LU93078I2 - Combimetinib, éventuellement sous toute forme protégée par le brevet de base, y compris les sels et solvates pharmaceutiquement acceptables, en particulier hémifumarate de cobimetinib - Google Patents
Combimetinib, éventuellement sous toute forme protégée par le brevet de base, y compris les sels et solvates pharmaceutiquement acceptables, en particulier hémifumarate de cobimetinib Download PDFInfo
- Publication number
- LU93078I2 LU93078I2 LU93078C LU93078C LU93078I2 LU 93078 I2 LU93078 I2 LU 93078I2 LU 93078 C LU93078 C LU 93078C LU 93078 C LU93078 C LU 93078C LU 93078 I2 LU93078 I2 LU 93078I2
- Authority
- LU
- Luxembourg
- Prior art keywords
- solvates
- pharmaceutically acceptable
- acceptable salts
- combimetinib
- possibly
- Prior art date
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
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- 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
- A61K31/397—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
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- 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
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- 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
- A61P35/00—Antineoplastic agents
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- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/06—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
-
- 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
- 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
- C07D401/06—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 linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D403/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
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- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US72457805P | 2005-10-07 | 2005-10-07 | |
US80284006P | 2006-05-23 | 2006-05-23 | |
PCT/US2006/039126 WO2007044515A1 (fr) | 2005-10-07 | 2006-10-05 | Inhibiteurs de mek et procedes pour les utiliser |
Publications (1)
Publication Number | Publication Date |
---|---|
LU93078I2 true LU93078I2 (fr) | 2016-07-19 |
Family
ID=37728416
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
LU93078C LU93078I2 (fr) | 2005-10-07 | 2016-05-19 | Combimetinib, éventuellement sous toute forme protégée par le brevet de base, y compris les sels et solvates pharmaceutiquement acceptables, en particulier hémifumarate de cobimetinib |
Country Status (32)
Country | Link |
---|---|
US (8) | US7803839B2 (fr) |
EP (1) | EP1934174B1 (fr) |
JP (8) | JP5129143B2 (fr) |
KR (2) | KR20130058072A (fr) |
CN (5) | CN103524392B (fr) |
AT (1) | ATE504565T1 (fr) |
AU (1) | AU2006302415B2 (fr) |
BR (1) | BRPI0617165B1 (fr) |
CA (3) | CA3052368A1 (fr) |
CY (2) | CY1111670T1 (fr) |
DE (1) | DE602006021205D1 (fr) |
DK (1) | DK1934174T3 (fr) |
EA (3) | EA025871B9 (fr) |
ES (1) | ES2365070T3 (fr) |
FR (1) | FR16C0021I2 (fr) |
GE (1) | GEP20125456B (fr) |
HK (2) | HK1119698A1 (fr) |
HR (1) | HRP20110498T1 (fr) |
HU (1) | HUS1600021I1 (fr) |
IL (5) | IL189900A (fr) |
LT (1) | LTC1934174I2 (fr) |
LU (1) | LU93078I2 (fr) |
MY (1) | MY162174A (fr) |
NL (1) | NL300809I2 (fr) |
NO (4) | NO347091B1 (fr) |
NZ (1) | NZ567140A (fr) |
PL (1) | PL1934174T3 (fr) |
PT (1) | PT1934174E (fr) |
RS (1) | RS51782B (fr) |
SI (1) | SI1934174T1 (fr) |
WO (1) | WO2007044515A1 (fr) |
ZA (1) | ZA200802075B (fr) |
Families Citing this family (242)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EA013212B1 (ru) * | 2004-10-20 | 2010-04-30 | Лаборатуар Сероно Са | 3-ариламинопиридиновые производные |
CA3052368A1 (fr) * | 2005-10-07 | 2007-04-19 | Exelixis, Inc. | Azetidines comme inhibiteurs de mek |
GB0601962D0 (en) | 2006-01-31 | 2006-03-15 | Ucb Sa | Therapeutic agents |
ATE539752T1 (de) * | 2006-08-16 | 2012-01-15 | Exelixis Inc | Verwendung von pi3k- und mek-modulatoren bei der krebsbehandlung |
EP2089359A2 (fr) | 2006-10-31 | 2009-08-19 | Takeda Pharmaceutical Company Limited | Inhibiteurs de kinase mapk/erk |
CN105106199A (zh) * | 2006-12-14 | 2015-12-02 | 埃克塞利希斯股份有限公司 | 使用mek抑制剂的方法 |
WO2008124085A2 (fr) * | 2007-04-03 | 2008-10-16 | Exelixis, Inc. | Méthodes d'utilisation de combinaisons d'inhibiteurs de mek et de jak-2 |
AP2009005047A0 (en) * | 2007-05-10 | 2009-12-31 | Pfizer Ltd | Azetidine derivatives and their use as prostaglandin E2 antagonists |
SG183023A1 (en) | 2007-07-16 | 2012-08-30 | Genentech Inc | Anti-cd79b antibodies and immunoconjugates and methods of use |
EP2641618A3 (fr) | 2007-07-16 | 2013-10-23 | Genentech, Inc. | Anticorps anti-CD79B humanisés et immuno-conjugués et procédés dýutilisation |
GB0714384D0 (en) | 2007-07-23 | 2007-09-05 | Ucb Pharma Sa | theraputic agents |
EP2240494B1 (fr) | 2008-01-21 | 2016-03-30 | UCB Biopharma SPRL | Dérivés de thiénopyridine utilisés comme inhibiteurs de mek |
IL295449A (en) | 2008-01-31 | 2022-10-01 | Genentech Inc | and fusion antibody-drug-cd79b engineered antibodies cysteine- |
EP2644204B1 (fr) | 2008-03-18 | 2017-04-19 | Genentech, Inc. | Combinaisons de conjugué de médicament-anticorps anti-HER2 et du pertuzumab |
GB0811304D0 (en) | 2008-06-19 | 2008-07-30 | Ucb Pharma Sa | Therapeutic agents |
US8841462B2 (en) * | 2008-07-01 | 2014-09-23 | Robert A. Heald | Bicyclic heterocycles as MEK kinase inhibitors |
MX2010014565A (es) | 2008-07-01 | 2011-03-04 | Genentech Inc | Isoindolona y metodos de uso. |
WO2010068738A1 (fr) | 2008-12-10 | 2010-06-17 | Dana-Farber Cancer Institute, Inc. | Mutations de mek conférant une résistance aux inhibiteurs de mek |
EP2405916B1 (fr) | 2009-03-12 | 2018-02-07 | Genentech, Inc. | Combinaison de composés inhibiteurs de la phosphoinositide 3-kinase et d'agents chimiothérapeutiques pour le traitement de tumeurs malignes hématopoïétiques |
BRPI1009022A2 (pt) | 2009-05-27 | 2016-03-08 | Hoffmann La Roche | "composto, composição farmacêutica, processo para produzir uma composição farmacêutica, uso de um composto, método para tratamento de uma doença ou transtorno e kit" |
US8263633B2 (en) | 2009-09-28 | 2012-09-11 | F. Hoffman-La Roche Ag | Benzoxepin PI3K inhibitor compounds and methods of use |
KR101428346B1 (ko) | 2009-09-28 | 2014-08-07 | 에프. 호프만-라 로슈 아게 | 벤즈옥사제핀 pi3k 억제 화합물 및 사용 방법 |
US20110086837A1 (en) * | 2009-10-12 | 2011-04-14 | Genentech, Inc. | Combinations of a pi3k inhibitor and a mek inhibitor |
WO2011054828A1 (fr) * | 2009-11-04 | 2011-05-12 | Novartis Ag | Derives sulfonamides heterocycliques utilises comme inhibiteurs de mek |
US20110165155A1 (en) | 2009-12-04 | 2011-07-07 | Genentech, Inc. | Methods of treating metastatic breast cancer with trastuzumab-mcc-dm1 |
EP2526102B1 (fr) | 2010-01-22 | 2017-03-08 | Fundación Centro Nacional de Investigaciones Oncológicas Carlos III | Inhibiteurs de la PI3 kinase |
BR112012019635A2 (pt) | 2010-02-22 | 2016-05-03 | Hoffmann La Roche | compostos inibidores de pirido[3,2-d] pirimidina pi3k delta e métodos de uso |
EP3028699B1 (fr) | 2010-02-25 | 2018-03-21 | Dana-Farber Cancer Institute, Inc. | Mutations braf conférant une résistance aux inhibiteurs de braf |
AU2011224410B2 (en) | 2010-03-09 | 2015-05-28 | Dana-Farber Cancer Institute, Inc. | Methods of diagnosing and treating cancer in patients having or developing resistance to a first cancer therapy |
WO2011121317A1 (fr) | 2010-04-01 | 2011-10-06 | Centro Nacional De Investigaciones Oncologicas (Cnio) | Imidazo[1,2-b][1,2,3]thiadiazoles en tant qu'inhibiteurs de la kinase protéique ou de la kinase lipidique |
BR112012025480A2 (pt) | 2010-04-07 | 2020-08-18 | F. Hoffmann - La Roche Ag | composto, composição farmacêutica composta de um composto, uso do composto e método de tratamento de uma doença ou distúrbio |
EA024730B1 (ru) | 2010-04-15 | 2016-10-31 | Медимьюн Лимитед | Пирролбензодиазепиновые соединения, их конъюгаты, фармацевтические композиции, содержащие указанные конъюгаты, и применение указанных конъюгатов |
CN110818724B (zh) | 2010-05-07 | 2020-11-13 | 吉利德康涅狄格有限公司 | 吡啶酮和氮杂吡啶酮化合物及使用方法 |
WO2012007493A1 (fr) | 2010-07-14 | 2012-01-19 | F. Hoffmann-La Roche Ag | Composés de purine sélectifs de la pi3k p110 delta, et procédés d'utilisation |
US9845489B2 (en) | 2010-07-26 | 2017-12-19 | Biomatrica, Inc. | Compositions for stabilizing DNA, RNA and proteins in saliva and other biological samples during shipping and storage at ambient temperatures |
CA2806670A1 (fr) | 2010-07-26 | 2012-02-09 | Biomatrica, Inc. | Compositions de stabilisation d'adn, d'arn, de proteines dans le sang et d'autres echantillons biologiques lors du transport et du stockage a temperatures ambiantes |
CN106220614B (zh) | 2010-09-01 | 2019-07-16 | 吉利德康涅狄格有限公司 | 吡啶酮/吡嗪酮、其制备方法及使用方法 |
KR101864908B1 (ko) | 2010-09-01 | 2018-06-05 | 질레드 코네티컷 인코포레이티드 | 피리다지논, 그의 제조 방법 및 사용 방법 |
WO2012052745A1 (fr) | 2010-10-21 | 2012-04-26 | Centro Nacional De Investigaciones Oncológicas (Cnio) | Combinaisons d'inhibiteurs de pi3k avec un second agent antitumoral |
US20140080810A1 (en) | 2010-11-15 | 2014-03-20 | Exelixis, Inc. | Benzoxazepines as Inhibitors of PI3K/mTOR and Methods of Their Use and Manufacture |
SI2651951T1 (sl) | 2010-12-16 | 2015-01-30 | F. Hoffmann-La Roche Ag | Tricikliäśne p13k inhibitorske spojine in postopki uporabe |
CN103476767B (zh) | 2011-02-09 | 2015-06-10 | 弗·哈夫曼-拉罗切有限公司 | 作为pi3激酶抑制剂的杂环化合物 |
BR112013024122A2 (pt) | 2011-03-21 | 2019-09-24 | Hoffmann La Roche | compostos de benzoxazepina seletivos para p110 delta pi3k e métodos de uso |
CN102718750B (zh) * | 2011-03-31 | 2015-03-11 | 中国人民解放军军事医学科学院毒物药物研究所 | 含吖啶环的氨基吡啶类衍生物及其用途 |
EP2694073B1 (fr) | 2011-04-01 | 2018-08-08 | Genentech, Inc. | Combinaisons de inhibiteurs d'akt et mek pour le traitement du cancer |
RS56759B1 (sr) | 2011-04-01 | 2018-04-30 | Genentech Inc | Kombinacija akt inhibitor jedinjenja i abiraterona za upotrebu pri terapeutskim tretiranjima |
EP2524918A1 (fr) | 2011-05-19 | 2012-11-21 | Centro Nacional de Investigaciones Oncológicas (CNIO) | Imidazopyrazines en tant qu'inhibiteurs de kinase |
CN103748099B (zh) | 2011-05-19 | 2016-08-17 | 卡洛斯三世国家癌症研究中心基金会 | 作为蛋白激酶抑制剂的大环化合物 |
RU2013154355A (ru) | 2011-06-03 | 2015-07-20 | Ф. Хоффманн-Ля Рош Аг | Способ лечения мезотелиомы ингибитором рi3к |
MY193562A (en) | 2011-08-01 | 2022-10-19 | Genentech Inc | Methods of treating cancer using pd-1 axis binding antagonists and mek inhibitors |
BR112014003296A2 (pt) | 2011-08-12 | 2017-03-14 | Hoffmann La Roche | composto, composição farmacêutica, processo para a preparação de uma composição farmacêutica, método para o tratamento de uma doença ou distúrbio, conjunto para o tratamento de uma condição mediada pela quinase pim e utilização do composto |
CA2845191A1 (fr) | 2011-09-27 | 2013-04-04 | F. Hoffmann-La Roche Ag | Composes de type pyrazol-4-yl-heterocyclyl-carboxamide et leurs methodes d'utilisation |
KR101877598B1 (ko) | 2011-10-14 | 2018-07-11 | 메디뮨 리미티드 | 피롤로벤조디아제핀 및 그의 컨주게이트 |
KR20140097205A (ko) * | 2011-10-28 | 2014-08-06 | 제넨테크, 인크. | 흑색종을 치료하는 치료 조합물 및 방법 |
UA111756C2 (uk) | 2011-11-03 | 2016-06-10 | Ф. Хоффманн-Ля Рош Аг | Сполуки гетероарилпіридону та азапіридону як інгібітори тирозинкінази брутона |
MX2014005289A (es) | 2011-11-03 | 2014-05-30 | Hoffmann La Roche | Compuestos de piperazina alquilados. |
BR112014010391A2 (pt) | 2011-11-03 | 2017-04-18 | Hoffmann La Roche | composto, composição farmacêutica, processo de produção de uma composição farmacêutica, método de tratamento, kit e uso de uma composição farmacêutica |
US8669251B2 (en) | 2011-11-03 | 2014-03-11 | Genentech, Inc. | 8-fluorophthalazin-1(2H)-one compounds |
EP2592103A1 (fr) | 2011-11-08 | 2013-05-15 | Adriacell S.p.A. | Dérivés d'aldéhyde de polymère |
JP2015501639A (ja) | 2011-11-23 | 2015-01-19 | アイジェニカ バイオセラピューティクス インコーポレイテッド | 抗cd98抗体およびその使用方法 |
WO2013082511A1 (fr) | 2011-12-02 | 2013-06-06 | Genentech, Inc. | Procédés pour surmonter la résistance tumorale aux antagonistes de vegf |
CN103204825B (zh) | 2012-01-17 | 2015-03-04 | 上海科州药物研发有限公司 | 作为蛋白激酶抑制剂的苯并噻唑化合物及其制备方法和用途 |
WO2013113102A1 (fr) | 2012-02-01 | 2013-08-08 | The Governors Of The University Of Alberta | Utilisation de pdgfr-a comme marqueur de diagnostic pour le cancer papillaire de la thyroïde |
US20150141470A1 (en) | 2012-05-08 | 2015-05-21 | The Broad Institute, Inc. | Diagnostic and treatment methods in patients having or at risk of developing resistance to cancer therapy |
SG10201706196XA (en) | 2012-06-08 | 2017-08-30 | Hoffmann La Roche | Mutant selectivity and combinations of a phosphoinositide 3 kinase inhibitor compound and chemotherapeutic agents for the treatment of cancer |
BR112014029674A2 (pt) | 2012-06-27 | 2017-06-27 | Hoffmann La Roche | composto, composição farmacêutica, método para o tratamento de uma doença, utilização de um composto, conjunto para o tratamento de uma condição mediada pela quinase pim e invenção |
EP2879708A4 (fr) | 2012-08-02 | 2016-03-16 | Genentech Inc | Anticorps et immunoconjugués anti-etbr |
RU2015106946A (ru) | 2012-08-02 | 2016-09-27 | Дженентек, Инк. | Антитела к рецептору эндотелина типа в (etbr) и их иммуноконъюгаты |
ES2765573T3 (es) | 2012-08-13 | 2020-06-09 | Univ Rockefeller | Tratamiento y diagnóstico de melanoma |
KR20210108502A (ko) | 2012-08-17 | 2021-09-02 | 에프. 호프만-라 로슈 아게 | 코비메티닙 및 베무라피닙을 투여함을 포함하는 흑색종의 조합 치료법 |
CN104583215B (zh) | 2012-08-30 | 2016-12-07 | 霍夫曼-拉罗奇有限公司 | 二噁烯并-和噁嗪-[2,3-d]嘧啶pi3k抑制剂化合物及使用方法 |
SI2900657T1 (sl) | 2012-09-26 | 2020-07-31 | F. Hoffmann-La Roche Ag | Ciklični eter pirazol-4-il-heterociklil-karboksamidne spojine in načini uporabe |
AU2013329311A1 (en) | 2012-10-09 | 2015-04-30 | Igenica Biotherapeutics, Inc. | Anti-C16orf54 antibodies and methods of use thereof |
AU2013328674B2 (en) | 2012-10-12 | 2017-06-22 | Medimmune Limited | Pyrrolobenzodiazepines and conjugates thereof |
LT2839860T (lt) | 2012-10-12 | 2019-07-10 | Medimmune Limited | Pirolobenzodiazepinai ir jų konjugatai |
US10695433B2 (en) | 2012-10-12 | 2020-06-30 | Medimmune Limited | Pyrrolobenzodiazepine-antibody conjugates |
ES2680153T3 (es) | 2012-10-12 | 2018-09-04 | Adc Therapeutics Sa | Conjugados de anticuerpos anti-PSMA-pirrolobenzodiazepinas |
MY186549A (en) * | 2012-10-12 | 2021-07-26 | Exelixis Inc | Novel process for making compounds for use in the treatment of cancer |
TR201815418T4 (tr) | 2012-10-12 | 2018-11-21 | Adc Therapeutics Sa | Pirrolobenzodiazepin -anti-psma antikor konjugatları. |
EP2906251B1 (fr) | 2012-10-12 | 2017-09-27 | ADC Therapeutics SA | Conjugués anticorps anti-cd22 - pyrrolobenzodiazépine |
EP2906296B1 (fr) | 2012-10-12 | 2018-03-21 | ADC Therapeutics SA | Conjugués anticorps - pyrrolobenzodiazépine |
HUE042731T2 (hu) | 2012-10-12 | 2019-07-29 | Adc Therapeutics Sa | Pirrolobenzodiazepin-antitest konjugátumok |
WO2014074785A1 (fr) | 2012-11-08 | 2014-05-15 | Ludwig Institute For Cancer Research Ltd. | Procédés de prédiction de l'issue et du traitement du cancer du sein |
WO2014078669A1 (fr) * | 2012-11-15 | 2014-05-22 | Duquesne University Of The Holy Ghost | Inhibiteurs de mek sous forme de promédicaments à base d'ester d'acide carboxylique |
TW201441193A (zh) * | 2012-12-06 | 2014-11-01 | Kyowa Hakko Kirin Co Ltd | 吡啶酮化合物 |
US9725703B2 (en) | 2012-12-20 | 2017-08-08 | Biomatrica, Inc. | Formulations and methods for stabilizing PCR reagents |
EP2935268B2 (fr) | 2012-12-21 | 2021-02-17 | MedImmune Limited | Pyrrolobenzodiazépines et conjugués associés |
US9567340B2 (en) | 2012-12-21 | 2017-02-14 | Medimmune Limited | Unsymmetrical pyrrolobenzodiazepines-dimers for use in the treatment of proliferative and autoimmune diseases |
RS58873B1 (sr) | 2013-02-22 | 2019-08-30 | Abbvie Stemcentrx Llc | Antidll3-antitelo-pbd konjugati i njihova upotreba |
JP2016509045A (ja) | 2013-02-22 | 2016-03-24 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | がんを治療し、薬剤耐性を防止する方法 |
EP2963114B1 (fr) | 2013-02-27 | 2018-12-12 | Daiichi Sankyo Company, Limited | Procédé de prédiction de la réactivité à un composé inhibant la voie de transduction du signal de mapk |
CA2905181C (fr) | 2013-03-13 | 2020-06-02 | Medimmune Limited | Pyrrolobenzodiazepines et ses conjugues servant a fournir une therapie ciblee |
KR102066318B1 (ko) | 2013-03-13 | 2020-01-14 | 메디뮨 리미티드 | 피롤로벤조디아제핀 및 그의 컨쥬게이트 |
US9821074B2 (en) | 2013-03-13 | 2017-11-21 | Genentech, Inc. | Pyrrolobenzodiazepines and conjugates thereof |
SG11201507477XA (en) | 2013-03-14 | 2015-10-29 | Genentech Inc | Combinations of a mek inhibitor compound with an her3/egfr inhibitor compound and methods of use |
EP2968346B1 (fr) | 2013-03-15 | 2024-02-07 | Cancer Research Technology, LLC | Procédés et compositions pour une modulation de cycle gamma-glutamyle |
EP2975936A4 (fr) | 2013-03-22 | 2017-03-15 | University of Hawaii | Nouveaux inhibiteurs de stats3 |
AU2014274660B2 (en) | 2013-06-06 | 2019-05-16 | Pierre Fabre Médicament | Anti-C10orf54 antibodies and uses thereof |
WO2015002729A2 (fr) | 2013-06-13 | 2015-01-08 | Biomatrica, Inc. | Stabilisation de cellules |
CA2912359A1 (fr) | 2013-07-03 | 2015-01-08 | F. Hoffmann-La Roche Ag | Composes heteroaryl pyridone et aza-pyridone amide |
ES2871418T3 (es) | 2013-08-28 | 2021-10-28 | Abbvie Stemcentrx Llc | Composiciones y métodos de conjugación de anticuerpos específicos de sitio |
US9532987B2 (en) | 2013-09-05 | 2017-01-03 | Genentech, Inc. | Use of a combination of a MEK inhibitor and an ERK inhibitor for treatment of hyperproliferative diseases |
WO2015052535A1 (fr) | 2013-10-11 | 2015-04-16 | Spirogen Sàrl | Conjugués anticorps-pyrrolobenzodiazépine |
WO2015052532A1 (fr) | 2013-10-11 | 2015-04-16 | Spirogen Sàrl | Conjugués anticorps-pyrrolobenzodiazépines |
GB201317982D0 (en) | 2013-10-11 | 2013-11-27 | Spirogen Sarl | Pyrrolobenzodiazepines and conjugates thereof |
WO2015052534A1 (fr) | 2013-10-11 | 2015-04-16 | Spirogen Sàrl | Conjugués anticorps-pyrrolobenzodiazépine |
CA2929918C (fr) | 2013-12-05 | 2018-01-23 | F. Hoffmann-La Roche Ag | Composes de pyridone heteroarylique et d'aza-pyridone a fonctionnalite electrophile |
JPWO2015108203A1 (ja) | 2014-01-15 | 2017-03-23 | 株式会社オーダーメードメディカルリサーチ | 抗slc6a6抗体を用いたがん治療用医薬組成物 |
CN104788365B (zh) * | 2014-01-16 | 2018-08-10 | 上海艾力斯医药科技有限公司 | 异烟酰胺衍生物、其制备方法及应用 |
MX2016012007A (es) | 2014-03-18 | 2016-12-05 | Hoffmann La Roche | Compuestos de oxepan-2-il-pirazol-4-il-heterociclil-carboxamida y metodos de uso. |
GB201406767D0 (en) | 2014-04-15 | 2014-05-28 | Cancer Rec Tech Ltd | Humanized anti-Tn-MUC1 antibodies anf their conjugates |
CA2946112C (fr) | 2014-04-18 | 2020-11-24 | The Governors Of The University Of Alberta | Therapie ciblee pour restaurer le transport de l'iode radioactif pour traiter le cancer de la thyroide |
WO2015164665A1 (fr) | 2014-04-25 | 2015-10-29 | Genentech, Inc. | Méthodes de traitement du cancer du sein précoce avec du trastuzumab-mcc-dm1 et du pertuzumab |
WO2015172073A1 (fr) | 2014-05-08 | 2015-11-12 | Cornell University | Gels bioadhésifs et procédés d'utilisation |
WO2015182734A1 (fr) * | 2014-05-30 | 2015-12-03 | 協和発酵キリン株式会社 | Composé hétérocyclique contenant de l'azote |
US10064404B2 (en) | 2014-06-10 | 2018-09-04 | Biomatrica, Inc. | Stabilization of thrombocytes at ambient temperatures |
JP6673896B2 (ja) | 2014-07-15 | 2020-03-25 | ジェネンテック, インコーポレイテッド | Pd−1軸結合アンタゴニスト及びmek阻害剤を使用した癌を処置するための組成物 |
WO2016037644A1 (fr) | 2014-09-10 | 2016-03-17 | Medimmune Limited | Pyrrolobenzodiazépines et leurs conjugués |
EP3191521A2 (fr) | 2014-09-12 | 2017-07-19 | F. Hoffmann-La Roche AG | Anticorps et conjugués modifiés génétiquement avec de la cystéine |
GB201416112D0 (en) | 2014-09-12 | 2014-10-29 | Medimmune Ltd | Pyrrolobenzodiazepines and conjugates thereof |
ES2830385T3 (es) | 2014-09-12 | 2021-06-03 | Genentech Inc | Anticuerpos e inmunoconjugados anti-HER2 |
BR112017004953A2 (pt) | 2014-09-17 | 2017-12-05 | Genentech Inc | imunoconjugado, formulação farmacêutica, método de tratamento e método de inibição da proliferação de uma célula |
EP3235820A1 (fr) | 2014-09-17 | 2017-10-25 | Genentech, Inc. | Pyrrolobenzodiazépines et conjugués à base de disulfure d'anticorps associés |
WO2016050921A1 (fr) | 2014-10-02 | 2016-04-07 | F. Hoffmann-La Roche Ag | Composés de pyrazole-carboxamide destinés à être utilisés dans le traitement de troubles médiés par la tyrosine kinase de bruton (btk) |
US20170224670A1 (en) | 2014-10-14 | 2017-08-10 | Exelixis, Inc. | Drug Combination to Treat Melanoma |
AU2015352545B2 (en) | 2014-11-25 | 2020-10-15 | Adc Therapeutics Sa | Pyrrolobenzodiazepine-antibody conjugates |
KR20170087500A (ko) | 2014-12-11 | 2017-07-28 | 피에르 파브르 메디카먼트 | 항-c10orf54 항체들 및 그들의 용도들 |
WO2016095088A1 (fr) * | 2014-12-15 | 2016-06-23 | Merck Sharp & Dohme Corp. | Inhibiteurs d'erk |
WO2016095089A1 (fr) | 2014-12-15 | 2016-06-23 | Merck Sharp & Dohme Corp. | Inhibiteurs d'erk |
RS60824B1 (sr) | 2014-12-18 | 2020-10-30 | Hoffmann La Roche | Tetrahidro-pirido[3,4-b]indoli kao modulatori estrogenih receptora i njihova upotreba |
GB201506402D0 (en) | 2015-04-15 | 2015-05-27 | Berkel Patricius H C Van And Howard Philip W | Site-specific antibody-drug conjugates |
GB201506411D0 (en) | 2015-04-15 | 2015-05-27 | Bergenbio As | Humanized anti-axl antibodies |
GB201506389D0 (en) | 2015-04-15 | 2015-05-27 | Berkel Patricius H C Van And Howard Philip W | Site-specific antibody-drug conjugates |
US11406715B2 (en) | 2015-05-30 | 2022-08-09 | Genentech, Inc. | Methods of treating HER2-positive metastatic breast cancer |
WO2016205176A1 (fr) | 2015-06-15 | 2016-12-22 | Genentech, Inc. | Anticorps et immunoconjugués |
SI3881833T1 (sl) | 2015-06-30 | 2024-03-29 | Genentech, Inc., | Tablete s takojšnjim sproščanjem, ki vsebujejo zdravilo in postopek za oblikovanje tablet |
AR105483A1 (es) * | 2015-06-30 | 2017-10-11 | Exelixis Inc | Sal de fumarato cristalina de (s)-[3,4-difluoro-2-(2-fluoro-4-yodofenilamino)fenil][3-hidroxi-3-(piperidin-2-il)azetidin-1-il]-metanona |
LT3317284T (lt) | 2015-07-02 | 2020-01-27 | F. Hoffmann-La Roche Ag | Benzoksazepino oksazolidinono junginiai ir jų naudojimo būdai |
CN111848643A (zh) | 2015-07-02 | 2020-10-30 | 豪夫迈·罗氏有限公司 | 苯并氧氮杂*噁唑烷酮化合物及其使用方法 |
US20190008859A1 (en) | 2015-08-21 | 2019-01-10 | Acerta Pharma B.V. | Therapeutic Combinations of a MEK Inhibitor and a BTK Inhibitor |
AR105910A1 (es) | 2015-09-04 | 2017-11-22 | Obi Pharma Inc | Matrices de glicano y método de uso |
US10959993B2 (en) | 2015-11-03 | 2021-03-30 | Genentech, Inc. | Combination of Bcl-2 inhibitor and MEK inhibitor for the treatment of cancer |
WO2017087280A1 (fr) | 2015-11-16 | 2017-05-26 | Genentech, Inc. | Procédés de traitement d'un cancer positif her2 |
PL3377107T3 (pl) | 2015-11-19 | 2020-12-14 | F. Hoffmann-La Roche Ag | Sposoby leczenia nowotworu przy użyciu inhibitorów b-raf i inhibitorów immunologicznego punktu kontrolnego |
KR102589056B1 (ko) | 2015-12-08 | 2023-10-12 | 바이오매트리카 인코포레이티드 | 적혈구 침강 속도의 감소 |
CN105330643B (zh) * | 2015-12-09 | 2017-12-05 | 苏州明锐医药科技有限公司 | 卡比替尼的制备方法 |
GB201601431D0 (en) | 2016-01-26 | 2016-03-09 | Medimmune Ltd | Pyrrolobenzodiazepines |
GB201602356D0 (en) | 2016-02-10 | 2016-03-23 | Medimmune Ltd | Pyrrolobenzodiazepine Conjugates |
GB201602359D0 (en) | 2016-02-10 | 2016-03-23 | Medimmune Ltd | Pyrrolobenzodiazepine Conjugates |
WO2017148837A1 (fr) | 2016-02-29 | 2017-09-08 | F. Hoffmann-La Roche Ag | Compositions de formes galéniques comprenant un inhibiteur de la tyrosine kinase de bruton |
US11883404B2 (en) | 2016-03-04 | 2024-01-30 | Taiho Pharmaceuticals Co., Ltd. | Preparation and composition for treatment of malignant tumors |
US10980894B2 (en) | 2016-03-29 | 2021-04-20 | Obi Pharma, Inc. | Antibodies, pharmaceutical compositions and methods |
TWI780045B (zh) | 2016-03-29 | 2022-10-11 | 台灣浩鼎生技股份有限公司 | 抗體、醫藥組合物及方法 |
WO2017180581A1 (fr) | 2016-04-15 | 2017-10-19 | Genentech, Inc. | Procédés diagnostiques et thérapeutiques relatifs au cancer |
KR20230110820A (ko) | 2016-04-22 | 2023-07-25 | 오비아이 파머 인코퍼레이티드 | 글로보 계열 항원을 통한 면역 활성화 또는 면역 조정에의한 암 면역요법 |
GB201607478D0 (en) | 2016-04-29 | 2016-06-15 | Medimmune Ltd | Pyrrolobenzodiazepine Conjugates |
CN106045969B (zh) * | 2016-05-27 | 2019-04-12 | 湖南欧亚药业有限公司 | 一种卡比替尼的合成方法 |
JP7018026B2 (ja) | 2016-06-16 | 2022-02-09 | エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト | ヘテロアリールエストロゲン受容体モジュレーター及びその使用 |
WO2017216280A1 (fr) | 2016-06-16 | 2017-12-21 | F. Hoffmann-La Roche Ag | Modulateurs des récepteurs des oestrogènes tétrahydro-pyrido[3,4-b]indoles et utilisations associées |
CN106220607B (zh) * | 2016-07-27 | 2018-09-18 | 成都百事兴科技实业有限公司 | 一种s-3-(哌啶-2-基)-氮杂环丁烷-3-醇的合成方法 |
CA3032049C (fr) | 2016-07-27 | 2023-11-07 | Obi Pharma, Inc. | Compositions de glycanes immunogenes/therapeutiques et utilisations associees |
EP3491026A4 (fr) | 2016-07-29 | 2020-07-29 | OBI Pharma, Inc. | Anticorps humains, compositions pharmaceutiques et procédés |
MX2019001635A (es) | 2016-08-12 | 2019-06-10 | Genentech Inc | Terapia de combinacion con un inhibidor de mek, un inhibidor del eje de pd-1, y un inhibidor de vegf. |
BR112019005815A2 (pt) | 2016-09-29 | 2019-06-25 | Genentech Inc | métodos de tratamento de um indivíduo com câncer de mama, kit para o tratamento de câncer de mama e combinação de fármacos para terapia de câncer de mama |
GB201617466D0 (en) | 2016-10-14 | 2016-11-30 | Medimmune Ltd | Pyrrolobenzodiazepine conjugates |
EP3541414A4 (fr) | 2016-11-21 | 2020-11-11 | OBI Pharma, Inc. | Molécules biologiques conjuguées, compositions pharmaceutiques et procédés |
LT3544636T (lt) | 2017-02-08 | 2021-06-25 | Adc Therapeutics Sa | Pirolobenzodiazepino-antikūno konjugatai |
GB201702031D0 (en) | 2017-02-08 | 2017-03-22 | Medlmmune Ltd | Pyrrolobenzodiazepine-antibody conjugates |
JP6704532B1 (ja) | 2017-02-08 | 2020-06-03 | アーデーセー セラピューティクス ソシエテ アノニム | ピロロベンゾジアゼピン抗体複合体 |
CN106866624B (zh) * | 2017-02-27 | 2017-12-26 | 济宁医学院 | 一种卡比替尼的化学合成方法 |
EP3612537B1 (fr) | 2017-04-18 | 2022-07-13 | Medimmune Limited | Conjugués de pyrrolobenzodiazépine |
WO2018193102A1 (fr) | 2017-04-20 | 2018-10-25 | Adc Therapeutics Sa | Polythérapie avec un conjugué anticorps anti-axl-médicament |
WO2018193104A1 (fr) | 2017-04-20 | 2018-10-25 | Adc Therapeutics Sa | Polythérapie avec un conjugué anticorps-médicament anti-cd25 |
UA127900C2 (uk) | 2017-06-14 | 2024-02-07 | Ейдісі Терапьютікс Са | Схема дозування для введення adc до cd19 |
EP3638372A1 (fr) | 2017-06-14 | 2020-04-22 | ADC Therapeutics SA | Régimes posologiques pour l'administration d'un cam anti-cd25 |
MX2020001880A (es) | 2017-08-18 | 2021-07-06 | Medimmune Ltd | Conjugados de pirrolobenzodiazepina. |
EP3679159A1 (fr) | 2017-09-08 | 2020-07-15 | H. Hoffnabb-La Roche Ag | Méthodes diagnostiques et thérapeutiques du cancer |
EP3752200A1 (fr) | 2018-02-13 | 2020-12-23 | Vib Vzw | Ciblage d'une maladie résiduelle minimale dans le cancer avec des antagonistes de rxr |
GB201803342D0 (en) | 2018-03-01 | 2018-04-18 | Medimmune Ltd | Methods |
MA52093A (fr) | 2018-03-19 | 2021-01-27 | Taiho Pharmaceutical Co Ltd | Composition pharmaceutique comprenant du sulfate d'alkyle de sodium |
EP3768306A1 (fr) | 2018-03-21 | 2021-01-27 | Colorado State University Research Foundation | Compositions de vaccins contre le cancer et leurs méthodes d'utilisation |
CN111902773A (zh) | 2018-03-26 | 2020-11-06 | 富士胶片株式会社 | 感光性树脂组合物及其制造方法、抗蚀剂膜、图案形成方法以及电子器件的制造方法 |
GB201806022D0 (en) | 2018-04-12 | 2018-05-30 | Medimmune Ltd | Pyrrolobenzodiazepines and conjugates thereof |
WO2019224275A1 (fr) | 2018-05-23 | 2019-11-28 | Adc Therapeutics Sa | Adjuvant moléculaire |
WO2020006176A1 (fr) | 2018-06-27 | 2020-01-02 | Obi Pharma, Inc. | Variants de glycosynthases pour génie des glycoprotéines et leurs procédés d'utilisation |
GB201811364D0 (en) | 2018-07-11 | 2018-08-29 | Adc Therapeutics Sa | Combination therapy |
EP3824287A1 (fr) | 2018-07-20 | 2021-05-26 | Pierre Fabre Médicament | Récepteur pour vista |
SG11202101518QA (en) | 2018-08-31 | 2021-03-30 | Adc Therapeutics Sa | Combination therapy |
CN112867803A (zh) | 2018-10-16 | 2021-05-28 | 诺华股份有限公司 | 单独的或与免疫标志物组合的肿瘤突变负荷作为生物标志物用于预测对靶向疗法的应答 |
JP7406264B2 (ja) * | 2018-11-20 | 2023-12-27 | エヌフレクション セラピューティクス インコーポレイテッド | 皮膚障害の処置のためのシアノアリール-アニリン化合物 |
MA54741A (fr) * | 2018-11-20 | 2021-11-24 | Nflection Therapeutics Inc | Composés thiényl-aniline destinés au traitement d'affections de la peau |
EP4233865A3 (fr) * | 2018-11-20 | 2023-09-27 | NFlection Therapeutics, Inc. | Composés aryl-aniline et hétéroaryl-aniline pour le traitement de cancers de la peau |
WO2020109251A1 (fr) | 2018-11-29 | 2020-06-04 | Adc Therapeutics Sa | Régime posologique |
GB201820725D0 (en) | 2018-12-19 | 2019-01-30 | Adc Therapeutics Sarl | Pyrrolobenzodiazepine resistance |
US20220347309A1 (en) | 2018-12-19 | 2022-11-03 | Adc Therapeutics Sa | Pyrrolobenzodiazepine resistance |
CA3124330A1 (fr) | 2018-12-21 | 2020-06-25 | Daiichi Sankyo Company, Limited | Combinaison d'un conjugue anticorps-medicament et d'un inhibiteur de kinase |
WO2020187674A1 (fr) | 2019-03-15 | 2020-09-24 | Sandoz Ag | Hémisuccinate de (s)-[3,4-difluoro-2-(2-fluoro-4-iodophénylamino)phényl][3-hydroxy-3-(pipéridin-2-yl) azétidin-1-yl]méthanone cristallin |
WO2020188015A1 (fr) | 2019-03-21 | 2020-09-24 | Onxeo | Molécule dbait associée à un inhibiteur de kinase pour le traitement du cancer |
PL3946464T3 (pl) | 2019-03-29 | 2022-12-19 | Medimmune Limited | Związki i ich koniugaty |
TWI735210B (zh) | 2019-04-26 | 2021-08-01 | 中國醫藥大學 | Adam9抑制劑作為免疫調節劑之用途 |
GB201908128D0 (en) | 2019-06-07 | 2019-07-24 | Adc Therapeutics Sa | Pyrrolobenzodiazepine-antibody conjugates |
AU2020292965A1 (en) | 2019-06-10 | 2022-01-27 | Adc Therapeutics Sa | Combination therapy comprising an anti-CD19 antibody drug conjugate and a PI3K inhibitor or a secondary agent |
SG11202113293XA (en) | 2019-06-10 | 2021-12-30 | Adc Therapeutics Sa | Combination therapy comprising an anti-cd25 antibody drug conjugate and a further agent |
CR20220029A (es) | 2019-07-22 | 2022-03-14 | Lupin Ltd | Compuestos macrocíclicos como agonistas de sting y métodos y usos de los mismos |
GB201912059D0 (en) | 2019-08-22 | 2019-10-09 | Bergenbio As | Combaination therapy of a patient subgroup |
WO2021080608A1 (fr) | 2019-10-25 | 2021-04-29 | Medimmune, Llc | Fraction ramifiée destinée à être utilisée dans des conjugués |
AU2020378630A1 (en) | 2019-11-08 | 2022-05-26 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
GB201917254D0 (en) | 2019-11-27 | 2020-01-08 | Adc Therapeutics Sa | Combination therapy |
WO2021119397A1 (fr) | 2019-12-13 | 2021-06-17 | Rgenix, Inc. | Sels métalliques et leurs utilisations |
CN111170990B (zh) * | 2020-01-16 | 2021-01-05 | 广州科锐特生物科技有限公司 | 一种3-哌啶-2-基-氮杂环丁烷-3-醇衍生物的制备方法 |
MX2022009052A (es) | 2020-01-22 | 2022-08-15 | Medimmune Ltd | Compuestos y conjugados de estos. |
WO2021148581A1 (fr) | 2020-01-22 | 2021-07-29 | Onxeo | Nouvelle molécule dbait et son utilisation |
TW202140076A (zh) | 2020-01-22 | 2021-11-01 | 英商梅迪繆思有限公司 | 化合物及其軛合物 |
GB202004189D0 (en) | 2020-03-23 | 2020-05-06 | Bergenbio As | Combination therapy |
WO2021206167A1 (fr) | 2020-04-10 | 2021-10-14 | 大鵬薬品工業株式会社 | Thérapie contre le cancer à l'aide d'un composé d'alcynyle benzène 3,5-disubstitué et un inhibiteur de mek |
IL297027A (en) | 2020-04-16 | 2022-12-01 | Regeneron Pharma | Diels-Alder compression methods |
GB202006072D0 (en) | 2020-04-24 | 2020-06-10 | Bergenbio Asa | Method of selecting patients for treatment with cmbination therapy |
EP3915576A1 (fr) | 2020-05-28 | 2021-12-01 | Fundació Privada Institut d'Investigació Oncològica de Vall-Hebron | Récepteurs d'antigène chimérique spécifiques pour p95her2 et leurs utilisations |
EP3939999A1 (fr) | 2020-07-14 | 2022-01-19 | Fundación del Sector Público Estatal Centro Nacional de Investigaciones Oncológicas Carlos III (F.S.P. CNIO) | Anticorps neutralisant la sous-unité alpha du récepteur de l'interleukine 11 (il11ra) et leurs utilisations |
GB202011993D0 (en) | 2020-07-31 | 2020-09-16 | Adc Therapeutics Sa | ANTI-IL 13Ra2 antibodies |
GB202012161D0 (en) | 2020-08-05 | 2020-09-16 | Adc Therapeutics Sa | Combination therapy |
MX2023001865A (es) | 2020-08-14 | 2023-05-09 | Guangzhou Lupeng Pharmaceutical Company Ltd | Composiciones de forma de dosificación que comprenden un inhibidor de btk y mutantes de este. |
GB202015226D0 (en) | 2020-09-25 | 2020-11-11 | Adc Therapeutics S A | Pyrrol obenzodiazepine-antibody conugates and uses thereof |
GB202015916D0 (en) | 2020-10-07 | 2020-11-18 | Adc Therapeutics Sa | Combination therapy |
US20230372528A1 (en) | 2020-10-16 | 2023-11-23 | University Of Georgia Research Foundation, Inc. | Glycoconjugates |
GB202102396D0 (en) | 2021-02-19 | 2021-04-07 | Adc Therapeutics Sa | Molecular adjuvant |
KR20230156731A (ko) | 2021-03-09 | 2023-11-14 | 제넨테크, 인크. | 뇌암 치료에 이용하기 위한 벨바라페닙 |
WO2022195551A1 (fr) | 2021-03-18 | 2022-09-22 | Novartis Ag | Biomarqueurs pour le cancer et leurs méthodes d'utilisation |
JP2024514112A (ja) | 2021-04-06 | 2024-03-28 | ジェネンテック, インコーポレイテッド | ベルバラフェニブおよびコビメチニブを用いた併用療法、またはベルバラフェニブ、コビメチニブおよびアテゾリズマブを用いた併用療法 |
GB202107706D0 (en) | 2021-05-28 | 2021-07-14 | Adc Therapeutics S A | Combination therapy |
GB202107713D0 (en) | 2021-05-28 | 2021-07-14 | Medimmune Ltd | Combination therapy |
GB202107709D0 (en) | 2021-05-28 | 2021-07-14 | Adc Therapeutics S A | Combination therapy |
KR20240008410A (ko) | 2021-06-09 | 2024-01-18 | 에프. 호프만-라 로슈 아게 | 암 치료를 위한 병용요법 |
WO2023274974A1 (fr) | 2021-06-29 | 2023-01-05 | Adc Therapeutics Sa | Polythérapie utilisant des conjugués anticorps-médicament |
WO2023057545A1 (fr) | 2021-10-06 | 2023-04-13 | Microquin Ltd. | Chalcones substitués |
CA3230652A1 (fr) | 2021-11-04 | 2023-05-11 | F. Hoffmann-La Roche Ag | Nouvelle utilisation d'un compose quinazolinone pour le traitement du cancer |
WO2023111213A1 (fr) | 2021-12-16 | 2023-06-22 | Rdp Pharma Ag | Polypeptides de pénétration cellulaire (cpps) et leur utilisation en thérapie humaine |
TW202342018A (zh) | 2022-03-04 | 2023-11-01 | 美商奇奈特生物製藥公司 | Mek激酶抑制劑 |
US11780800B1 (en) | 2022-03-17 | 2023-10-10 | Springworks Therapeutics, Inc. | Fluorinated phenylamino compounds and pharmaceutical compositions |
EP4253418A1 (fr) | 2022-03-29 | 2023-10-04 | Fundació Privada Institut d'Investigació Oncològica de Vall-Hebron | Cellules immunitaires exprimant des récepteurs d'antigène chimérique et anticorps bispécifiques et leurs utilisations |
GB202209285D0 (en) | 2022-06-24 | 2022-08-10 | Bergenbio Asa | Dosage regimen for AXL inhibitor |
WO2024033381A1 (fr) | 2022-08-10 | 2024-02-15 | Vib Vzw | Inhibition de tcf4/itf2 dans le traitement du cancer |
Family Cites Families (62)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4510139A (en) | 1984-01-06 | 1985-04-09 | Sterling Drug Inc. | Substituted aminobenzamides and their use as agents which inhibit lipoxygenase activity |
US5155110A (en) | 1987-10-27 | 1992-10-13 | Warner-Lambert Company | Fenamic acid hydroxamate derivatives having cyclooxygenase and 5-lipoxygenase inhibition |
JPH03192592A (ja) | 1989-12-21 | 1991-08-22 | Matsushita Electric Ind Co Ltd | 磁気テープ記録再生装置 |
AU685933B2 (en) | 1994-04-01 | 1998-01-29 | Shionogi & Co., Ltd. | Oxime derivative and bactericide containing the same as active ingredient |
AU6966696A (en) | 1995-10-05 | 1997-04-28 | Warner-Lambert Company | Method for treating and preventing inflammation and atherosclerosis |
WO1998037881A1 (fr) | 1997-02-28 | 1998-09-03 | Warner Lambert Company | Methode de traitement ou de prevention du choc septique par administration d'un inhibiteur mek |
EP0993439B1 (fr) | 1997-07-01 | 2004-09-29 | Warner-Lambert Company LLC | Derives d'acide benzhydroxamique phenylamino 4-bromo ou 4-iodo et utilisation de ces derniers en tant qu'inhibiteurs de mek |
WO1999001421A1 (fr) * | 1997-07-01 | 1999-01-14 | Warner-Lambert Company | Derives d'acide benzoique 2-(4-bromo ou 4-iodo phenylamino) et utilisation de ces derniers en tant qu'inhibiteurs de mek |
US6974878B2 (en) | 2001-03-21 | 2005-12-13 | Symyx Technologies, Inc. | Catalyst ligands, catalytic metal complexes and processes using same |
CA2346684A1 (fr) | 1998-12-15 | 2000-06-22 | Warner-Lambert Company | Technique de prevention du rejet de greffe par utilisation d'un inhibiteur du mek |
CA2346448A1 (fr) * | 1998-12-16 | 2000-06-22 | Warner-Lambert Company | Traitement de l'arthrite a l'aide d'inhibiteurs de la mek |
EE200100339A (et) | 1998-12-22 | 2002-10-15 | Warner-Lambert Company | Kombineeritud kemoteraapia |
KR20000047461A (ko) | 1998-12-29 | 2000-07-25 | 성재갑 | 트롬빈 억제제 |
WO2000040235A2 (fr) | 1999-01-07 | 2000-07-13 | Warner-Lambert Company | Traitement de l'asthme a l'aide d'inhibiteurs de mek |
EP1140067A1 (fr) | 1999-01-07 | 2001-10-10 | Warner-Lambert Company | Methode antivirale utilisant des inhibiteurs de mek |
CA2348236A1 (fr) | 1999-01-13 | 2000-07-20 | Stephen Douglas Barrett | 4-arylamino, 4-aryloxy, et 4-arylthio diarylamines et leurs derives comme inhibiteurs selectifs de mek |
CA2355470C (fr) * | 1999-01-13 | 2008-09-30 | Warner-Lambert Company | Les benzoheterocycles et leur utilisation comme inhibiteurs de mek |
WO2000041505A2 (fr) * | 1999-01-13 | 2000-07-20 | Warner-Lambert Company | 4'heteroaryle diarylamines |
NZ513432A (en) | 1999-01-13 | 2004-02-27 | Warner Lambert Co | 1-heterocycle substituted diarylamines |
ATE309205T1 (de) | 1999-01-13 | 2005-11-15 | Warner Lambert Co | Benzenesulfonamid-derivative und ihre verwendung als mek-inhibitoren |
JP2003504400A (ja) | 1999-07-16 | 2003-02-04 | ワーナー−ランバート・カンパニー | Mek阻害剤を用いた慢性痛の治療方法 |
DK1202724T3 (da) | 1999-07-16 | 2004-01-26 | Warner Lambert Co | Fremgangsmåde til behandling af kronisk smerte under anvendelse af mek-inhibitorer |
PL352705A1 (en) | 1999-07-16 | 2003-09-08 | Warner-Lambert Company | Method for treating chronic pain using mek inhibitors |
HUP0202319A3 (en) | 1999-07-16 | 2004-12-28 | Warner Lambert Co | Use of mek inhibitors for the preparation of pharmaceutical compositions treating chronic pain |
MX226123B (es) | 1999-09-17 | 2005-02-07 | Millennium Pharm Inc | Benzamidas e inhibidores del factor xa relacionadas. |
JP2003527379A (ja) | 2000-03-15 | 2003-09-16 | ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー | Mex阻害物質としての5−アミド置換ジアリールアミン類 |
AR033517A1 (es) | 2000-04-08 | 2003-12-26 | Astrazeneca Ab | Derivados de piperidina, proceso para su preparacion y uso de estos derivados en la fabricacion de medicamentos |
DZ3401A1 (fr) | 2000-07-19 | 2002-01-24 | Warner Lambert Co | Esters oxygenes d'acides 4-iodophenylamino benzhydroxamiques |
IL149462A0 (en) | 2001-05-09 | 2002-11-10 | Warner Lambert Co | Method of treating or inhibiting neutrophil chemotaxis by administering a mek inhibitor |
DE10141266A1 (de) | 2001-08-21 | 2003-03-06 | Syntec Ges Fuer Chemie Und Tec | Elektrolumineszierende Derivate der 2,5-Diamino-terephthalsäure und deren Verwendung in organischen Leuchtdioden |
JP2003192592A (ja) | 2001-10-17 | 2003-07-09 | Sankyo Co Ltd | 医薬組成物 |
IL160967A0 (en) | 2001-10-31 | 2004-08-31 | Pfizer Prod Inc | Nicotinic acetylcholine receptor agonists in the treatment of restless legs syndrome |
JP2005515253A (ja) | 2002-01-23 | 2005-05-26 | ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー | N−(4−置換フェニル)−アントラニル酸ヒドロキサメートエステル |
DOP2003000556A (es) | 2002-01-23 | 2003-10-31 | Warner Lambert Co | Esteres hidroxamato de acido n-(4-fenil-sustituido)-antranilico. |
KR20040098013A (ko) | 2002-03-13 | 2004-11-18 | 어레이 바이오파마 인크. | Mek 억제제로서의 n3 알킬화된 벤즈이미다졸 유도체 |
US7235537B2 (en) | 2002-03-13 | 2007-06-26 | Array Biopharma, Inc. | N3 alkylated benzimidazole derivatives as MEK inhibitors |
SI1482932T1 (sl) * | 2002-03-13 | 2010-02-26 | Array Biopharma Inc | N3-alkilirani derivati benzimidazola kot inhibitorji mek |
AU2003238915B2 (en) | 2002-06-11 | 2008-02-21 | Merck & Co., Inc. | (halo-benzo carbonyl)heterobicyclic p38 kinase inhibiting agents |
GB0214268D0 (en) * | 2002-06-20 | 2002-07-31 | Celltech R&D Ltd | Chemical compounds |
US20050004186A1 (en) | 2002-12-20 | 2005-01-06 | Pfizer Inc | MEK inhibiting compounds |
WO2004078116A2 (fr) | 2003-03-03 | 2004-09-16 | Array Biopharma, Inc. | Inhibiteurs de la p 38 et leurs procedes d'utilisation |
JP2005162727A (ja) | 2003-03-18 | 2005-06-23 | Sankyo Co Ltd | スルファミド誘導体及びその医薬組成物 |
TW200505834A (en) | 2003-03-18 | 2005-02-16 | Sankyo Co | Sulfamide derivative and the pharmaceutical composition thereof |
GB0308185D0 (en) * | 2003-04-09 | 2003-05-14 | Smithkline Beecham Corp | Novel compounds |
BRPI0410653A (pt) * | 2003-06-20 | 2006-07-04 | Celltech R&D Ltd | composto, composição farmacêutica, e, uso de um composto ou um sal, solvato, hidrato ou n-óxido farmaceuticamente aceitável do mesmo |
WO2005000818A1 (fr) | 2003-06-27 | 2005-01-06 | Warner-Lambert Company Llc | Derives de 4-[phenylamino (substitue)]-2-pyridone a substitution en 5 en tant qu'inhibiteurs de la mek |
US20050049276A1 (en) * | 2003-07-23 | 2005-03-03 | Warner-Lambert Company, Llc | Imidazopyridines and triazolopyridines |
WO2005007616A1 (fr) * | 2003-07-23 | 2005-01-27 | Warner-Lambert Company Llc | Derives de diphenylaminocetone utiles comme inhibiteurs de mek |
ES2331246T3 (es) | 2003-07-24 | 2009-12-28 | Warner-Lambert Company Llc | Derivados de benzamidazol como inhibidores del mek. |
US7144907B2 (en) * | 2003-09-03 | 2006-12-05 | Array Biopharma Inc. | Heterocyclic inhibitors of MEK and methods of use thereof |
US7538120B2 (en) | 2003-09-03 | 2009-05-26 | Array Biopharma Inc. | Method of treating inflammatory diseases |
WO2005028426A1 (fr) | 2003-09-19 | 2005-03-31 | Chugai Seiyaku Kabushiki Kaisha | Nouveau derive de 4-phenylamino-benzaldoxime et son utilisation en tant qu'inhibiteur de mek |
US7517994B2 (en) | 2003-11-19 | 2009-04-14 | Array Biopharma Inc. | Heterocyclic inhibitors of MEK and methods of use thereof |
AU2004293436B2 (en) | 2003-11-19 | 2010-12-09 | Array Biopharma Inc. | Heterocyclic inhibitors of MEK and methods of use thereof |
EP1694673B1 (fr) * | 2003-12-08 | 2008-01-16 | F.Hoffmann-La Roche Ag | Derives de thiazole |
TWI361066B (en) | 2004-07-26 | 2012-04-01 | Chugai Pharmaceutical Co Ltd | 5-substituted-2-phenylamino benzamides as mek inhibitors |
PE20060572A1 (es) | 2004-07-27 | 2006-06-27 | Novartis Ag | Compuestos de benzoimidazolona como inhibidores de hsp90 |
EA013212B1 (ru) * | 2004-10-20 | 2010-04-30 | Лаборатуар Сероно Са | 3-ариламинопиридиновые производные |
WO2006061712A2 (fr) | 2004-12-10 | 2006-06-15 | Pfizer Inc. | Utilisation d'inhibiteurs de mek dans le traitement d'une croissance cellulaire anormale |
US7547782B2 (en) * | 2005-09-30 | 2009-06-16 | Bristol-Myers Squibb Company | Met kinase inhibitors |
CA3052368A1 (fr) * | 2005-10-07 | 2007-04-19 | Exelixis, Inc. | Azetidines comme inhibiteurs de mek |
ATE539752T1 (de) * | 2006-08-16 | 2012-01-15 | Exelixis Inc | Verwendung von pi3k- und mek-modulatoren bei der krebsbehandlung |
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