JP2014524469A5 - - Google Patents

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Publication number
JP2014524469A5
JP2014524469A5 JP2014527196A JP2014527196A JP2014524469A5 JP 2014524469 A5 JP2014524469 A5 JP 2014524469A5 JP 2014527196 A JP2014527196 A JP 2014527196A JP 2014527196 A JP2014527196 A JP 2014527196A JP 2014524469 A5 JP2014524469 A5 JP 2014524469A5
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JP
Japan
Prior art keywords
pharmaceutical composition
cancer
administered
leukemia
antimetabolite
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.)
Withdrawn
Application number
JP2014527196A
Other languages
English (en)
Japanese (ja)
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JP2014524469A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2012/051316 external-priority patent/WO2013028505A1/en
Publication of JP2014524469A publication Critical patent/JP2014524469A/ja
Publication of JP2014524469A5 publication Critical patent/JP2014524469A5/ja
Withdrawn legal-status Critical Current

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JP2014527196A 2011-08-19 2012-08-17 代謝拮抗剤とhsp90阻害剤の組み合わせ癌療法 Withdrawn JP2014524469A (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201161525375P 2011-08-19 2011-08-19
US61/525,375 2011-08-19
US201161555787P 2011-11-04 2011-11-04
US61/555,787 2011-11-04
PCT/US2012/051316 WO2013028505A1 (en) 2011-08-19 2012-08-17 Combination cancer therapy of hsp90 inhibitor with antimetabolite

Publications (2)

Publication Number Publication Date
JP2014524469A JP2014524469A (ja) 2014-09-22
JP2014524469A5 true JP2014524469A5 (OSRAM) 2015-09-10

Family

ID=46759073

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014527196A Withdrawn JP2014524469A (ja) 2011-08-19 2012-08-17 代謝拮抗剤とhsp90阻害剤の組み合わせ癌療法

Country Status (7)

Country Link
US (1) US20140296176A1 (OSRAM)
EP (1) EP2744494A1 (OSRAM)
JP (1) JP2014524469A (OSRAM)
AU (1) AU2012299177A1 (OSRAM)
CA (1) CA2844809A1 (OSRAM)
EA (1) EA201490472A1 (OSRAM)
WO (1) WO2013028505A1 (OSRAM)

Families Citing this family (17)

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Publication number Priority date Publication date Assignee Title
PL2035396T3 (pl) 2006-05-25 2014-10-31 Synta Pharmaceuticals Corp Związki triazolowe modulujące aktywność hsp90
EP2323737A2 (en) 2008-08-08 2011-05-25 Synta Pharmaceuticals Corp. Triazole compounds that modulate hsp90 activity
EP2560640A1 (en) 2010-04-19 2013-02-27 Synta Pharmaceuticals Corp. Cancer therapy using a combination of a hsp90 inhibitory compounds and a egfr inhibitor
US9439899B2 (en) 2011-11-02 2016-09-13 Synta Pharmaceuticals Corp. Cancer therapy using a combination of HSP90 inhibitors with topoisomerase I inhibitors
US20140286902A1 (en) 2011-11-02 2014-09-25 Synta Pharmaceuticals Corp. Combination therapy of hsp90 inhibitors with platinum-containing agents
CA2854188A1 (en) 2011-11-14 2013-05-23 Synta Pharmaceuticals Corp. Combination therapy of hsp90 inhibitors with braf inhibitors
US20140079636A1 (en) * 2012-04-16 2014-03-20 Dinesh U. Chimmanamada Targeted therapeutics
WO2014018862A1 (en) * 2012-07-27 2014-01-30 Corning Incorporated Pharmaceutical compositions comprising a heat shock protein inhibitor and a|purine de novo synthesis inhibitor for treating rheumatoid arthritis or cancer
DK3179992T3 (da) 2014-08-11 2022-07-11 Acerta Pharma Bv Terapeutisk kombination af en btk-inhibitor, en pd-1-inhibitor og/eller en pd-l1-inhibitor
WO2016024232A1 (en) 2014-08-11 2016-02-18 Acerta Pharma B.V. Therapeutic combinations of a btk inhibitor, a pi3k inhibitor, a jak-2 inhibitor and/or a cdk 4/6 inhibitor
DK3179991T3 (da) 2014-08-11 2021-12-06 Acerta Pharma Bv Terapeutiske kombinationer af en btk-inhibitor og en bcl-2-inhibitor
JP6869899B2 (ja) 2015-02-13 2021-05-12 サン・ファーマシューティカル・インダストリーズ・リミテッド 静脈内注入剤形
WO2018236796A1 (en) * 2017-06-20 2018-12-27 Tarveda Therapeutics, Inc. Combination therapies comprising targeted therapeutics
AU2018289349A1 (en) 2017-06-20 2020-01-02 Madrigal Pharmaceuticals, Inc. Combination therapies comprising targeted therapeutics
KR20200016875A (ko) 2017-06-20 2020-02-17 마드리갈 파마슈티칼스 인코포레이티드 표적화 치료제
CN115957328A (zh) * 2022-07-13 2023-04-14 杭州百可生物科技有限公司 一种用于治疗白血病的药物组合物以及白血病的治疗方法
CN121041304A (zh) * 2025-11-06 2025-12-02 哈尔滨医科大学 Cct018159与奈拉滨联合用药在制备急性白血病药物中的应用

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US3536809A (en) 1969-02-17 1970-10-27 Alza Corp Medication method
US3598123A (en) 1969-04-01 1971-08-10 Alza Corp Bandage for administering drugs
US3845770A (en) 1972-06-05 1974-11-05 Alza Corp Osmatic dispensing device for releasing beneficial agent
US3916899A (en) 1973-04-25 1975-11-04 Alza Corp Osmotic dispensing device with maximum and minimum sizes for the passageway
US4008719A (en) 1976-02-02 1977-02-22 Alza Corporation Osmotic system having laminar arrangement for programming delivery of active agent
IE58110B1 (en) 1984-10-30 1993-07-14 Elan Corp Plc Controlled release powder and process for its preparation
US5073543A (en) 1988-07-21 1991-12-17 G. D. Searle & Co. Controlled release formulations of trophic factors in ganglioside-lipsome vehicle
IT1229203B (it) 1989-03-22 1991-07-25 Bioresearch Spa Impiego di acido 5 metiltetraidrofolico, di acido 5 formiltetraidrofolico e dei loro sali farmaceuticamente accettabili per la preparazione di composizioni farmaceutiche in forma a rilascio controllato attive nella terapia dei disturbi mentali organici e composizioni farmaceutiche relative.
US5120548A (en) 1989-11-07 1992-06-09 Merck & Co., Inc. Swelling modulated polymeric drug delivery device
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US5591767A (en) 1993-01-25 1997-01-07 Pharmetrix Corporation Liquid reservoir transdermal patch for the administration of ketorolac
IT1270594B (it) 1994-07-07 1997-05-07 Recordati Chem Pharm Composizione farmaceutica a rilascio controllato di moguisteina in sospensione liquida
US20050020534A1 (en) * 2003-05-30 2005-01-27 Kosan Biosciences, Inc. Method for treating diseases using HSP90-inhibiting agents in combination with antimetabolites
PT1817295E (pt) * 2004-11-18 2013-02-18 Synta Pharmaceuticals Corp Compostos de triazol que modulam a actividade da hsp90
WO2012068487A1 (en) * 2010-11-18 2012-05-24 Synta Pharmaceuticals Corp. Preselection of subjects for therapeutic treatment with oxygen sensitive agents based on hypoxic status

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