[go: up one dir, main page]

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=google_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

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/535Heterocyclic 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
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

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)
IL (1) IL219105A0 (fr)
MA (1) MA33974B1 (fr)
MX (1) MX345155B (fr)
NZ (1) NZ599939A (fr)
PE (1) PE20121816A1 (fr)
PH (1) PH12012500709A1 (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
CA2729914A1 (fr) 2008-07-11 2010-01-14 Novartis Ag Combinaison de (a) un inhibiteur de phosphoinositide 3-kinase et de (b) un modulateur de voie ras/raf/mek
PL2385832T3 (pl) 2009-01-08 2016-01-29 Curis Inc Inhibitory 3-kinazy fosfoinozytydowej z grupą wiążącą cynk
PH12012501361A1 (en) 2009-12-31 2012-10-22 Centro Nac De Investigaciones Oncologicas Cnio Tricyclic compounds for use as kinase inhibitors
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
KR101902325B1 (ko) 2011-04-01 2018-09-28 쿠리스 인코퍼레이션 아연 결합 모이어티를 갖는 포스포이노시티드 3-키나아제 억제제
BR112014002353B1 (pt) * 2011-08-01 2022-09-27 Genentech, Inc Usos de antagonistas de ligação do eixo pd-1 e inibidores de mek, composições farmacêuticas, e kit
KR20140072028A (ko) * 2011-08-31 2014-06-12 노파르티스 아게 Pi3k- 및 mek-억제제의 상승작용적 조합물
JP6062442B2 (ja) 2011-10-13 2017-01-18 ジェネンテック, インコーポレイテッド 薬剤誘発性低酸症の治療
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
CA2869152A1 (fr) * 2012-04-06 2013-10-10 Sanofi Methodes de traitement du cancer a l'aide d'un inhibiteur de pi3k et d'un inhibiteur de mek
JP6093757B2 (ja) * 2012-04-19 2017-03-08 国立大学法人九州大学 医薬組成物
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
RU2015106946A (ru) 2012-08-02 2016-09-27 Дженентек, Инк. Антитела к рецептору эндотелина типа в (etbr) и их иммуноконъюгаты
US9464141B2 (en) 2012-08-02 2016-10-11 Genentech, Inc. Anti-ETBR antibodies and immunoconjugates
RS59113B1 (sr) * 2012-08-17 2019-09-30 Hoffmann La Roche Kombinovane terapije za melanom koje uključuju davanje kobimetiniba i vemurafiniba
WO2014152358A2 (fr) * 2013-03-14 2014-09-25 Genentech, Inc. Combinaisons d'un composé inhibiteur de mek avec un composé inhibiteur de her3/egfr et procédés d'utilisation
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
US9962385B2 (en) 2014-02-07 2018-05-08 Verastem, Inc. Methods and compositions for treating abnormal cell growth
CN116617401A (zh) 2014-07-15 2023-08-22 豪夫迈·罗氏有限公司 使用pd-1轴结合拮抗剂和mek抑制剂治疗癌症的组合物
CN113620978A (zh) * 2014-09-11 2021-11-09 加利福尼亚大学董事会 mTORC1抑制剂
AU2019340376B2 (en) 2018-09-11 2024-12-19 Curis Inc. Combination therapy with a phosphoinositide 3-kinase inhibitor with a zinc binding moiety
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
EP0754684A4 (fr) * 1994-04-01 1998-05-13 Shionogi & Co Derive d'oxime et bactericide le contenant en tant qu'ingredient actif
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
JP4617299B2 (ja) * 2003-03-03 2011-01-19 アレイ バイオファーマ、インコーポレイテッド p38阻害剤及びその使用法
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
JP4931419B2 (ja) * 2003-09-19 2012-05-16 中外製薬株式会社 新規4−フェニルアミノ−ベンズアルドオキシム誘導体並びにそのmek阻害剤としての使用
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
CN103524392B (zh) * 2005-10-07 2018-06-01 埃克塞利希斯股份有限公司 作为用于治疗增生性疾病的mek 抑制剂的吖丁啶
WO2007129161A2 (fr) * 2006-04-26 2007-11-15 F. Hoffmann-La Roche Ag Composés pharmaceutiques
CA2658725A1 (fr) * 2006-08-16 2008-02-21 Exelixis, Inc. Procedes d'utilisation de modulateurs pi3k etmek
ES2544082T3 (es) * 2006-12-07 2015-08-27 F. Hoffmann-La Roche Ag Compuestos inhibidores de fosfoinosítido 3-quinasa y métodos de uso
KR101584823B1 (ko) 2007-09-12 2016-01-22 제넨테크, 인크. 포스포이노시타이드 3-키나제 저해제 화합물과 화학치료제의 배합물 및 이의 사용방법
BR112013025397A2 (pt) * 2011-04-01 2019-09-24 Deepak Sampath combinação de um composto, composto de fórmula i ou um sal farmaceuticamente aceitável do mesmo, uso, kit, produto, método para tratamento de um distúrbio hiperproliferativo e método para tratamento de uma doença ou afecção modulada por quinase akt em um mamífero

Also Published As

Publication number Publication date
CN102740851A (zh) 2012-10-17
TWI428336B (zh) 2014-03-01
AU2010314287A2 (en) 2012-07-12
KR101489045B1 (ko) 2015-02-02
BR112012008483A2 (pt) 2019-09-24
JP2015038110A (ja) 2015-02-26
EP2488178A1 (fr) 2012-08-22
US20110086837A1 (en) 2011-04-14
MX2012004286A (es) 2012-05-22
RU2563193C2 (ru) 2015-09-20
HK1175125A1 (en) 2013-06-28
AU2010314287A1 (en) 2012-05-03
AR078588A1 (es) 2011-11-16
IL219105A0 (en) 2012-06-28
EP2488178B1 (fr) 2016-11-16
MX345155B (es) 2017-01-18
PH12012500709A1 (en) 2012-10-29
CN102740851B (zh) 2013-12-18
ECSP12011865A (es) 2012-06-29
KR20120064132A (ko) 2012-06-18
CL2012000913A1 (es) 2012-09-14
CO6531463A2 (es) 2012-09-28
ES2609767T3 (es) 2017-04-24
NZ599939A (en) 2014-02-28
JP2013507415A (ja) 2013-03-04
WO2011054620A1 (fr) 2011-05-12
TW201118082A (en) 2011-06-01
RU2012118974A (ru) 2013-11-20
PE20121816A1 (es) 2013-01-02
ZA201202618B (en) 2014-10-29
CA2776944A1 (fr) 2011-05-12
CR20120173A (es) 2012-07-04
JP5745678B2 (ja) 2015-07-08

Similar Documents

Publication Publication Date Title
MA33974B1 (fr) Combinaisons d'un inhibiteur de pi3k et d'un inhibiteur de mek
EA201490194A1 (ru) Комбинированная терапия, включающая ингибитор cdk4/6 и ингибитор pi3k для применения в лечении рака
EA201200473A1 (ru) Замещенные (гетероарилметил)тиогидантоины
EA201201464A1 (ru) Новая комбинированная терапия для лечения онкологических и фиброзных заболеваний
EA200802118A1 (ru) Обладающие ингибирующей активностью в отношении mnk1/mnk2 тиенопиримидины, предназначенные для применения в фармацевтических композициях
DE502007002289D1 (de) Methacrylatharze zur herstellung von fahrbahnmarkierungen
MX2009011226A (es) Inhibidores especificos pdgfrbeta.
BRPI0510177A (pt) heterociclos monocìclicos como inibidores de cinase
EA201290184A1 (ru) Бензодиазепиновый ингибитор бромодомена
GT200800202A (es) Quinazolinas para la inhibicion de pdk1
EA201101117A1 (ru) Ингибиторы дпп-4 для лечения диабета у детей
TR201900306T4 (tr) Mek inhibitörlerini kullanma yöntemleri.
HRP20192130T1 (hr) Kombinacijska terapija za liječenje pacijenata s neurološkim poremećajima i moždanim udarom
BR112015026297A2 (pt) terapia combinada composta por um inibidor tor quinase e um composto de 5-quinazolinona substituído para o tratamento de câncer
MX385872B (es) Uso de un anticuerpo que tiene la capacidad para ligarse a clnd 6 en el tratamiento o prevención de cáncer
MX2011010908A (es) Anticuerpos anti-tnf-alfa y sus usos.
NZ588033A (en) Methods of treating a mif-mediated disorder
MX2010003013A (es) Inhibicion de angiogenesis.
MX2013007171A (es) Inductor de autofagia y terapia de combinacion inhibidora para el tratamiento de neoplasias.
CR20120653A (es) Compuestos heterocíclicos, su preparación y su aplicación terapéutica
EA200802072A1 (ru) Ликопин для лечения нарушения обмена веществ
MX2011006725A (es) Combinacion de inhibidores de aurora cinasa y anticuerpos anti-cd20.
BR112014004577A2 (pt) inibidor pi3k para uso no tratamento de câncer ósseo ou para prevenção por metástase de células cancerosas primárias para os ossos
EA201200087A1 (ru) 2-карбоксамиды циклоаминомочевин, которые являются ингибиторами pi3k
MX2010007669A (es) Metodos para inhibir la angiogenesis utilizando antagonistas de egfl8.