CR20120173A - 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
CR20120173A
CR20120173A CR20120173A CR20120173A CR20120173A CR 20120173 A CR20120173 A CR 20120173A CR 20120173 A CR20120173 A CR 20120173A CR 20120173 A CR20120173 A CR 20120173A CR 20120173 A CR20120173 A CR 20120173A
Authority
CR
Costa Rica
Prior art keywords
inhibitor
combinations
pi3k
mek
kinase
Prior art date
Application number
CR20120173A
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=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CR20120173(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 CR20120173A publication Critical patent/CR20120173A/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

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Bioinformatics & Cheminformatics (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

La invención se refiere a métodos para tratar un paciente que tiene tumores sólidos localmente avanzados o matastásicos 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.
CR20120173A 2009-10-12 2012-04-10 Combinaciones de un inhibidor de pi3k y un inhibidor de mek CR20120173A (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
CR20120173A true CR20120173A (es) 2012-07-04

Family

ID=43072663

Family Applications (1)

Application Number Title Priority Date Filing Date
CR20120173A CR20120173A (es) 2009-10-12 2012-04-10 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)
IL (1) IL219105A0 (es)
MA (1) MA33974B1 (es)
MX (1) MX345155B (es)
NZ (1) NZ599939A (es)
PE (1) PE20121816A1 (es)
PH (1) PH12012500709A1 (es)
RU (1) RU2563193C2 (es)
TW (1) TWI428336B (es)
WO (1) WO2011054620A1 (es)
ZA (1) ZA201202618B (es)

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RU2508110C2 (ru) 2008-07-11 2014-02-27 Новартис Аг КОМБИНАЦИЯ (А) ИНГИБИТОРА ФОСФОИНОЗИТ-3-КИНАЗЫ И (Б) МОДУЛЯТОРА ПУТИ Ras/Raf/Mek
DK2385832T3 (en) 2009-01-08 2015-09-21 Curis Inc Phosphoinositid-3-kinase-inhibitorer med en zink-bindingsdel
PH12012501361A1 (en) 2009-12-31 2012-10-22 Centro Nac De Investigaciones Oncologicas Cnio Tricyclic compounds for use as kinase inhibitors
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
PL3111938T3 (pl) 2011-04-01 2019-09-30 Curis, Inc. Inhibitor 3-kinazy fosfoinozytydowej z grupą wiążącą cynk
EA026924B1 (ru) * 2011-08-01 2017-05-31 Дженентек, Инк. Способы лечения рака с использованием антагонистов, связывающихся с осью pd-1, и ингибиторов mek
MX2014002471A (es) * 2011-08-31 2014-03-27 Novartis Ag Combinaciones sinergicas de los inhibidores de p13k y mek.
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
CA2850034A1 (en) * 2011-10-28 2013-05-02 Genentech, Inc. Therapeutic combinations and methods of treating melanoma
WO2013082511A1 (en) 2011-12-02 2013-06-06 Genentech, Inc. Methods for overcoming tumor resistance to vegf antagonists
EP2854854A1 (en) * 2012-04-06 2015-04-08 Sanofi Methods for treating cancer using pi3k inhibitor and mek inhibitor
US9566307B2 (en) 2012-04-19 2017-02-14 Kyushu University, National University Corporation Pharmaceutical composition
KR101915942B1 (ko) 2012-06-08 2018-11-06 에프. 호프만-라 로슈 아게 암의 치료를 위한 포스포이노시타이드 3 키나제 억제제 화합물 및 화학치료제의 돌연변이체 선택성 및 조합물
MX2015001407A (es) 2012-08-02 2015-05-08 Genentech Inc Inmunoconjugados y anticuerpos anti-etbr.
BR112015002193A2 (pt) 2012-08-02 2017-07-04 Genentech Inc anticorpos anti-etbr e imunoconjugados
SI2884979T1 (sl) 2012-08-17 2019-10-30 Hoffmann La Roche Kombinirana zdravljenja melanoma, ki vključujejo dajanje kobimetiniba in vemurafeniba
BR112015022576A2 (pt) * 2013-03-14 2017-10-24 Genentech Inc produto farmacêutico e seu uso, kit e método para tratar uma disfunção hiperproliferativa
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
ES2779975T3 (es) * 2014-02-07 2020-08-21 Verastem Inc Métodos y composiciones para tratar el crecimiento celular anormal
EP3563870A1 (en) 2014-07-15 2019-11-06 F. Hoffmann-La Roche AG Methods of treating cancer using pd-1 axis binding antagonists and mek inhibitors
CN113620978A (zh) * 2014-09-11 2021-11-09 加利福尼亚大学董事会 mTORC1抑制剂
CN113164466B (zh) 2018-09-11 2025-07-08 柯瑞斯公司 使用具有锌结合部分的磷酸肌醇3-激酶抑制剂的联合治疗
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
WO2021047783A1 (en) 2019-09-13 2021-03-18 The Institute Of Cancer Research: Royal Cancer Hospital Vs-6063 in combination with ch5126766 for the treatment of cancer
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
US20110086837A1 (en) 2011-04-14
KR101489045B1 (ko) 2015-02-02
AU2010314287A1 (en) 2012-05-03
AU2010314287A2 (en) 2012-07-12
WO2011054620A1 (en) 2011-05-12
MX2012004286A (es) 2012-05-22
RU2563193C2 (ru) 2015-09-20
CA2776944A1 (en) 2011-05-12
HK1175125A1 (en) 2013-06-28
MA33974B1 (fr) 2013-02-01
ES2609767T3 (es) 2017-04-24
RU2012118974A (ru) 2013-11-20
CL2012000913A1 (es) 2012-09-14
KR20120064132A (ko) 2012-06-18
JP5745678B2 (ja) 2015-07-08
AR078588A1 (es) 2011-11-16
CN102740851A (zh) 2012-10-17
IL219105A0 (en) 2012-06-28
BR112012008483A2 (pt) 2019-09-24
EP2488178A1 (en) 2012-08-22
ZA201202618B (en) 2014-10-29
CN102740851B (zh) 2013-12-18
NZ599939A (en) 2014-02-28
PE20121816A1 (es) 2013-01-02
MX345155B (es) 2017-01-18
JP2013507415A (ja) 2013-03-04
ECSP12011865A (es) 2012-06-29
PH12012500709A1 (en) 2012-10-29
CO6531463A2 (es) 2012-09-28
JP2015038110A (ja) 2015-02-26
TWI428336B (zh) 2014-03-01
EP2488178B1 (en) 2016-11-16
TW201118082A (en) 2011-06-01

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