LU92681I2 - Nintédanib, its tautomers and its salts, in particular Nintédanib and its pharmaceutically acceptable salts, in particular Nintédanib Esilate - Google Patents
Nintédanib, its tautomers and its salts, in particular Nintédanib and its pharmaceutically acceptable salts, in particular Nintédanib EsilateInfo
- Publication number
- LU92681I2 LU92681I2 LU92681C LU92681C LU92681I2 LU 92681 I2 LU92681 I2 LU 92681I2 LU 92681 C LU92681 C LU 92681C LU 92681 C LU92681 C LU 92681C LU 92681 I2 LU92681 I2 LU 92681I2
- Authority
- LU
- Luxembourg
- Prior art keywords
- nintédanib
- salts
- esilate
- tautomers
- pharmaceutically acceptable
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
- 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
- A61P25/00—Drugs for disorders of the nervous 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- 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
- A61P35/04—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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- 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
-
- 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
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/32—Oxygen atoms
- C07D209/34—Oxygen atoms in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Cardiology (AREA)
- Ophthalmology & Optometry (AREA)
- Heart & Thoracic Surgery (AREA)
- Rheumatology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Neurology (AREA)
- Hematology (AREA)
- Pain & Pain Management (AREA)
- Diabetes (AREA)
- Biomedical Technology (AREA)
- Oncology (AREA)
- Neurosurgery (AREA)
- Transplantation (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19949208A DE19949208A1 (en) | 1999-10-13 | 1999-10-13 | New 3-(amino-methylene)-2-indolinone derivatives are kinase inhibitors and cell proliferation inhibitors useful e.g. for treating tumors, metastasis, rheumatoid arthritis or psoriasis |
DE2000142696 DE10042696A1 (en) | 2000-08-31 | 2000-08-31 | New 3-(amino-methylene)-2-indolinone derivatives are kinase inhibitors and cell proliferation inhibitors useful e.g. for treating tumors, metastasis, rheumatoid arthritis or psoriasis |
PCT/EP2000/009867 WO2001027081A1 (en) | 1999-10-13 | 2000-10-09 | 6-position substituted indoline, production and use thereof as a medicament |
Publications (2)
Publication Number | Publication Date |
---|---|
LU92681I2 true LU92681I2 (en) | 2015-05-18 |
LU92681I9 LU92681I9 (en) | 2019-01-03 |
Family
ID=26006858
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
LU92681C LU92681I2 (en) | 1999-10-13 | 2015-03-16 | Nintédanib, its tautomers and its salts, in particular Nintédanib and its pharmaceutically acceptable salts, in particular Nintédanib Esilate |
Country Status (42)
Families Citing this family (101)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19816624A1 (en) * | 1998-04-15 | 1999-10-21 | Boehringer Ingelheim Pharma | Novel substituted indolinones, their preparation and their use as pharmaceuticals |
DK1415987T3 (en) | 2000-10-20 | 2007-07-02 | Eisai R&D Man Co Ltd | Nitrogen-containing aromatic ring compounds for use as anticancer agents |
US6638965B2 (en) | 2000-11-01 | 2003-10-28 | Boehringer Ingelheim Pharma Kg | Substituted indolinones, preparation thereof and their use as pharmaceutical compositions |
DE10117204A1 (en) | 2001-04-06 | 2002-10-10 | Boehringer Ingelheim Pharma | Indolinones substituted in the 6-position, their preparation and their use as medicaments |
ATE330608T1 (en) | 2001-06-29 | 2006-07-15 | Ab Science | THE USE OF N-PHENYL-2-PYRIMIDINE-AMINE DERIVATIVES FOR THE TREATMENT OF INFLAMMATORY DISEASES |
WO2003004007A2 (en) | 2001-06-29 | 2003-01-16 | Ab Science | Use of tyrosine kinase inhibitors for treating inflammatory bowel diseases (ibd) |
DE60227709D1 (en) * | 2001-06-29 | 2008-08-28 | Ab Science | THE USE OF C-CRITERIA FOR THE TREATMENT OF AUTOIMMUNE DISEASES |
DK1401413T3 (en) | 2001-06-29 | 2007-03-26 | Ab Science | Use of tyrosine kinase inhibitors for the treatment of allergic diseases |
JP2005500041A (en) | 2001-06-29 | 2005-01-06 | アブ サイエンス | Potent, selective and non-toxic C-KIT inhibitor |
US20030091974A1 (en) * | 2001-06-29 | 2003-05-15 | Alain Moussy | Method for screening compounds capable of depleting mast cells |
WO2003027102A1 (en) * | 2001-09-27 | 2003-04-03 | Allergan, Inc. | 3-(arylamino)methylene-1, 3-dihydro-2h-indol-2-ones as kinase inhibitors |
US20030187026A1 (en) | 2001-12-13 | 2003-10-02 | Qun Li | Kinase inhibitors |
US6797825B2 (en) | 2001-12-13 | 2004-09-28 | Abbott Laboratories | Protein kinase inhibitors |
JP4363985B2 (en) | 2001-12-27 | 2009-11-11 | セラヴァンス, インコーポレーテッド | Indoline derivatives useful as protein kinase inhibitors |
SE0302546D0 (en) | 2003-09-24 | 2003-09-24 | Astrazeneca Ab | New compounds |
ITBO20020198A1 (en) * | 2002-04-12 | 2003-10-13 | Univ Bologna | DERIVATIVES 2, 5 BIS DIAMMINO 1, 4 BENZOCHENIONIC USEFUL FOR THE TREATMENT OF ALZHEIMER DISEASE, METHOD FOR THEIR PREPARATION AND |
US7514468B2 (en) | 2002-07-23 | 2009-04-07 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Indolinone derivatives substituted in the 6 position, the preparation thereof and their use as pharmaceutical compositions |
US7169936B2 (en) | 2002-07-23 | 2007-01-30 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Indolinone derivatives substituted in the 6-position, their preparation and their use as medicaments |
DE10233500A1 (en) * | 2002-07-24 | 2004-02-19 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | 3-Z- [1- (4- (N - ((4-methyl-piperazin-1-yl) -methylcarbonyl) -N-methyl-amino) -anilino) -1-phenyl-methylene] -6-methoxycarbonyl- 2-indolinone monoethanesulfonate and its use as a medicament |
DE10237423A1 (en) | 2002-08-16 | 2004-02-19 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Treating immunological (or related) diseases, e.g. inflammatory bowel disease, rheumatoid arthritis or psoriasis, comprises administration of 3-methylene-2-indolinone derivative or quinazoline compound |
US20040204458A1 (en) | 2002-08-16 | 2004-10-14 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Use of Lck inhibitors for treatment of immunologic diseases |
US7148249B2 (en) * | 2002-09-12 | 2006-12-12 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Indolinones substituted by heterocycles, the preparation thereof and their use as medicaments |
JP4879492B2 (en) * | 2002-11-27 | 2012-02-22 | アラーガン、インコーポレイテッド | Kinase inhibitors for the treatment of diseases |
US20050043233A1 (en) * | 2003-04-29 | 2005-02-24 | Boehringer Ingelheim International Gmbh | Combinations for the treatment of diseases involving cell proliferation, migration or apoptosis of myeloma cells or angiogenesis |
EP1683785B1 (en) | 2003-11-11 | 2013-10-16 | Eisai R&D Management Co., Ltd. | Urea derivative and process for producing the same |
SE0401790D0 (en) * | 2004-07-07 | 2004-07-07 | Forskarpatent I Syd Ab | Tamoxifen response in pre- and postmenopausal breast cancer patients |
US20060058311A1 (en) * | 2004-08-14 | 2006-03-16 | Boehringer Ingelheim International Gmbh | Combinations for the treatment of diseases involving cell proliferation |
WO2006030941A1 (en) | 2004-09-13 | 2006-03-23 | Eisai R & D Management Co., Ltd. | Simultaneous use of sulfonamide-containing compound and angiogenesis inhibitor |
US8772269B2 (en) | 2004-09-13 | 2014-07-08 | Eisai R&D Management Co., Ltd. | Use of sulfonamide-including compounds in combination with angiogenesis inhibitors |
AU2005283422C1 (en) | 2004-09-17 | 2017-02-02 | Eisai R & D Management Co., Ltd. | Medicinal composition |
PE20060777A1 (en) * | 2004-12-24 | 2006-10-06 | Boehringer Ingelheim Int | INDOLINONE DERIVATIVES FOR THE TREATMENT OR PREVENTION OF FIBROTIC DISEASES |
EP2281901B1 (en) | 2005-08-02 | 2013-11-27 | Eisai R&D Management Co., Ltd. | Anti-tumour pharmaceutical composition with angiogenesis inhibitors |
WO2007057397A1 (en) * | 2005-11-15 | 2007-05-24 | Boehringer Ingelheim International Gmbh | Treatment of cancer |
US20090209580A1 (en) | 2006-05-18 | 2009-08-20 | Eisai R & D Management Co., Ltd. | Antitumor agent for thyroid cancer |
EP1870400A1 (en) * | 2006-06-08 | 2007-12-26 | Boehringer Ingelheim Pharma GmbH & Co. KG | Salts and crystalline salt forms of an 2-indolinone derivative |
JP5368096B2 (en) | 2006-08-28 | 2013-12-18 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | Anti-tumor agent for undifferentiated gastric cancer |
CA2676796C (en) | 2007-01-29 | 2016-02-23 | Eisai R & D Management Co., Ltd. | Composition for treatment of undifferentiated gastric cancer |
WO2008152013A1 (en) * | 2007-06-12 | 2008-12-18 | Boehringer Ingelheim International Gmbh | Indolinone derivatives and their use in treating disease-states such as cancer |
CA2687909C (en) | 2007-06-21 | 2015-09-15 | Janssen Pharmaceutica Nv | Indolin-2-ones and aza-indolin-2-ones |
WO2009060945A1 (en) | 2007-11-09 | 2009-05-14 | Eisai R & D Management Co., Ltd. | Combination of anti-angiogenic substance and anti-tumor platinum complex |
PE20091445A1 (en) * | 2007-12-03 | 2009-10-19 | Boehringer Ingelheim Int | INDOLINONE DERIVATIVES AND PROCEDURE FOR ITS MANUFACTURE |
AU2008333286B2 (en) | 2007-12-03 | 2014-08-14 | Boehringer Ingelheim International Gmbh | Process for the manufacture of an indolinone derivative |
US20110178099A1 (en) | 2008-06-06 | 2011-07-21 | Boehringer Ingelheim International Gmbh | Pharmaceutical combination |
CA2731919A1 (en) | 2008-07-29 | 2010-02-04 | Boehringer Ingelheim International Gmbh | New compounds |
JP2012515184A (en) | 2009-01-14 | 2012-07-05 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | How to treat colorectal cancer |
US8802384B2 (en) | 2009-03-12 | 2014-08-12 | Boehringer Ingelheim International Gmbh | Method or system using biomarkers for the monitoring of a treatment |
WO2010108503A1 (en) | 2009-03-24 | 2010-09-30 | Life & Brain Gmbh | Promotion of neuronal integration in neural stem cell grafts |
EP2429520A1 (en) | 2009-05-14 | 2012-03-21 | Boehringer Ingelheim International GmbH | New combination therapy in treatment of oncological and fibrotic diseases |
US20120107304A1 (en) | 2010-04-27 | 2012-05-03 | Boehringer Ingelheim International Gmbh | Combination therapy in treatment of oncological and fibrotic diseases |
KR101677790B1 (en) | 2010-06-25 | 2016-11-18 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | Antitumor agent using compounds having kinase inhibitory effect in combination |
WO2012068441A2 (en) | 2010-11-19 | 2012-05-24 | Ratiopharm Gmbh | Intedanib salts and solid state forms thereof |
CN103402519B (en) | 2011-04-18 | 2015-11-25 | 卫材R&D管理有限公司 | tumor therapeutic agent |
JP6038128B2 (en) | 2011-06-03 | 2016-12-07 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | A biomarker for predicting and evaluating the reactivity of thyroid and renal cancer subjects to lenvatinib compounds |
WO2013059740A1 (en) | 2011-10-21 | 2013-04-25 | Foundation Medicine, Inc. | Novel alk and ntrk1 fusion molecules and uses thereof |
PT2807160T (en) | 2012-01-26 | 2019-10-28 | Angion Biomedica Corp | Antifibrotic compounds and uses thereof |
ES2949394T3 (en) | 2012-11-05 | 2023-09-28 | Found Medicine Inc | Novel fusion molecules and their uses |
AU2013337277B2 (en) | 2012-11-05 | 2018-03-08 | Foundation Medicine, Inc. | Novel NTRK1 fusion molecules and uses thereof |
EP2930167B1 (en) * | 2012-12-06 | 2018-11-21 | KBP Biosciences Co., Ltd. | An indolinone derivative as tyrosine kinase inhibitor |
JPWO2014098176A1 (en) | 2012-12-21 | 2017-01-12 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | Amorphous quinoline derivative and method for producing the same |
AU2014207342C1 (en) | 2013-01-18 | 2019-04-04 | Foundation Medicine, Inc. | Methods of treating cholangiocarcinoma |
US20140350022A1 (en) | 2013-05-10 | 2014-11-27 | Boehringer Ingelheim International Gmbh | Efficacious treatment of NSCLC and predictive clinical marker of the responsiveness of a tumour to a treatment |
CN105264380B (en) | 2013-05-14 | 2017-09-05 | 卫材R&D管理有限公司 | Pleasure is cut down for the biological marker of Buddhist nun's compound response for predicting and evaluating carcinoma of endometrium subject |
CN104003925B (en) * | 2013-06-05 | 2016-03-30 | 四川大学 | Oxindole compounds or derivatives thereof and uses thereof |
WO2015009889A1 (en) * | 2013-07-18 | 2015-01-22 | Concert Pharmaceuticals, Inc. | Deuterated intedanib derivatives and their use for the treatment of proliferative disorders |
CA2919498C (en) | 2013-07-31 | 2023-07-25 | Windward Pharma, Inc. | Aerosol nintedanib compounds and uses thereof |
HRP20221047T1 (en) | 2014-08-28 | 2022-11-11 | Eisai R&D Management Co., Ltd. | High-purity quinoline derivative and method for manufacturing same |
CN104262232B (en) * | 2014-09-09 | 2016-05-04 | 苏州明锐医药科技有限公司 | The preparation method of Ni Taidani |
HUE064614T2 (en) | 2015-02-25 | 2024-04-28 | Eisai R&D Man Co Ltd | Method for suppressing bitterness of quinoline derivative |
AU2015384801B2 (en) | 2015-03-04 | 2022-01-06 | Eisai R&D Management Co., Ltd. | Combination of a PD-1 antagonist and a VEGFR/FGFR/RET tyrosine kinase inhibitor for treating cancer |
WO2016178064A1 (en) | 2015-05-06 | 2016-11-10 | Suven Life Sciences Limited | Polymorph of nintedanib ethanesulphonate, processes and intermediates thereof |
CN104844499B (en) * | 2015-06-05 | 2017-03-08 | 北京康立生医药技术开发有限公司 | One kettle way prepares the synthetic method of Nintedanib |
KR20240043821A (en) * | 2015-06-06 | 2024-04-03 | 클라우드브레이크 테라퓨틱스, 엘엘씨 | Compositions and methods for treating pterygium |
US11369623B2 (en) | 2015-06-16 | 2022-06-28 | Prism Pharma Co., Ltd. | Anticancer combination of a CBP/catenin inhibitor and an immune checkpoint inhibitor |
CN105126909B (en) * | 2015-07-13 | 2018-01-23 | 淮海工学院 | Application of the immobilized palladium catalyst in the synthesis of the nitrobenzene methyl of 4 phenylacetylene base 3 |
CZ308695B6 (en) | 2015-07-29 | 2021-03-03 | Zentiva, K.S. | Process for preparing methyl (Z) -3 - [[4- [methyl [2- (4-methyl-1-piperazinyl) acetyl] amino] phenyl] amino] phenylmethylene) -oxindole-6-carboxylate (intedanib, nintedanib) |
CN106467500A (en) * | 2015-08-14 | 2017-03-01 | 廊坊百瑞化工有限公司 | A kind of one pot synthesis synthesize the new method of Nintedanib key intermediate |
SG11201805423TA (en) | 2015-12-24 | 2018-07-30 | Respivert Ltd | Indolinones compounds and their use in the treatment of fibrotic diseases |
CZ2016104A3 (en) | 2016-02-24 | 2017-09-06 | Zentiva, K.S. | Crystalline modifications of methyl (3Z)-3- {[(4-{methyl[(4-methylpiperazin-1yl)acetyl]amino}phenyl)amino](phenyl)methylidene}-2oxo-2,3-dihydro-1H-indole-6-carboxylate and the methods of their preparation |
EP3426649B1 (en) | 2016-03-08 | 2020-07-22 | Respivert Limited | Indole derivatives and their use as protein kinase inhibitors |
US20190160054A1 (en) | 2016-04-13 | 2019-05-30 | Boehringer Ingelheim International Gmbh | Pharmaceutical combination of nintedanib, trifluridine and tipiracil for treating colorectal cancer |
EP3246029A1 (en) | 2016-05-19 | 2017-11-22 | Boehringer Ingelheim International Gmbh | Pharmaceutical combination of nintedanib and capecitabine for the treatment of colorectal cancer |
EP3464240A1 (en) | 2016-05-27 | 2019-04-10 | Boehringer Ingelheim International GmbH | Use of ecm biomarkers for the determining the treatment onset with nintedanib and pirfenidone |
JP2019523225A (en) | 2016-06-01 | 2019-08-22 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Use of ECM biomarkers to determine initiation of treatment with nintedanib and pirfenidone |
KR20240052865A (en) | 2016-06-02 | 2024-04-23 | 에이디에스 테라퓨틱스 엘엘씨 | Compositions and methods of using nintedanib for improving glaucoma surgery success |
US10159660B2 (en) | 2016-07-29 | 2018-12-25 | Oncternal Therapeutics, Inc. | Uses of indolinone compounds |
CN106748961A (en) * | 2016-11-30 | 2017-05-31 | 瑞阳制药有限公司 | The impurity compound of Nintedanib, preparation method, using and its detection method |
CN106748960A (en) * | 2016-11-30 | 2017-05-31 | 瑞阳制药有限公司 | The potential impurity compound of Nintedanib, preparation method, using and its detection method |
WO2018108669A1 (en) | 2016-12-12 | 2018-06-21 | Boehringer Ingelheim International Gmbh | Nintedanib for use in methods for the treatment of interstitial lung diseases by coadministration with olodaterol |
WO2018177893A1 (en) | 2017-03-28 | 2018-10-04 | Boehringer Ingelheim International Gmbh | Nintedanib for use in methods for the treatment of muscular dystrophy |
CN111278442B (en) | 2017-10-23 | 2023-06-06 | 勃林格殷格翰国际有限公司 | Novel combinations of active agents for the treatment of progressive fibrotic interstitial lung disease (PF-ILD) |
JP7382317B2 (en) | 2017-11-17 | 2023-11-16 | フェルミオン オサケ ユキチュア | Synthesis of 2-indolinone derivatives known as intermediates for producing nintedanib |
JP7061310B2 (en) * | 2018-04-05 | 2022-04-28 | 国立大学法人 大分大学 | Pharmaceuticals for the prevention and treatment of chronic fatty diseases |
CN108358827A (en) * | 2018-05-07 | 2018-08-03 | 日照市普达医药科技有限公司 | It is a kind of to treat psoriasic 2- oxo-indoles analog derivative and preparation method thereof |
WO2020070331A1 (en) * | 2018-10-05 | 2020-04-09 | Ichnos Sciences S.A. | Indolinone compounds for use as map4k1 inhibitors |
CN115361950A (en) | 2020-04-01 | 2022-11-18 | 勃林格殷格翰国际有限公司 | Use of biomarkers in the treatment of fibrotic disorders |
CN111848490B (en) * | 2020-08-24 | 2021-09-24 | 江西国药有限责任公司 | Preparation method of high-purity ethanesulfonic acid nintedanib |
CN112574094B (en) * | 2020-12-14 | 2022-07-01 | 成都大学 | Indolone derivatives and pharmaceutical use thereof |
KR20220107973A (en) | 2021-01-25 | 2022-08-02 | 주식회사 나이벡 | Peptides for prevention and treatment of fibrosis |
EP4098246A1 (en) | 2021-05-31 | 2022-12-07 | Lotus Pharmaceutical Co., Ltd. | Formulation of nintedanib |
CN115703758B (en) * | 2021-08-12 | 2024-03-26 | 中国医学科学院药物研究所 | Compounds used as kinase inhibitors, preparation method and application thereof |
WO2024037982A1 (en) | 2022-08-16 | 2024-02-22 | Boehringer Ingelheim International Gmbh | Pharmaceutical formulations of nintedanib for intraocular use |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL96047C (en) * | 1956-06-08 | |||
AU684950B2 (en) * | 1994-05-06 | 1998-01-08 | Alcon Laboratories, Inc. | Use of vitamin E tocopheryl derivatives in ophthalmic compositions |
US5880141A (en) * | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
CA2214759C (en) * | 1996-01-17 | 2004-05-18 | Taiho Pharmaceutical Co., Ltd. | Intimal hypertrophy inhibitors |
GB9718913D0 (en) * | 1997-09-05 | 1997-11-12 | Glaxo Group Ltd | Substituted oxindole derivatives |
DE19815020A1 (en) * | 1998-04-03 | 1999-10-07 | Boehringer Ingelheim Pharma | New substituted indolinones, their production and their use as medicines |
DE19816624A1 (en) * | 1998-04-15 | 1999-10-21 | Boehringer Ingelheim Pharma | Novel substituted indolinones, their preparation and their use as pharmaceuticals |
DE19824922A1 (en) * | 1998-06-04 | 1999-12-09 | Boehringer Ingelheim Pharma | Novel substituted indolinones, their preparation and their use as pharmaceuticals |
GB9904933D0 (en) * | 1999-03-04 | 1999-04-28 | Glaxo Group Ltd | Compounds |
-
2000
- 2000-09-10 UA UA2002053890A patent/UA75054C2/en unknown
- 2000-10-09 DE DE50015711T patent/DE50015711D1/en not_active Expired - Lifetime
- 2000-10-09 HU HU0204587A patent/HU230416B1/en active Protection Beyond IP Right Term
- 2000-10-09 AU AU10233/01A patent/AU781939B2/en active Active
- 2000-10-09 SK SK646-2002A patent/SK287312B6/en not_active IP Right Cessation
- 2000-10-09 KR KR1020027004701A patent/KR100835546B1/en active IP Right Grant
- 2000-10-09 CZ CZ20021410A patent/CZ301073B6/en unknown
- 2000-10-09 EE EEP200200197A patent/EE05427B1/en active Protection Beyond IP Right Term
- 2000-10-09 BR BRPI0014735-4 patent/BRPI0014735B8/en active IP Right Grant
- 2000-10-09 PL PL355433A patent/PL207445B1/en not_active IP Right Cessation
- 2000-10-09 ES ES00971347T patent/ES2331459T3/en not_active Expired - Lifetime
- 2000-10-09 EP EP09164507A patent/EP2157081A1/en not_active Withdrawn
- 2000-10-09 NZ NZ518489A patent/NZ518489A/en not_active IP Right Cessation
- 2000-10-09 WO PCT/EP2000/009867 patent/WO2001027081A1/en active IP Right Grant
- 2000-10-09 EA EA200200380A patent/EA006080B1/en not_active IP Right Cessation
- 2000-10-09 SI SI200031039T patent/SI1224170T1/en unknown
- 2000-10-09 AT AT00971347T patent/ATE439342T1/en active
- 2000-10-09 RS YUP-266/02A patent/RS51013B/en unknown
- 2000-10-09 PT PT00971347T patent/PT1224170E/en unknown
- 2000-10-09 CA CA002387013A patent/CA2387013C/en not_active Expired - Lifetime
- 2000-10-09 KR KR1020077017807A patent/KR100857734B1/en active IP Right Grant
- 2000-10-09 CN CNB008158681A patent/CN100455568C/en not_active Expired - Lifetime
- 2000-10-09 JP JP2001530102A patent/JP4021664B2/en not_active Expired - Lifetime
- 2000-10-09 ME MEP-454/08A patent/MEP45408A/en unknown
- 2000-10-09 DK DK00971347.0T patent/DK1224170T5/en active
- 2000-10-09 MX MXPA02002799A patent/MXPA02002799A/en active IP Right Grant
- 2000-10-09 IL IL14875600A patent/IL148756A0/en active IP Right Grant
- 2000-10-09 EP EP00971347.0A patent/EP1224170B9/en not_active Expired - Lifetime
- 2000-10-11 PE PE2000001088A patent/PE20010671A1/en not_active IP Right Cessation
- 2000-10-11 EG EG2000101293A patent/EG25931A/en active
- 2000-10-11 MY MYPI20004762A patent/MY127956A/en unknown
- 2000-10-12 TW TW089121320A patent/TWI268922B/en active
- 2000-10-12 CO CO00077925A patent/CO5261488A1/en not_active Application Discontinuation
- 2000-10-13 AR ARP000105394A patent/AR026036A1/en active Pending
-
2001
- 2001-02-06 SA SA01210704A patent/SA01210704B1/en unknown
-
2002
- 2002-03-19 IL IL148756A patent/IL148756A/en active Protection Beyond IP Right Term
- 2002-04-05 BG BG106587A patent/BG65983B1/en active Active
- 2002-04-10 HR HR20020306A patent/HRP20020306B1/en not_active IP Right Cessation
- 2002-04-11 NO NO20021719A patent/NO322746B1/en active Protection Beyond IP Right Term
-
2003
- 2003-06-30 HK HK03104649.4A patent/HK1052505B/en not_active IP Right Cessation
-
2007
- 2007-08-15 JP JP2007211755A patent/JP2007302697A/en active Pending
-
2009
- 2009-11-06 CY CY20091101152T patent/CY1110067T1/en unknown
-
2015
- 2015-03-13 CY CY2015009C patent/CY2015009PI1/en unknown
- 2015-03-16 FR FR15C0024C patent/FR15C0024I2/en active Active
- 2015-03-16 BE BE2015C018C patent/BE2015C018I2/fr unknown
- 2015-03-16 NL NL300725C patent/NL300725I2/en unknown
- 2015-03-16 LU LU92681C patent/LU92681I2/en unknown
- 2015-03-18 NO NO2015009C patent/NO2015009I1/en unknown
-
2016
- 2016-05-13 HU HUS1600022C patent/HUS1600022I1/en unknown
-
2023
- 2023-09-05 NO NO2023033C patent/NO2023033I1/en unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
LU92681I2 (en) | Nintédanib, its tautomers and its salts, in particular Nintédanib and its pharmaceutically acceptable salts, in particular Nintédanib Esilate | |
LU91501I2 (en) | Sugammadex and its pharmaceutically acceptable salts-BRIDION | |
LU92182I2 (en) | Dapagliflozin and its pharmaceutically acceptable salts | |
LU91280I2 (en) | Sorafenib and pharmaceutically acceptable salts | |
LU91363I2 (en) | Methoxy polyethylene glycol-epoetin beta and its pharmaceutically acceptable salts (MIRCERA) | |
LU91650I2 (en) | Saxagliptin and pharmaceutically acceptable salts thereof, including saxagliptin hydrochloride - Onglyza-saxagliptin | |
LU92381I2 (en) | Macitentan and its pharmaceutically acceptable derivatives (OPSUMIT) | |
NO2011002I1 (en) | Regadenosone and its salts. | |
LU91076I2 (en) | Tulathromycin and its pharmaceutically acceptable salts (draxxin). | |
DK1177178T3 (en) | Heterocyclic substituted benzimidazoles, their preparation and use | |
NO2008001I1 (en) | Vildagliptin and pharmaceutically acceptable salts thereof | |
LU92513I2 (en) | SOFOSBUVIR AND ITS PHARMACEUTICALLY ACCEPTABLE DERIVATIVES (SOLVALDI) | |
NO20025154L (en) | Imidazopyrimidine derivatives and triazole pyrimidine derivatives | |
DK1354888T3 (en) | Glucopyranosyloxypyrazole derivatives and their use in drugs | |
LU91624I2 (en) | Canakinumab and its pharmaceutically acceptable derivatives (ILARIS®) | |
IS6385A (en) | New uses and new N-azabicyclo-amide derivatives | |
ZA200501677B (en) | Hydantoin derivatives and their use as TACE inhibitors. | |
IL156131A0 (en) | Tetrahydropyridine derivatives, their preparation and their use as cell proliferation inhibitors | |
LU91345I2 (en) | Rufinamide and its pharmaceutically acceptable salts (inovelon) | |
DE60023642D1 (en) | ROLLING MILL | |
AU5066900A (en) | Benzimidazole derivatives and their use as methionyl t-rna synthetase inhibitors | |
NO20015897L (en) | Indolylpiperidine derivatives as antihistaminic and antiallergic agents | |
NO20024598L (en) | Pharmaceutically active pyrrolidine derivatives | |
ZA200207489B (en) | Apomorphine derivatives and methods for their use. | |
NO20016419L (en) | Melagatran in substantially crystalline form |