IN2012DN03012A - - Google Patents
Download PDFInfo
- Publication number
- IN2012DN03012A IN2012DN03012A IN3012DEN2012A IN2012DN03012A IN 2012DN03012 A IN2012DN03012 A IN 2012DN03012A IN 3012DEN2012 A IN3012DEN2012 A IN 3012DEN2012A IN 2012DN03012 A IN2012DN03012 A IN 2012DN03012A
- Authority
- IN
- India
- Prior art keywords
- methods
- inhibitors
- kinase
- assays
- synthesizing
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 abstract 3
- 238000000034 method Methods 0.000 abstract 3
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 238000003556 assay Methods 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 229940043355 kinase inhibitor Drugs 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 abstract 1
- 102000004169 proteins and genes Human genes 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
- 230000002194 synthesizing effect Effects 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
- A61K31/505—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
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- 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
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- 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
- 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
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
-
- 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
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
- 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
- C07D401/02—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Pulmonology (AREA)
- Pain & Pain Management (AREA)
- Transplantation (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Abstract
Described herein are kinase inhibitor compounds, methods for synthesizing such inhibitors, and methods for using such inhibitors in the treatment of diseases. Further described herein are methods, assays and systems for determining an appropriate inhibitor of a protein, including a kinase.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25078709P | 2009-10-12 | 2009-10-12 | |
| US12/581,044 US7718662B1 (en) | 2009-10-12 | 2009-10-16 | Pyrazolo-pyrimidine inhibitors of bruton's tyrosine kinase |
| US12/581,062 US7741330B1 (en) | 2009-10-12 | 2009-10-16 | Pyrazolo-pyrimidine inhibitors of Bruton's tyrosine kinase |
| PCT/US2010/052377 WO2011046964A2 (en) | 2009-10-12 | 2010-10-12 | Inhibitors of bruton's tyrosine kinase |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IN2012DN03012A true IN2012DN03012A (en) | 2015-07-31 |
Family
ID=42166572
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IN3012DEN2012 IN2012DN03012A (en) | 2009-10-12 | 2010-10-12 |
Country Status (21)
| Country | Link |
|---|---|
| US (4) | US7718662B1 (en) |
| EP (2) | EP2393816A4 (en) |
| JP (2) | JP5717109B2 (en) |
| KR (1) | KR20120097376A (en) |
| CN (1) | CN102656173B (en) |
| AU (1) | AU2010306921C1 (en) |
| BR (1) | BR112012008624A2 (en) |
| CA (1) | CA2776543A1 (en) |
| CL (1) | CL2012000917A1 (en) |
| CO (1) | CO6531429A2 (en) |
| CR (1) | CR20120244A (en) |
| EA (1) | EA021715B1 (en) |
| ES (1) | ES2590905T3 (en) |
| IL (1) | IL219076A (en) |
| IN (1) | IN2012DN03012A (en) |
| MX (1) | MX2012004258A (en) |
| NZ (1) | NZ599396A (en) |
| PH (1) | PH12012500712A1 (en) |
| SG (1) | SG10201506776RA (en) |
| WO (1) | WO2011046964A2 (en) |
| ZA (1) | ZA201202552B (en) |
Families Citing this family (142)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL2526934T4 (en) | 2006-09-22 | 2016-09-30 | Bruton tyrosine kinase inhibitors | |
| US8809273B2 (en) | 2007-03-28 | 2014-08-19 | Pharmacyclics, Inc. | Inhibitors of Bruton's tyrosine kinase |
| US20100101977A1 (en) * | 2008-06-05 | 2010-04-29 | United Comb & Novelty Corporation | Stackable Packaging For Lipped Containers |
| US11351168B1 (en) | 2008-06-27 | 2022-06-07 | Celgene Car Llc | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
| AU2009262068C1 (en) | 2008-06-27 | 2015-07-02 | Celgene Car Llc | Heteroaryl compounds and uses thereof |
| US8338439B2 (en) | 2008-06-27 | 2012-12-25 | Celgene Avilomics Research, Inc. | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
| EP3311818A3 (en) * | 2008-07-16 | 2018-07-18 | Pharmacyclics, LLC | Inhibitors of bruton's tyrosine kinase for the treatment of solid tumors |
| CN102482277B (en) | 2009-05-05 | 2017-09-19 | 达纳-法伯癌症研究所有限公司 | Epidermal growth factor receptor inhibitors and methods of treating disorders |
| US7718662B1 (en) * | 2009-10-12 | 2010-05-18 | Pharmacyclics, Inc. | Pyrazolo-pyrimidine inhibitors of bruton's tyrosine kinase |
| EP2575818A4 (en) | 2010-06-03 | 2013-11-06 | Pharmacyclics Inc | USE OF INHIBITORS OF BRUTON TYROSINE KINASE (BTK) |
| WO2012003544A1 (en) * | 2010-07-09 | 2012-01-12 | The Walter And Eliza Hall Institute Of Medical Research | Protein kinase inhibitors and methods of treatment |
| RU2013109393A (en) | 2010-08-10 | 2014-09-20 | Сэлджин Авиаломикс Ресеарч, Инк. | BTK INHIBITOR SALT |
| CA2815858C (en) | 2010-11-01 | 2018-10-16 | Celgene Avilomics Research, Inc. | Heterocyclic compounds and uses thereof |
| WO2012061303A1 (en) | 2010-11-01 | 2012-05-10 | Avila Therapeutics, Inc. | Heteroaryl compounds and uses thereof |
| JP5957003B2 (en) | 2010-11-10 | 2016-07-27 | セルジーン アヴィロミクス リサーチ, インコーポレイテッド | Mutant selective EGFR inhibitor and use thereof |
| PT2693881T (en) | 2011-04-01 | 2019-12-09 | Univ Utah Res Found | Substituted n-phenylpyrimidin-2-amine analogs as inhibitors of the axl kinase |
| CN103889962B (en) * | 2011-04-01 | 2017-05-03 | 犹他大学研究基金会 | Substituted n-(3-(pyrimidin-4-yl)phenyl)acrylamide analogs as tyrosine receptor kinase BTK inhibitors |
| JP6068451B2 (en) * | 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 | Kinase inhibitor |
| PL2710005T3 (en) | 2011-05-17 | 2017-07-31 | Principia Biopharma Inc. | Tyrosine kinase inhibitors |
| WO2012158795A1 (en) * | 2011-05-17 | 2012-11-22 | Principia Biopharma Inc. | Pyrazolopyrimidine derivatives as tyrosine kinase inhibitors |
| CA2840413A1 (en) * | 2011-06-28 | 2013-01-03 | Pharmacyclics, Inc. | Methods and compositions for inhibition of bone resorption |
| BR112014000653A2 (en) * | 2011-07-13 | 2017-02-14 | Pharmacyclics Inc | bruton tyrosine kinase inhibitors |
| US9416132B2 (en) | 2011-07-21 | 2016-08-16 | Tolero Pharmaceuticals, Inc. | Substituted imidazo[1,2-b]pyridazines as protein kinase inhibitors |
| TW201325593A (en) | 2011-10-28 | 2013-07-01 | Celgene Avilomics Res Inc | Methods of treating a BRUTON'S tyrosine kinase disease or disorder |
| 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 |
| TW201336847A (en) * | 2012-02-07 | 2013-09-16 | Taiho Pharmaceutical Co Ltd | Quinolyl pyrrolopyrimidine compound or salt thereof |
| TWI496783B (en) * | 2012-02-23 | 2015-08-21 | Taiho Pharmaceutical Co Ltd | Quinolylpyrrolopyrimidine condensed cyclic compounds or salts |
| EP2825042B1 (en) | 2012-03-15 | 2018-08-01 | Celgene CAR LLC | Salts of an epidermal growth factor receptor kinase inhibitor |
| KR102081042B1 (en) | 2012-03-15 | 2020-02-26 | 셀젠 카르 엘엘씨 | Solid forms of an epidermal growth factor receptor kinase inhibitor |
| US9522917B2 (en) | 2012-04-11 | 2016-12-20 | Acerta Pharma B.V. | Bruton's tyrosine kinase inhibitors for hematopoietic mobilization |
| WO2013157021A1 (en) | 2012-04-20 | 2013-10-24 | Advinus Therapeutics Limited | Bicyclic compounds, compositions and medicinal applications thereof |
| EP2838898B1 (en) | 2012-04-20 | 2017-01-18 | Advinus Therapeutics Limited | Substituted hetero-bicyclic compounds, compositions and medicinal applications thereof |
| CA2874211A1 (en) * | 2012-05-31 | 2013-12-05 | Pharmascience Inc. | Protein kinase inhibitors |
| US9296753B2 (en) | 2012-06-04 | 2016-03-29 | Pharmacyclics Llc | Crystalline forms of a Bruton's tyrosine kinase inhibitor |
| EP3550031A1 (en) | 2012-07-24 | 2019-10-09 | Pharmacyclics, LLC | Mutations associated with resistance to inhibitors of bruton's tyrosine kinase (btk) |
| KR102203990B1 (en) | 2012-09-10 | 2021-01-18 | 프린시피아 바이오파마, 인코퍼레이티드 | Pyrazolopyrimidine compounds as kinase inhibitors |
| JP6313772B2 (en) | 2012-10-04 | 2018-04-18 | ユニヴァーシティー オブ ユタ リサーチ ファウンデーション | Substituted N- (3- (pyrimidin-4-yl) phenyl) acrylamide analogs that are tyrosine receptor kinase BTK inhibitors |
| KR102194611B1 (en) | 2012-10-04 | 2020-12-23 | 유니버시티 오브 유타 리서치 파운데이션 | Substituted n-(3-(pyrimidin-4-yl)phenyl)acrylamide analogs as tyrosine receptor kinase btk inhibitors |
| MX2015006168A (en) | 2012-11-15 | 2015-08-10 | Pharmacyclics Inc | Pyrrolopyrimidine compounds as kinase inhibitors. |
| CN103848810A (en) * | 2012-11-30 | 2014-06-11 | 北京赛林泰医药技术有限公司 | Bruton's tyrosine kinases inhibitor |
| WO2014100748A1 (en) | 2012-12-21 | 2014-06-26 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| EP2953457B1 (en) | 2013-02-08 | 2020-04-08 | Celgene CAR LLC | Erk inhibitors and uses thereof |
| BR112015018222A2 (en) * | 2013-02-22 | 2017-07-18 | Taiho Pharmaceutical Co Ltd | method for producing a tricyclic compound, and tricyclic compound which may be produced by said production method |
| KR20210149232A (en) | 2013-03-14 | 2021-12-08 | 스미토모 다이니폰 파마 온콜로지, 인크. | Jak2 and alk2 inhibitors and methods for their use |
| JP6777398B2 (en) * | 2013-03-15 | 2020-10-28 | ヤンセン ファーマシューティカ エヌ.ベー. | Methods and intermediates for preparing drugs |
| WO2014152114A1 (en) * | 2013-03-15 | 2014-09-25 | Boehringer Ingelheim International Gmbh | Heteroaromatic compounds as btk inhibitors |
| WO2014168986A1 (en) | 2013-04-08 | 2014-10-16 | Brown Dennis M | Therapeutic benefit of suboptimally administered chemical compounds |
| US8957080B2 (en) | 2013-04-09 | 2015-02-17 | Principia Biopharma Inc. | Tyrosine kinase inhibitors |
| KR101793807B1 (en) | 2013-04-25 | 2017-11-03 | 베이진 엘티디 | Fused heterocyclic compounds as protein kinase inhibitors |
| GB201309085D0 (en) | 2013-05-20 | 2013-07-03 | Redx Pharma Ltd | Compounds |
| CN105764502A (en) | 2013-07-26 | 2016-07-13 | 现代化制药公司 | Combination methods for improving the therapeutic benefit of bisantrene and analogs and derivatives thereof |
| EP3027192A4 (en) | 2013-08-02 | 2017-03-22 | Pharmacyclics, LLC | Methods for the treatment of solid tumors |
| EP3033079B1 (en) | 2013-08-12 | 2018-10-31 | Pharmacyclics LLC | Methods for the treatment of her2 amplified cancer |
| RU2689158C2 (en) * | 2013-08-22 | 2019-05-24 | Тайхо Фармасьютикал Ко., Лтд. | Novel quinoline-substituted compound |
| EP3508204A1 (en) | 2013-08-23 | 2019-07-10 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| US9492471B2 (en) | 2013-08-27 | 2016-11-15 | Celgene Avilomics Research, Inc. | Methods of treating a disease or disorder associated with Bruton'S Tyrosine Kinase |
| BR112016005408B1 (en) | 2013-09-13 | 2023-03-21 | Beigene Switzerland Gmbh | ANTI-PD1, F(AB) OR F(AB)2 ANTIBODIES AND REFERRED USE ANTIBODY FOR TREATMENT OF CANCER OR VIRAL INFECTION |
| JP2016531941A (en) | 2013-09-30 | 2016-10-13 | ファーマサイクリックス エルエルシー | Inhibitor of breton-type tyrosine kinase |
| WO2015057992A1 (en) | 2013-10-16 | 2015-04-23 | Izumi Raquel | Btk inhibitors for hematopoietic mobilization |
| RU2653504C2 (en) * | 2013-12-13 | 2018-05-10 | Ф. Хоффманн-Ля Рош Аг | Bruton's tyrosine kinase inhibitors |
| US9415049B2 (en) | 2013-12-20 | 2016-08-16 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| AU2015225745B2 (en) * | 2014-02-03 | 2017-04-20 | Cadila Healthcare Limited | Heterocyclic compounds |
| BR112016018948B1 (en) | 2014-02-21 | 2023-01-17 | Principia Biopharma Inc | USE OF COMPOUND OR PHARMACEUTICALLY ACCEPTABLE SALT, SULFONIC ACID OR CARBOXYLIC ACID SALT OF COMPOUND, AMORPHOUS FORM OF PHARMACEUTICALLY ACCEPTABLE SALT OF COMPOUND, PHARMACEUTICAL COMPOSITION AND USE THEREOF |
| JP2017509336A (en) | 2014-03-20 | 2017-04-06 | ファーマサイクリックス エルエルシー | Mutations associated with phospholipase C gamma 2 and resistance |
| WO2015181633A2 (en) | 2014-04-11 | 2015-12-03 | Acerta Pharma B.V. | Methods of blocking the cxcr-4/sdf-1 signaling pathway with inhibitors of bruton's tyrosine kinase |
| EP3134418A4 (en) | 2014-04-23 | 2018-01-03 | The Research Foundation for The State University of New York | A rapid and efficient bioorthogonal ligation reaction and boron-containing heterocycles useful in conjuction therewith |
| CN105017256A (en) * | 2014-04-29 | 2015-11-04 | 浙江导明医药科技有限公司 | Polyfluorinated compound Bruton tyrosine kinase inhibitor |
| CN106458919B (en) * | 2014-05-13 | 2019-03-15 | 广东东阳光药业有限公司 | A kind of preparation method of intermediate |
| CN104086551B (en) * | 2014-06-06 | 2016-09-21 | 人福医药集团股份公司 | Compound and its production and use |
| GB201410430D0 (en) | 2014-06-11 | 2014-07-23 | Redx Pharma Ltd | Compounds |
| KR102130600B1 (en) | 2014-07-03 | 2020-07-08 | 베이진 엘티디 | Anti-PD-L1 Antibodies and Their Use as Therapeutics and Diagnostics |
| WO2016019233A1 (en) | 2014-08-01 | 2016-02-04 | Pharmacyclics Llc | Inhibitors of bruton's tyrosine kinase |
| EP3193877A4 (en) | 2014-08-07 | 2018-04-04 | Pharmacyclics LLC | Novel formulations of a bruton's tyrosine kinase inhibitor |
| WO2016025561A1 (en) | 2014-08-13 | 2016-02-18 | Celgene Avilomics Research, Inc. | Forms and compositions of an erk inhibitor |
| WO2016050422A1 (en) * | 2014-10-01 | 2016-04-07 | Ratiopharm Gmbh | Acid addition salt of ibrutinib |
| TW201702218A (en) | 2014-12-12 | 2017-01-16 | 美國杰克森實驗室 | Compositions and methods relating to the treatment of cancer, autoimmune disease, and neurodegenerative disease |
| EA036269B1 (en) | 2014-12-18 | 2020-10-21 | Принсипиа Биофарма Инк. | Treatment of pemphigus |
| EP3042903B1 (en) | 2015-01-06 | 2019-08-14 | Impetis Biosciences Ltd. | Substituted hetero-bicyclic compounds, compositions and medicinal applications thereof |
| MA41350A (en) * | 2015-01-14 | 2017-11-21 | Janssen Pharmaceutica Nv | SUMMARY OF A BRUTON TYROSINE KINASE INHIBITOR |
| CN105481862B (en) * | 2015-01-21 | 2018-08-21 | 中国科学院合肥物质科学研究院 | novel inhibitors of F L T3 kinase and uses thereof |
| WO2016115869A1 (en) * | 2015-01-21 | 2016-07-28 | 中国科学院合肥物质科学研究院 | Novel inhibitor of flt3 kinase and use thereof |
| CN105859721B (en) * | 2015-01-22 | 2018-04-17 | 浙江京新药业股份有限公司 | A kind of Yi Bulu replaces the preparation method of Buddhist nun |
| CN107207519B (en) * | 2015-02-12 | 2019-11-08 | 正大天晴药业集团股份有限公司 | The preparation method of ibrutinib |
| CN107613769A (en) | 2015-02-17 | 2018-01-19 | 润新生物公司 | Certain chemical entities, compositions and methods |
| IL315294A (en) | 2015-03-03 | 2024-10-01 | Pharmacyclics Llc | Pharmaceutical formulations of proton tyrosine kinase inhibitor |
| US10045990B2 (en) | 2015-03-04 | 2018-08-14 | Arizona Board Of Regents On Behalf Of Arizona State University | ERBB4 inhibitors and methods of use thereof |
| 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 |
| CN106146508A (en) * | 2015-03-19 | 2016-11-23 | 浙江导明医药科技有限公司 | The drug combination optimized and treatment cancer and the purposes of autoimmune disease thereof |
| CN106146516B (en) * | 2015-04-20 | 2019-02-15 | 北京睿创康泰医药研究院有限公司 | The preparation method of Buddhist nun's impurity of the drug is replaced according to Shandong |
| JP6646072B2 (en) * | 2015-06-03 | 2020-02-14 | プリンシピア バイオファーマ インコーポレイテッド | Tyrosine kinase inhibitor |
| US9394312B1 (en) * | 2015-06-14 | 2016-07-19 | Mark Quang Nguyen | Ibrutinib prodrugs, pharmaceutical compositions thereof, and methods of use |
| TW201718572A (en) | 2015-06-24 | 2017-06-01 | 普林斯匹亞生物製藥公司 | Tyrosine kinase inhibitors |
| CN108431007B (en) | 2015-09-16 | 2022-06-07 | 洛克索肿瘤学股份有限公司 | Pyrazolopyrimidine derivatives as BTK inhibitors for the treatment of cancer |
| MY202026A (en) | 2015-12-16 | 2024-03-29 | Loxo Oncology Inc | Compounds useful as kinase inhibitors |
| KR102687603B1 (en) | 2015-12-24 | 2024-07-24 | 다케다 야쿠힌 고교 가부시키가이샤 | Co-crystals, methods for their preparation, and medicines containing co-crystals |
| KR102688907B1 (en) * | 2016-01-05 | 2024-07-29 | 지앙수 헨그루이 파마슈티컬스 컴퍼니 리미티드 | Crystalline forms of BTK kinase inhibitors and methods for their preparation |
| JP7109365B2 (en) * | 2016-01-19 | 2022-07-29 | ヤンセン ファーマシューティカ エヌ.ベー. | Formulations/compositions containing BTK inhibitors |
| KR102699906B1 (en) * | 2016-01-21 | 2024-08-29 | 즈보 바이오폴라 창쉥 파마수티컬 컴퍼니 리미티드 | Bruton's tyrosine kinase inhibitor |
| US10793566B2 (en) | 2016-01-21 | 2020-10-06 | Zibo Biopolar Changsheng Pharmaceutical Co. Ltd. | Bruton's tyrosine kinase inhibitors |
| CN106995446B (en) * | 2016-01-22 | 2021-07-02 | 山东新时代药业有限公司 | Preparation method of Bruton's tyrosine kinase inhibitor |
| KR102416971B1 (en) | 2016-03-11 | 2022-07-04 | 엔젤 파마슈티칼 컴퍼니, 리미티드 | Compounds and methods for modulating Brutonian tyrosine kinases |
| CN111153906B (en) * | 2016-05-16 | 2020-09-11 | 苏州信诺维医药科技有限公司 | Pyrazolopyrimidine derivatives as BTK inhibitors, process for their preparation and pharmaceutical compositions containing them |
| KR102391693B1 (en) | 2016-06-29 | 2022-04-29 | 프린시피아 바이오파마, 인코퍼레이티드 | 2-[3-[4-amino-3-(2-fluoro-4-phenoxy-phenyl)pyrazolo[3,4-D]pyrimidin-1-yl]piperidine-1-carbonyl] Modified release formulation of -4-methyl-4-[4-(oxetan-3-yl)piperazin-1-yl]pent-2-ennitrile |
| US10864203B2 (en) | 2016-07-05 | 2020-12-15 | Beigene, Ltd. | Combination of a PD-1 antagonist and a RAF inhibitor for treating cancer |
| CN109843858B (en) * | 2016-08-15 | 2023-05-05 | 润新生物公司 | Certain chemical entities, compositions and methods |
| KR20250052473A (en) | 2016-08-16 | 2025-04-18 | 베이진 스위찰랜드 게엠베하 | (S)-7-(1-Acryloylpiperidin-4-yl)-2-(4-Phenoxyphenyl)-4,5,6,7-tetra-Hydrazolo[1,5-a]Pyrimidine-3-Carboxamide, Preparation, and Uses Thereof |
| HUE065528T2 (en) | 2016-08-19 | 2024-06-28 | Beigene Switzerland Gmbh | Combination of zanubrutinib with an anti-cd20 or an anti-pd-1 antibody for use in treating cancer |
| IL292938A (en) | 2016-09-19 | 2022-07-01 | Mei Pharma Inc | Combined treatment |
| JOP20190073A1 (en) | 2016-10-31 | 2019-04-07 | Taiho Pharmaceutical Co Ltd | Selective inhibitor of exon 20 insertion mutant egfr |
| JOP20190113A1 (en) * | 2016-11-18 | 2019-05-15 | Biocad Joint Stock Co | Inhibitors of bruton’s tyrosine kinase |
| US11590167B2 (en) | 2016-12-03 | 2023-02-28 | Juno Therapeutic, Inc. | Methods and compositions for use of therapeutic T cells in combination with kinase inhibitors |
| EP3573989A4 (en) | 2017-01-25 | 2020-11-18 | Beigene, Ltd. | CRYSTALLINE FORMS OF (S) -7- (1- (BUT-2-YNOYL) -PIPERIDINE-4-YL) -2- (4-PHENOXYPHENYL) -4,5,6,7-TETRAHYDROPYRAZOLO [1,5-A ] PYRIMIDINE-3-CARBOXAMIDE, MANUFACTURING AND USES THEREOF |
| WO2018145280A1 (en) * | 2017-02-09 | 2018-08-16 | 合肥合源药业有限公司 | Flt3 kinase inhibitor or crystal forms of salt thereof and preparation method therefor |
| KR102757960B1 (en) | 2017-06-26 | 2025-01-22 | 베이진 엘티디 | Immunotherapy for hepatocellular carcinoma (HCC) |
| WO2019034009A1 (en) | 2017-08-12 | 2019-02-21 | Beigene, Ltd. | Btk INHIBITORS WITH IMPROVED DUAL SELECTIVITY |
| AU2018325819B2 (en) | 2017-09-01 | 2024-02-01 | Taiho Pharmaceutical Co., Ltd. | Exon 18 and/or exon 21 mutant EGFR selective inhibitor |
| TW201922256A (en) | 2017-10-27 | 2019-06-16 | 中國大陸商浙江導明醫藥科技有限公司 | Methods for treating lymphoid malignancies |
| US11786529B2 (en) | 2017-11-29 | 2023-10-17 | Beigene Switzerland Gmbh | Treatment of indolent or aggressive B-cell lymphomas using a combination comprising BTK inhibitors |
| CN108191871B (en) * | 2018-01-02 | 2020-02-18 | 成都倍特药业有限公司 | Novel Bruton's tyrosine kinase inhibitor and preparation method and application thereof |
| EP3773591A4 (en) | 2018-04-05 | 2021-12-22 | Sumitomo Dainippon Pharma Oncology, Inc. | AXL KINASE INHIBITORS AND THEIR USES |
| US20210113562A1 (en) | 2018-04-13 | 2021-04-22 | Sumitomo Dainippon Pharma Oncology, Inc. | Pim kinase inhibitors for treatment of myeloproliferative neoplasms and fibrosis associated with cancer |
| AU2019310590A1 (en) | 2018-07-26 | 2021-01-14 | Sumitomo Pharma Oncology, Inc. | Methods for treating diseases associated with abnormal acvr1 expression and acvr1 inhibitors for use in the same |
| CN109134472B (en) * | 2018-09-20 | 2020-02-11 | 浙江理工大学 | Synthesis process of 3- (4-phenoxyphenyl) -1H-pyrazolo [3,4-d ] pyrimidine-4-amine |
| CN110964016B (en) * | 2018-09-29 | 2021-05-28 | 南京药捷安康生物科技有限公司 | Amino-norbornane derivative and preparation method and application thereof |
| CN109369654A (en) * | 2018-11-20 | 2019-02-22 | 山东大学 | 1,3-Disubstituted-4-aminopyrazolopyrimidine compounds and preparation method and application thereof |
| WO2020131674A1 (en) | 2018-12-19 | 2020-06-25 | Array Biopharma Inc. | 7-((3,5-dimethoxyphenyl)amino)quinoxaline derivatives as fgfr inhibitors for treating cancer |
| JP2022515198A (en) | 2018-12-19 | 2022-02-17 | アレイ バイオファーマ インコーポレイテッド | Substituted pyrazolo [1,5-a] pyridine compound as an inhibitor of FGFR tyrosine kinase |
| CN111454268B (en) * | 2019-01-18 | 2023-09-08 | 明慧医药(上海)有限公司 | Cyclic molecules as inhibitors of bruton's tyrosine kinase |
| CN113412262A (en) | 2019-02-12 | 2021-09-17 | 大日本住友制药肿瘤公司 | Formulations comprising heterocyclic protein kinase inhibitors |
| WO2020239103A1 (en) * | 2019-05-31 | 2020-12-03 | 四川海思科制药有限公司 | Btk inhibitor ring derivative, preparation method therefor and pharmaceutical application thereof |
| WO2020249001A1 (en) | 2019-06-10 | 2020-12-17 | 百济神州瑞士有限责任公司 | Oral solid tablet comprising bruton's tyrosine kinase inhibitor and preparation method therefor |
| CN110606848A (en) * | 2019-08-27 | 2019-12-24 | 药雅科技(上海)有限公司 | 5-azaindole derivative Bruton's tyrosine kinase inhibitor and preparation method and application thereof |
| CA3154257A1 (en) | 2019-10-14 | 2021-04-22 | Principia Biopharma Inc. | Methods for treating immune thrombocytopenia by administering (r)-2-[3-[4-amino-3-(2-fluoro-4-phenoxy-phenyl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carbonyl]-4-methyl-4-[4-(oxetan-3-yl)piperazin-1-yl]pent-2-enenitrile |
| CN115038700B (en) | 2019-11-08 | 2025-07-25 | 内尔维亚诺医疗科学公司 | Geminally disubstituted heterocyclic compounds and their use as IDH inhibitors |
| TWI883107B (en) | 2020-01-20 | 2025-05-11 | 美商普林斯匹亞生物製藥公司 | Therapeutic tyrosine kinase inhibitors for relapsing multiple sclerosis (rms) |
| TW202140484A (en) | 2020-01-22 | 2021-11-01 | 美商普林斯匹亞生物製藥公司 | Crystalline forms of 2-[3-[4-amino-3- (2-fluoro-4-phenoxy-phenyl)-1h- pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1- carbonyl]-4-methyl-4-[4-(oxetan-3- yl)piperazin-1-yl]pent-2-enenitrile |
| CN113943294A (en) * | 2020-07-15 | 2022-01-18 | 成都海博为药业有限公司 | Compound serving as BTK inhibitor and preparation method and application thereof |
| WO2022111447A1 (en) * | 2020-11-25 | 2022-06-02 | 四川海思科制药有限公司 | Method for preparing btk degrading agent |
| AU2021398051A1 (en) | 2020-12-10 | 2023-07-27 | Principia Biopharma Inc. | Crystal form of tolebrutinib, preparation method therefor and use thereof |
| CN113004246B (en) * | 2021-02-22 | 2022-02-01 | 广西医科大学 | 1,3, 5-triazine-2-amine-4, 6 substituted derivative or pharmaceutically acceptable salt and application thereof |
| US11786531B1 (en) | 2022-06-08 | 2023-10-17 | Beigene Switzerland Gmbh | Methods of treating B-cell proliferative disorder |
| CN120302975A (en) | 2022-10-31 | 2025-07-11 | 住友制药美国公司 | PIM1 inhibitors for the treatment of myeloproliferative neoplasms |
Family Cites Families (85)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2008A (en) * | 1841-03-18 | Gas-lamp eok conducting gas pkom ah elevated buhner to one below it | ||
| US3598123A (en) | 1969-04-01 | 1971-08-10 | Alza Corp | Bandage for administering drugs |
| US3993073A (en) | 1969-04-01 | 1976-11-23 | Alza Corporation | Novel drug delivery device |
| US3598122A (en) | 1969-04-01 | 1971-08-10 | Alza Corp | Bandage for administering drugs |
| US3710795A (en) | 1970-09-29 | 1973-01-16 | Alza Corp | Drug-delivery device with stretched, rate-controlling membrane |
| US4069307A (en) | 1970-10-01 | 1978-01-17 | Alza Corporation | Drug-delivery device comprising certain polymeric materials for controlled release of drug |
| US3731683A (en) | 1971-06-04 | 1973-05-08 | Alza Corp | Bandage for the controlled metering of topical drugs to the skin |
| US3742951A (en) | 1971-08-09 | 1973-07-03 | Alza Corp | Bandage for controlled release of vasodilators |
| US3996934A (en) | 1971-08-09 | 1976-12-14 | Alza Corporation | Medical bandage |
| BE795384A (en) | 1972-02-14 | 1973-08-13 | Ici Ltd | DRESSINGS |
| US3921636A (en) | 1973-01-15 | 1975-11-25 | Alza Corp | Novel drug delivery device |
| US3993072A (en) | 1974-08-28 | 1976-11-23 | Alza Corporation | Microporous drug delivery device |
| US4151273A (en) | 1974-10-31 | 1979-04-24 | The Regents Of The University Of California | Increasing the absorption rate of insoluble drugs |
| US3972995A (en) | 1975-04-14 | 1976-08-03 | American Home Products Corporation | Dosage form |
| US4077407A (en) | 1975-11-24 | 1978-03-07 | Alza Corporation | Osmotic devices having composite walls |
| US4031894A (en) | 1975-12-08 | 1977-06-28 | Alza Corporation | Bandage for transdermally administering scopolamine to prevent nausea |
| US4060084A (en) | 1976-09-07 | 1977-11-29 | Alza Corporation | Method and therapeutic system for providing chemotherapy transdermally |
| US4201211A (en) | 1977-07-12 | 1980-05-06 | Alza Corporation | Therapeutic system for administering clonidine transdermally |
| JPS5562012A (en) | 1978-11-06 | 1980-05-10 | Teijin Ltd | Slow-releasing preparation |
| US4230105A (en) | 1978-11-13 | 1980-10-28 | Merck & Co., Inc. | Transdermal delivery of drugs |
| US4229447A (en) | 1979-06-04 | 1980-10-21 | American Home Products Corporation | Intraoral methods of using benzodiazepines |
| CA1146866A (en) | 1979-07-05 | 1983-05-24 | Yamanouchi Pharmaceutical Co. Ltd. | Process for the production of sustained release pharmaceutical composition of solid medical material |
| US4291015A (en) | 1979-08-14 | 1981-09-22 | Key Pharmaceuticals, Inc. | Polymeric diffusion matrix containing a vasodilator |
| US4327725A (en) | 1980-11-25 | 1982-05-04 | Alza Corporation | Osmotic device with hydrogel driving member |
| US4476116A (en) | 1982-12-10 | 1984-10-09 | Syntex (U.S.A.) Inc. | Polypeptides/chelating agent nasal compositions having enhanced peptide absorption |
| US5116817A (en) | 1982-12-10 | 1992-05-26 | Syntex (U.S.A.) Inc. | LHRH preparations for intranasal administration |
| US4596795A (en) | 1984-04-25 | 1986-06-24 | The United States Of America As Represented By The Secretary, Dept. Of Health & Human Services | Administration of sex hormones in the form of hydrophilic cyclodextrin derivatives |
| US4624848A (en) | 1984-05-10 | 1986-11-25 | Ciba-Geigy Corporation | Active agent containing hydrogel devices wherein the active agent concentration profile contains a sigmoidal concentration gradient for improved constant release, their manufacture and use |
| GB8518301D0 (en) | 1985-07-19 | 1985-08-29 | Fujisawa Pharmaceutical Co | Hydrodynamically explosive systems |
| JPH0778017B2 (en) | 1985-12-28 | 1995-08-23 | 住友製薬株式会社 | Pulsed and sustained release formulation |
| US4755386A (en) | 1986-01-22 | 1988-07-05 | Schering Corporation | Buccal formulation |
| US5312325A (en) | 1987-05-28 | 1994-05-17 | Drug Delivery Systems Inc | Pulsating transdermal drug delivery system |
| US4968509A (en) | 1987-07-27 | 1990-11-06 | Mcneilab, Inc. | Oral sustained release acetaminophen formulation and process |
| US5033252A (en) | 1987-12-23 | 1991-07-23 | Entravision, Inc. | Method of packaging and sterilizing a pharmaceutical product |
| US5052558A (en) | 1987-12-23 | 1991-10-01 | Entravision, Inc. | Packaged pharmaceutical product |
| IL92966A (en) | 1989-01-12 | 1995-07-31 | Pfizer | Dispensing devices powered by hydrogel |
| US5739136A (en) | 1989-10-17 | 1998-04-14 | Ellinwood, Jr.; Everett H. | Intraoral dosing method of administering medicaments |
| US5017381A (en) | 1990-05-02 | 1991-05-21 | Alza Corporation | Multi-unit pulsatile delivery system |
| US5633009A (en) | 1990-11-28 | 1997-05-27 | Sano Corporation | Transdermal administration of azapirones |
| ATE159426T1 (en) | 1991-04-16 | 1997-11-15 | Nippon Shinyaku Co Ltd | METHOD FOR PRODUCING A SOLID DISPERSION |
| DE69231313T2 (en) | 1991-11-22 | 2001-03-15 | Procter & Gamble Pharmaceuticals, Inc. | Medicines containing risedronate with delayed drug delivery |
| US5229135A (en) | 1991-11-22 | 1993-07-20 | Prographarm Laboratories | Sustained release diltiazem formulation |
| US5340591A (en) | 1992-01-24 | 1994-08-23 | Fujisawa Pharmaceutical Co., Ltd. | Method of producing a solid dispersion of the sparingly water-soluble drug, nilvadipine |
| US5461140A (en) | 1992-04-30 | 1995-10-24 | Pharmaceutical Delivery Systems | Bioerodible polymers for solid controlled release pharmaceutical compositions |
| US5260068A (en) | 1992-05-04 | 1993-11-09 | Anda Sr Pharmaceuticals Inc. | Multiparticulate pulsatile drug delivery system |
| US5281420A (en) | 1992-05-19 | 1994-01-25 | The Procter & Gamble Company | Solid dispersion compositions of tebufelone |
| US5323907A (en) | 1992-06-23 | 1994-06-28 | Multi-Comp, Inc. | Child resistant package assembly for dispensing pharmaceutical medications |
| AU4198793A (en) | 1992-07-24 | 1994-01-27 | Takeda Chemical Industries Ltd. | Microparticle preparation and production thereof |
| US5700485A (en) | 1992-09-10 | 1997-12-23 | Children's Medical Center Corporation | Prolonged nerve blockade by the combination of local anesthetic and glucocorticoid |
| KR100291362B1 (en) | 1992-10-16 | 2001-09-17 | 니뽄 신야쿠 가부시키가이샤 | Preparation of wax matrix |
| US5260069A (en) | 1992-11-27 | 1993-11-09 | Anda Sr Pharmaceuticals Inc. | Pulsatile particles drug delivery system |
| US5686105A (en) | 1993-10-19 | 1997-11-11 | The Procter & Gamble Company | Pharmaceutical dosage form with multiple enteric polymer coatings for colonic delivery |
| US6326469B1 (en) | 1994-04-22 | 2001-12-04 | Sugen, Inc. | Megakaryocytic protein tyrosine kinases |
| US5665378A (en) | 1994-09-30 | 1997-09-09 | Davis; Roosevelt | Transdermal therapeutic formulation |
| US5567441A (en) | 1995-03-24 | 1996-10-22 | Andrx Pharmaceuticals Inc. | Diltiazem controlled release formulation |
| KR19990014865A (en) | 1995-05-17 | 1999-02-25 | 피터 이. 브래이브맨 | Compositions containing fatty acids to enhance digestion and absorption in the small intestine |
| SE9502244D0 (en) | 1995-06-20 | 1995-06-20 | Bioglan Ab | A composition and a process for the preparation thereof |
| US5837284A (en) | 1995-12-04 | 1998-11-17 | Mehta; Atul M. | Delivery of multiple doses of medications |
| US5858401A (en) | 1996-01-22 | 1999-01-12 | Sidmak Laboratories, Inc. | Pharmaceutical composition for cyclosporines |
| US6923983B2 (en) | 1996-02-19 | 2005-08-02 | Acrux Dds Pty Ltd | Transdermal delivery of hormones |
| US6929801B2 (en) | 1996-02-19 | 2005-08-16 | Acrux Dds Pty Ltd | Transdermal delivery of antiparkinson agents |
| US6458373B1 (en) | 1997-01-07 | 2002-10-01 | Sonus Pharmaceuticals, Inc. | Emulsion vehicle for poorly soluble drugs |
| HUP0001507A3 (en) * | 1997-03-19 | 2002-01-28 | Abbott Gmbh & Co Kg | Pyrrolo [2,3-d] pyrimidine derivatives, process for their preparation, their use and pharmaceutical compositions containing them |
| US5840329A (en) | 1997-05-15 | 1998-11-24 | Bioadvances Llc | Pulsatile drug delivery system |
| US6391452B1 (en) | 1997-07-18 | 2002-05-21 | Bayer Corporation | Compositions for nasal drug delivery, methods of making same, and methods of removing residual solvent from pharmaceutical preparations |
| US5869090A (en) | 1998-01-20 | 1999-02-09 | Rosenbaum; Jerry | Transdermal delivery of dehydroepiandrosterone |
| US6946144B1 (en) | 1998-07-08 | 2005-09-20 | Oryxe | Transdermal delivery system |
| BR9913887A (en) * | 1998-09-18 | 2001-10-23 | Basf Ag | Compound, and, methods of inhibiting protein kinase activity, treating a patient who has a condition that is mediated by protein kinase activity and decreasing fertility in a patient |
| ES2307482T3 (en) | 1999-02-10 | 2008-12-01 | Pfizer Products Inc. | SOLID PHARMACEUTICAL DISPERSIONS. |
| US6395300B1 (en) | 1999-05-27 | 2002-05-28 | Acusphere, Inc. | Porous drug matrices and methods of manufacture thereof |
| US6660744B1 (en) * | 1999-09-17 | 2003-12-09 | Abbott Gmbh & Co. Kg | Pyrazolopyrimidines as therapeutic agents |
| US6921763B2 (en) | 1999-09-17 | 2005-07-26 | Abbott Laboratories | Pyrazolopyrimidines as therapeutic agents |
| WO2001082901A1 (en) | 2000-04-28 | 2001-11-08 | Zengen, Inc. | New antibodies to biological membranes |
| US6465014B1 (en) | 2001-03-21 | 2002-10-15 | Isp Investments Inc. | pH-dependent sustained release, drug-delivery composition |
| MXPA03008560A (en) | 2001-03-22 | 2004-06-30 | Abbot Gmbh & Co Kg | Single-stage pfc + ballast control circuit/general purpose power converter. |
| US6960563B2 (en) | 2001-08-31 | 2005-11-01 | Morton Grove Pharmaceuticals, Inc. | Spontaneous emulsions containing cyclosporine |
| EP1715871A1 (en) * | 2003-12-22 | 2006-11-02 | Gilead Sciences, Inc. | Kinase inhibitor phosphonate conjugates |
| US20070281907A1 (en) * | 2003-12-22 | 2007-12-06 | Watkins William J | Kinase Inhibitor Phosphonate Conjugates |
| EP1730148A4 (en) * | 2004-02-03 | 2009-08-19 | Abbott Lab | Aminobenzoxazoles as therapeutic agents |
| US9512125B2 (en) * | 2004-11-19 | 2016-12-06 | The Regents Of The University Of California | Substituted pyrazolo[3.4-D] pyrimidines as anti-inflammatory agents |
| ES2423010T3 (en) * | 2006-04-04 | 2013-09-17 | The Regents Of The University Of California | Pyrazolopyrimidine derivatives for use as kinase antagonists |
| PL2526934T4 (en) | 2006-09-22 | 2016-09-30 | Bruton tyrosine kinase inhibitors | |
| CA3143428A1 (en) * | 2007-03-28 | 2008-10-09 | Pharmacyclics Llc | 8-amino-3-substituted-imidazo[1,5-a]pyrazine and use thereof as inhibitors of bruton's tyrosine kinase |
| US7718662B1 (en) | 2009-10-12 | 2010-05-18 | Pharmacyclics, Inc. | Pyrazolo-pyrimidine inhibitors of bruton's tyrosine kinase |
| NZ599343A (en) | 2009-10-14 | 2014-05-30 | Merck Sharp & Dohme | Substituted piperidines that increase p53 activity and the uses thereof |
-
2009
- 2009-10-16 US US12/581,044 patent/US7718662B1/en active Active
- 2009-10-16 US US12/581,062 patent/US7741330B1/en active Active
-
2010
- 2010-10-12 CA CA2776543A patent/CA2776543A1/en not_active Abandoned
- 2010-10-12 EP EP10823966A patent/EP2393816A4/en not_active Withdrawn
- 2010-10-12 PH PH1/2012/500712A patent/PH12012500712A1/en unknown
- 2010-10-12 ES ES13166272.8T patent/ES2590905T3/en active Active
- 2010-10-12 WO PCT/US2010/052377 patent/WO2011046964A2/en not_active Application Discontinuation
- 2010-10-12 SG SG10201506776RA patent/SG10201506776RA/en unknown
- 2010-10-12 MX MX2012004258A patent/MX2012004258A/en active IP Right Grant
- 2010-10-12 KR KR20127011767A patent/KR20120097376A/en not_active Ceased
- 2010-10-12 BR BR112012008624A patent/BR112012008624A2/en not_active IP Right Cessation
- 2010-10-12 JP JP2012534294A patent/JP5717109B2/en active Active
- 2010-10-12 AU AU2010306921A patent/AU2010306921C1/en not_active Ceased
- 2010-10-12 EP EP13166272.8A patent/EP2650294B1/en active Active
- 2010-10-12 IN IN3012DEN2012 patent/IN2012DN03012A/en unknown
- 2010-10-12 US US12/903,101 patent/US9012463B2/en active Active
- 2010-10-12 EA EA201270553A patent/EA021715B1/en unknown
- 2010-10-12 CN CN201080056387.2A patent/CN102656173B/en not_active Expired - Fee Related
- 2010-10-12 NZ NZ59939610A patent/NZ599396A/en not_active IP Right Cessation
-
2012
- 2012-04-05 IL IL219076A patent/IL219076A/en active IP Right Grant
- 2012-04-09 CO CO12057551A patent/CO6531429A2/en active IP Right Grant
- 2012-04-10 ZA ZA2012/02552A patent/ZA201202552B/en unknown
- 2012-04-11 CL CL2012000917A patent/CL2012000917A1/en unknown
- 2012-05-11 CR CR20120244A patent/CR20120244A/en unknown
-
2013
- 2013-11-20 US US14/085,722 patent/US20140080844A1/en not_active Abandoned
-
2015
- 2015-03-10 JP JP2015047643A patent/JP2015134802A/en active Pending
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| IN2012DN03012A (en) | ||
| PH12014500122A1 (en) | Inhibitors of bruton's tyrosine kinase | |
| MX2009010284A (en) | Inhibitors of bruton's tyrosine kinase. | |
| MA32934B1 (en) | Counter fittings for HSP90 | |
| TN2011000293A1 (en) | Protein kinase inhibitors | |
| UA99284C2 (en) | P70 s6 kinase inhibitors | |
| MX355728B (en) | Kinase inhibitors. | |
| SG179085A1 (en) | Pi3 kinase inhibitors and uses thereof | |
| TW200801008A (en) | Protein kinase inhibitors | |
| ECSP13012394A (en) | NEW FORMS OF MODIFIED RELEASE DOSAGE OF AN XANTINA OXIDORREDUCTASA INHIBITOR OR XANTINA OXIDASA INHIBITORS | |
| PH12014501122A1 (en) | Methods of treatment using an antibody against interferon gamma | |
| MX353984B (en) | Multispecific antibodies. | |
| EA201171367A1 (en) | VINYLINDASOLYL COMPOUNDS | |
| BR112012011528A2 (en) | methods for inhibiting a protein kinase and for treating a disease associated with kinase activity, and, compound | |
| MX2009010924A (en) | System and method for providing adjustable ballast factor. | |
| EA200900091A1 (en) | NEW INDICATIONS FOR THE USE OF DIRECT THROMBIN INHIBITORS IN THE TREATMENT OF CARDIOVASCULAR DISEASES | |
| GEP20125647B (en) | Kinesin inhibitors as cancer therapeutics | |
| MX2009004030A (en) | Antimicrobial articles and method of manufacture. | |
| MA32933B1 (en) | A combination of hspo90 inhibitors and herceptin | |
| MX2010001582A (en) | Predictive markers for egfr inhibitors treatment. | |
| MX2012001875A (en) | Process for the preparation of cathepsin s inhibitors. | |
| ATE499138T1 (en) | IMPLANTABLE DEVICE | |
| MX2010001578A (en) | Egfr inhibitor treatment marker. | |
| UA102516C2 (en) | 7-substituted indole mcl-1 inhibitors | |
| UA36281U (en) | Use of vinboron for treating memory disorders |