TN2015000168A1 - Inhibiteurs de la tyrosine kinase de bruton - Google Patents
Inhibiteurs de la tyrosine kinase de brutonInfo
- Publication number
- TN2015000168A1 TN2015000168A1 TNP2015000168A TN2015000168A TN2015000168A1 TN 2015000168 A1 TN2015000168 A1 TN 2015000168A1 TN P2015000168 A TNP2015000168 A TN P2015000168A TN 2015000168 A TN2015000168 A TN 2015000168A TN 2015000168 A1 TN2015000168 A1 TN 2015000168A1
- Authority
- TN
- Tunisia
- Prior art keywords
- tyrosine kinase
- inhibitors
- compounds
- disclosed
- conditions
- Prior art date
Links
- 102000001714 Agammaglobulinaemia Tyrosine Kinase Human genes 0.000 title abstract 3
- 108010029445 Agammaglobulinaemia Tyrosine Kinase Proteins 0.000 title abstract 3
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 238000000034 method Methods 0.000 abstract 2
- 208000023275 Autoimmune disease Diseases 0.000 abstract 1
- 229940124291 BTK inhibitor Drugs 0.000 abstract 1
- 206010025323 Lymphomas Diseases 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 229940124597 therapeutic agent Drugs 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Transplantation (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Epidemiology (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Il est divulgué dans le présent mémoire des composés qui forment des liaisons covalentes avec la tyrosine-kinase de Bruton (BTK) . Des procédés pour la préparation des composés sont divulgués. Il est également divulgué des compositions pharmaceutiques qui comprennent les composés. Il est divulgué des procédés d'utilisation des inhibiteurs de BTK, seuls ou en association avec d'autres agents thérapeutiques, pour le traitement de maladies ou affections auto-immunes, de maladies ou affections hétéroimmunes,d'un cancer, y compris d'un lymphome, et de maladies ou d'affections inflammatoires. (Formule I) .
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261721920P | 2012-11-02 | 2012-11-02 | |
| US201361772028P | 2013-03-04 | 2013-03-04 | |
| PCT/IB2013/059846 WO2014068527A1 (fr) | 2012-11-02 | 2013-11-01 | Inhibiteurs de la tyrosine kinase de bruton |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TN2015000168A1 true TN2015000168A1 (fr) | 2016-10-03 |
Family
ID=49596360
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TNP2015000168A TN2015000168A1 (fr) | 2012-11-02 | 2015-04-30 | Inhibiteurs de la tyrosine kinase de bruton |
Country Status (27)
| Country | Link |
|---|---|
| US (4) | US20150291554A1 (fr) |
| EP (1) | EP2914586B1 (fr) |
| JP (1) | JP6178861B2 (fr) |
| KR (1) | KR101668574B1 (fr) |
| CN (1) | CN105008344B (fr) |
| AP (1) | AP2015008381A0 (fr) |
| AU (1) | AU2013340345B2 (fr) |
| BR (1) | BR112015009624A2 (fr) |
| CA (1) | CA2888960C (fr) |
| CL (1) | CL2015001168A1 (fr) |
| CO (1) | CO7350624A2 (fr) |
| CR (1) | CR20150228A (fr) |
| DO (1) | DOP2015000100A (fr) |
| EA (1) | EA201500393A1 (fr) |
| ES (1) | ES2625944T3 (fr) |
| GE (1) | GEP201606597B (fr) |
| HK (1) | HK1211293A1 (fr) |
| IL (1) | IL238571A0 (fr) |
| MD (1) | MD20150035A2 (fr) |
| MX (1) | MX2015005422A (fr) |
| NI (1) | NI201500059A (fr) |
| PE (1) | PE20151070A1 (fr) |
| PH (1) | PH12015500940A1 (fr) |
| SG (1) | SG11201502893WA (fr) |
| TN (1) | TN2015000168A1 (fr) |
| TW (1) | TWI518080B (fr) |
| WO (1) | WO2014068527A1 (fr) |
Families Citing this family (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20140045813A1 (en) | 2012-08-10 | 2014-02-13 | Boehringer Ingelheim International Gmbh | Heteroaromatic compounds as btk inhibitors |
| SMT201900344T1 (it) | 2012-09-10 | 2019-07-11 | Principia Biopharma Inc | Composti di pirazolopirimidina come inibitori di chinasi |
| CN103848810A (zh) * | 2012-11-30 | 2014-06-11 | 北京赛林泰医药技术有限公司 | 鲁顿酪氨酸激酶抑制剂 |
| EP2970163B1 (fr) | 2013-03-14 | 2018-02-28 | Boehringer Ingelheim International GmbH | Dérivés de 5-thiazolecarboxamide et leur utilisation en tant qu'inhibiteurs de la btk |
| US9156847B2 (en) * | 2013-03-15 | 2015-10-13 | Janssen Pharmaceutica Nv | Processes and intermediates for preparing a medicament |
| CN112608298A (zh) * | 2013-03-15 | 2021-04-06 | 詹森药业有限公司 | 用于制备药物的方法和中间体 |
| WO2014152114A1 (fr) | 2013-03-15 | 2014-09-25 | Boehringer Ingelheim International Gmbh | Composés hétéroaromatiques en tant qu'inhibiteurs de btk |
| IL299897B2 (en) | 2013-08-19 | 2024-02-01 | Taris Biomedical Llc | Devices and methods for administering multiple units of drug |
| MX2016004030A (es) * | 2013-09-30 | 2016-10-26 | Beijing Synercare Pharma Tech Co Ltd | Inhibidores sustituidos de nicotinamida de btk y su preparacion y uso en el tratamiento del cancer, inflamacion y enfermedad autoinmune. |
| WO2015116485A1 (fr) * | 2014-01-29 | 2015-08-06 | Boehringer Ingelheim International Gmbh | Composés de pyrazole utilisés en tant qu'inhibiteurs de btk |
| CN112353806A (zh) | 2014-02-21 | 2021-02-12 | 普林斯匹亚生物制药公司 | Btk抑制剂的盐和固体形式 |
| WO2015185998A2 (fr) * | 2014-04-11 | 2015-12-10 | Acerta Pharma B.V. | Procédés de blocage de la voie de signalisation des cxcr-4/sdf-1 à l'aide d'inhibiteurs de kinase x de moelle osseuse |
| CN105085474B (zh) * | 2014-05-07 | 2018-05-18 | 北京赛林泰医药技术有限公司 | 鲁顿酪氨酸激酶抑制剂 |
| GB201410430D0 (en) | 2014-06-11 | 2014-07-23 | Redx Pharma Ltd | Compounds |
| CN106687446B (zh) * | 2014-07-18 | 2020-04-28 | 百济神州(北京)生物科技有限公司 | 作为t790m/wt-egfr的选择性和不可逆的激酶抑制剂的5-氨基-4-氨甲酰基-吡唑化合物及其用途 |
| WO2016019237A2 (fr) * | 2014-07-31 | 2016-02-04 | Pharmacyclics Llc | Inhibiteurs de la tyrosine kinase de bruton |
| CN105884747B (zh) * | 2014-08-28 | 2021-01-05 | 首药控股(北京)有限公司 | 一种制备布鲁顿酪氨酸激酶(btk)激酶抑制剂的制备方法 |
| CA2970723C (fr) | 2014-12-18 | 2023-09-05 | Principia Biopharma Inc. | Traitement du pemphigus |
| WO2016192074A1 (fr) * | 2015-06-04 | 2016-12-08 | Merck Sharp & Dohme Corp. | Inhibiteurs de la btk |
| US20180305350A1 (en) | 2015-06-24 | 2018-10-25 | Principia Biopharma Inc. | Tyrosine kinase inhibitors |
| HK1258779A1 (zh) | 2015-09-16 | 2019-11-22 | Loxo Oncology Inc. | 用於治療癌症的作為btk抑制劑的吡唑並嘧啶衍生物 |
| CN108884076B (zh) * | 2015-11-17 | 2021-07-30 | 默克专利有限公司 | 使用具有btk抑制活性的嘧啶和吡啶化合物治疗多发性硬化症的方法 |
| SI3390395T1 (sl) * | 2015-12-16 | 2020-11-30 | Loxo Oncology, Inc. | Spojine uporabne kot inhibitorji kinaz |
| CA3005268C (fr) | 2015-12-16 | 2024-04-30 | Boehringer Ingelheim International Gmbh | Composes heteroaromatiques utilises en tant qu'inhibiteurs de la btk |
| US10570118B2 (en) | 2016-01-13 | 2020-02-25 | Boehringer Ingelheim International Gmbh | Isoquinolones as BTK inhibitors |
| CN107021963A (zh) | 2016-01-29 | 2017-08-08 | 北京诺诚健华医药科技有限公司 | 吡唑稠环类衍生物、其制备方法及其在治疗癌症、炎症和免疫性疾病上的应用 |
| MA43753A (fr) | 2016-03-24 | 2018-11-28 | Mission Therapeutics Ltd | Dérivés 1-cyano-pyrrolidine comme inhibiteurs de dbu |
| JP6953445B2 (ja) * | 2016-05-16 | 2021-10-27 | スーチョウ、シノベント、ファーマスーティカルズ、カンパニー、リミテッドSuzhou Sinovent Pharmaceuticals Co., Ltd. | Btk阻害剤としての5−アミノピラゾールカルボキサミド誘導体およびその製造方法および医薬組成物 |
| JP7129704B2 (ja) | 2016-06-29 | 2022-09-02 | プリンシピア バイオファーマ インコーポレイテッド | 2-[3-[4-アミノ-3-(2-フルオロ-4-フェノキシ-フェニル)ピラゾロ[3,4-d]ピリミジン-1-イル]ピペリジン-1-カルボニル]-4-メチル-4-[4-(オキセタン-3-イル)ピペラジン-1-イル]ペント-2-エネニトリルの放出調節製剤 |
| GB201616511D0 (en) | 2016-09-29 | 2016-11-16 | Mission Therapeutics Limited | Novel compounds |
| GB201616627D0 (en) | 2016-09-30 | 2016-11-16 | Mission Therapeutics Limited | Novel compounds |
| TWI771327B (zh) * | 2016-10-05 | 2022-07-21 | 英商使命醫療公司 | 新穎化合物 |
| WO2018102785A2 (fr) | 2016-12-03 | 2018-06-07 | Juno Therapeutics, Inc. | Méthodes et compositions pour l'utilisation de lymphocytes t thérapeutiques en association avec des inhibiteurs de kinase |
| EP3824906A1 (fr) | 2016-12-21 | 2021-05-26 | Amgen Inc. | Formulations d'anticorps anti-tnf alpha |
| MX2020003671A (es) | 2017-10-06 | 2020-08-03 | Forma Therapeutics Inc | Inhibicion de peptidasa especifica de ubiquitina 30. |
| WO2019091441A1 (fr) * | 2017-11-10 | 2019-05-16 | 苏州信诺维医药科技有限公司 | Composé 5-amino pyrazole carboxamide en tant qu'inhibiteur de btk et son procédé de préparation |
| WO2019091438A1 (fr) * | 2017-11-10 | 2019-05-16 | 苏州信诺维医药科技有限公司 | Dispersion solide amorphe d'un composé de 5-aminopyrazole carboxamide comme inhibiteur de btk |
| CN111225669B (zh) * | 2017-11-10 | 2020-12-29 | 苏州信诺维医药科技有限公司 | 作为btk抑制剂的5-氨基吡唑甲酰胺化合物的晶型i |
| CN108530436B (zh) * | 2018-05-17 | 2020-12-29 | 黄传满 | 一种吡唑类化合物及其制备方法和应用 |
| IL278291B2 (en) | 2018-05-17 | 2023-10-01 | Forma Therapeutics Inc | Fused bicyclic compounds useful as ubiquitin-specific peptidase 30 inhibitors |
| PL3860989T3 (pl) | 2018-10-05 | 2023-07-10 | Forma Therapeutics, Inc. | Sprzężone piroliny, które działają jako inhibitory proteazy 30 swoistej dla ubikwityny (usp30) |
| KR102533599B1 (ko) * | 2019-03-14 | 2023-05-17 | 칼리코 라이프 사이언시스 엘엘씨 | 단백질 티로신 포스파타제 억제제 및 이의 사용 방법 |
| BR112021018168B1 (pt) | 2019-03-21 | 2023-11-28 | Onxeo | Composição farmacêutica, combinação e kit compreendendo uma molécula dbait e um inibidor de quinase para o tratamento de câncer |
| CN120136774A (zh) * | 2019-05-21 | 2025-06-13 | 詹森药业有限公司 | 用于制备btk抑制剂的方法和中间体 |
| WO2021076514A1 (fr) | 2019-10-14 | 2021-04-22 | Principia Biopharma Inc. | Procédé de traitement de la thrombocytopénie immunitaire par l'administration de (r)-2-[3-[4-amino-3-(2-fluoro-4-phénoxy-phényl)pyrazolo[3,4-d]pyrimidine-1-yl]pipéridine-1-carbonyle]-4-méthyl-4-[4-(oxétane-3-yl)pipérazine-1-yl]pent-2-ènenitrile |
| CN114761006A (zh) | 2019-11-08 | 2022-07-15 | Inserm(法国国家健康医学研究院) | 对激酶抑制剂产生耐药性的癌症的治疗方法 |
| WO2021148581A1 (fr) | 2020-01-22 | 2021-07-29 | Onxeo | Nouvelle molécule dbait et son utilisation |
| WO2021150723A1 (fr) | 2020-01-22 | 2021-07-29 | Principia Biopharma Inc. | Formes cristallines de 2-[3-[4-amino-3-(2-fluoro-4-phénoxy-phényle) -1h-pyrazolo [3,4-d]pyrimidine-1-yl]pipéridine-1-carbonyl]-4-méthyl-4-[4-(oxétane-3-yl]pipéridine-1-carbonyl]-4-méthyl-4-[4- (oxétane-3-yl)) pipérazine-1-yl] pent-2-enenitrile |
| TWI809489B (zh) * | 2020-09-10 | 2023-07-21 | 美商絡速藥業公司 | 用於製備(s)-5-胺基-3-(4-((5-氟-2-甲氧基苯甲醯胺基)甲基)苯基)-1-(1,1,1-三氟丙烷-2-基)-1h-吡唑-4-甲醯胺之方法及中間體 |
| MX2023002953A (es) * | 2020-09-11 | 2023-06-01 | Calico Life Sciences Llc | Inhibidores de proteína tirosina fosfatasa y métodos para su uso. |
| WO2022140246A1 (fr) | 2020-12-21 | 2022-06-30 | Hangzhou Jijing Pharmaceutical Technology Limited | Procédés et composés destinés à l'autophagie ciblée |
| WO2023284765A1 (fr) * | 2021-07-16 | 2023-01-19 | 深圳市塔吉瑞生物医药有限公司 | Composé pyrazole substitué, composition le contenant et son utilisation |
| CN116554102B (zh) * | 2022-01-28 | 2025-10-03 | 深圳海博为药业有限公司 | 一种作为btk抑制剂的化合物及其制备方法和应用 |
| CA3243695A1 (fr) * | 2022-02-04 | 2023-08-10 | Retune Pharma Inc | Certaines entités chimiques, compositions et procédés |
| WO2024153226A1 (fr) * | 2023-01-19 | 2024-07-25 | 北京普祺医药科技股份有限公司 | Composé cyclique fusionné au pyrazole, composition pharmaceutique et utilisation de celui-ci |
| WO2024153237A1 (fr) * | 2023-01-19 | 2024-07-25 | 北京普祺医药科技股份有限公司 | Inhibiteurs de tyrosine kinase igf-1r, composition pharmaceutique et leur utilisation |
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| GB9608435D0 (en) * | 1996-04-24 | 1996-06-26 | Celltech Therapeutics Ltd | Chemical compounds |
| EP1436265A4 (fr) * | 2001-09-27 | 2004-12-15 | Smithkline Beecham Corp | Composes chimiques |
| AU2007235237B2 (en) * | 2006-04-11 | 2011-08-18 | Vertex Pharmaceuticals Incorporated | Thiazoles, imidazoles, and pyrazoles useful as inhibitors of protein kinases |
| PL2529622T3 (pl) | 2006-09-22 | 2018-07-31 | Pharmacyclics Llc | Inhibitory kinazy tyrozynowej brutona |
| FR2908409B1 (fr) | 2006-11-10 | 2009-01-09 | Sanofi Aventis Sa | Pyrazoles substituees,compositions les contenant,procede de fabrication et utilisation |
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| PT2324008E (pt) | 2008-07-24 | 2012-06-25 | Nerviano Medical Sciences Srl | 3,4-diarilpirazoles como inibidores da proteína quinase |
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| CN103848810A (zh) * | 2012-11-30 | 2014-06-11 | 北京赛林泰医药技术有限公司 | 鲁顿酪氨酸激酶抑制剂 |
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-
2013
- 2013-11-01 HK HK15112141.6A patent/HK1211293A1/xx unknown
- 2013-11-01 SG SG11201502893WA patent/SG11201502893WA/en unknown
- 2013-11-01 MX MX2015005422A patent/MX2015005422A/es unknown
- 2013-11-01 ES ES13792494.0T patent/ES2625944T3/es active Active
- 2013-11-01 CA CA2888960A patent/CA2888960C/fr not_active Expired - Fee Related
- 2013-11-01 AU AU2013340345A patent/AU2013340345B2/en not_active Ceased
- 2013-11-01 MD MDA20150035A patent/MD20150035A2/ro not_active Application Discontinuation
- 2013-11-01 PE PE2015000569A patent/PE20151070A1/es not_active Application Discontinuation
- 2013-11-01 AP AP2015008381A patent/AP2015008381A0/xx unknown
- 2013-11-01 BR BR112015009624A patent/BR112015009624A2/pt active Search and Examination
- 2013-11-01 EP EP13792494.0A patent/EP2914586B1/fr active Active
- 2013-11-01 EA EA201500393A patent/EA201500393A1/ru unknown
- 2013-11-01 CN CN201380065731.8A patent/CN105008344B/zh not_active Expired - Fee Related
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- 2013-11-01 US US14/439,478 patent/US20150291554A1/en not_active Abandoned
- 2013-11-01 WO PCT/IB2013/059846 patent/WO2014068527A1/fr not_active Ceased
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2015
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- 2015-04-30 TN TNP2015000168A patent/TN2015000168A1/fr unknown
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2017
- 2017-06-16 US US15/624,969 patent/US10266513B2/en active Active
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2019
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2020
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