ECSP12011865A - Combinaciones de un inhibidor de pi3k y un inhibidor de mek - Google Patents

Combinaciones de un inhibidor de pi3k y un inhibidor de mek

Info

Publication number
ECSP12011865A
ECSP12011865A ECSP12011865A ECSP12011865A EC SP12011865 A ECSP12011865 A EC SP12011865A EC SP12011865 A ECSP12011865 A EC SP12011865A EC SP12011865 A ECSP12011865 A EC SP12011865A
Authority
EC
Ecuador
Prior art keywords
inhibitor
combinations
pi3k
mek
kinase
Prior art date
Application number
Other languages
English (en)
Inventor
Marcia Belvin
Iris T Chan
Lori Friedman
Klaus P Hoeflich
John Prescott
Jeffrey Wallin
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=43072663&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ECSP12011865(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of ECSP12011865A publication Critical patent/ECSP12011865A/es

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Abstract

La invención se refiere a métodos para tratar un paciente que tiene tumores sólidos localmente avanzados o metastásicos con una combinación de un inhibidor de fosfatidilinositol-3-quinasa (PI 3-quinasa o PI3K) y un inhibidor de proteína-quinasa-quinasa activada con mitógeno (MEK) aquí descritos.
ECSP12011865 2009-10-12 2012-05-03 Combinaciones de un inhibidor de pi3k y un inhibidor de mek ECSP12011865A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US25085209P 2009-10-12 2009-10-12

Publications (1)

Publication Number Publication Date
ECSP12011865A true ECSP12011865A (es) 2012-06-29

Family

ID=43072663

Family Applications (1)

Application Number Title Priority Date Filing Date
ECSP12011865 ECSP12011865A (es) 2009-10-12 2012-05-03 Combinaciones de un inhibidor de pi3k y un inhibidor de mek

Country Status (24)

Country Link
US (1) US20110086837A1 (es)
EP (1) EP2488178B1 (es)
JP (2) JP2013507415A (es)
KR (1) KR101489045B1 (es)
CN (1) CN102740851B (es)
AR (1) AR078588A1 (es)
AU (1) AU2010314287A1 (es)
BR (1) BR112012008483A2 (es)
CA (1) CA2776944A1 (es)
CL (1) CL2012000913A1 (es)
CO (1) CO6531463A2 (es)
CR (1) CR20120173A (es)
EC (1) ECSP12011865A (es)
ES (1) ES2609767T3 (es)
HK (1) HK1175125A1 (es)
IL (1) IL219105A0 (es)
MA (1) MA33974B1 (es)
MX (1) MX345155B (es)
NZ (1) NZ599939A (es)
PE (1) PE20121816A1 (es)
RU (1) RU2563193C2 (es)
TW (1) TWI428336B (es)
WO (1) WO2011054620A1 (es)
ZA (1) ZA201202618B (es)

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WO2012098387A1 (en) 2011-01-18 2012-07-26 Centro Nacional De Investigaciones Oncológicas (Cnio) 6, 7-ring-fused triazolo [4, 3 - b] pyridazine derivatives as pim inhibitors
EP2694075B1 (en) 2011-04-01 2016-04-27 Curis, Inc. Phosphoinositide 3-kinase inhibitor with a zinc binding moiety
AU2012290121B2 (en) 2011-08-01 2015-11-26 Genentech, Inc. Methods of treating cancer using PD-1 axis binding antagonists and MEK inhibitors
BR112014004587A2 (pt) 2011-08-31 2017-03-14 Novartis Ag combinações sinérgicas de inibidores de pi3k- e de mek
RU2603462C2 (ru) 2011-10-13 2016-11-27 Дженентек, Инк. Лечение фармакологически индуцированной гипохлоргидрии
EP2776051A4 (en) * 2011-10-28 2015-06-17 Hoffmann La Roche THERAPEUTIC COMBINATIONS AND METHOD FOR THE TREATMENT OF MELANOMA
WO2013082511A1 (en) 2011-12-02 2013-06-06 Genentech, Inc. Methods for overcoming tumor resistance to vegf antagonists
CN104334192A (zh) * 2012-04-06 2015-02-04 赛诺菲 使用pi3k抑制剂和mek抑制剂治疗癌症的方法
JP6093757B2 (ja) * 2012-04-19 2017-03-08 国立大学法人九州大学 医薬組成物
MX2014014831A (es) 2012-06-08 2015-02-12 Hoffmann La Roche Selectividad de mutante y combinaciones de un compuesto inhibidor de fosfoinositida 3 cinasa y agentes quimioterapeuticos para el tratamiento de cancer.
AR091961A1 (es) 2012-08-02 2015-03-11 Genentech Inc Inmunoconjugados y anticuerpos anti-etbr (receptor de endotelina b)
WO2014022680A1 (en) 2012-08-02 2014-02-06 Genentech, Inc. Anti-etbr antibodies and immunoconjugates
BR112015003418A2 (pt) * 2012-08-17 2017-07-04 Hoffmann La Roche produto farmacêutico, conjunto, métodos para estender a duração da resposta ao tratamento, de retardar ou prevenir o desenvolvimento de resistência ao tratamento, para a seleção de uma terapia e para otimizar a eficácia terapêutica.
US20140271634A1 (en) * 2013-03-14 2014-09-18 The Regents Of The University Of California Combinations of a mek inhibitor compound with an her3/egfr inhibitor compound and methods of use
US9532987B2 (en) 2013-09-05 2017-01-03 Genentech, Inc. Use of a combination of a MEK inhibitor and an ERK inhibitor for treatment of hyperproliferative diseases
JP2017505321A (ja) * 2014-02-07 2017-02-16 ベラステム・インコーポレーテッドＶｅｒａｓｔｅｍ，Ｉｎｃ． 異常な細胞成長を処置するための方法および組成物
MX2017000546A (es) 2014-07-15 2017-03-08 Genentech Inc Composiciones para el tratamiento del cancer mediante el uso de antagonistas de union al eje de pd-1 e inhibidores de mek.
CN113620978A (zh) * 2014-09-11 2021-11-09 加利福尼亚大学董事会 mTORC1抑制剂
MX2021002742A (es) 2018-09-11 2021-08-11 Curis Inc Terapia combinada con un inhibidor de la fosfoinositida 3-quinasa con un resto de unión a zinc.
CN110420330B (zh) * 2019-07-19 2020-05-29 南京医科大学 一种pi3k与mth1靶向药组合物的制药用途
JP2022547358A (ja) 2019-09-13 2022-11-14 ジ インスティテュート オブ キャンサー リサーチ：ロイヤル キャンサー ホスピタル 治療組成物、組み合わせ、及び使用方法
US11873296B2 (en) 2022-06-07 2024-01-16 Verastem, Inc. Solid forms of a dual RAF/MEK inhibitor

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Also Published As

Publication number Publication date
RU2012118974A (ru) 2013-11-20
MX2012004286A (es) 2012-05-22
RU2563193C2 (ru) 2015-09-20
IL219105A0 (en) 2012-06-28
CL2012000913A1 (es) 2012-09-14
ES2609767T3 (es) 2017-04-24
JP2013507415A (ja) 2013-03-04
HK1175125A1 (en) 2013-06-28
NZ599939A (en) 2014-02-28
MX345155B (es) 2017-01-18
MA33974B1 (fr) 2013-02-01
KR101489045B1 (ko) 2015-02-02
TWI428336B (zh) 2014-03-01
EP2488178B1 (en) 2016-11-16
KR20120064132A (ko) 2012-06-18
US20110086837A1 (en) 2011-04-14
AU2010314287A2 (en) 2012-07-12
BR112012008483A2 (pt) 2019-09-24
CO6531463A2 (es) 2012-09-28
CA2776944A1 (en) 2011-05-12
TW201118082A (en) 2011-06-01
CN102740851B (zh) 2013-12-18
JP5745678B2 (ja) 2015-07-08
EP2488178A1 (en) 2012-08-22
WO2011054620A1 (en) 2011-05-12
CN102740851A (zh) 2012-10-17
AU2010314287A1 (en) 2012-05-03
JP2015038110A (ja) 2015-02-26
AR078588A1 (es) 2011-11-16
ZA201202618B (en) 2014-10-29
PE20121816A1 (es) 2013-01-02
CR20120173A (es) 2012-07-04

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