JP2011527704A5 - - Google Patents

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Publication number
JP2011527704A5
JP2011527704A5 JP2011517646A JP2011517646A JP2011527704A5 JP 2011527704 A5 JP2011527704 A5 JP 2011527704A5 JP 2011517646 A JP2011517646 A JP 2011517646A JP 2011517646 A JP2011517646 A JP 2011517646A JP 2011527704 A5 JP2011527704 A5 JP 2011527704A5
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Japan
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weight
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JP2011517646A
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English (en)
Japanese (ja)
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JP2011527704A (ja
JP5596680B2 (ja
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Priority claimed from US12/171,515 external-priority patent/US8026271B2/en
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Publication of JP2011527704A5 publication Critical patent/JP2011527704A5/ja
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Publication of JP5596680B2 publication Critical patent/JP5596680B2/ja
Expired - Fee Related legal-status Critical Current
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JP2011517646A 2008-07-11 2009-07-10 経口抗がん製剤 Expired - Fee Related JP5596680B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US12/171,515 2008-07-11
US12/171,515 US8026271B2 (en) 2008-07-11 2008-07-11 Formulations of indol-3-yl-2-oxoacetamide compounds
PCT/US2009/050210 WO2010006234A2 (en) 2008-07-11 2009-07-10 Anticancer oral formulation

Publications (3)

Publication Number Publication Date
JP2011527704A JP2011527704A (ja) 2011-11-04
JP2011527704A5 true JP2011527704A5 (https=) 2012-08-16
JP5596680B2 JP5596680B2 (ja) 2014-09-24

Family

ID=41505721

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011517646A Expired - Fee Related JP5596680B2 (ja) 2008-07-11 2009-07-10 経口抗がん製剤

Country Status (8)

Country Link
US (1) US8026271B2 (https=)
EP (1) EP2310363B1 (https=)
JP (1) JP5596680B2 (https=)
KR (1) KR101627382B1 (https=)
CN (1) CN102159541B (https=)
ES (1) ES2426599T3 (https=)
TW (1) TWI384984B (https=)
WO (1) WO2010006234A2 (https=)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8026271B2 (en) * 2008-07-11 2011-09-27 National Health Research Institutes Formulations of indol-3-yl-2-oxoacetamide compounds
CN104945420A (zh) 2009-06-29 2015-09-30 因塞特公司 作为pi3k抑制剂的嘧啶酮类
WO2011075643A1 (en) 2009-12-18 2011-06-23 Incyte Corporation Substituted heteroaryl fused derivatives as pi3k inhibitors
US8680108B2 (en) * 2009-12-18 2014-03-25 Incyte Corporation Substituted fused aryl and heteroaryl derivatives as PI3K inhibitors
AR081823A1 (es) 2010-04-14 2012-10-24 Incyte Corp DERIVADOS FUSIONADOS COMO INHIBIDORES DE PI3Kd
US9062055B2 (en) 2010-06-21 2015-06-23 Incyte Corporation Fused pyrrole derivatives as PI3K inhibitors
EP2655374B1 (en) 2010-12-20 2019-10-23 Incyte Holdings Corporation N-(1-(substituted-phenyl)ethyl)-9h-purin-6-amines as pi3k inhibitors
US9108984B2 (en) 2011-03-14 2015-08-18 Incyte Corporation Substituted diamino-pyrimidine and diamino-pyridine derivatives as PI3K inhibitors
WO2012135009A1 (en) 2011-03-25 2012-10-04 Incyte Corporation Pyrimidine-4,6-diamine derivatives as pi3k inhibitors
DK2707101T3 (da) * 2011-05-12 2019-05-13 Proteostasis Therapeutics Inc Proteostaseregulatorer
KR102507287B1 (ko) 2011-09-02 2023-03-07 인사이트 홀딩스 코포레이션 Pi3k 억제제로서 헤테로시클릴아민
AR090548A1 (es) 2012-04-02 2014-11-19 Incyte Corp Azaheterociclobencilaminas biciclicas como inhibidores de pi3k
WO2015073528A1 (en) 2013-11-12 2015-05-21 Proteostasis Therapeutics, Inc. Proteasome activity enhancing compounds
WO2015191677A1 (en) 2014-06-11 2015-12-17 Incyte Corporation Bicyclic heteroarylaminoalkyl phenyl derivatives as pi3k inhibitors
SI3831833T1 (sl) 2015-02-27 2023-03-31 Incyte Holdings Corporation Postopki za pripravo inhibitorja PI3K
US9732097B2 (en) 2015-05-11 2017-08-15 Incyte Corporation Process for the synthesis of a phosphoinositide 3-kinase inhibitor
US9988401B2 (en) 2015-05-11 2018-06-05 Incyte Corporation Crystalline forms of a PI3K inhibitor
CA3101323A1 (en) 2018-06-01 2019-12-05 Incyte Corporation Dosing regimen for the treatment of pi3k related disorders

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6979456B1 (en) * 1998-04-01 2005-12-27 Jagotec Ag Anticancer compositions
US6372251B2 (en) * 1999-06-11 2002-04-16 Abbott Laboratories Formulations comprising lipid-regulating agents
US20040092428A1 (en) * 2001-11-27 2004-05-13 Hongming Chen Oral pharmaceuticals formulation comprising paclitaxel, derivatives and methods of administration thereof
US6903104B2 (en) * 2001-12-06 2005-06-07 National Health Research Institutes Indol-3-YL-2-oxoacetamide compounds and methods of use thereof
MX2007006183A (es) * 2004-11-24 2007-09-11 Merck & Co Inc Formulaciones farmaceuticas liquidas y semisolidas para administracion oral de una amida sustituida.
US20060134204A1 (en) * 2004-12-21 2006-06-22 Wong Patrick S Complexes made using low solubility drugs
TWI376239B (en) * 2006-02-01 2012-11-11 Andrew Xian Chen Vitamin e succinate stabilized pharmaceutical compositions, methods for the preparation and the use thereof
AU2007325628A1 (en) * 2006-11-28 2008-06-05 Marinus Pharmaceuticals Nanoparticulate formulations and methods for the making and use thereof
AU2008206294A1 (en) * 2007-01-16 2008-07-24 Bipar Sciences, Inc. Formulations for cancer treatment
US8026271B2 (en) * 2008-07-11 2011-09-27 National Health Research Institutes Formulations of indol-3-yl-2-oxoacetamide compounds

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