MA33974B1 - Combinaisons d'un inhibiteur de pi3k et d'un inhibiteur de mek - Google Patents

Combinaisons d'un inhibiteur de pi3k et d'un inhibiteur de mek

Info

Publication number
MA33974B1
MA33974B1 MA34821A MA34821A MA33974B1 MA 33974 B1 MA33974 B1 MA 33974B1 MA 34821 A MA34821 A MA 34821A MA 34821 A MA34821 A MA 34821A MA 33974 B1 MA33974 B1 MA 33974B1
Authority
MA
Morocco
Prior art keywords
inhibitor
combinations
pi3k
mek
kinase inhibitor
Prior art date
Application number
MA34821A
Other languages
Arabic (ar)
English (en)
Inventor
Marcia Belvin
Iris T Chan
Lori Friedman
Klause 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=MA33974(B1) "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 MA33974B1 publication Critical patent/MA33974B1/fr

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

L'invention concerne des procédés de traitement d'un patient présentant des tumeurs solides localement avancées ou métastasiques par une combinaison d'un inhibiteur de phosphatidylinositol 3-kinase (pi 3-kinase ou pi3k) et un inhibiteur de kinase de kinase de protéine activée par le mitogène.
MA34821A 2009-10-12 2010-10-11 Combinaisons d'un inhibiteur de pi3k et d'un inhibiteur de mek MA33974B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US25085209P 2009-10-12 2009-10-12
PCT/EP2010/065149 WO2011054620A1 (fr) 2009-10-12 2010-10-11 Combinaisons d'un inhibiteur de pi3k et d'un inhibiteur de mek

Publications (1)

Publication Number Publication Date
MA33974B1 true MA33974B1 (fr) 2013-02-01

Family

ID=43072663

Family Applications (1)

Application Number Title Priority Date Filing Date
MA34821A MA33974B1 (fr) 2009-10-12 2010-10-11 Combinaisons d'un inhibiteur de pi3k et d'un inhibiteur de mek

Country Status (24)

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

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BRPI0915901A2 (pt) 2008-07-11 2015-10-27 Novartis Ag combinação de (a) um inibidor de fosfoinositídeo 3-quinase e (b) um modulador da via ras/raf/mek
MX2011007326A (es) 2009-01-08 2011-10-19 Curis Inc Inhibidores de fosfoinositida 3-quinasa con una porcion de enlace de cinc.
WO2011080510A1 (fr) 2009-12-31 2011-07-07 Centro Nacional De Investigaciones Oncológicas (Cnio) Composés tricycliques pour une utilisation comme inhibiteurs de la kinase
WO2012098387A1 (fr) 2011-01-18 2012-07-26 Centro Nacional De Investigaciones Oncológicas (Cnio) Dérivés de triazolo[4,3-b]pyridazines au cycle 6,7 fusionné utilisés en tant qu'inhibiteurs de pim
PL2694075T3 (pl) 2011-04-01 2016-09-30 Inhibitor 3-kinazy fosfoinozytydowej z grupą wiążącą cynk
MY193562A (en) * 2011-08-01 2022-10-19 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
US20130096116A1 (en) 2011-10-13 2013-04-18 Genentech, Inc. Treatment of pharmacological-induced hypochlorhydria
KR20140097205A (ko) * 2011-10-28 2014-08-06 제넨테크, 인크. 흑색종을 치료하는 치료 조합물 및 방법
WO2013082511A1 (fr) 2011-12-02 2013-06-06 Genentech, Inc. Procédés pour surmonter la résistance tumorale aux antagonistes de vegf
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
US9566307B2 (en) 2012-04-19 2017-02-14 Kyushu University, National University Corporation Pharmaceutical composition
SG10201706196XA (en) 2012-06-08 2017-08-30 Hoffmann La Roche Mutant selectivity and combinations of a phosphoinositide 3 kinase inhibitor compound and chemotherapeutic agents for the treatment of cancer
EP2879708A4 (fr) 2012-08-02 2016-03-16 Genentech Inc Anticorps et immunoconjugués anti-etbr
RU2015106946A (ru) 2012-08-02 2016-09-27 Дженентек, Инк. Антитела к рецептору эндотелина типа в (etbr) и их иммуноконъюгаты
KR20210108502A (ko) * 2012-08-17 2021-09-02 에프. 호프만-라 로슈 아게 코비메티닙 및 베무라피닙을 투여함을 포함하는 흑색종의 조합 치료법
SG11201507477XA (en) * 2013-03-14 2015-10-29 Genentech Inc 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
EP3102232B1 (fr) 2014-02-07 2020-02-05 Verastem, Inc. Méthodes et composition de traitement de croissance cellulaire anormale
JP6673896B2 (ja) 2014-07-15 2020-03-25 ジェネンテック， インコーポレイテッド Ｐｄ−１軸結合アンタゴニスト及びｍｅｋ阻害剤を使用した癌を処置するための組成物
CN113620978A (zh) * 2014-09-11 2021-11-09 加利福尼亚大学董事会 mTORC1抑制剂
EA202190748A1 (ru) 2018-09-11 2021-07-22 Кьюрис Инк. Комбинированная терапия ингибитором фосфоинозитид-3-киназы с цинк-связывающей группировкой
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

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1470356A1 (de) * 1964-01-15 1970-04-30 Thomae Gmbh Dr K Neue Thieno[3,2-d]pyrimidine und Verfahren zu ihrer Herstellung
BE754606A (fr) * 1969-08-08 1971-02-08 Thomae Gmbh Dr K Nouvelles 2-aminoalcoylamino-thieno(3,2-d)pyrimidines et leurs procedesde fabrication
BE759493A (fr) * 1969-11-26 1971-05-25 Thomae Gmbh Dr K Nouvelles 2-(5-nitro-2-furyl)-thieno(3,2-d) pyrimidines et procedes pour les fabriquer
US3763156A (en) * 1970-01-28 1973-10-02 Boehringer Sohn Ingelheim 2-heterocyclic amino-4-morpholinothieno(3,2-d)pyrimidines
CH592668A5 (fr) * 1973-10-02 1977-10-31 Delalande Sa
GB1570494A (en) * 1975-11-28 1980-07-02 Ici Ltd Thienopyrimidine derivatives and their use as pesticides
US4510139A (en) * 1984-01-06 1985-04-09 Sterling Drug Inc. Substituted aminobenzamides and their use as agents which inhibit lipoxygenase activity
AU685933B2 (en) * 1994-04-01 1998-01-29 Shionogi & Co., Ltd. Oxime derivative and bactericide containing the same as active ingredient
US6974878B2 (en) * 2001-03-21 2005-12-13 Symyx Technologies, Inc. Catalyst ligands, catalytic metal complexes and processes using same
US6608053B2 (en) * 2000-04-27 2003-08-19 Yamanouchi Pharmaceutical Co., Ltd. Fused heteroaryl derivatives
US7498304B2 (en) * 2000-06-16 2009-03-03 Curis, Inc. Angiogenesis-modulating compositions and uses
DZ3401A1 (fr) * 2000-07-19 2002-01-24 Warner Lambert Co Esters oxygenes d'acides 4-iodophenylamino benzhydroxamiques
US7235537B2 (en) * 2002-03-13 2007-06-26 Array Biopharma, Inc. N3 alkylated benzimidazole derivatives as MEK inhibitors
WO2004078116A2 (fr) * 2003-03-03 2004-09-16 Array Biopharma, Inc. Inhibiteurs de la p 38 et leurs procedes d'utilisation
US20050049276A1 (en) * 2003-07-23 2005-03-03 Warner-Lambert Company, Llc Imidazopyridines and triazolopyridines
US7144907B2 (en) * 2003-09-03 2006-12-05 Array Biopharma Inc. Heterocyclic inhibitors of MEK and methods of use thereof
US7538120B2 (en) * 2003-09-03 2009-05-26 Array Biopharma Inc. Method of treating inflammatory diseases
WO2005028426A1 (fr) * 2003-09-19 2005-03-31 Chugai Seiyaku Kabushiki Kaisha Nouveau derive de 4-phenylamino-benzaldoxime et son utilisation en tant qu'inhibiteur de mek
US7517994B2 (en) * 2003-11-19 2009-04-14 Array Biopharma Inc. Heterocyclic inhibitors of MEK and methods of use thereof
GB0423653D0 (en) 2004-10-25 2004-11-24 Piramed Ltd Pharmaceutical compounds
CA3052368A1 (fr) 2005-10-07 2007-04-19 Exelixis, Inc. Azetidines comme inhibiteurs de mek
RU2439074C2 (ru) 2006-04-26 2012-01-10 Ф. Хоффманн-Ля Рош Аг ПРОИЗВОДНОЕ ТИЕНО[3,2-d]ПИРИМИДИНА В КАЧЕСТВЕ ИНГИБИТОРА ФОСФАТИДИЛИНОЗИТОЛ-3-КИНАЗЫ (РI3К)
ATE539752T1 (de) * 2006-08-16 2012-01-15 Exelixis Inc Verwendung von pi3k- und mek-modulatoren bei der krebsbehandlung
ES2544082T3 (es) * 2006-12-07 2015-08-27 F. Hoffmann-La Roche Ag Compuestos inhibidores de fosfoinosítido 3-quinasa y métodos de uso
EP2205242B1 (fr) * 2007-09-12 2015-04-15 Genentech, Inc. Combinaisons de composés inhibiteurs des phosphoinositide 3-kinases et agents chimiothérapeutiques, et leurs procédés d'utilisation
EP2694073B1 (fr) * 2011-04-01 2018-08-08 Genentech, Inc. Combinaisons de inhibiteurs d'akt et mek pour le traitement du cancer

Also Published As

Publication number Publication date
MX345155B (es) 2017-01-18
AR078588A1 (es) 2011-11-16
TW201118082A (en) 2011-06-01
AU2010314287A1 (en) 2012-05-03
HK1175125A1 (en) 2013-06-28
CA2776944A1 (fr) 2011-05-12
KR20120064132A (ko) 2012-06-18
JP2015038110A (ja) 2015-02-26
ES2609767T3 (es) 2017-04-24
MX2012004286A (es) 2012-05-22
RU2563193C2 (ru) 2015-09-20
EP2488178A1 (fr) 2012-08-22
EP2488178B1 (fr) 2016-11-16
CO6531463A2 (es) 2012-09-28
JP2013507415A (ja) 2013-03-04
CL2012000913A1 (es) 2012-09-14
AU2010314287A2 (en) 2012-07-12
NZ599939A (en) 2014-02-28
WO2011054620A1 (fr) 2011-05-12
BR112012008483A2 (pt) 2019-09-24
ECSP12011865A (es) 2012-06-29
TWI428336B (zh) 2014-03-01
ZA201202618B (en) 2014-10-29
US20110086837A1 (en) 2011-04-14
CR20120173A (es) 2012-07-04
CN102740851B (zh) 2013-12-18
JP5745678B2 (ja) 2015-07-08
IL219105A0 (en) 2012-06-28
RU2012118974A (ru) 2013-11-20
KR101489045B1 (ko) 2015-02-02
CN102740851A (zh) 2012-10-17
PE20121816A1 (es) 2013-01-02

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