WO2015095834A3 - Traitements du cancer faisant appel à des inhibiteurs des familles erk1/2 et bcl-2 - Google Patents
Traitements du cancer faisant appel à des inhibiteurs des familles erk1/2 et bcl-2 Download PDFInfo
- Publication number
- WO2015095834A3 WO2015095834A3 PCT/US2014/071736 US2014071736W WO2015095834A3 WO 2015095834 A3 WO2015095834 A3 WO 2015095834A3 US 2014071736 W US2014071736 W US 2014071736W WO 2015095834 A3 WO2015095834 A3 WO 2015095834A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- cancer
- subject
- erk1
- bcl
- effects
- Prior art date
Links
Classifications
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- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
- A61K31/353—3,4-Dihydrobenzopyrans, e.g. chroman, catechin
-
- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
- A61K31/63—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide
- A61K31/635—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide having a heterocyclic ring, e.g. sulfadiazine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
Abstract
La présente invention concerne, inter alia, des méthodes pour le traitement ou l'amélioration des effets d'un cancer chez un sujet qui a besoin d'un tel traitement. Ces méthodes consistent à administrer au sujet une quantité efficace de (i) un inhibiteur de l'ERK1/2 (tel que le BVD-523) ou son sel pharmaceutiquement acceptable, et (ii) un inhibiteur de la famille BCL-2 (tel que le navitoclax) ou son sel pharmaceutiquement acceptable, pour traiter ou améliorer les effets du cancer. L'invention concerne également des kits et des compositions pharmaceutiques pour le traitement ou l'amélioration des effets d'un cancer chez un sujet et des méthodes permettant de sélectionner un sujet atteint d'un cancer qui pourrait bénéficier d'une pharmacothérapie comprenant une association médicamenteuse.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361919148P | 2013-12-20 | 2013-12-20 | |
US61/919,148 | 2013-12-20 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2015095834A2 WO2015095834A2 (fr) | 2015-06-25 |
WO2015095834A3 true WO2015095834A3 (fr) | 2015-08-27 |
Family
ID=53403900
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2014/071736 WO2015095834A2 (fr) | 2013-12-20 | 2014-12-19 | Traitements du cancer faisant appel à des inhibiteurs des familles erk1/2 et bcl-2 |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2015095834A2 (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP7427212B2 (ja) | 2013-12-20 | 2024-02-05 | バイオメッド バレー ディスカバリーズ,インコーポレイティド | 非erk mapk経路阻害剤耐性のがんを処置するための方法および組成物 |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8703777B2 (en) | 2008-01-04 | 2014-04-22 | Intellikine Llc | Certain chemical entities, compositions and methods |
US8193182B2 (en) | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
US8809349B2 (en) | 2011-01-10 | 2014-08-19 | Infinity Pharmaceuticals, Inc. | Processes for preparing isoquinolinones and solid forms of isoquinolinones |
US8828998B2 (en) | 2012-06-25 | 2014-09-09 | Infinity Pharmaceuticals, Inc. | Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors |
WO2015160975A2 (fr) | 2014-04-16 | 2015-10-22 | Infinity Pharmaceuticals, Inc. | Polythérapies |
JP2018528206A (ja) * | 2015-08-28 | 2018-09-27 | ノバルティス アーゲー | Mdm2阻害剤およびその組み合わせ物 |
KR20180096621A (ko) * | 2015-12-18 | 2018-08-29 | 이그니타, 인코포레이티드 | 암의 치료용 조합물 |
CN109640999A (zh) | 2016-06-24 | 2019-04-16 | 无限药品股份有限公司 | 组合疗法 |
CN115279375A (zh) | 2019-11-05 | 2022-11-01 | 艾伯维公司 | 用于以navitoclax治疗骨髓纤维化和mpn相关病症的给药方案 |
IT201900023895A1 (it) * | 2019-12-13 | 2021-06-13 | Univ Degli Studi Padova | Combinazione comprendente il composto bh3-mimetico abt-199 (venetoclax) e almeno un inibitore della produzione di nadph e/o suoi sali o derivati farmaceuticamente accettabili, composizioni farmaceutiche che comprendano tale combinazione e uso nel trattamento dei linfomi non-hodgkin a cellule b, preferibilmente nel trattamento del linfoma diffuso a grandi cellule b (dlbcl) |
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2014
- 2014-12-19 WO PCT/US2014/071736 patent/WO2015095834A2/fr active Application Filing
Non-Patent Citations (4)
Title |
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JAIN ET AL.: "Phase II study of the oral MEK inhibitor selumetinib in advanced acute myelogenous leukemia: a University of Chicago phase II consortium trial.", CLIN CANCER RES., vol. 20, no. 2, 31 October 2013 (2013-10-31), pages 490 - 498, XP055221318 * |
MELCHER ET AL.: "Spectral karyotyping of the human colon cancer cell lines SW480 and SW620.", CYTOGENET CELL GENET., vol. 88, no. 1-2, 2000, pages 145 - 52 * |
MORRIS ET AL.: "Discovery of a novel ERK inhibitor with activity in models of acquired resistance to BRAF and MEK inhibitors.", C ANCER DISCOV., vol. 3, no. 7, July 2013 (2013-07-01), pages 742 - 50, XP055219076 * |
SALE ET AL.: "That which does not kill me makes me stronger; combining ERK1/2 pathway inhibitors and BH3 mimetics to kill tumour cells and prevent acquired resistance.", BR J PHARMACOL., vol. 169, no. 8, August 2013 (2013-08-01), pages 1708 - 1722, XP055221313 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP7427212B2 (ja) | 2013-12-20 | 2024-02-05 | バイオメッド バレー ディスカバリーズ,インコーポレイティド | 非erk mapk経路阻害剤耐性のがんを処置するための方法および組成物 |
Also Published As
Publication number | Publication date |
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WO2015095834A2 (fr) | 2015-06-25 |
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