Publication number
JP2014507412A5
JP2014507412A5 JP2013549503A JP2013549503A JP2014507412A5 JP 2014507412 A5 JP2014507412 A5 JP 2014507412A5 JP 2013549503 A JP2013549503 A JP 2013549503A JP 2013549503 A JP2013549503 A JP 2013549503A JP 2014507412 A5 JP2014507412 A5 JP 2014507412A5
Authority
JP
Japan
Prior art keywords
cancer
combination
chloro
methyl
days
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
JP2013549503A
Other languages
English (en)
Japanese (ja)
Other versions
JP2014507412A (ja
JP6100700B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2012/020863 external-priority patent/WO2012097021A1/en
Publication of JP2014507412A publication Critical patent/JP2014507412A/ja
Publication of JP2014507412A5 publication Critical patent/JP2014507412A5/ja
Application granted granted Critical
Publication of JP6100700B2 publication Critical patent/JP6100700B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2013549503A 2011-01-11 2012-01-11 組合せ Active JP6100700B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161431508P 2011-01-11 2011-01-11
US61/431,508 2011-01-11
PCT/US2012/020863 WO2012097021A1 (en) 2011-01-11 2012-01-11 Combination

Publications (3)

Publication Number Publication Date
JP2014507412A JP2014507412A (ja) 2014-03-27
JP2014507412A5 true JP2014507412A5 (enExample) 2015-03-05
JP6100700B2 JP6100700B2 (ja) 2017-03-22

Family

ID=46507420

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2013549503A Active JP6100700B2 (ja) 2011-01-11 2012-01-11 組合せ

Country Status (15)

Country Link
US (6) US20130288984A1 (enExample)
EP (1) EP2663189B1 (enExample)
JP (1) JP6100700B2 (enExample)
KR (1) KR20140053836A (enExample)
CN (1) CN103298345B (enExample)
AU (1) AU2012205601B2 (enExample)
BR (1) BR112013017722A2 (enExample)
CA (1) CA2824201A1 (enExample)
EA (1) EA029000B1 (enExample)
ES (1) ES2689760T3 (enExample)
IL (1) IL227097B (enExample)
MX (1) MX356704B (enExample)
SG (2) SG10201600077RA (enExample)
WO (1) WO2012097021A1 (enExample)
ZA (1) ZA201304139B (enExample)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109674801A (zh) * 2013-10-01 2019-04-26 诺华股份有限公司 组合
KR20210063475A (ko) * 2013-11-07 2021-06-01 데시페라 파마슈티칼스, 엘엘씨. 암치료에 유용한 tie2 키나아제의 억제 방법
AU2019215081B2 (en) 2018-01-31 2024-07-25 Deciphera Pharmaceuticals, Llc. Combination therapy for the treatment of gastrointestinal stromal tumors
CN111886006B (zh) 2018-01-31 2024-07-09 德西费拉制药有限责任公司 治疗肥大细胞增多症的组合疗法
WO2020185812A1 (en) 2019-03-11 2020-09-17 Teva Pharmaceuticals International Gmbh Solid state forms of ripretinib
WO2021030405A1 (en) 2019-08-12 2021-02-18 Deciphera Pharmaceuticals, Llc Ripretinib for treating gastrointestinal stromal tumors
MX2022001863A (es) 2019-08-12 2022-05-30 Deciphera Pharmaceuticals Llc Metodos para tratar los tumores del estroma gastrointestinal.
FI4084779T3 (fi) 2019-12-30 2024-12-16 Deciphera Pharmaceuticals Llc 1-(4-bromi-5-(1-etyyli-7-(metyyliamino)-2-okso-1,2-dihydro-1,6-naftyridin-3-yyli)-2-fluorifenyyli)-3-fenyyliurean koostumuksia
CN119970649A (zh) 2019-12-30 2025-05-13 德西费拉制药有限责任公司 非晶型激酶抑制剂制剂及其使用方法
US11779572B1 (en) 2022-09-02 2023-10-10 Deciphera Pharmaceuticals, Llc Methods of treating gastrointestinal stromal tumors

Family Cites Families (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5604213A (en) 1992-03-31 1997-02-18 British Technology Group Limited 17-substituted steroids useful in cancer treatment
US5681835A (en) 1994-04-25 1997-10-28 Glaxo Wellcome Inc. Non-steroidal ligands for the estrogen receptor
GB9716557D0 (en) 1997-08-06 1997-10-08 Glaxo Group Ltd Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity
US6328590B1 (en) 2000-07-20 2001-12-11 Emc Corporation Methods and apparatus for controlling attachment of an electronic module with a circuit board connector
EP1740579B1 (en) * 2004-03-24 2015-08-19 AbbVie Inc. Tricyclic pyrazole kinase inhibitors
CA2584246C (en) 2004-10-13 2011-08-09 Pharmacia & Upjohn Company Llc Crystalline forms of 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6h)-yl]-n-(2-hydroxyethyl)-4-methylbenzamide
US7709517B2 (en) 2005-05-13 2010-05-04 The Regents Of The University Of California Diarylhydantoin compounds
JP2009506069A (ja) * 2005-08-26 2009-02-12 ブレインセルス,インコーポレイティド ムスカリン性受容体調節による神経発生
EP1840114A1 (en) 2006-03-30 2007-10-03 LTB4 Sweden AB Crystalline Leukotriene B4
CN101415411A (zh) 2006-04-05 2009-04-22 诺瓦提斯公司 用于治疗癌症的治疗剂组合
WO2007122686A1 (ja) 2006-04-14 2007-11-01 Eisai R & D Management Co., Ltd. ベンズイミダゾール化合物
CN104306977A (zh) 2006-08-25 2015-01-28 库伽尔生物科技公司 治疗癌症的方法和组合物
US20080051380A1 (en) 2006-08-25 2008-02-28 Auerbach Alan H Methods and compositions for treating cancer
JP4299327B2 (ja) 2006-08-31 2009-07-22 トヨタ自動車株式会社 可変バルブタイミング装置
US8828451B2 (en) * 2006-10-04 2014-09-09 University Of South Florida Akt sensitization of cancer cells
EP2079714B1 (de) 2006-10-13 2012-09-26 Basf Se Hydrate des 2-chlor-5-ý3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluormethyl)-1-(2h)-pyrimidinyl¨-4-fluor-n-ýýmethyl-(1-methylethyl)amino¨sulfonyl¨benzamids
AR064010A1 (es) 2006-12-06 2009-03-04 Merck & Co Inc Inhibidores de la actividad de la akt
UY30892A1 (es) 2007-02-07 2008-09-02 Smithkline Beckman Corp Inhibidores de la actividad akt
BRPI0818533B8 (pt) 2007-10-11 2021-05-25 Astrazeneca Ab composto, composição farmacêutica, uso de um composto, e, processo para a preparação de um composto
WO2009067453A1 (en) * 2007-11-19 2009-05-28 Syndax Pharmaceuticals, Inc. Combinations of hdac inhibitors and proteasome inhibitors
DE102008044901A1 (de) 2008-08-29 2010-03-04 Siemens Aktiengesellschaft Verfahren und Vorrichtung zur Auswahl eines Bestrahlungsplans sowie Bestrahlungsanlage
WO2010088331A1 (en) 2009-01-30 2010-08-05 Glaxosmithkline Llc Crystalline n-{(1-s)-2-amino-1-[(3-fluorophenyl)methyl]ethyl}-5-chloro-4-(4-chloro-1-methyl-1h-pyrazol-5-yl)-2-thiophenecarboxamide hydrochloride
AU2010264698C1 (en) 2009-06-26 2013-05-16 Novartis Ag 1, 3-disubstituted imidazolidin-2-one derivatives as inhibitors of CYP 17
ES2530436T3 (es) 2009-10-08 2015-03-02 Glaxosmithkline Llc Combinación
SG194045A1 (en) 2011-04-01 2013-11-29 Genentech Inc Combinations of akt inhibitor compounds and abiraterone, and methods of use
CN103813788A (zh) 2011-05-03 2014-05-21 罗切斯特大学 治疗前列腺癌的方法
JP2014520863A (ja) 2011-07-13 2014-08-25 ファーマサイクリックス,インク. Bruton型チロシンキナーゼの阻害剤
SI2766381T1 (sl) 2011-10-10 2016-11-30 Zach System, Z.I. Postopek za pripravo 17-substituiranih steroidov
PL2785349T5 (pl) 2011-11-30 2023-01-30 Astrazeneca Ab Kombinacja do leczenia nowotworu
KR20150015021A (ko) 2012-06-04 2015-02-09 파마시클릭스, 인코포레이티드 브루톤 타이로신 키나아제 저해제의 결정 형태
MX2016004265A (es) 2013-10-01 2016-07-08 Novartis Ag Combinacion.

Similar Documents

Publication Publication Date Title
JP2014507412A5 (enExample)
RU2015154275A (ru) Комбинации антитела против pd-l1 и ингибитора mek и/или ингибитора braf
HRP20201681T1 (hr) Inhibitor aurora a kinaze
JP2011126896A5 (enExample)
JP2014511840A5 (enExample)
JP2016503399A5 (enExample)
RU2018138828A (ru) Уменьшение массы опухоли путем введения ccr1 антагонистов в комбинации с pd-1 ингибиторами или pd-l1 ингибиторами
JP2012255026A5 (enExample)
JP2013509429A5 (enExample)
JP2018168191A5 (enExample)
JP2015511609A5 (enExample)
RU2015119218A (ru) Комбинация
JP2013518107A5 (enExample)
JP2017511360A5 (enExample)
JP2014510729A5 (enExample)
FI3429571T3 (fi) Lsd1-inhibiittorien yhdistelmiä käytettäväksi kasvaintautien hoitamisessa
HRP20191617T1 (hr) Kombinacija koja sadrži inhibitor mek i inhibitor b-raf
JP2012193216A5 (enExample)
RU2017102319A (ru) Прерывистое введение ингибитора mdm2
JP2012516344A5 (enExample)
RU2015121424A (ru) Комбинированная терапия
JP6014142B2 (ja) N−ヒドロキシ−4−{2−[3−(n,n−ジメチルアミノメチル)ベンゾフラン−2−イルカルボニルアミノ]エトキシ}ベンズアミドの投与に関するスキーム
RU2016116789A (ru) Комбинация энзалутамида и афурезертиба для лечения рака
ME02119B (me) Spojevi korisni za inhibiranje chk1
JP2015537009A5 (enExample)