DK3179991T3 - Terapeutiske kombinationer af en btk-inhibitor og en bcl-2-inhibitor - Google Patents
Terapeutiske kombinationer af en btk-inhibitor og en bcl-2-inhibitor Download PDFInfo
- Publication number
- DK3179991T3 DK3179991T3 DK15757002.9T DK15757002T DK3179991T3 DK 3179991 T3 DK3179991 T3 DK 3179991T3 DK 15757002 T DK15757002 T DK 15757002T DK 3179991 T3 DK3179991 T3 DK 3179991T3
- Authority
- DK
- Denmark
- Prior art keywords
- inhibitor
- bcl
- therapeutic combinations
- btk
- btk inhibitor
- Prior art date
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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61K31/4468—Non condensed piperidines, e.g. piperocaine having a nitrogen directly attached in position 4, e.g. clebopride, fentanyl
-
- 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
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- 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
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- A61K31/33—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
- A61K31/52—Purines, e.g. adenine
-
- 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
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/66—Phosphorus compounds
- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Endocrinology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462035795P | 2014-08-11 | 2014-08-11 | |
| US201462088240P | 2014-12-05 | 2014-12-05 | |
| US201562115497P | 2015-02-12 | 2015-02-12 | |
| US201562181160P | 2015-06-17 | 2015-06-17 | |
| PCT/IB2015/056126 WO2016024230A1 (en) | 2014-08-11 | 2015-08-11 | Therapeutic combinations of a btk inhibitor, a pi3k inhibitor, a jak-2 inhibitor, and/or a bcl-2 inhibitor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DK3179991T3 true DK3179991T3 (da) | 2021-12-06 |
Family
ID=54015145
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK15757002.9T DK3179991T3 (da) | 2014-08-11 | 2015-08-11 | Terapeutiske kombinationer af en btk-inhibitor og en bcl-2-inhibitor |
Country Status (17)
| Country | Link |
|---|---|
| US (3) | US20170231986A1 (da) |
| EP (1) | EP3179991B1 (da) |
| AR (1) | AR101505A1 (da) |
| CY (1) | CY1125588T1 (da) |
| DK (1) | DK3179991T3 (da) |
| ES (1) | ES2900184T3 (da) |
| HR (1) | HRP20211813T1 (da) |
| HU (1) | HUE056329T2 (da) |
| LT (1) | LT3179991T (da) |
| MA (1) | MA40596B1 (da) |
| PL (1) | PL3179991T3 (da) |
| PT (1) | PT3179991T (da) |
| RS (1) | RS62713B1 (da) |
| SI (1) | SI3179991T1 (da) |
| SM (1) | SMT202100674T1 (da) |
| TW (1) | TW201618772A (da) |
| WO (1) | WO2016024230A1 (da) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101537148B1 (ko) | 2010-05-31 | 2015-07-15 | 오노 야꾸힝 고교 가부시키가이샤 | 푸리논 유도체 |
| US9199997B2 (en) | 2011-11-29 | 2015-12-01 | Ono Pharmaceutical Co., Ltd. | Purinone derivative hydrochloride |
| US9416131B2 (en) | 2014-03-25 | 2016-08-16 | Ono Pharmaceutical Co., Ltd. | Prophylactic agent and/or therapeutic agent for diffuse large B-cell lymphoma |
| HRP20211813T1 (hr) * | 2014-08-11 | 2022-03-04 | Acerta Pharma B.V. | Terapeutske kombinacije inhibitora btk i inhibitora bcl-2 |
| US10239879B2 (en) | 2015-04-09 | 2019-03-26 | Ono Pharmaceutical Co., Ltd. | Process for producing purinone derivative |
| JP6785804B2 (ja) * | 2015-06-23 | 2020-11-18 | ギリアド サイエンシズ, インコーポレイテッド | B細胞悪性腫瘍を治療するための組合せ療法 |
| EP3331531A1 (en) * | 2015-08-03 | 2018-06-13 | Gilead Sciences, Inc. | Combination therapies for treating cancers |
| KR102494039B1 (ko) | 2016-03-28 | 2023-01-30 | 프레시지 바이오싸이언시스, 인크. | 암 치료를 위한 제약학적 조합물 |
| EP3481397A1 (en) * | 2016-07-06 | 2019-05-15 | Concert Pharmaceuticals Inc. | Deuterated venetoclax |
| US10925880B2 (en) | 2016-09-23 | 2021-02-23 | Bayer Pharma Aktiengesellschaft | Combination of PI3K-inhibitors |
| WO2018102785A2 (en) | 2016-12-03 | 2018-06-07 | Juno Therapeutics, Inc. | Methods and compositions for use of therapeutic t cells in combination with kinase inhibitors |
| NZ754944A (en) | 2016-12-07 | 2023-02-24 | Beigene Ltd | Imidazo [1,5-a] pyrazine derivatives as pi3kdelta inhibitors |
| JP7368856B2 (ja) | 2017-07-25 | 2023-10-25 | トゥルーバインディング,インコーポレイテッド | Tim-3とそのリガンドとの相互作用の遮断によるがん治療 |
| US11351176B2 (en) | 2017-08-14 | 2022-06-07 | Mei Pharma, Inc. | Combination therapy |
| MX2020002630A (es) * | 2017-09-08 | 2020-07-20 | Beigene Ltd | Derivados de imidazo[1,5-a]pirazina como inhibidores de fosfatidilinositol-4,5-bisfosfato 3-quinasadelta. |
| US10588916B2 (en) | 2017-10-31 | 2020-03-17 | Unity Biotechnology, Inc. | Technology to inhibit vascular changes that lead to vision loss in the eye |
| TW201924721A (zh) * | 2017-12-08 | 2019-07-01 | 韓商保寧製藥股份公司 | 包含pi3激酶抑制劑與bcl-2抑制劑的組成物 |
| US20190240198A1 (en) * | 2018-02-05 | 2019-08-08 | Dean G. Tang | Formulations and methods for the treatment of cancers |
| US20190328729A1 (en) | 2018-04-26 | 2019-10-31 | Emory University | Uses of Bcl-2 Antagonists for Treating Cancer and Diagnostics Related Thereto |
| CN110772521A (zh) * | 2018-07-31 | 2020-02-11 | 苏州亚盛药业有限公司 | Bcl-2抑制剂或Bcl-2/Bcl-xL抑制剂与BTK抑制剂的组合产品及其用途 |
| MX2020009759A (es) | 2018-07-31 | 2020-10-08 | Ascentage Pharma Suzhou Co Ltd | Efecto antitumoral sinergico de un inhibidor de bcl-2 combinado con rituximab y/o bendamustina o un inhibidor de bcl-2 combinado con chop. |
| CA3094449C (en) | 2018-07-31 | 2023-02-28 | Ascentage Pharma (Suzhou) Co., Ltd. | Combination product of bcl-2 inhibitor and mdm2 inhibitor and use thereof in the prevention and/or treatment of diseases |
| US11491167B2 (en) | 2018-07-31 | 2022-11-08 | Ascentage Pharma (Suzhou) Co., Ltd. | Combination product of Bcl-2 inhibitor and chemotherapeutic agent and use thereof in the prevention and/or treatment of diseases |
| CN113164487B (zh) * | 2018-10-12 | 2024-11-26 | 内布拉斯加大学董事委员会 | 磷酸二酯酶抑制剂 |
| WO2020132563A1 (en) * | 2018-12-21 | 2020-06-25 | Mei Pharma, Inc. | Combination therapy |
| CN111377929A (zh) * | 2018-12-28 | 2020-07-07 | 南京艾德凯腾生物医药有限责任公司 | 一种可用于治疗白血病阿卡替尼(Acalabrutinib)制备的方法 |
| WO2020223609A1 (en) * | 2019-05-01 | 2020-11-05 | New York University | Methods and compositions for sensitizing cancer cells to drug-induced apoptosis |
| CN112294966B (zh) * | 2019-07-31 | 2021-12-17 | 苏州亚盛药业有限公司 | Bcl-2/Bcl-xL抑制剂与化疗药的组合产品及其在预防和/或治疗疾病中的用途 |
| TWI772992B (zh) * | 2019-12-03 | 2022-08-01 | 大陸商蘇州亞盛藥業有限公司 | 作為bcl-2抑制劑的n-(苯基磺醯基)苯甲醯胺及相關化合物 |
| JOP20220168A1 (ar) * | 2020-01-08 | 2023-01-30 | Telios Pharma Inc | طرق علاج الطحال |
| US20240024314A1 (en) | 2020-01-08 | 2024-01-25 | Telios Pharma, Inc. | Methods of Treating Splenomegaly |
| KR20210095495A (ko) * | 2020-01-23 | 2021-08-02 | 주식회사 바이오웨이 | 신규한 퀴나졸리논 화합물 및 이를 포함하는 약학적 조성물 |
| CA3167134A1 (en) * | 2020-02-07 | 2021-08-12 | University Health Network (Uhn) | Methods for enhancing t cells using venetoclax |
| MX2022013006A (es) | 2020-04-15 | 2023-01-11 | Beigene Ltd | Inhibidor de bcl-2. |
| CA3185040A1 (en) | 2020-05-26 | 2021-12-02 | Truebinding, Inc. | Methods of treating inflammatory diseases by blocking galectin-3 |
| WO2022056092A1 (en) * | 2020-09-11 | 2022-03-17 | Cti Biopharma Corp. | Methods of treating viral infection |
| KR20240016335A (ko) * | 2021-06-02 | 2024-02-06 | 베이진 스위찰랜드 게엠베하 | Bcl-2 억제제를 이용한 b-세포 악성 종양의 치료 방법 |
| JP2024520630A (ja) * | 2021-06-04 | 2024-05-24 | ヤンセン ファーマシューティカ エヌ.ベー. | ブルトン型チロシンキナーゼの阻害剤及びその使用方法 |
| WO2025124429A1 (zh) * | 2023-12-11 | 2025-06-19 | 北京康辰药业股份有限公司 | 芳香胺化合物及其药物组合物、应用 |
Family Cites Families (132)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20010085824A (ko) | 1998-09-18 | 2001-09-07 | 스타르크, 카르크 | 단백질 키나아제 억제제로서의 피롤로피리미딘 |
| DE60037455T2 (de) | 1999-09-17 | 2008-11-27 | Abbott Gmbh & Co. Kg | Kinaseinhibitoren als arzneimittel |
| US6921763B2 (en) | 1999-09-17 | 2005-07-26 | Abbott Laboratories | Pyrazolopyrimidines as therapeutic agents |
| US6998391B2 (en) | 2002-02-07 | 2006-02-14 | Supergen.Inc. | Method for treating diseases associated with abnormal kinase activity |
| US7405295B2 (en) | 2003-06-04 | 2008-07-29 | Cgi Pharmaceuticals, Inc. | Certain imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of Bruton's tyrosine kinase by such compounds |
| US7393848B2 (en) | 2003-06-30 | 2008-07-01 | Cgi Pharmaceuticals, Inc. | Certain heterocyclic substituted imidazo[1,2-A]pyrazin-8-ylamines and methods of inhibition of Bruton's tyrosine kinase by such compounds |
| TWI372050B (en) | 2003-07-03 | 2012-09-11 | Astex Therapeutics Ltd | (morpholin-4-ylmethyl-1h-benzimidazol-2-yl)-1h-pyrazoles |
| BRPI0415395A (pt) | 2003-10-15 | 2006-12-12 | Osi Pharm Inc | composto, métodos para inibir a atividade da proteìna quinase e para tratar um paciente que tenha uma condição que seja mediada pela atividade da proteìna quinase, e, composição |
| AP2139A (en) | 2004-04-02 | 2010-08-21 | Osi Pharm Inc | 6,6-bicyclic ring substituted heterobicyclic protein kinase inhibitors. |
| RS55551B1 (sr) | 2004-05-13 | 2017-05-31 | Icos Corp | Hinazolinoni kao inhibitori humane fosfatidilinozitol 3-kinaze delta |
| MX2007005857A (es) | 2004-11-17 | 2007-10-10 | Mikana Therapeutics Inc | Inhibidores de cinasa. |
| CA2586612C (en) | 2004-11-18 | 2016-10-11 | Synta Pharmaceuticals Corp. | Triazole compounds that modulate hsp90 activity |
| PT2383268E (pt) | 2005-02-04 | 2015-12-21 | Astrazeneca Ab | Derivados de pirazolilaminopiridina úteis como inibidores de quinase |
| EP1858644B1 (en) | 2005-02-18 | 2012-11-21 | The Hong Kong Polytechnic University | Method for asymmetric hydrosilylation of ketones |
| KR20140025610A (ko) | 2005-09-30 | 2014-03-04 | 미카나 테라퓨틱스, 인크. | 치환된 피라졸 화합물 |
| HRP20120824T1 (hr) | 2005-10-28 | 2012-11-30 | Astrazeneca Ab | Derivati 4-(3-aminopirazol) pirimidina za uporabu kao inhibitori tirozin kinaze u lijeäśenju karcinoma |
| PL1951729T3 (pl) | 2005-11-16 | 2015-02-27 | Cti Biopharma Corp | Pochodne pirymidyny połączone przez atom tlenu |
| PL1951724T3 (pl) | 2005-11-17 | 2011-09-30 | Osi Pharmaceuticals Llc | SKONDENSOWANE BICYKLICZNE INHIBITORY mTOR |
| CA2630562C (en) | 2005-11-22 | 2013-12-31 | Merck & Co., Inc. | Tricyclic compounds useful as inhibitors of kinases |
| PE20070855A1 (es) | 2005-12-02 | 2007-10-14 | Bayer Pharmaceuticals Corp | Derivados de 4-amino-pirrolotriazina sustituida como inhibidores de quinasas |
| AR057960A1 (es) | 2005-12-02 | 2007-12-26 | Osi Pharm Inc | Inhibidores de proteina quinasa biciclicos |
| SI2426129T1 (sl) | 2005-12-13 | 2017-02-28 | Incyte Holdings Corporation | Heteroarilno substituirani pirolo(2,3-b)piridini in pirolo(2,3-b)pirimidini kot zaviralci janusove kinaze |
| US8399442B2 (en) | 2005-12-30 | 2013-03-19 | Astex Therapeutics Limited | Pharmaceutical compounds |
| EP1996193A2 (en) | 2006-03-13 | 2008-12-03 | OSI Pharmaceuticals, Inc. | Combined treatment with an egfr kinase inhibitor and an agent that sensitizes tumor cells to the effects of egfr kinase inhibitors |
| PL2529622T3 (pl) | 2006-09-22 | 2018-07-31 | Pharmacyclics Llc | Inhibitory kinazy tyrozynowej brutona |
| US8486941B2 (en) | 2007-03-12 | 2013-07-16 | Ym Biosciences Australia Pty Ltd | Phenyl amino pyrimidine compounds and uses thereof |
| US8193199B2 (en) | 2007-03-23 | 2012-06-05 | Amgen Inc. | Heterocyclic compounds and their uses |
| US20120101114A1 (en) | 2007-03-28 | 2012-04-26 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
| CA2681756C (en) | 2007-03-28 | 2015-02-24 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
| EP2166849A4 (en) | 2007-06-11 | 2010-09-15 | Miikana Therapeutics Inc | SUBSTITUTED PYRAZOL COMPOUNDS |
| CL2008001709A1 (es) | 2007-06-13 | 2008-11-03 | Incyte Corp | Compuestos derivados de pirrolo [2,3-b]pirimidina, moduladores de quinasas jak; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como cancer, psoriasis, artritis reumatoide, entre otras. |
| MX342814B (es) | 2007-06-13 | 2016-10-13 | Incyte Holdings Corp | Sales de inhibidor de janus cinasa (r)-3-(4-7h-pirrolo[2,3-d]pirim idin-4-il)-1h-pirazol-1-il)-3-ciclopentilpropanitrilo. |
| US20100272717A1 (en) | 2007-12-13 | 2010-10-28 | Novartis Ag | Combinations of therapeutic agents for treating cancer |
| US8193182B2 (en) | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
| SI2288610T1 (sl) | 2008-03-11 | 2016-11-30 | Incyte Holdings Corporation | Derivati azetidina in ciklobutana kot inhibitorji jak |
| RU2536584C2 (ru) | 2008-06-27 | 2014-12-27 | Авила Терапьютикс, Инк. | Гетероарильные соединения и их применение |
| US9095592B2 (en) | 2008-11-07 | 2015-08-04 | The Research Foundation For The State University Of New York | Bruton's tyrosine kinase as anti-cancer drug target |
| EP2373313A4 (en) | 2008-11-26 | 2012-06-13 | Miikana Therapeutics Inc | SUBSTITUTED PYRAZOL COMPOUNDS |
| US20100160322A1 (en) | 2008-12-04 | 2010-06-24 | Abbott Laboratories | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| US8557983B2 (en) | 2008-12-04 | 2013-10-15 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| US8563735B2 (en) | 2008-12-05 | 2013-10-22 | Abbvie Inc. | Bcl-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases |
| US8586754B2 (en) | 2008-12-05 | 2013-11-19 | Abbvie Inc. | BCL-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases |
| PA8851101A1 (es) | 2008-12-16 | 2010-07-27 | Lilly Co Eli | Compuesto amino pirazol |
| JOP20190230A1 (ar) | 2009-01-15 | 2017-06-16 | Incyte Corp | طرق لاصلاح مثبطات انزيم jak و المركبات الوسيطة المتعلقة به |
| CA2747837A1 (en) | 2009-01-19 | 2010-07-22 | Abbott Laboratories | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| US8673891B2 (en) | 2009-02-06 | 2014-03-18 | Nippon Shinyaku Co., Ltd. | Aminopyrazine derivative and medicine |
| EP2401267B1 (en) | 2009-02-27 | 2014-01-15 | Ambit Biosciences Corporation | Jak kinase modulating quinazoline derivatives and their use in methods |
| JP5656976B2 (ja) | 2009-04-29 | 2015-01-21 | ローカス ファーマシューティカルズ インコーポレイテッド | ピロロトリアジン化合物 |
| HUE046493T2 (hu) | 2009-05-22 | 2020-03-30 | Incyte Holdings Corp | 3-[4-(7H-Pirrolo[2,3-d]pirimidin-4-il)-lH-pirazol-l-il]oktán- vagy heptán-nitril JAK inhibitorokként |
| US8546399B2 (en) | 2009-05-26 | 2013-10-01 | Abbvie Inc. | Apoptosis inducing agents for the treatment of cancer and immune and autoimmune diseases |
| PT2435432E (pt) | 2009-05-26 | 2015-10-13 | Abbvie Bahamas Ltd | Agentes indutores de apoptose para o tratamento de cancro e doenças imunes e autoimunes |
| US9034875B2 (en) | 2009-05-26 | 2015-05-19 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| US20120157500A1 (en) | 2009-08-24 | 2012-06-21 | Weikang Tao | Jak inhibition blocks rna interference associated toxicities |
| EA022488B1 (ru) | 2009-09-03 | 2016-01-29 | Бристол-Майерс Сквибб Кампани | Ингибиторы jak2 и их применение для лечения миелопролиферативных заболеваний и злокачественной опухоли |
| JP5946768B2 (ja) | 2009-10-09 | 2016-07-06 | インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation | 3−(4−(7H−ピロロ[2,3−d]ピリミジン−4−イル)−1H−ピラゾール−1−イル)−3−シクロペンチルプロパンニトリルのヒドロキシル、ケト及びグルクロニド誘導体 |
| MX2012009208A (es) | 2010-02-08 | 2012-09-07 | Msd Oss Bv | Compuestos de 8-metil-1-fenil-imidazol[1, 5-a]pirazina. |
| UY33288A (es) | 2010-03-25 | 2011-10-31 | Glaxosmithkline Llc | Derivados de indolina inhibidores de la proteina quinasa r del reticulo endoplasmatico |
| EP2571357B1 (en) | 2010-05-21 | 2016-07-06 | Infinity Pharmaceuticals, Inc. | Chemical compounds, compositions and methods for kinase modulation |
| KR101537148B1 (ko) | 2010-05-31 | 2015-07-15 | 오노 야꾸힝 고교 가부시키가이샤 | 푸리논 유도체 |
| MX387728B (es) | 2010-06-03 | 2025-03-18 | Pharmacyclics Llc | El uso de inhibidores de la tirosina quinasa de bruton (btk). |
| US20120053189A1 (en) | 2010-06-28 | 2012-03-01 | Pharmacyclics, Inc. | Btk inhibitors for the treatment of immune mediated conditions |
| AU2011289604C1 (en) | 2010-08-10 | 2016-04-21 | Celgene Avilomics Research, Inc. | Besylate salt of a BTK inhibitor |
| JP5668756B2 (ja) | 2010-08-11 | 2015-02-12 | 日本新薬株式会社 | 悪性リンパ腫治療剤 |
| JPWO2012020786A1 (ja) | 2010-08-11 | 2013-10-28 | 日本新薬株式会社 | 医薬組成物 |
| WO2012030944A2 (en) | 2010-09-01 | 2012-03-08 | Ambit Biosciences Corporation | Quinoline and isoquinoline compounds and methods of use thereof |
| US20130225614A1 (en) | 2010-09-01 | 2013-08-29 | Ambit Biosciences Corporation | 4-azolylaminoquinazoline derivatives and methods of use thereof |
| US8703943B2 (en) | 2010-09-01 | 2014-04-22 | Ambit Biosciences Corporation | Optically active pyrazolylaminoquinazoline, and pharmaceutical compositions and methods of use thereof |
| RU2598345C2 (ru) | 2010-10-29 | 2016-09-20 | Эббви Инк. | Твердые дисперсии, содержащие средства, вызывающие апоптоз |
| UA113500C2 (xx) | 2010-10-29 | 2017-02-10 | Одержані екструзією розплаву тверді дисперсії, що містять індукуючий апоптоз засіб | |
| US20120128665A1 (en) | 2010-11-18 | 2012-05-24 | Synta Pharmaceuticals Corp. | Preselection of subjects for therapeutic treatment based on hypoxic status |
| JP2014503500A (ja) | 2010-11-18 | 2014-02-13 | シンタ ファーマスーティカルズ コーポレーション | 低酸素状態に基づく酸素感受性薬剤による治療に適した被験体の事前選択 |
| TWI535701B (zh) | 2010-11-23 | 2016-06-01 | 艾伯維巴哈馬有限公司 | 使用選擇性bcl-2抑制劑之治療方法 |
| NZ610151A (en) | 2010-11-23 | 2015-06-26 | Abbvie Inc | Salts and crystalline forms of an apoptosis-inducing agent |
| SG190950A1 (en) | 2010-12-03 | 2013-07-31 | Ym Biosciences Australia Pty | Treatment of jak2-mediated conditions |
| SG10201600179RA (en) | 2011-01-10 | 2016-02-26 | Infinity Pharmaceuticals Inc | Processes for preparing isoquinolinones and solid forms of isoquinolinones |
| CA2827739A1 (en) | 2011-02-24 | 2012-10-18 | Synta Pharmaceuticals Corp. | Prostate cancer therapy with hsp90 inhibitory compounds |
| WO2012116247A1 (en) | 2011-02-25 | 2012-08-30 | Synta Pharmaceuticals Corp. | Hsp90 inhibitory compounds in treating jak/stat signaling-mediated cancers |
| CA2831843A1 (en) | 2011-04-04 | 2012-10-11 | Pharmascience Inc. | Protein kinase inhibitors |
| CA2760174A1 (en) | 2011-12-01 | 2013-06-01 | Pharmascience Inc. | Protein kinase inhibitors and uses thereof |
| WO2012155063A1 (en) | 2011-05-11 | 2012-11-15 | Synta Pharmaceuticals Corp. | Treating cancer with an hsp90 inhibitory compound |
| PL2710007T3 (pl) | 2011-05-17 | 2020-06-01 | The Regents Of The University Of California | Inhibitory kinazy |
| EP2714039A1 (en) | 2011-05-23 | 2014-04-09 | Synta Pharmaceuticals Corp. | Combination therapy of hsp90 inhibitory compounds with mek inhibitors |
| EP2714038A1 (en) | 2011-05-24 | 2014-04-09 | Synta Pharmaceuticals Corp. | Combination therapy of hsp90 inhibitory compounds with mtor/pi3k inhibitors |
| US20140194388A1 (en) | 2011-05-26 | 2014-07-10 | Synta Pharmaceuticals Corp. | Combination therapy of hsp90 inhibitory compounds with chk inhibitors |
| US20130178483A1 (en) | 2011-06-28 | 2013-07-11 | Pharmacyclics, Inc. | Methods and Compositions for Inhibition of Bone Resorption |
| WO2013006864A2 (en) | 2011-07-07 | 2013-01-10 | Synta Pharmaceuticals Corp. | Treating cancer with hsp90 inhibitory compounds |
| JP2014520863A (ja) | 2011-07-13 | 2014-08-25 | ファーマサイクリックス,インク. | Bruton型チロシンキナーゼの阻害剤 |
| MX2014000648A (es) | 2011-07-19 | 2014-09-25 | Infinity Pharmaceuticals Inc | Compuestos heterociclicos y sus usos. |
| EP2548877A1 (en) | 2011-07-19 | 2013-01-23 | MSD Oss B.V. | 4-(5-Membered fused pyridinyl)benzamides as BTK-inhibitors |
| EP2734520B1 (en) | 2011-07-19 | 2016-09-14 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| EP2734522B1 (en) | 2011-07-19 | 2018-10-31 | Merck Sharp & Dohme B.V. | 4-imidazopyridazin-1-yl-benzamides and 4-imidazotriazin-1-yl-benzamides as btk-inhibitors |
| US20140155406A1 (en) | 2011-07-19 | 2014-06-05 | Petrus Antonius De Adrianus Man | 4-imidazopyridazin-1-yl-benzamides and 4-imidazotriazin-1-yl-benzamides btk inhibitors |
| WO2013028505A1 (en) | 2011-08-19 | 2013-02-28 | Synta Pharmaceuticals Corp. | Combination cancer therapy of hsp90 inhibitor with antimetabolite |
| KR20140075693A (ko) | 2011-08-29 | 2014-06-19 | 인피니티 파마슈티칼스, 인코포레이티드 | 헤테로사이클릭 화합물 및 그의 용도 |
| CA3110966A1 (en) | 2011-10-19 | 2013-04-25 | Pharmacyclics Llc | Use of inhibitors of bruton's tyrosine kinase (btk) |
| US8628752B2 (en) | 2011-10-28 | 2014-01-14 | Synta Pharmaceuticals Corp. | Methods of identifying HSP90 inhibitors with less ocular toxicity |
| EP2776025A1 (en) | 2011-11-02 | 2014-09-17 | Synta Pharmaceuticals Corp. | Combination therapy of hsp90 inhibitors with platinum-containing agents |
| AU2012332421A1 (en) | 2011-11-02 | 2014-06-05 | Synta Pharmaceuticals Corp. | Cancer therapy using a combination of Hsp90 inhibitors with topoisomerase I inhibitors |
| CA2854188A1 (en) | 2011-11-14 | 2013-05-23 | Synta Pharmaceuticals Corp. | Combination therapy of hsp90 inhibitors with braf inhibitors |
| US9199997B2 (en) | 2011-11-29 | 2015-12-01 | Ono Pharmaceutical Co., Ltd. | Purinone derivative hydrochloride |
| US20140212425A1 (en) | 2011-12-05 | 2014-07-31 | Immunomedics, Inc. | Therapeutic use of anti-cd22 antibodies for inducing trogocytosis |
| US8377946B1 (en) | 2011-12-30 | 2013-02-19 | Pharmacyclics, Inc. | Pyrazolo[3,4-d]pyrimidine and pyrrolo[2,3-d]pyrimidine compounds as kinase inhibitors |
| US8940742B2 (en) | 2012-04-10 | 2015-01-27 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| US20140079636A1 (en) | 2012-04-16 | 2014-03-20 | Dinesh U. Chimmanamada | Targeted therapeutics |
| US20150099721A1 (en) | 2012-05-10 | 2015-04-09 | Synta Pharmaceuticals Corp. | Treating cancer with hsp90 inhibitory compounds |
| WO2013170182A1 (en) | 2012-05-11 | 2013-11-14 | Synta Pharmaceuticals Corp. | Treating cancer with an hsp90 inhibitory compound |
| WO2013173436A1 (en) | 2012-05-16 | 2013-11-21 | Synta Pharmaceuticals Corp. | Pre-selection of subjects for therapeutic treatment with an hsp90 inhibitor based on hypoxic status |
| UA125503C2 (uk) | 2012-06-13 | 2022-04-13 | Інсайт Холдинґс Корпорейшн | Заміщені трициклічні сполуки як інгібітори fgfr |
| 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 |
| EP3492472A1 (en) | 2012-08-17 | 2019-06-05 | Concert Pharmaceuticals Inc. | Deuterated baricitinib with improved metabolic stability as jak1 and jak2 kinase inhibitor for treating e.g. rheumatoid arthritis |
| EP2892557A1 (en) * | 2012-09-07 | 2015-07-15 | Genentech, Inc. | Combination therapy of a type ii anti-cd20 antibody with a selective bcl-2 inhibitor |
| TW201441234A (zh) | 2013-01-23 | 2014-11-01 | Merck Sharp & Dohme | Btk抑制劑 |
| KR20160006668A (ko) | 2013-03-14 | 2016-01-19 | 파마싸이클릭스 엘엘씨 | 브루톤 티로신 키나제 억제제와 cyp3a4 억제제의 배합물 |
| WO2014143807A2 (en) | 2013-03-15 | 2014-09-18 | Stromatt Scott | Anti-cd37 antibody and bcr pathway antagonist combination therapy for treatment of b-cell malignancies and disorders |
| CA2908375A1 (en) * | 2013-04-08 | 2014-10-16 | Pharmacyclics Llc | Ibrutinib combination therapy |
| CA2902686C (en) | 2013-04-25 | 2017-01-24 | Beigene, Ltd. | Fused heterocyclic compounds as protein kinase inhibitors |
| US20160113932A1 (en) * | 2013-05-30 | 2016-04-28 | Infinity Pharmaceuticals, Inc. | Treatment of cancers using pi3 kinase isoform modulators |
| US20150005277A1 (en) | 2013-06-28 | 2015-01-01 | Beigene, Ltd. | Protein Kinase Inhibitors and Uses Thereof |
| WO2015018522A1 (en) | 2013-08-06 | 2015-02-12 | Oncoethix Sa | Bet-bromodomain inhibitor shows synergism with several anti-cancer agents in pre-clinical models of diffuse large b-cell lymphoma (dlbcl) |
| CA2927794A1 (en) * | 2013-10-25 | 2015-04-30 | Pharmacyclics Llc | Treatment using bruton's tyrosine kinase inhibitors and immunotherapy |
| CN105979948A (zh) * | 2013-12-05 | 2016-09-28 | 安塞塔制药公司 | Pi3k抑制剂和btk抑制剂的治疗组合 |
| TW201613644A (en) * | 2014-06-17 | 2016-04-16 | Acerta Pharma Bv | Therapeutic combinations of a BTK inhibitor, a PI3K inhibitor, and/or a JAK-2 inhibitor |
| MX2017001656A (es) | 2014-08-08 | 2017-07-24 | Pharmacyclics Llc | Combinaciones de inhibidor de tirosina cinasa de bruton y usos de estas. |
| US20170224819A1 (en) | 2014-08-11 | 2017-08-10 | Acerta Pharma B.V. | Therapeutic Combinations of a BTK Inhibitor, a PI3K Inhibitor, a JAK-2 Inhibitor, and/or a CDK 4/6 Inhibitor |
| US20170231995A1 (en) * | 2014-08-11 | 2017-08-17 | Acerta Pharma B.V. | BTK Inhibitors to Treat Solid Tumors Through Modulation of the Tumor Microenvironment |
| SMT202200285T1 (it) * | 2014-08-11 | 2022-09-14 | Acerta Pharma Bv | Combinazioni terapeutiche di un inibitore di btk, un inibitore di pd-1 e/o un inibitore di pd-l1 |
| HRP20211813T1 (hr) * | 2014-08-11 | 2022-03-04 | Acerta Pharma B.V. | Terapeutske kombinacije inhibitora btk i inhibitora bcl-2 |
| US9717745B2 (en) * | 2015-03-19 | 2017-08-01 | Zhejiang DTRM Biopharma Co. Ltd. | Pharmaceutical compositions and their use for treatment of cancer and autoimmune diseases |
| SI3613745T1 (sl) * | 2015-07-02 | 2021-12-31 | Acerta Pharma B.V. | Trdne oblike in formulacije (S)-4-(8-amino-3-(1-(but-2-inoil)pirolidin- 2-il)imidazo(1,5-a)pirazin-1-il)-n-(piridin-2-il)benzamida |
| US20170071962A1 (en) * | 2015-09-11 | 2017-03-16 | Acerta Pharma B.V. | Therapeutic Combinations of a Proteasome Inhibitor and a BTK Inhibitor |
| US20190201409A1 (en) * | 2016-09-19 | 2019-07-04 | Mei Pharma, Inc. | Combination therapy |
| WO2018134786A1 (en) * | 2017-01-19 | 2018-07-26 | Acerta Pharma B.V. | Compositions and methods for the assessment of drug target occupancy for bruton's tyrosine kinase |
-
2015
- 2015-08-11 HR HRP20211813TT patent/HRP20211813T1/hr unknown
- 2015-08-11 LT LTEPPCT/IB2015/056126T patent/LT3179991T/lt unknown
- 2015-08-11 EP EP15757002.9A patent/EP3179991B1/en active Active
- 2015-08-11 SI SI201531754T patent/SI3179991T1/sl unknown
- 2015-08-11 US US15/503,217 patent/US20170231986A1/en not_active Abandoned
- 2015-08-11 AR ARP150102592A patent/AR101505A1/es unknown
- 2015-08-11 TW TW104126105A patent/TW201618772A/zh unknown
- 2015-08-11 SM SM20210674T patent/SMT202100674T1/it unknown
- 2015-08-11 ES ES15757002T patent/ES2900184T3/es active Active
- 2015-08-11 MA MA40596A patent/MA40596B1/fr unknown
- 2015-08-11 PT PT157570029T patent/PT3179991T/pt unknown
- 2015-08-11 RS RS20211442A patent/RS62713B1/sr unknown
- 2015-08-11 HU HUE15757002A patent/HUE056329T2/hu unknown
- 2015-08-11 WO PCT/IB2015/056126 patent/WO2016024230A1/en not_active Ceased
- 2015-08-11 PL PL15757002T patent/PL3179991T3/pl unknown
- 2015-08-11 DK DK15757002.9T patent/DK3179991T3/da active
-
2018
- 2018-05-17 US US15/982,525 patent/US11166951B2/en active Active
-
2021
- 2021-07-08 US US17/370,827 patent/US11654143B2/en active Active
-
2022
- 2022-01-04 CY CY20221100007T patent/CY1125588T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US11654143B2 (en) | 2023-05-23 |
| EP3179991A1 (en) | 2017-06-21 |
| SMT202100674T1 (it) | 2022-01-10 |
| EP3179991B1 (en) | 2021-10-06 |
| US20180250298A1 (en) | 2018-09-06 |
| HUE056329T2 (hu) | 2022-02-28 |
| MA40596B1 (fr) | 2021-12-31 |
| SI3179991T1 (sl) | 2022-04-29 |
| US20170231986A1 (en) | 2017-08-17 |
| LT3179991T (lt) | 2021-11-10 |
| PL3179991T3 (pl) | 2022-02-14 |
| ES2900184T3 (es) | 2022-03-16 |
| HRP20211813T1 (hr) | 2022-03-04 |
| WO2016024230A1 (en) | 2016-02-18 |
| PT3179991T (pt) | 2021-11-26 |
| RS62713B1 (sr) | 2022-01-31 |
| TW201618772A (zh) | 2016-06-01 |
| US20220088013A1 (en) | 2022-03-24 |
| AR101505A1 (es) | 2016-12-21 |
| CY1125588T1 (el) | 2024-02-16 |
| US11166951B2 (en) | 2021-11-09 |
| MA40596A (fr) | 2021-05-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DK3179991T3 (da) | Terapeutiske kombinationer af en btk-inhibitor og en bcl-2-inhibitor | |
| DK3368069T3 (da) | Anvendelse af myostatininhibitorer og kombinationsterapier | |
| DK3210977T3 (da) | Hidtil ukendt aminoalkylbenzothiazepinderivat og anvendelse deraf | |
| DK3747472T3 (da) | Terapeutiske kombinationer af en cd19-hæmmer og en btk-hæmmer | |
| DK3179992T3 (da) | Terapeutisk kombination af en btk-inhibitor, en pd-1-inhibitor og/eller en pd-l1-inhibitor | |
| DK3129018T3 (da) | Behandling af NAFLD og NASH | |
| DK3160966T3 (da) | Mnk-inhibitorer og fremgangsmåder forbundet dermed | |
| DK3215147T3 (da) | Neurodæmpende norketamin-forbindelser og fremgangsmåder | |
| DK3725357T3 (da) | Opholdsstrukturer og relaterede fremgangsmåder | |
| DK3305935T3 (da) | Fladt stålprodukt med høj styrke og anvendelse af et fladt stålprodukt med høj styrke | |
| DK3185868T3 (da) | Hidtil ukendte ULK1-inhibitorer og fremgangsmåder til anvendelse af samme | |
| DK3160956T3 (da) | Inhibitorer af lysin-specifik demethylase-1 | |
| DK3218358T3 (da) | Ifluorometyl-aminopyridiner og difluorometyl-aminopyrimidiner | |
| DK2937422T3 (da) | Fremgangsmåde og et kit til ikke-invasiv detektering af patogene genmutationer for fosterdøvhed | |
| DK3193611T3 (da) | Mk2-inhibitorer og anvendelser deraf | |
| DK3511319T3 (da) | Hæmmere af lysinspecifik demethylase-1 | |
| DK3288553T3 (da) | Kombinationer af cannabinoider og n-acylethanolaminer | |
| DK3140310T3 (da) | Syntese af boronatsalte og brug deraf | |
| DK3089971T3 (da) | Forbindelser og fremgangsmåder til anvendelse | |
| DK3099800T3 (da) | Ekspression og oprensning af crm197 og beslægtede proteiner | |
| DK3209773T3 (da) | Prolintolerante tripeptidylpeptidaser og anvendelser deraf | |
| DK3129149T3 (da) | Fremgangsmåde til demontering og montering af en ringbandage | |
| DK3474883T3 (da) | Komplementinhibitorer og anvendelser deraf | |
| DK3215493T3 (da) | Syntese af copanlisib og dihydrochloridsalt deraf | |
| DK3142659T3 (da) | Hiv-1 proteasehæmmere og anvendelser deraf |