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MX2014014831A - Selectividad de mutante y combinaciones de un compuesto inhibidor de fosfoinositida 3 cinasa y agentes quimioterapeuticos para el tratamiento de cancer. - Google Patents

Selectividad de mutante y combinaciones de un compuesto inhibidor de fosfoinositida 3 cinasa y agentes quimioterapeuticos para el tratamiento de cancer.

Info

Publication number
MX2014014831A
MX2014014831A MX2014014831A MX2014014831A MX2014014831A MX 2014014831 A MX2014014831 A MX 2014014831A MX 2014014831 A MX2014014831 A MX 2014014831A MX 2014014831 A MX2014014831 A MX 2014014831A MX 2014014831 A MX2014014831 A MX 2014014831A
Authority
MX
Mexico
Prior art keywords
chemotherapeutic agents
phosphoinositide
cancer
combinations
treatment
Prior art date
Application number
MX2014014831A
Other languages
English (en)
Inventor
Jeffrey Wallin
Marcia Belvin
Lori Friedman
Deepak Sampath
Original Assignee
Hoffmann La Roche
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of MX2014014831A publication Critical patent/MX2014014831A/es

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    • AHUMAN NECESSITIES
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/553Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
    • AHUMAN NECESSITIES
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    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/13Amines
    • A61K31/135Amines having aromatic rings, e.g. ketamine, nortriptyline
    • A61K31/138Aryloxyalkylamines, e.g. propranolol, tamoxifen, phenoxybenzamine
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    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/337Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
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    • A61K31/357Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having two or more oxygen atoms in the same ring, e.g. crown ethers, guanadrel
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    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41961,2,4-Triazoles
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    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
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Abstract

Se proporcionan métodos y composiciones para tratar trastornos hiperproliferativos en pacientes con un inhibidor de PI3K, GDC-0032 como un agente único o en combinación con agentes quimioterapéuticos. (ver fórmula).
MX2014014831A 2012-06-08 2013-06-07 Selectividad de mutante y combinaciones de un compuesto inhibidor de fosfoinositida 3 cinasa y agentes quimioterapeuticos para el tratamiento de cancer. MX2014014831A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201261657484P 2012-06-08 2012-06-08
US201361808727P 2013-04-05 2013-04-05
PCT/EP2013/061765 WO2013182668A1 (en) 2012-06-08 2013-06-07 Mutant selectivity and combinations of a phosphoinositide 3 kinase inhibitor compound and chemotherapeutic agents for the treatment of cancer

Publications (1)

Publication Number Publication Date
MX2014014831A true MX2014014831A (es) 2015-02-12

Family

ID=48652013

Family Applications (2)

Application Number Title Priority Date Filing Date
MX2014014831A MX2014014831A (es) 2012-06-08 2013-06-07 Selectividad de mutante y combinaciones de un compuesto inhibidor de fosfoinositida 3 cinasa y agentes quimioterapeuticos para el tratamiento de cancer.
MX2018004832A MX2018004832A (es) 2012-06-08 2014-12-04 Selectividad de mutante y combinaciones de un compuesto inhibidor de fosfoinositida 3 cinasa y agentes quimioterapeuticos para el tratamiento de cancer.

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MX2018004832A MX2018004832A (es) 2012-06-08 2014-12-04 Selectividad de mutante y combinaciones de un compuesto inhibidor de fosfoinositida 3 cinasa y agentes quimioterapeuticos para el tratamiento de cancer.

Country Status (15)

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US (3) US9107926B2 (es)
EP (2) EP3545968A1 (es)
JP (3) JP5933830B2 (es)
KR (3) KR101915942B1 (es)
CN (2) CN109939236A (es)
AU (2) AU2013273489B9 (es)
BR (1) BR112014028376A2 (es)
CA (1) CA2871359A1 (es)
HK (1) HK1202265A1 (es)
IL (1) IL235963A0 (es)
MX (2) MX2014014831A (es)
NZ (1) NZ702244A (es)
RU (1) RU2665949C2 (es)
SG (2) SG11201407537YA (es)
WO (1) WO2013182668A1 (es)

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