CL2017003445A1 - Formas solidas y formulaciones de compuestos de imidazopirazina. - Google Patents
Formas solidas y formulaciones de compuestos de imidazopirazina.Info
- Publication number
- CL2017003445A1 CL2017003445A1 CL2017003445A CL2017003445A CL2017003445A1 CL 2017003445 A1 CL2017003445 A1 CL 2017003445A1 CL 2017003445 A CL2017003445 A CL 2017003445A CL 2017003445 A CL2017003445 A CL 2017003445A CL 2017003445 A1 CL2017003445 A1 CL 2017003445A1
- Authority
- CL
- Chile
- Prior art keywords
- solid forms
- formulations
- pharmaceutical
- modes
- crystalline solid
- Prior art date
Links
- 239000007787 solid Substances 0.000 title abstract 3
- 239000000203 mixture Substances 0.000 title abstract 2
- 238000009472 formulation Methods 0.000 title 1
- 150000005235 imidazopyrazines Chemical class 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000003638 chemical reducing agent Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed 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
- A61K31/4985—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
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/04—Antipruritics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Hematology (AREA)
- Communicable Diseases (AREA)
- Heart & Thoracic Surgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Virology (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Inorganic Chemistry (AREA)
- Molecular Biology (AREA)
- Pain & Pain Management (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Vascular Medicine (AREA)
- Obesity (AREA)
- Ophthalmology & Optometry (AREA)
- Neurology (AREA)
Abstract
<p>EN ALGUNAS MODALIDADES, LA INVENCIÓN SE RELACIONA CON FORMAS SÓLIDAS CRISTALINAS, COMO POLIMORFAS, HIDRATOS Y SALES, DE (S)-4-(8-AMINO-3-(1-(BUT-2-INOIL)PIRROLIDIN-2-IL)IMIDAZO[1,5-A]PIRAZIN-1-IL)-N-(PIRIDIN-2- IL)BENZAMIDA. EN ALGUNAS MODALIDADES, LA INVENCIÓN SE RELACIONA ADEMÁS CON COMPOSICIONES FARMACÉUTICAS QUE CONTIENEN FORMAS SÓLIDAS CRISTALINAS, Y MÉTODOS DE TRATAMIENTO DE TRASTORNOS O AFECCIONES MEDIANTE LA ADMINISTRACIÓN A UN SUJETO DE UNA COMPOSICIÓN FARMACÉUTICA QUE INCLUYE LAS FORMAS, COMO COMPOSICIONES FARMACÉUTICAS Y MÉTODOS DE ELIMINACIÓN DE LOS EFECTOS DE AGENTES REDUCTORES DE ÁCIDO.</p>
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201562188468P | 2015-07-02 | 2015-07-02 | |
US201562271708P | 2015-12-28 | 2015-12-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
CL2017003445A1 true CL2017003445A1 (es) | 2018-05-11 |
Family
ID=56363881
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CL2017003445A CL2017003445A1 (es) | 2015-07-02 | 2017-12-28 | Formas solidas y formulaciones de compuestos de imidazopirazina. |
Country Status (29)
Country | Link |
---|---|
US (7) | US9796721B2 (es) |
EP (4) | EP4209493A1 (es) |
JP (3) | JP6829215B2 (es) |
KR (2) | KR102688052B1 (es) |
CN (2) | CN108349978B (es) |
AU (3) | AU2016286548B2 (es) |
CA (1) | CA2991096A1 (es) |
CL (1) | CL2017003445A1 (es) |
CY (3) | CY1124519T1 (es) |
DK (3) | DK3613745T3 (es) |
ES (3) | ES2946489T3 (es) |
FI (1) | FI3954690T3 (es) |
HK (1) | HK1250511A1 (es) |
HR (3) | HRP20230417T1 (es) |
HU (3) | HUE062258T2 (es) |
IL (3) | IL274066B (es) |
LT (3) | LT3317281T (es) |
MA (1) | MA50817B1 (es) |
MD (1) | MD3317281T2 (es) |
MX (2) | MX2020014163A (es) |
MY (1) | MY193514A (es) |
PL (3) | PL3954690T3 (es) |
PT (3) | PT3954690T (es) |
RS (3) | RS62455B1 (es) |
RU (1) | RU2018103913A (es) |
SG (1) | SG10201913796UA (es) |
SI (3) | SI3954690T1 (es) |
WO (1) | WO2017002095A1 (es) |
ZA (2) | ZA201800329B (es) |
Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HRP20211813T1 (hr) * | 2014-08-11 | 2022-03-04 | Acerta Pharma B.V. | Terapeutske kombinacije inhibitora btk i inhibitora bcl-2 |
KR102688052B1 (ko) | 2015-07-02 | 2024-07-25 | 아세르타 파마. 비.브이. | (S)-4-(8-아미노-3-(1-(부트-2-이노일)피롤리딘-2-일)이미다조[1,5-a]피라진-1-일)-N-(피리딘-2-일)벤즈아마이드의 고체 형태 및 제제 |
CN108137605B (zh) | 2016-10-05 | 2021-07-13 | 杭州领业医药科技有限公司 | Acp-196的晶型及其制备方法和药物组合物 |
WO2018115965A1 (en) * | 2016-12-23 | 2018-06-28 | Acerta Pharma Bv | Solid forms of imidazopyrazine compounds |
US10899770B2 (en) | 2017-02-20 | 2021-01-26 | Hangzhou Solipharma Co., Ltd. | Crystal form of ACP-196 salt and preparation method, pharmaceutical composition, and use thereof |
MX2019011491A (es) * | 2017-03-27 | 2020-01-23 | Tesaro Inc | Formulaciones de niraparib. |
MX2019011496A (es) | 2017-03-27 | 2020-01-23 | Tesaro Inc | Composiciones de niraparib. |
US10717740B2 (en) | 2017-06-13 | 2020-07-21 | Dr. Reddy's Laboratories Limited. | Solid forms of acalabrutinib and process for preparation thereof |
CA3073293A1 (en) * | 2017-08-29 | 2019-03-07 | Apotex Inc. | Novel crystalline forms of acalabrutinib |
AU2018341479B2 (en) | 2017-09-26 | 2022-02-17 | Tesaro, Inc. | Niraparib formulations |
WO2019105359A1 (zh) * | 2017-11-30 | 2019-06-06 | 苏州科睿思制药有限公司 | Acalabrutinib的晶型及其制备方法和用途 |
WO2019134455A1 (zh) | 2018-01-05 | 2019-07-11 | 苏州科睿思制药有限公司 | Acalabrutinib的新晶型及其制备方法和用途 |
WO2019159097A1 (en) * | 2018-02-14 | 2019-08-22 | Sun Pharmaceutical Industries Limited | Crystalline polymorphic forms of acalabrutinib |
CN110650960B (zh) * | 2018-04-26 | 2021-08-24 | 苏州科睿思制药有限公司 | Acalabrutinib的新晶型及其制备方法和用途 |
EP3587421A1 (en) | 2018-06-29 | 2020-01-01 | Sandoz AG | Crystalline forms of (s)-4-(8-amino-3-(1-(but-2-ynoyl)pyrrolidin-2-yl)imidazo[1,5-alpha]pyrazin-1-yl-n-(pyridin-2-yl)benzamide |
BR112021003480A2 (pt) | 2018-08-29 | 2021-05-18 | Acerta Pharma B.V. | processos para a preparação de 4-{8-amino-3-[(2s)-1-(but-2-inoil)-pirrolidin-2-il]imidazo[1,5-a]-pirazin-1-il}-n-(piridin-2-il)-benzamida |
WO2020053795A2 (en) | 2018-09-13 | 2020-03-19 | Fresenius Kabi Oncology Ltd. | Process for the preparation of acalabrutinib and its intermediates |
US20220002302A1 (en) * | 2018-09-25 | 2022-01-06 | Cipla Limited | Novel polymorphs of acalabrutinib, a bruton's tyrosine kinase inhibitor |
US20220153744A1 (en) | 2019-03-27 | 2022-05-19 | Assia Chemical Industries Ltd. | Solid state forms of acalabrutinib |
WO2020225831A1 (en) * | 2019-05-09 | 2020-11-12 | Msn Laboratories Private Limited, R&D Center | Improved process for the preparation of 4-{8-amino-3-[(2s)-1-(but-2-ynoyl)pyrrolidin-2-yl] imidazo[1,5-a]pyrazin-1-yl)}-n-(pyridine-2-yl)benzamide |
WO2021135346A1 (zh) * | 2019-12-31 | 2021-07-08 | 苏州科睿思制药有限公司 | Acalabrutinib的新晶型及其制备方法和用途 |
WO2021239893A1 (en) | 2020-05-29 | 2021-12-02 | Bend Research, Inc. | Amorphous solid dispersion of acalabrutinib |
CN115916161A (zh) * | 2020-06-19 | 2023-04-04 | 安塞塔制药公司 | 阿卡拉布替尼马来酸盐剂型 |
CN112028896A (zh) * | 2020-10-14 | 2020-12-04 | 奥锐特药业(天津)有限公司 | 阿卡替尼的新晶型及其制备方法 |
WO2022153330A1 (en) * | 2021-01-13 | 2022-07-21 | Natco Pharma Limited | Pharmaceutical compositions comprising acalabrutinib |
WO2023014817A1 (en) | 2021-08-03 | 2023-02-09 | Syros Pharmaceuticals, Inc. | Compositions and methods for treating lymphomas with a cdk7 inhibitor in combination with a btk inhibitor |
WO2023205279A1 (en) * | 2022-04-19 | 2023-10-26 | The Johns Hopkins University | Improved raman spectroscopy with the addition of aromatic compounds |
WO2024164066A1 (en) * | 2023-02-09 | 2024-08-15 | Apotex Inc | Crystalline forms of acalabrutinib maleate |
Family Cites Families (48)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001081031A (ja) | 1999-08-30 | 2001-03-27 | Schering Ag | 溶解性および経口吸収性を改善したベンズアミド誘導体含有製剤 |
US6921763B2 (en) | 1999-09-17 | 2005-07-26 | Abbott Laboratories | Pyrazolopyrimidines as therapeutic agents |
CZ2002934A3 (cs) | 1999-09-17 | 2002-07-17 | Abbott Gmbh & Co. Kg | Inhibitory kinázy jako terapeutická činidla |
US6998391B2 (en) | 2002-02-07 | 2006-02-14 | Supergen.Inc. | Method for treating diseases associated with abnormal kinase activity |
WO2005037836A2 (en) | 2003-10-15 | 2005-04-28 | Osi Pharmaceuticals, Inc. | Imidazo ‘1, 5 - a ! pyrazine tyrosine kinase inhibitors |
DK1740591T3 (da) | 2004-04-02 | 2009-10-26 | Osi Pharm Inc | Heterobicykliske proteinkinaseinhibitorer substitueret med en 6,6-biocyclisk ring |
ITMI20051231A1 (it) | 2005-06-29 | 2006-12-30 | Pharmaproducts Uk Ltd | Formulazioni farmaceutiche contenenti colostro e calcio folinato per il trattamento delle affezioni del cavo orale |
JP5269595B2 (ja) | 2005-09-09 | 2013-08-21 | アンジェリーニ ラボファーム リミテッド ライアビリティ カンパニー | 1日1回投与用トラゾドン組成物 |
EP1951724B1 (en) | 2005-11-17 | 2011-04-27 | OSI Pharmaceuticals, Inc. | FUSED BICYCLIC mTOR INHIBITORS |
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 |
WO2007106503A2 (en) | 2006-03-13 | 2007-09-20 | Osi Pharmaceuticals, Inc. | Combined treatment with an egfr kinase inhibitor and an agent that sensitizes tumor cells to the effects of egfr kinase inhibitors |
EP2201840B1 (en) | 2006-09-22 | 2011-11-02 | Pharmacyclics, Inc. | Inhibitors of Bruton's Tyrosine Kinase |
US20120101114A1 (en) | 2007-03-28 | 2012-04-26 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
EP2954900A1 (en) | 2007-03-28 | 2015-12-16 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
US8088824B2 (en) * | 2007-08-15 | 2012-01-03 | Reata Pharmaceuticals Inc. | Forms of CDDO methyl ester |
CA2708149A1 (en) | 2007-12-13 | 2009-06-18 | Novartis Ag | Combinations of therapeutic agents for treating cancer |
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 |
US8299077B2 (en) | 2009-03-02 | 2012-10-30 | Roche Palo Alto Llc | Inhibitors of Bruton's tyrosine kinase |
EP2424368B1 (en) | 2009-04-29 | 2014-12-31 | Locus Pharmaceuticals, Inc. | Pyrrolotriazine compounds |
RU2560162C2 (ru) | 2010-02-08 | 2015-08-20 | Мерк Шарп и Доум Б.В. | СОЕДИНЕНИЯ 8-МЕТИЛ-1-ФЕНИЛИМИДАЗО[1, 5-а]ПИРАЗИНА |
CN102190594A (zh) * | 2010-03-17 | 2011-09-21 | 上海医药工业研究院 | 阿戈美拉汀氯化氢水合物及其制备方法 |
UY33288A (es) | 2010-03-25 | 2011-10-31 | Glaxosmithkline Llc | Derivados de indolina inhibidores de la proteina quinasa r del reticulo endoplasmatico |
MY189483A (en) | 2010-05-31 | 2022-02-16 | Ono Pharmaceutical Co | Purinone derivative |
CA3113343A1 (en) | 2010-06-03 | 2011-12-08 | Pharmacyclics Llc | Use of inhibitors of bruton's tyrosine kinase (btk) in the treatment of follicular lymphoma |
US20120053189A1 (en) | 2010-06-28 | 2012-03-01 | Pharmacyclics, Inc. | Btk inhibitors for the treatment of immune mediated conditions |
JP6068451B2 (ja) | 2011-05-17 | 2017-01-25 | ザ・リージエンツ・オブ・ザ・ユニバーシテイ・オブ・カリフオルニア | キナーゼ阻害剤 |
EP2726077A4 (en) | 2011-06-28 | 2014-12-10 | Pharmacyclics Inc | METHODS AND COMPOSITIONS FOR INHIBITING BONE RESORPTION |
AU2012283775A1 (en) | 2011-07-13 | 2014-01-23 | Pharmacyclics Llc | Inhibitors of Bruton's tyrosine kinase |
CA2841887A1 (en) | 2011-07-19 | 2013-01-24 | Merck Sharp & Dohme B.V. | 4-imidazopyridazin-1-yl-benzamides and 4-imidazotriazin-1-yl-benzamides as btk - inhibitors |
US9290504B2 (en) * | 2011-07-19 | 2016-03-22 | Merck Sharp & Dohme B.V. | 4-imidazopyridazin-1-yl-benzamides and 4-imidazotriazin-1-yl-benzamides as Btk inhibitors |
EP2548877A1 (en) * | 2011-07-19 | 2013-01-23 | MSD Oss B.V. | 4-(5-Membered fused pyridinyl)benzamides as BTK-inhibitors |
MX361772B (es) | 2011-10-19 | 2018-12-17 | Pharmacyclics Llc | Uso de inhibidores de la tirosina cinasa de bruton (btk). |
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 |
NZ703124A (en) * | 2012-05-23 | 2016-07-29 | Nerviano Medical Sciences Srl | Process for the preparation of n-[5-(3,5-difluoro-benzyl)-1h-indazol-3-yl]-4-(4-methyl-piperazin-1-yl)-2-(tetrahydro-pyran-4-ylamino)-benzamide |
US20140206681A1 (en) | 2013-01-23 | 2014-07-24 | Ronald M. Kim | Btk inhibitors |
CN105073115A (zh) | 2013-03-14 | 2015-11-18 | 药品循环有限责任公司 | 布鲁顿氏酪氨酸激酶抑制剂和cyp3a4抑制剂的组合 |
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 |
MX2015014171A (es) | 2013-04-08 | 2015-12-16 | Bayer Pharma AG | Uso de 2,3-dihidroimidazo[1,2-c]quinazolinas sustituidas. |
EP2983670A4 (en) | 2013-04-08 | 2017-03-08 | Pharmacyclics LLC | Ibrutinib combination therapy |
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) |
WO2015057992A1 (en) * | 2013-10-16 | 2015-04-23 | Izumi Raquel | Btk inhibitors for hematopoietic mobilization |
WO2015083008A1 (en) | 2013-12-05 | 2015-06-11 | Acerta Pharma B.V. | Therapeutic combination of a pi3k inhibitor and a btk inhibitor |
WO2015086642A1 (en) | 2013-12-13 | 2015-06-18 | F. Hoffmann-La Roche Ag | Inhibitors of bruton's tyrosine kinase |
WO2015110923A2 (en) | 2014-01-21 | 2015-07-30 | Acerta Pharma B.V. | Methods of treating chronic lymphocytic leukemia and small lymphocytic leukemia usng a btk inhibitor |
FR3021783B1 (fr) | 2014-06-02 | 2016-05-13 | Morpho | Procede de validation de l'authenticite d'un element du corps humain |
KR102688052B1 (ko) | 2015-07-02 | 2024-07-25 | 아세르타 파마. 비.브이. | (S)-4-(8-아미노-3-(1-(부트-2-이노일)피롤리딘-2-일)이미다조[1,5-a]피라진-1-일)-N-(피리딘-2-일)벤즈아마이드의 고체 형태 및 제제 |
-
2016
- 2016-07-01 KR KR1020187003310A patent/KR102688052B1/ko active IP Right Grant
- 2016-07-01 EP EP23157244.7A patent/EP4209493A1/en active Pending
- 2016-07-01 SI SI201631705T patent/SI3954690T1/sl unknown
- 2016-07-01 PL PL21182842.1T patent/PL3954690T3/pl unknown
- 2016-07-01 RS RS20211291A patent/RS62455B1/sr unknown
- 2016-07-01 LT LTEP16735945.4T patent/LT3317281T/lt unknown
- 2016-07-01 SG SG10201913796UA patent/SG10201913796UA/en unknown
- 2016-07-01 IL IL274066A patent/IL274066B/en unknown
- 2016-07-01 US US15/200,875 patent/US9796721B2/en active Active
- 2016-07-01 PT PT211828421T patent/PT3954690T/pt unknown
- 2016-07-01 MA MA50817A patent/MA50817B1/fr unknown
- 2016-07-01 EP EP19196939.3A patent/EP3613745B1/en active Active
- 2016-07-01 DK DK19196939.3T patent/DK3613745T3/da active
- 2016-07-01 HU HUE21182842A patent/HUE062258T2/hu unknown
- 2016-07-01 EP EP21182842.1A patent/EP3954690B1/en active Active
- 2016-07-01 MX MX2020014163A patent/MX2020014163A/es unknown
- 2016-07-01 MX MX2018000179A patent/MX2018000179A/es unknown
- 2016-07-01 PT PT167359454T patent/PT3317281T/pt unknown
- 2016-07-01 PL PL19196939T patent/PL3613745T3/pl unknown
- 2016-07-01 EP EP16735945.4A patent/EP3317281B1/en active Active
- 2016-07-01 ES ES21182842T patent/ES2946489T3/es active Active
- 2016-07-01 LT LTEP19196939.3T patent/LT3613745T/lt unknown
- 2016-07-01 PT PT191969393T patent/PT3613745T/pt unknown
- 2016-07-01 WO PCT/IB2016/053988 patent/WO2017002095A1/en active Application Filing
- 2016-07-01 LT LTEP21182842.1T patent/LT3954690T/lt unknown
- 2016-07-01 HU HUE16735945A patent/HUE049989T2/hu unknown
- 2016-07-01 CN CN201680050713.6A patent/CN108349978B/zh active Active
- 2016-07-01 RS RS20230367A patent/RS64195B1/sr unknown
- 2016-07-01 FI FIEP21182842.1T patent/FI3954690T3/fi active
- 2016-07-01 JP JP2017568182A patent/JP6829215B2/ja active Active
- 2016-07-01 AU AU2016286548A patent/AU2016286548B2/en active Active
- 2016-07-01 ES ES16735945T patent/ES2797987T3/es active Active
- 2016-07-01 MY MYPI2017001918A patent/MY193514A/en unknown
- 2016-07-01 RU RU2018103913A patent/RU2018103913A/ru unknown
- 2016-07-01 SI SI201631364T patent/SI3613745T1/sl unknown
- 2016-07-01 RS RS20200681A patent/RS60411B1/sr unknown
- 2016-07-01 DK DK21182842.1T patent/DK3954690T3/da active
- 2016-07-01 HR HRP20230417TT patent/HRP20230417T1/hr unknown
- 2016-07-01 SI SI201630805T patent/SI3317281T1/sl unknown
- 2016-07-01 PL PL16735945T patent/PL3317281T3/pl unknown
- 2016-07-01 CN CN202110761102.5A patent/CN113480542A/zh active Pending
- 2016-07-01 ES ES19196939T patent/ES2895802T3/es active Active
- 2016-07-01 KR KR1020247024480A patent/KR20240115937A/ko active Search and Examination
- 2016-07-01 HR HRP20211511TT patent/HRP20211511T1/hr unknown
- 2016-07-01 IL IL293821A patent/IL293821A/en unknown
- 2016-07-01 DK DK16735945.4T patent/DK3317281T3/da active
- 2016-07-01 HU HUE19196939A patent/HUE056008T2/hu unknown
- 2016-07-01 CA CA2991096A patent/CA2991096A1/en active Pending
- 2016-07-01 MD MDE20180479T patent/MD3317281T2/ro unknown
-
2017
- 2017-09-18 US US15/707,508 patent/US10167291B2/en active Active
- 2017-12-28 CL CL2017003445A patent/CL2017003445A1/es unknown
- 2017-12-28 IL IL256633A patent/IL256633B/en active IP Right Grant
-
2018
- 2018-01-17 ZA ZA2018/00329A patent/ZA201800329B/en unknown
- 2018-07-31 HK HK18109886.8A patent/HK1250511A1/zh unknown
- 2018-11-01 US US16/177,927 patent/US10640509B2/en active Active
-
2020
- 2020-01-16 ZA ZA2020/00300A patent/ZA202000300B/en unknown
- 2020-04-30 US US16/863,033 patent/US11059829B2/en active Active
- 2020-06-10 HR HRP20200934TT patent/HRP20200934T1/hr unknown
- 2020-07-02 CY CY20201100611T patent/CY1124519T1/el unknown
- 2020-11-24 AU AU2020277123A patent/AU2020277123B2/en active Active
-
2021
- 2021-01-21 JP JP2021007689A patent/JP7091494B2/ja active Active
- 2021-06-10 US US17/344,233 patent/US20220177476A1/en not_active Abandoned
- 2021-10-19 CY CY20211100904T patent/CY1124815T1/el unknown
-
2022
- 2022-01-27 US US17/586,726 patent/US11820777B2/en active Active
- 2022-06-15 JP JP2022096907A patent/JP2022120156A/ja active Pending
- 2022-12-23 AU AU2022291635A patent/AU2022291635B2/en active Active
-
2023
- 2023-06-01 CY CY20231100260T patent/CY1126103T1/el unknown
- 2023-10-16 US US18/487,254 patent/US20240199622A1/en active Pending
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CL2017003445A1 (es) | Formas solidas y formulaciones de compuestos de imidazopirazina. | |
CO2017005483A2 (es) | Forma cristalina de sulfato de hidrógeno de (s)-n-(5-((r)-2-(2,5-difluorofenil)-pirrolidin-1- il)-pirazol[1,5-a]pirimidin-3-il)-3-hidroxipirrolidina-1-carboxamida | |
CL2017003496A1 (es) | Formas cristalinas de un inhibidor de tirosina quinasa de bruton. | |
TR201904455T4 (tr) | Nükleer taşıma modülatörleri olarak 1,2,4-triazoller ve bunların kullanımları. | |
NZ708593A (en) | Novel pyrazole derivative | |
ECSP16005566A (es) | Sulfonamidas como moduladores de canales de sodio | |
CL2012000059A1 (es) | Compuestos derivados de pirazolo[1,5-a]pirimidina; proceso de preparacion; composicion farmaceutica que los comprende; y su uso como inhbidores de trk-quinasa para el tratamiento de enfermedades o trastornos tales como dolor, cancer, inflamacion; entre otras. | |
DOP2014000008A (es) | 4-imidazopiridazina-1-il-benzamidas y 4-imidazotriazina-1-il-benzamidas como inhibidores de btk | |
DOP2013000105A (es) | Derivados de 2,3-dihidroimidazo[1,2-c]quinazolina sustituidos con aminoalcoholes que son de utilidad para tratar trastornos hiperproliferativos y enfermedades asociadas a la angiogénesis | |
EA201591541A1 (ru) | Ингибиторы бета-секретазы 1 (bace 1) | |
EA201492216A1 (ru) | Ингибиторы бромодомена и их применение | |
EA201291310A1 (ru) | Композиция ингибитора jak для местного применения | |
EA201591804A1 (ru) | Производные 2-((4-амино-3-(3-фтор-5-гидроксифенил)-1h-пиразоло[3,4-d]пиримидин-1-ил)метил)-3-(2-(трифторметил)бензил)хиназолин-4(3h)-она и их применение в качестве ингибиторов фосфоинозитид-3-киназы | |
BR112015000229A2 (pt) | formulações aquosas estáveis de etanercept | |
CU24330B1 (es) | Derivados del ácido 4-((1,1) bifenil-4-il)-3-(3-fosfonopropanamido) butanoico, activos como inhibidores de nep (endopeptidasa neutral) | |
GT200500026A (es) | Derivados de beta-aminoacidos como inhibidores del factor xa. | |
EA201492097A1 (ru) | 5-амино[1,4]тиазины в качестве ингибиторов бета-секретазы 1 | |
PA8589601A1 (es) | Derivados de indazol como antagonistas del crf | |
CU20170086A7 (es) | Pirazolpiridinaminas como inhibidores de mknk1 y mknk2 | |
EA201590066A1 (ru) | Дифторгексагидроциклопентаоксазинилы и дифторгексагидробензоксазинилы в качестве ингибиторов бета-секретазы 1 | |
EA201891319A1 (ru) | Соединения алкилдигидрохинолинсульфонамида | |
EA201490045A1 (ru) | Дейтерированные 1-пиперазино-3-фенилинданы, применяемые для лечения шизофрении | |
PE20211391A1 (es) | Procedimiento para la preparacion de (3s)-3-(4-cloro-3-{[(2s,3r)-2-(4-clorofenil)-4,4,4-trifluor-3-metilbutanoil]amino}fenil)-3-acido ciclopropilpropanoico y su forma cristalina para uso como principio activo farmaceutico | |
BR112019007591A2 (pt) | inibidores de bromodomínios | |
CL2008002060A1 (es) | Compuestos derivados de sulfonamida, inhibidores de la produccion de beta amiloide; metodo de preparacion; composicion farmaceutica; kit farmaceutico; y uso en el tratamiento de enfermedades tales como alzheimer, angiopatia amiloide, sindrome de down, entre otras. |