US6569868B2
(en)
|
1998-04-16 |
2003-05-27 |
Sugen, Inc. |
2-indolinone derivatives as modulators of protein kinase activity
|
US20040226056A1
(en)
*
|
1998-12-22 |
2004-11-11 |
Myriad Genetics, Incorporated |
Compositions and methods for treating neurological disorders and diseases
|
EP1147214B1
(fr)
|
1999-01-13 |
2011-01-05 |
The Research Foundation Of State University Of New York |
Nouveau procede d'identification d'inhibiteurs de proteines kinase
|
UA73976C2
(uk)
*
|
2000-02-15 |
2005-10-17 |
Суджен, Інк. |
Заміщені піролом 2-індолінони, фармацевтична композиція, спосіб модуляції каталітичної активності протеїнкінази та спосіб лікування або профілактики захворювання, пов'язаного з протеїнкіназою
|
US7030219B2
(en)
|
2000-04-28 |
2006-04-18 |
Johns Hopkins University |
B7-DC, Dendritic cell co-stimulatory molecules
|
MY128449A
(en)
|
2000-05-24 |
2007-02-28 |
Sugen Inc |
Prodrugs of 3-(pyrrol-2-ylmethylidene)-2-indolinone derivatives
|
US6706709B2
(en)
|
2000-06-02 |
2004-03-16 |
Sugen, Inc. |
Indolinone derivatives as protein kinase/phosphatase inhibitors
|
CA2414468A1
(fr)
*
|
2000-06-30 |
2002-01-10 |
Sugen, Inc. |
4-heteroaryl-3-heteroarylidenyl-2-indolinones et leur utilisation comme inhibiteurs des proteine kinases
|
HU230302B1
(hu)
|
2000-10-20 |
2015-12-28 |
Eisai R&D Management Co., Ltd. |
Nitrogéntartalmú aromás származékok és ezeket tartalmazó gyógyászati készítmények
|
JP2004518669A
(ja)
*
|
2000-12-20 |
2004-06-24 |
スージェン・インコーポレーテッド |
4−アリール置換インドリノン
|
AR042586A1
(es)
*
|
2001-02-15 |
2005-06-29 |
Sugen Inc |
3-(4-amidopirrol-2-ilmetiliden)-2-indolinona como inhibidores de la protein quinasa; sus composiciones farmaceuticas; un metodo para la modulacion de la actividad catalitica de la proteinquinasa; un metodo para tratar o prevenir una afeccion relacionada con la proteinquinasa
|
EP1247809A3
(fr)
*
|
2001-03-30 |
2003-12-17 |
Pfizer Products Inc. |
Dérivés de triazine et leur application comme inhibiteurs de sorbitol-déhydrogénase
|
WO2002096361A2
(fr)
|
2001-05-30 |
2002-12-05 |
Sugen, Inc. |
Derives de 5-aralkylsulfonyl-3-(pyrrol-2-ylmethylidene)-2-indolinone utilises comme inhibiteurs de kinase
|
DE60227709D1
(de)
*
|
2001-06-29 |
2008-08-28 |
Ab Science |
Die verwendung von c-kithemmern zur behandlung von autoimmunerkrankungen
|
EP1419151B1
(fr)
|
2001-08-15 |
2014-02-26 |
Pharmacia & Upjohn Company LLC |
Cristaux comprenant un sel d'acide malique de n- [2-(diethylamino)ethyl] -5- [(5-fluoro-1,2-dihydro-2-oxo-3h-indol-3-ylidene)methyl] -2,4-dimethyl-1h-pyrrole-3-carboxamide, procedes de preparation associes et compositions correspondantes
|
AR038957A1
(es)
*
|
2001-08-15 |
2005-02-02 |
Pharmacia Corp |
Terapia de combinacion para el tratamiento del cancer
|
JP2005506982A
(ja)
|
2001-09-10 |
2005-03-10 |
スージェン・インコーポレーテッド |
キナーゼ阻害剤としての3−(4,5,6,7−テトラヒドロインドール−2−イルメチリデン)−2−インドリノン誘導体
|
JP2005508953A
(ja)
*
|
2001-10-10 |
2005-04-07 |
スージェン・インコーポレーテッド |
キナーゼ阻害剤としての3−[4−(置換ヘテロサイクリル)−ピロール−2−イルメチリデン]−2−インドリノン誘導体
|
US7005445B2
(en)
|
2001-10-22 |
2006-02-28 |
The Research Foundation Of State University Of New York |
Protein kinase and phosphatase inhibitors and methods for designing them
|
EP1444204A4
(fr)
*
|
2001-10-22 |
2009-11-04 |
Univ New York State Res Found |
Inhibiteurs de proteines kinases et de proteines phosphatases, methodes d'identification et methodes d'utilisation associees
|
US20030080191A1
(en)
*
|
2001-10-26 |
2003-05-01 |
Allen Lubow |
Method and apparatus for applying bar code information to products during production
|
TWI259081B
(en)
*
|
2001-10-26 |
2006-08-01 |
Sugen Inc |
Treatment of acute myeloid leukemia with indolinone compounds
|
US6797825B2
(en)
|
2001-12-13 |
2004-09-28 |
Abbott Laboratories |
Protein kinase inhibitors
|
US20030187026A1
(en)
|
2001-12-13 |
2003-10-02 |
Qun Li |
Kinase inhibitors
|
US7156308B2
(en)
*
|
2001-12-17 |
2007-01-02 |
International Barcode Corporation |
Double-sided bar code doubling as a single bar code
|
US20050131733A1
(en)
*
|
2001-12-17 |
2005-06-16 |
Allen Lubow |
Sealable individual bar coded packets
|
HUP0500111A3
(en)
|
2001-12-27 |
2009-10-28 |
Theravance |
Indolinone derivatives useful as protein kinase inhibitors
|
JP2005528344A
(ja)
*
|
2002-02-15 |
2005-09-22 |
ファルマシア・アンド・アップジョン・カンパニー・エルエルシー |
インドリノン誘導体の製造法
|
US20040018528A1
(en)
*
|
2002-05-17 |
2004-01-29 |
Sugen, Inc. |
Novel biomarkers of tyrosine kinase inhibitor exposure and activity in mammals
|
ITMI20021620A1
(it)
*
|
2002-07-23 |
2004-01-23 |
Novuspharma Spa |
Composto ad ativita' antitumorale
|
WO2004016211A2
(fr)
*
|
2002-08-08 |
2004-02-26 |
Vanderbilt University |
Antagonistes pi3k utilises en tant que radiosensibilisateurs
|
WO2004015082A2
(fr)
*
|
2002-08-09 |
2004-02-19 |
Theravance, Inc. |
Polypeptides de fusion d'oncokinase associes a des troubles hyperproliferatifs, acides nucleiques codant pour lesdits polypeptides et leurs methodes de detection et d'identification
|
US20040121407A1
(en)
*
|
2002-09-06 |
2004-06-24 |
Elixir Pharmaceuticals, Inc. |
Regulation of the growth hormone/IGF-1 axis
|
TW200418836A
(en)
*
|
2002-09-10 |
2004-10-01 |
Pharmacia Italia Spa |
Formulations comprising an indolinone compound
|
JP2006510727A
(ja)
*
|
2002-11-15 |
2006-03-30 |
エクセリクシス, インク. |
キナーゼモジュレーター
|
AR042042A1
(es)
*
|
2002-11-15 |
2005-06-08 |
Sugen Inc |
Administracion combinada de una indolinona con un agente quimioterapeutico para trastornos de proliferacion celular
|
US7452913B2
(en)
*
|
2003-02-24 |
2008-11-18 |
Pharmacia & Upjohn Company |
Polymorphs of pyrrole substituted 2-indolinone protein kinase inhibitors
|
US20040209937A1
(en)
*
|
2003-02-24 |
2004-10-21 |
Sugen, Inc. |
Treatment of excessive osteolysis with indolinone compounds
|
EP2476667B1
(fr)
|
2003-02-26 |
2014-07-16 |
Sugen, Inc. |
Composés d'aminohétéroaryle utilisés en tant qu'inhibiteurs de protéine kinase
|
US20040266843A1
(en)
*
|
2003-03-07 |
2004-12-30 |
Sugen, Inc. |
Sulfonamide substituted indolinones as inhibitors of DNA dependent protein kinase (DNA-PK)
|
US7157577B2
(en)
*
|
2003-03-07 |
2007-01-02 |
Sugen Inc. |
5-sulfonamido-substituted indolinone compounds as protein kinase inhibitors
|
JPWO2004080462A1
(ja)
*
|
2003-03-10 |
2006-06-08 |
エーザイ株式会社 |
c−Kitキナーゼ阻害剤
|
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
|
DE10334582A1
(de)
*
|
2003-07-28 |
2005-02-24 |
Basf Ag |
Verfahren zur Herstellung von Maleinsäureanhydrid
|
WO2005023765A1
(fr)
*
|
2003-09-11 |
2005-03-17 |
Pharmacia & Upjohn Company Llc |
Methode de catalyse de reactions d'amidation au moyen de co2
|
PT1670785E
(pt)
*
|
2003-10-02 |
2010-09-16 |
Pharmacia & Upjohn Co Llc |
Sais e polimorfos de um composto de indolinona substituída com pirrole
|
DK1680140T3
(da)
*
|
2003-10-16 |
2011-06-14 |
Imclone Llc |
Fibrolast-vækstfaktorreceptor-1-inhibitorer og fremgangsmåde til behandling deraf
|
EP1699421B1
(fr)
|
2003-11-07 |
2014-05-21 |
Novartis Vaccines and Diagnostics, Inc. |
Sels de lactate de composés de quinolinone et leur utilisation pharmaceutique
|
US7683172B2
(en)
|
2003-11-11 |
2010-03-23 |
Eisai R&D Management Co., Ltd. |
Urea derivative and process for preparing the same
|
US20080044881A1
(en)
*
|
2003-11-26 |
2008-02-21 |
Congxin Liang |
Advanced Indolinone Based Protein Kinase Inhibitors
|
US20050171182A1
(en)
*
|
2003-12-11 |
2005-08-04 |
Roger Briesewitz |
Methods and compositions for use in the treatment of mutant receptor tyrosine kinase driven cellular proliferative diseases
|
US20050152943A1
(en)
*
|
2003-12-23 |
2005-07-14 |
Medtronic Vascular, Inc. |
Medical devices to treat or inhibit restenosis
|
WO2005118543A1
(fr)
*
|
2004-06-03 |
2005-12-15 |
Ono Pharmaceutical Co., Ltd. |
Inhibiteur des kinases et utilisation de cet inhibiteur
|
WO2006002422A2
(fr)
|
2004-06-24 |
2006-01-05 |
Novartis Vaccines And Diagnostics Inc. |
Composes utilises pour l'immunopotentialisation
|
SE0401790D0
(sv)
*
|
2004-07-07 |
2004-07-07 |
Forskarpatent I Syd Ab |
Tamoxifen response in pre- and postmenopausal breast cancer patients
|
US20060009510A1
(en)
*
|
2004-07-09 |
2006-01-12 |
Pharmacia & Upjohn Company Llc |
Method of synthesizing indolinone compounds
|
PL1786785T3
(pl)
*
|
2004-08-26 |
2010-08-31 |
Pfizer |
Enancjomerycznie czyste związki aminoheteroarylowe jako kinazy białkowe
|
ATE428421T1
(de)
|
2004-09-17 |
2009-05-15 |
Eisai R&D Man Co Ltd |
Medizinische zusammensetzung mit verbesserter stabilität und reduzierten gelierungseigenschaften
|
CN100432071C
(zh)
*
|
2004-11-05 |
2008-11-12 |
中国科学院上海药物研究所 |
取代1h-吲哚-2-酮类化合物及其制备方法和用途
|
GT200500321A
(es)
*
|
2004-11-09 |
2006-09-04 |
|
Compuestos y composiciones como inhibidores de proteina kinase.
|
BRPI0607579A2
(pt)
*
|
2005-03-23 |
2009-09-15 |
Pfizer Prod Inc |
uso de anticorpo anti-ctla4 e indolinona para a preparação de medicamentos para o tratamento de cáncer
|
EA012970B1
(ru)
|
2005-04-26 |
2010-02-26 |
Пфайзер Инк. |
Антитела против р-кадгерина
|
KR20070119745A
(ko)
*
|
2005-05-12 |
2007-12-20 |
화이자 인코포레이티드 |
수니티닙 말레이트를 사용하는 항암 병행 요법
|
ATE539064T1
(de)
|
2005-05-18 |
2012-01-15 |
Array Biopharma Inc |
Heterozyklische inhibitoren von mek und verwendungsverfahren damit
|
SG154451A1
(en)
|
2005-05-23 |
2009-08-28 |
Novartis Ag |
Crystalline and other forms of 4-amino-5-fluoro-3-[6-(4-methylpiperazin-1- yl)-1h-benzimidazol-2-yl]-1h-quinolin-2-one lactic acid salts
|
BRPI0611419A2
(pt)
*
|
2005-05-26 |
2010-09-08 |
Scripps Research Inst |
composto, sal, tautÈmero ou pró-fármaco, método para a modulação da atividade catalìtica de uma proteìna cinase e processo para a sìntese de uma pirrolil-indolinona
|
WO2007015569A1
(fr)
|
2005-08-01 |
2007-02-08 |
Eisai R & D Management Co., Ltd. |
Procédé de prédiction de l’efficacité d’un inhibiteur de vascularisation
|
EP1925676A4
(fr)
|
2005-08-02 |
2010-11-10 |
Eisai R&D Man Co Ltd |
Procédé d'analyse de l' effet d 'un inhibiteur de vascularisation
|
AP2013006963A0
(en)
|
2005-09-07 |
2013-07-31 |
Amgen Fremont Inc |
Human monoclonal antibodies to activin receptor-like Kinase-1
|
EP2112148A1
(fr)
|
2005-09-19 |
2009-10-28 |
Pfizer Products Inc. |
Sels solides de 2-indolinone à substitution pyrrole
|
JPWO2007052849A1
(ja)
*
|
2005-11-07 |
2009-04-30 |
エーザイ・アール・アンド・ディー・マネジメント株式会社 |
血管新生阻害物質とc−kitキナーゼ阻害物質との併用
|
UA96139C2
(uk)
|
2005-11-08 |
2011-10-10 |
Дженентек, Інк. |
Антитіло до нейропіліну-1 (nrp1)
|
BRPI0620939A2
(pt)
*
|
2005-12-29 |
2011-11-29 |
Scripps Research Inst |
derivados de aminoácido de indolinona com base em inibidores de proteìna quinase
|
JO2660B1
(en)
|
2006-01-20 |
2012-06-17 |
نوفارتيس ايه جي |
Pi-3 inhibitors and methods of use
|
CN101007801A
(zh)
*
|
2006-01-27 |
2007-08-01 |
上海恒瑞医药有限公司 |
吡咯取代的2-二氢吲哚酮衍生物、其制法与医药上的用途
|
AR060358A1
(es)
|
2006-04-06 |
2008-06-11 |
Novartis Vaccines & Diagnostic |
Quinazolinas para la inhibicion de pdk 1
|
TW200813091A
(en)
|
2006-04-10 |
2008-03-16 |
Amgen Fremont Inc |
Targeted binding agents directed to uPAR and uses thereof
|
CN101472915A
(zh)
|
2006-04-19 |
2009-07-01 |
诺瓦提斯公司 |
吲唑化合物和抑制cdc7的方法
|
EP2021338A1
(fr)
|
2006-05-09 |
2009-02-11 |
Pfizer Products Inc. |
Dérivés d'acide cycloalkylaminé et compositions pharmaceutiques à base de ceux-ci
|
ES2556173T3
(es)
|
2006-05-18 |
2016-01-13 |
Eisai R&D Management Co., Ltd. |
Agente antitumoral para un cáncer de tiroides
|
DE102006024834B4
(de)
*
|
2006-05-24 |
2010-07-01 |
Schebo Biotech Ag |
Neue Indol-Pyrrol-Derivate und deren Verwendungen
|
US20090203693A1
(en)
*
|
2006-06-29 |
2009-08-13 |
Eisai R & D Management Co., Ltd. |
Therapeutic agent for liver fibrosis
|
US7838542B2
(en)
|
2006-06-29 |
2010-11-23 |
Kinex Pharmaceuticals, Llc |
Bicyclic compositions and methods for modulating a kinase cascade
|
WO2008008981A1
(fr)
|
2006-07-13 |
2008-01-17 |
Zymogenetics, Inc. |
Traitement de combinaison d'interleukine 21 et d'inhibiteur de tyrosine kinase
|
CL2007002225A1
(es)
|
2006-08-03 |
2008-04-18 |
Astrazeneca Ab |
Agente de union especifico para un receptor del factor de crecimiento derivado de plaquetas (pdgfr-alfa); molecula de acido nucleico que lo codifica; vector y celula huesped que la comprenden; conjugado que comprende al agente; y uso del agente de un
|
MX2009001349A
(es)
|
2006-08-04 |
2009-04-17 |
Takeda Pharmaceutical |
Derivado heterociclico fusionado y su uso.
|
JP5227321B2
(ja)
|
2006-08-23 |
2013-07-03 |
クドス ファーマシューティカルズ リミテッド |
Mtor阻害剤としての2−メチルモルホリンピリド−、ピラゾ−及びピリミド−ピリミジン誘導体
|
US8865737B2
(en)
|
2006-08-28 |
2014-10-21 |
Eisai R&D Management Co., Ltd. |
Antitumor agent for undifferentiated gastric cancer
|
PL2079727T3
(pl)
|
2006-09-15 |
2016-08-31 |
Xcovery Inc |
Inhibitory kinazy
|
US7750007B2
(en)
|
2006-11-06 |
2010-07-06 |
Supergen, Inc. |
Imidazo[1,2-beta]pyridazine and pyrazolo[1,5-alpha]pyrimidine derivatives and their use as protein kinase inhibitors
|
JP4623604B2
(ja)
*
|
2006-11-06 |
2011-02-02 |
株式会社セラバリューズ |
新規なオキシインドール誘導体
|
ATE547411T1
(de)
|
2006-12-04 |
2012-03-15 |
Jiangsu Simcere Pharmaceutical R & D Co Ltd |
3-pyrrolo-cyclohexylen-2-dihydroindolinonderiva e und anwendungen davon
|
WO2008093855A1
(fr)
|
2007-01-29 |
2008-08-07 |
Eisai R & D Management Co., Ltd. |
Composition destinée au traitement d'un cancer de l'estomac de type indifférencié
|
WO2008096218A1
(fr)
|
2007-02-06 |
2008-08-14 |
Pfizer Inc. |
Dérivés de 2-amino-5,7-dihydro-6h-pyrrolo[3,4-d]pyrimidine en tant qu'inhibiteurs de la hsp 90 pour le traitement du cancer
|
WO2008114819A1
(fr)
|
2007-03-20 |
2008-09-25 |
Dainippon Sumitomo Pharma Co., Ltd. |
Nouveau composé d'adénine
|
US20090004213A1
(en)
|
2007-03-26 |
2009-01-01 |
Immatics Biotechnologies Gmbh |
Combination therapy using active immunotherapy
|
US20090042906A1
(en)
*
|
2007-04-26 |
2009-02-12 |
Massachusetts Institute Of Technology |
Methods for treating cancers associated with constitutive egfr signaling
|
WO2008138184A1
(fr)
|
2007-05-14 |
2008-11-20 |
Shanghai Hengrui Pharmaceutical Co.Ltd. |
Dérivés de pyrrolo-azacycles, leur procédé de fabrication et leur utilisation en tant qu'inhibiteurs de protéine kinases
|
WO2008145398A1
(fr)
*
|
2007-06-01 |
2008-12-04 |
Pfizer Italia S.R.L. |
Dérivés de la 2-indoline substituée par 4-arylpyrrole, actifs en tant qu'inhibiteurs de protéine kinase
|
CL2008001626A1
(es)
|
2007-06-05 |
2009-06-05 |
Takeda Pharmaceuticals Co |
Compuestos derivados de heterociclos fusionados, agente farmaceutico que los comprende y su uso en la profilaxis y tratamiento del cancer.
|
EP2181987B9
(fr)
|
2007-08-23 |
2014-09-03 |
Takeda Pharmaceutical Company Limited |
2-Carbonylaminobenzothiazoles et leur utilisation dans la prévention ou le traitement du cancer
|
US20090062368A1
(en)
*
|
2007-08-29 |
2009-03-05 |
Protia, Llc |
Deuterium-enriched sunitinib
|
DK2197878T3
(en)
*
|
2007-09-06 |
2016-11-14 |
Boston Biomedical Inc |
FORMATIONS OF kinase inhibitors AND USE THEREOF FOR THE TREATMENT OF CANCER AND OTHER DISEASES RELATED TO kinases
|
KR101494734B1
(ko)
|
2007-10-11 |
2015-02-26 |
아스트라제네카 아베 |
단백질 키나제 b 억제제로서 피롤로[2,3-d]피리미딘 유도체
|
CN101848895B
(zh)
|
2007-11-09 |
2013-10-23 |
卫材R&D管理有限公司 |
血管新生抑制物质和抗肿瘤性铂络合物的组合使用
|
US20100256392A1
(en)
*
|
2007-11-21 |
2010-10-07 |
Teva Pharmaceutical Industries Ltd. |
Polymorphs of sunitinib base and processes for preparation thereof
|
EP2220071A2
(fr)
|
2007-11-21 |
2010-08-25 |
Teva Pharmaceutical Industries Ltd. |
Hémi-l-malate de sunitinib, polymorphes et leur préparation, polymorphes de malate de sunitinib racémique, compositions contenant une base de sunitinib et de l'acide malique et leur préparation
|
EP2229380A1
(fr)
*
|
2007-12-12 |
2010-09-22 |
Medichem, S.A. |
Formes polymorphes d'une 2-indolinone substituée par 3-pyrrole
|
ES2437141T3
(es)
|
2007-12-19 |
2014-01-09 |
Genentech, Inc. |
5-Anilinoimidazopiridinas y métodos de uso
|
PE20091523A1
(es)
|
2007-12-20 |
2009-10-29 |
Novartis Ag |
Derivados de tiazol como inhibidores de la enzima fosfatidilinositol 3-cinasa (pi3k)
|
WO2009082687A1
(fr)
|
2007-12-21 |
2009-07-02 |
Genentech, Inc. |
Azaindolizines et procédés d'utilisation
|
AU2009210098B2
(en)
*
|
2008-01-29 |
2013-06-13 |
Eisai R & D Management Co., Ltd. |
Combined use of angiogenesis inhibitor and taxane
|
EA201001125A1
(ru)
*
|
2008-02-13 |
2011-04-29 |
Рациофарм Гмбх |
Фармацевтические композиции, включающие n-[2-(диэтиламино)этил]-5-[(5-фтор-1,2-дигидро-2-оксо-3н-индол-3-илиден)метил]-2,4-диметил-1н-пиррол-3-карбоксамид
|
EP2090306A1
(fr)
|
2008-02-13 |
2009-08-19 |
Ratiopharm GmbH |
Compositions pharmaceutiques comportant du N-[2-(diethylamino)ethyl]-5-[5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide
|
EP2113248A1
(fr)
|
2008-04-29 |
2009-11-04 |
Ratiopharm GmbH |
Composition pharmaceutique comportant du N-[2-(diethylamino)ethyl]-5-[5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2-dimethyl-1H-pyrrole-3-carboxamide
|
CN101255154B
(zh)
*
|
2008-02-18 |
2011-09-07 |
靳广毅 |
一种取代的2-吲哚啉酮衍生物和制备方法及其应用
|
CN101983195A
(zh)
*
|
2008-02-21 |
2011-03-02 |
基因里克斯(英国)有限公司 |
新型多晶型物及其制备方法
|
EP2098521A1
(fr)
*
|
2008-03-06 |
2009-09-09 |
Ratiopharm GmbH |
Formules cristallines de N-[2-(diéthylamino)éthyl]-5-[5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidène)méthyl]-2,4-diméthyl-1H-pyrrole-3-carboxamide
|
US20090247767A1
(en)
*
|
2008-03-31 |
2009-10-01 |
Teva Pharmaceutical Industries Ltd. |
Processes for preparing sunitinib and salts thereof
|
EP2280960A1
(fr)
|
2008-04-16 |
2011-02-09 |
Natco Pharma Limited |
Nouvelles formes polymorphes du sunitinib base
|
US8158656B2
(en)
*
|
2008-05-16 |
2012-04-17 |
Shenzhen Chipscreen Biosciences Ltd. |
2-indolinone derivatives as multi-target protein kinase inhibitors and histone deacetylase inhibitors
|
KR101375156B1
(ko)
*
|
2008-05-23 |
2014-03-18 |
쟝수 치아타이 티안큉 파마수티컬 주식회사 |
디하이드로인돌리논 유도체들
|
WO2009154697A2
(fr)
|
2008-05-28 |
2009-12-23 |
Massachusetts Institute Of Technology |
Activateurs de la voie de la disc-1 dans le contrôle de la neurogenèse
|
AR072117A1
(es)
*
|
2008-06-13 |
2010-08-04 |
Medichem Sa |
Procedimiento para preparar una sal de malato 3-pirrol sustituido 2-indolinona, intermediario de sintesis y una composicion farmaceutica que la comprende.
|
KR20110036055A
(ko)
*
|
2008-06-23 |
2011-04-06 |
낫코 파마 리미티드 |
고순도의 수니티닙 및 이의 약학적으로 허용가능한 염의 개선된 제조 방법
|
EP2138167A1
(fr)
|
2008-06-24 |
2009-12-30 |
ratiopharm GmbH |
Compositions pharmaceutiques comportant du N-[2-(diethylamino)ethyl]-5-[5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide
|
WO2009156837A2
(fr)
*
|
2008-06-26 |
2009-12-30 |
Medichem, S.A. |
Forme amorphe d'un sel de malate de 2-indolinone à substitution 3-pyrrole
|
EP2307421A4
(fr)
*
|
2008-06-30 |
2011-07-13 |
Cylene Pharmaceuticals Inc |
Composés d'oxindole
|
CA2729303A1
(fr)
|
2008-06-30 |
2010-01-14 |
Angioblast Systems, Inc. |
Traitement de maladies oculaires et d'une neovascularisation excessive utilisant un traitement combine
|
DE102008031038A1
(de)
|
2008-06-30 |
2009-12-31 |
Alexander Priv.-Doz. Dr. Dömling |
Sutent zur Anwendung in der Organtransplantation
|
EP2318364A2
(fr)
*
|
2008-07-02 |
2011-05-11 |
Generics [UK] Limited |
Preparation des derives de 2-indolinone substitue par 3-pyrrole
|
US20110257237A1
(en)
*
|
2008-07-10 |
2011-10-20 |
Generics [Uk] Limited |
Process for the preparation of crystalline forms of sunitinib malate
|
WO2010010454A2
(fr)
|
2008-07-24 |
2010-01-28 |
Medichem, S.A. |
Formes cristallines d’un sel de malate de 2-indolinone à substitution 3-pyrrole
|
WO2010011834A2
(fr)
*
|
2008-07-24 |
2010-01-28 |
Teva Pharmaceutical Industries Ltd. |
Sunitinib et ses sels et leurs polymorphes
|
US8993615B2
(en)
*
|
2008-08-08 |
2015-03-31 |
The Johns Hopkins University |
Compositions and methods for treatment of neurodegenerative disease
|
JP2012500855A
(ja)
*
|
2008-08-25 |
2012-01-12 |
アンプリミューン、インコーポレーテッド |
Pd−1アンタゴニストおよび感染性疾患を処置するための方法
|
PL2350129T3
(pl)
|
2008-08-25 |
2015-12-31 |
Amplimmune Inc |
Kompozycje antagonistów PD-1 i sposoby stosowania
|
CN102197034A
(zh)
*
|
2008-08-25 |
2011-09-21 |
基因里克斯(英国)有限公司 |
舒尼替尼的新型多晶型物及其制备方法
|
JP2012500837A
(ja)
*
|
2008-08-25 |
2012-01-12 |
ジェネリクス・(ユーケー)・リミテッド |
新規な結晶型およびその調製方法
|
CN102171208A
(zh)
*
|
2008-09-05 |
2011-08-31 |
帝国创新有限公司 |
用作体内显像剂的靛红衍生物
|
KR20110057244A
(ko)
|
2008-09-19 |
2011-05-31 |
메디뮨 엘엘씨 |
Dll4에 대한 항체 및 이의 용도
|
CN102177155A
(zh)
*
|
2008-10-10 |
2011-09-07 |
麦迪凯姆股份公司 |
一种3-吡咯取代的2-吲哚酮苹果酸盐的制备工艺
|
EP2181991A1
(fr)
|
2008-10-28 |
2010-05-05 |
LEK Pharmaceuticals D.D. |
Nouveaux sels de sunitinib
|
EP2186809A1
(fr)
|
2008-11-13 |
2010-05-19 |
LEK Pharmaceuticals D.D. |
Nouvelle forme cristalline du malate de sunitinib
|
US20100222371A1
(en)
*
|
2008-11-20 |
2010-09-02 |
Children's Medical Center Corporation |
Prevention of surgical adhesions
|
JP5579619B2
(ja)
|
2008-12-01 |
2014-08-27 |
武田薬品工業株式会社 |
複素環化合物およびその用途
|
JO3101B1
(ar)
|
2008-12-02 |
2017-09-20 |
Takeda Pharmaceuticals Co |
مشتقات بنزوثيازول كعوامل مضادة للسرطان
|
TW201028410A
(en)
|
2008-12-22 |
2010-08-01 |
Astrazeneca Ab |
Chemical compounds 610
|
AU2009331528A1
(en)
|
2008-12-23 |
2011-08-11 |
Astrazeneca Ab |
Targeted binding agents directed to alpha5beta1 and uses thereof
|
EP2896618A1
(fr)
|
2009-01-02 |
2015-07-22 |
Hetero Research Foundation |
Polymorphes du malate de sunitinib
|
EA038195B1
(ru)
|
2009-01-16 |
2021-07-22 |
Экселиксис, Инк. |
Малатная соль n-(4-{[6,7-бис-(метилокси)хинолин-4-ил]окси}фенил)-n'-(4-фторфенил)циклопропан-1,1-дикарбоксамида и ее применение для лечения рака почек и печени
|
KR101984053B1
(ko)
|
2009-02-05 |
2019-05-30 |
이뮤노젠 아이엔씨 |
신규한 벤조디아제핀 유도체
|
CA2748943A1
(fr)
|
2009-02-09 |
2010-08-12 |
Supergen, Inc. |
Inhibiteurs pyrrolopyrimidinyle de l'axi kinase
|
WO2010098888A1
(fr)
*
|
2009-02-27 |
2010-09-02 |
Massachusetts Institute Of Technology |
Utilisations de produits chimiques pour moduler la signalisation par gsk–3 pour le traitement d'un trouble bipolaire et autres troubles cérébraux
|
WO2010098866A1
(fr)
|
2009-02-27 |
2010-09-02 |
Supergen, Inc. |
Inhibiteurs cyclopentathiophène/cyclohexathiophène de l'adn méthyltransférase
|
ES2529205T3
(es)
|
2009-03-13 |
2015-02-17 |
Cellzome Limited |
Derivados de pirimidina como inhibidores de mTOR
|
WO2010108503A1
(fr)
|
2009-03-24 |
2010-09-30 |
Life & Brain Gmbh |
Promotion de l'intégration neuronale dans des greffons de cellules souches neurales
|
WO2010118986A1
(fr)
|
2009-04-14 |
2010-10-21 |
Cellzome Limited |
Composés de pyrimidine substitués par fluoro en tant qu'inhibiteurs de jak3
|
WO2010120386A1
(fr)
|
2009-04-17 |
2010-10-21 |
Nektar Therapeutics |
Conjugués inhibiteur de protéine tyrosine kinase-oligomère
|
EP2255792A1
(fr)
|
2009-05-20 |
2010-12-01 |
Ratiopharm GmbH |
Composition pharmaceutique pour n-[2-(diethylamino)ethyl]5-[(fluoro-1,2-dihydro-2-oxo-3H-indole-3-ylidene) methyl]-2,4-dimenthyl-1h-pyrrole-3-carboxamide
|
US8211901B2
(en)
|
2009-05-22 |
2012-07-03 |
Shenzhen Chipscreen Biosciences Ltd. |
Naphthamide derivatives as multi-target protein kinase inhibitors and histone deacetylase inhibitors
|
EP2264027A1
(fr)
*
|
2009-05-27 |
2010-12-22 |
Ratiopharm GmbH |
Processus pour la préparation de N-[2-(diethylamino)ethyl]-5-[5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide
|
US8389580B2
(en)
|
2009-06-02 |
2013-03-05 |
Duke University |
Arylcyclopropylamines and methods of use
|
CN101906076B
(zh)
|
2009-06-04 |
2013-03-13 |
深圳微芯生物科技有限责任公司 |
作为蛋白激酶抑制剂和组蛋白去乙酰化酶抑制剂的萘酰胺衍生物、其制备方法及应用
|
US8293753B2
(en)
|
2009-07-02 |
2012-10-23 |
Novartis Ag |
Substituted 2-carboxamide cycloamino ureas
|
WO2011004200A1
(fr)
|
2009-07-10 |
2011-01-13 |
Generics [Uk] Limited |
Nouveaux dérivés de pyrrole
|
FR2948940B1
(fr)
*
|
2009-08-04 |
2011-07-22 |
Servier Lab |
Nouveaux derives dihydroindolones, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
|
EP2475648A1
(fr)
|
2009-09-11 |
2012-07-18 |
Cellzome Limited |
Composés de pyrimidine ortho-substitués en tant qu'inhibiteurs de jak
|
CA2774634A1
(fr)
|
2009-09-16 |
2011-03-24 |
Ranbaxy Laboratories Limited |
Sels de sunitinib
|
CN102666545B
(zh)
|
2009-10-20 |
2016-04-06 |
塞尔卓姆有限公司 |
作为jak抑制剂的杂环吡唑并嘧啶类似物
|
WO2011058521A2
(fr)
|
2009-11-12 |
2011-05-19 |
Ranbaxy Laboratories Limited |
Procédé de préparation de la forme cristalline i du sel d'acide l-malique de sunitinib
|
EP2501694A1
(fr)
|
2009-11-19 |
2012-09-26 |
Ranbaxy Laboratories Limited |
Procédé de préparation de la forme cristalline ii du sel d'acide malique l du sunitinib
|
WO2011066389A1
(fr)
|
2009-11-24 |
2011-06-03 |
Medimmmune, Limited |
Agents de liaison ciblés dirigés contre b7-h1
|
WO2011068233A1
(fr)
|
2009-12-03 |
2011-06-09 |
Dainippon Sumitomo Pharma Co., Ltd. |
Imidazoquinolines agissant par l'intermédiaire des récepteurs de type toll (tlr)
|
WO2011095802A1
(fr)
|
2010-02-02 |
2011-08-11 |
Generics [Uk] Limited |
Procédé hplc pour l'analyse de sunitinib
|
WO2011100325A2
(fr)
|
2010-02-09 |
2011-08-18 |
Sicor Inc. |
Polymorphes de sels de sunitinib
|
KR20130009760A
(ko)
|
2010-02-10 |
2013-01-23 |
이뮤노젠 아이엔씨 |
Cd20 항체 및 이의 용도
|
RU2012139182A
(ru)
|
2010-02-22 |
2014-03-27 |
Ф. Хоффманн-Ля Рош Аг |
ПИРИДО[3,2-d]ПИРИМИДИНЫ - ИНГИБИТОРЫ PI3К ДЕЛЬТА И СПОСОБЫ ИХ ПРИМЕНЕНИЯ
|
WO2011104555A2
(fr)
|
2010-02-25 |
2011-09-01 |
Generics [Uk] Limited |
Nouveau procédé
|
CA2792039A1
(fr)
|
2010-03-04 |
2011-09-09 |
Ranbaxy Laboratories Limited |
Procede de preparation directe de sel d'acide malique de sunitinib
|
WO2011107585A1
(fr)
|
2010-03-04 |
2011-09-09 |
Cellzome Limited |
Dérivés d'urée substituée par un morpholino en tant qu'inhibiteurs de mtor
|
CN102858739A
(zh)
*
|
2010-03-10 |
2013-01-02 |
斯索恩有限公司 |
酰胺化吡咯甲酸酯化合物的方法
|
WO2011114246A1
(fr)
|
2010-03-18 |
2011-09-22 |
Ranbaxy Laboratories Limited |
Procédé pour la préparation du sel de l'acide maléique du sunitinib
|
WO2011119777A2
(fr)
|
2010-03-23 |
2011-09-29 |
The Johns Hopkins University |
Compositions et méthodes de traitement d'une maladie neurodégénérative
|
WO2011128699A2
(fr)
|
2010-04-16 |
2011-10-20 |
Generics [Uk] Limited |
Procédés inédits
|
BR112012027803A2
(pt)
|
2010-04-30 |
2016-08-09 |
Cellzome Ltd |
compostos de pirazol como inibidores de jak
|
WO2011138565A1
(fr)
|
2010-05-05 |
2011-11-10 |
Biorebus |
Association pharmaceutique contenant l'acide lipoïque, l'acide hydroxycitrique et une somatostatine a titre de principes actifs
|
EP2392324A1
(fr)
|
2010-06-01 |
2011-12-07 |
Societe De Coordination De Recherches Therapeutiques |
Complexes de rhénium et leur utilisation pharmaceutique
|
SA111320519B1
(ar)
|
2010-06-11 |
2014-07-02 |
Astrazeneca Ab |
مركبات بيريميدينيل للاستخدام كمثبطات atr
|
MX2012014776A
(es)
|
2010-06-25 |
2013-01-29 |
Eisai R&D Man Co Ltd |
Agente antitumoral que emplea compuestos con efecto inhibidor de cinasas combinados.
|
EP2588105A1
(fr)
|
2010-07-01 |
2013-05-08 |
Cellzome Limited |
Triazolopyridines en tant qu'inhibiteurs de tyk2
|
NZ605449A
(en)
|
2010-07-09 |
2015-03-27 |
Genentech Inc |
Anti-neuropilin antibodies and methods of use
|
AR082418A1
(es)
|
2010-08-02 |
2012-12-05 |
Novartis Ag |
Formas cristalinas de 1-(4-metil-5-[2-(2,2,2-trifluoro-1,1-dimetil-etil)-piridin-4-il]-tiazol-2-il)-amida de 2-amida del acido (s)-pirrolidin-1,2-dicarboxilico
|
WO2012022681A2
(fr)
|
2010-08-20 |
2012-02-23 |
Cellzome Limited |
Analogues de la hétérocyclyl pyrazolopyrimidine comme inhibiteurs sélectifs de la jak
|
US8426418B2
(en)
|
2010-08-27 |
2013-04-23 |
CollabRx Inc. |
Method to treat melanoma in BRAF inhibitor-resistant subjects
|
WO2012042421A1
(fr)
|
2010-09-29 |
2012-04-05 |
Pfizer Inc. |
Procédé de traitement de la croissance cellulaire anormale
|
CN103328465B
(zh)
|
2010-11-01 |
2015-05-27 |
神隆(昆山)生化科技有限公司 |
使用2-甲硅烷氧基-吡咯类制备3-((吡咯-2-基)亚甲基)-2-吡咯酮类的方法
|
WO2012059941A1
(fr)
*
|
2010-11-04 |
2012-05-10 |
Ind-Swift Laboratories Limited |
Procédé pour préparation de malate de sunitinib et sels correspondants
|
CN103298794A
(zh)
|
2010-11-09 |
2013-09-11 |
塞尔卓姆有限公司 |
作为tyk2抑制剂的吡啶化合物及其氮杂类似物
|
EP2640384A1
(fr)
|
2010-11-18 |
2013-09-25 |
Synta Pharmaceuticals Corp. |
Présélection de patients pour un traitement thérapeutique fondé sur un état hypoxique, avec des agents sensibles à l'oxygène
|
EP2640360A2
(fr)
|
2010-11-19 |
2013-09-25 |
Forsight Vision4, Inc. |
Formulations d'agents thérapeutiques pour des dispositifs implantés
|
AR083868A1
(es)
|
2010-12-03 |
2013-03-27 |
Lilly Co Eli |
Compuestos de oxazol[5,4-b]piridin-5-ilo
|
US10220020B2
(en)
|
2010-12-23 |
2019-03-05 |
Nektar Therapeutics |
Polymer-des-ethyl sunitinib conjugates
|
WO2012088529A1
(fr)
|
2010-12-23 |
2012-06-28 |
Nektar Therapeutics |
Conjugués polymère-sunitinib
|
PT2670753T
(pt)
|
2011-01-31 |
2017-01-10 |
Novartis Ag |
Novos derivados heterocíclicos
|
CN103702686B
(zh)
|
2011-02-15 |
2016-11-23 |
伊缪诺金公司 |
缀合物的制备方法
|
DK2675793T3
(en)
|
2011-02-17 |
2018-11-12 |
Cancer Therapeutics Crc Pty Ltd |
FAK INHIBITORS
|
CN103534240B
(zh)
|
2011-02-17 |
2015-12-09 |
癌症疗法Crc私人有限公司 |
选择性fak抑制剂
|
GB201103578D0
(en)
|
2011-03-02 |
2011-04-13 |
Sabrepharm Ltd |
Dipyridinium derivatives
|
US8630703B2
(en)
|
2011-03-09 |
2014-01-14 |
Technion Research & Development Foundation Limited |
Treatment utilizing hydrophobic weak bases chemotherapeutic agents and illumination
|
CN102115469A
(zh)
*
|
2011-03-21 |
2011-07-06 |
浙江大学 |
吲哚啉-2-酮类衍生物的制备和用途
|
US20140163023A1
(en)
|
2011-04-04 |
2014-06-12 |
Cellzome Limited |
Dihydropyrrolo pyrimidine derivatives as mtor inhibitors
|
KR20140027972A
(ko)
*
|
2011-04-08 |
2014-03-07 |
베타 파마, 인크. |
신규 인돌리논 단백질 키나제 억제제
|
WO2012143320A1
(fr)
|
2011-04-18 |
2012-10-26 |
Cellzome Limited |
Composés (7h-pyrrolo[2,3-d]pyrimidin-2-yl)amine comme inhibiteurs de la jak3
|
RU2580609C2
(ru)
|
2011-04-18 |
2016-04-10 |
Эйсай Ар Энд Ди Менеджмент Ко., Лтд. |
Противоопухолевое терапевтическое средство
|
CN102898402B
(zh)
*
|
2011-04-26 |
2016-01-20 |
北京大学 |
一种苯并异硒唑酮修饰的吡咯甲酸酯取代的吲哚酮类化合物及其应用
|
ES2705950T3
(es)
|
2011-06-03 |
2019-03-27 |
Eisai R&D Man Co Ltd |
Biomarcadores para predecir y valorar la capacidad de respuesta de sujetos con cáncer de tiroides y de riñón a compuestos de lenvatinib
|
EP3812387A1
(fr)
|
2011-07-21 |
2021-04-28 |
Sumitomo Dainippon Pharma Oncology, Inc. |
Inhibiteurs de protéine kinase hétérocycliques
|
AU2012288892B2
(en)
|
2011-07-28 |
2016-04-21 |
Cellzome Limited |
Heterocyclyl pyrimidine analogues as JAK inhibitors
|
WO2013017480A1
(fr)
|
2011-07-29 |
2013-02-07 |
Cellzome Limited |
Dérivés de pyrazolo[4,3-c]pyridine en tant qu'inhibiteurs de jak
|
WO2013017479A1
(fr)
|
2011-07-29 |
2013-02-07 |
Cellzome Limited |
Dérivés de pyrazolo[4,3-c]pyridine en tant qu'inhibiteurs de jak
|
EP2739252A4
(fr)
|
2011-08-05 |
2015-08-12 |
Forsight Vision4 Inc |
Administration de petites molécules à l'aide d'un dispositif thérapeutique implantable
|
JP2014531449A
(ja)
|
2011-09-20 |
2014-11-27 |
セルゾーム リミティッド |
キナーゼ阻害剤としてのピラゾロ[4,3―c]ピリジン誘導体
|
ES2609606T3
(es)
|
2011-09-21 |
2017-04-21 |
Cellzome Limited |
Derivados de urea y carbamato de 2-morfolino-1,3,5-triazina como inhibidores de mTOR para el tratamiento de enfermedades inmunológicas o proliferativas
|
MX341577B
(es)
|
2011-10-07 |
2016-08-25 |
Cellzome Ltd |
Derivados biciclicos de pirimidin-urea o carbamato sustituidos con morfolino como inhibidores del blanco de rapamicina de mamifero.
|
CN102499917B
(zh)
|
2011-10-25 |
2014-12-17 |
澳门大学 |
吲哚酮类化合物在制备神经保护药物中的应用
|
CN104039790B
(zh)
|
2011-10-28 |
2016-04-13 |
诺华股份有限公司 |
嘌呤衍生物及它们在治疗疾病中的应用
|
CN103130774B
(zh)
*
|
2011-11-22 |
2016-06-22 |
齐鲁制药有限公司 |
具有酪氨酸激酶抑制作用的化合物及其制备方法和应用
|
CN103127096B
(zh)
*
|
2011-12-02 |
2015-11-25 |
杨子娇 |
吡咯基取代的吲哚类化合物在治疗青光眼病的应用
|
WO2013092854A1
(fr)
|
2011-12-23 |
2013-06-27 |
Cellzome Limited |
Dérivés de pyrimidine-2,4-diamine en tant qu'inhibiteurs de kinase
|
US20130178520A1
(en)
|
2011-12-23 |
2013-07-11 |
Duke University |
Methods of treatment using arylcyclopropylamine compounds
|
CN102491932A
(zh)
*
|
2011-12-26 |
2012-06-13 |
天津科技大学 |
一种3-吲哚啉酮类衍生物及其制备方法及其应用
|
US9206163B2
(en)
|
2012-03-23 |
2015-12-08 |
Laurus Labs Private Ltd. |
Process for the preparation of sunitinib and its acid addition salts thereof
|
IN2014MN02105A
(fr)
|
2012-04-20 |
2015-09-11 |
Annji Pharm Co Ltd |
|
CN102653521B
(zh)
*
|
2012-04-27 |
2014-08-06 |
首都师范大学 |
吲哚-2-酮的哌嗪硫代甲酰肼衍生物及其制备方法和用途
|
PL399027A1
(pl)
|
2012-04-27 |
2013-10-28 |
Instytut Farmaceutyczny |
Sposób otrzymywania N-[2-(dietylamino)etylo]-5-formylo-2,4-dimetylo-1H-pirolo-3-karboksyamidu o wysokiej czystosci i jego zastosowanie do wytwarzania sunitynibu
|
SG10201603896RA
(en)
|
2012-05-04 |
2016-07-28 |
Pfizer |
Prostate-associated antigens and vaccine-based immunotherapy regimens
|
EP2849756A1
(fr)
|
2012-05-16 |
2015-03-25 |
Novartis AG |
Régime posologique pour un inhibiteur de pi-3 kinase
|
BR112014030278A2
(pt)
|
2012-06-08 |
2017-06-27 |
Sutro Biopharma Inc |
anticorpo, e, composição.
|
EP3135690A1
(fr)
|
2012-06-26 |
2017-03-01 |
Sutro Biopharma, Inc. |
Proteines fc modifiees contenant des residus specifiques d'acides amines non naturels, leurs conjugues, leurs procedes de preparation et leurs procedes d'utilisation
|
US9238644B2
(en)
|
2012-08-17 |
2016-01-19 |
Cancer Therapeutics Crc Pty Limited |
VEGFR3 inhibitors
|
EP2887965A1
(fr)
|
2012-08-22 |
2015-07-01 |
ImmunoGen, Inc. |
Dérivés de benzodiazépine cytotoxique
|
AU2013308494B2
(en)
|
2012-08-31 |
2018-03-01 |
Sutro Biopharma, Inc. |
Modified amino acids comprising an azido group
|
WO2014041349A1
(fr)
|
2012-09-12 |
2014-03-20 |
Cancer Therapeutics Crc Pty Ltd |
Pyrimidines ou pyridazines tétrahydropyran-4-yléthylamino- ou tétrahydropyranyl-4-éthyloxy utiles comme inhibiteurs de l'isoprényl-cystéine-carboxy-méthyl-transférase
|
WO2014045101A1
(fr)
|
2012-09-21 |
2014-03-27 |
Cellzome Gmbh |
Dérivés de tétrazolo quinoxaline utilisés comme inhibiteurs de la tankyrase
|
ES2644758T3
(es)
|
2012-10-16 |
2017-11-30 |
Tolero Pharmaceuticals, Inc. |
Moduladores de PKM2 y métodos para su uso
|
US9260426B2
(en)
|
2012-12-14 |
2016-02-16 |
Arrien Pharmaceuticals Llc |
Substituted 1H-pyrrolo [2, 3-b] pyridine and 1H-pyrazolo [3, 4-b] pyridine derivatives as salt inducible kinase 2 (SIK2) inhibitors
|
JPWO2014098176A1
(ja)
|
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 |
キノリン誘導体のアモルファス及びその製造方法
|
EP3566750A3
(fr)
|
2013-02-28 |
2020-04-08 |
ImmunoGen, Inc. |
Conjugués comprenant des agents de liaison cellulaire et des agents cytotoxiques
|
EP2961435B1
(fr)
|
2013-02-28 |
2019-05-01 |
ImmunoGen, Inc. |
Conjugués comprenant des agents de liaison cellulaire (cba) et des agents cytotoxiques
|
US20160031888A1
(en)
*
|
2013-03-13 |
2016-02-04 |
Boston Biomedical, Inc. |
3-(aryl or heteroaryl) methyleneindolin-2-one derivatives as inhibitors of cancer stem cell pathway kinases for the treatment of cancer
|
DK2970205T3
(da)
|
2013-03-14 |
2019-07-29 |
Tolero Pharmaceuticals Inc |
JAK2- og ALK2-inhibitorer og fremgangsmåder til anvendelse deraf
|
AU2014236455B2
(en)
|
2013-03-14 |
2018-07-12 |
Forsight Vision4, Inc. |
Systems for sustained intraocular delivery of low solubility compounds from a port delivery system implant
|
AR095443A1
(es)
|
2013-03-15 |
2015-10-14 |
Fundación Centro Nac De Investig Oncológicas Carlos Iii |
Heterociclos condensados con acción sobre atr
|
US9206188B2
(en)
|
2013-04-18 |
2015-12-08 |
Arrien Pharmaceuticals Llc |
Substituted pyrrolo[2,3-b]pyridines as ITK and JAK inhibitors
|
CN104119321B
(zh)
*
|
2013-04-28 |
2017-09-08 |
齐鲁制药有限公司 |
二氢吲哚酮衍生物的二马来酸盐及其多晶型物
|
KR102204279B1
(ko)
|
2013-05-14 |
2021-01-15 |
에자이 알앤드디 매니지먼트 가부시키가이샤 |
자궁내막암 대상의 렌바티닙 화합물에 대한 반응성을 예측 및 평가하기 위한 생체표지
|
WO2014194030A2
(fr)
|
2013-05-31 |
2014-12-04 |
Immunogen, Inc. |
Conjugués comprenant des agents de liaison cellulaire et des agents cytotoxiques
|
WO2015006555A2
(fr)
|
2013-07-10 |
2015-01-15 |
Sutro Biopharma, Inc. |
Anticorps comprenant plusieurs résidus d'acides aminés non naturels site-spécifiques, des procédés permettant leur préparation et leurs méthodes d'utilisation
|
FR3008411B1
(fr)
*
|
2013-07-12 |
2015-07-03 |
Servier Lab |
Nouveau sel de la 3-[(3-{[4-(4-morpholinylmethyl)-1h-pyrrol-2-yl]methylene}-2-oxo-2,3-dihydro-1h-indol-5-yl)methyl]-1,3-thiazolidine-2,4-dione, sa preparation, et les formulations qui le contiennent
|
PT3039424T
(pt)
|
2013-08-28 |
2020-09-03 |
Crown Bioscience Inc Taicang |
Assinaturas de expressão genética que permitem prever a resposta de um sujeito a um inibidor multiquinase e métodos de utilização do mesmo
|
WO2015054658A1
(fr)
|
2013-10-11 |
2015-04-16 |
Sutro Biopharma, Inc. |
Acides aminés modifiés comprenant des groupes fonctionnels de tétrazine, procédés de préparation et procédés d'utilisation associés
|
US9604968B2
(en)
|
2013-10-18 |
2017-03-28 |
Sun Pharmaceutical Industries Limited |
Pure crystalline Form II of L-malic acid salt of sunitinib and processes for its preparation
|
US9278955B2
(en)
|
2013-10-18 |
2016-03-08 |
Sun Pharmaceutical Industries Limited |
Ascorbic acid salt of sunitinib
|
NZ718652A
(en)
|
2013-11-01 |
2019-06-28 |
Pfizer |
Vectors for expression of prostate-associated antigens
|
EP3076969B1
(fr)
|
2013-12-06 |
2021-09-01 |
Novartis AG |
Schéma posologique d'un inhibiteur de la phosphatidylinositol 3-kinase sélectif de l'isoforme alpha
|
CN104829596B
(zh)
*
|
2014-02-10 |
2017-02-01 |
石家庄以岭药业股份有限公司 |
吡咯取代吲哚酮类衍生物、其制备方法、包含该衍生物的组合物、及其用途
|
CN103923014A
(zh)
*
|
2014-05-05 |
2014-07-16 |
宁夏宝马药业有限公司 |
环肌酸制备方法
|
US9474756B2
(en)
|
2014-08-08 |
2016-10-25 |
Forsight Vision4, Inc. |
Stable and soluble formulations of receptor tyrosine kinase inhibitors, and methods of preparation thereof
|
EP3825305A1
(fr)
|
2014-08-28 |
2021-05-26 |
Eisai R&D Management Co., Ltd. |
Procédé de fabrication de lenvatinib
|
TWI595006B
(zh)
|
2014-12-09 |
2017-08-11 |
禮納特神經系統科學公司 |
抗pd-1抗體類和使用彼等之方法
|
SG11201705767PA
(en)
|
2015-01-13 |
2017-08-30 |
Univ Kyoto |
Agent for preventing and/or treating amyotrophic lateral sclerosis
|
WO2016136745A1
(fr)
|
2015-02-25 |
2016-09-01 |
エーザイ・アール・アンド・ディー・マネジメント株式会社 |
Procédé de suppression de l'amertume d'un dérivé de quinoléine
|
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
|
RU2717829C2
(ru)
|
2015-04-20 |
2020-03-26 |
Толеро Фармасьютикалз, Инк. |
Прогнозирование ответа на альвоцидиб с помощью анализа профиля митохондрий
|
WO2016184793A1
(fr)
|
2015-05-15 |
2016-11-24 |
INSERM (Institut National de la Santé et de la Recherche Médicale) |
Méthodes de traitement de patients souffrant d'un adénocarcinome rénal métastatique résistant aux inhibiteurs du vegfr
|
MX2017014645A
(es)
|
2015-05-18 |
2018-01-23 |
Tolero Pharmaceuticals Inc |
Profarmacos de alvocidib que tienen una biodisponibilidad aumentada.
|
GB201510019D0
(en)
|
2015-06-09 |
2015-07-22 |
Cancer Therapeutics Crc Pty Ltd |
Compounds
|
BR112017027227B1
(pt)
|
2015-06-16 |
2023-12-12 |
Eisai R&D Management Co., Ltd |
Agente anti-câncer
|
EP3331510A4
(fr)
|
2015-08-03 |
2019-04-03 |
Tolero Pharmaceuticals, Inc. |
Thérapies combinatoires pour le traitement du cancer
|
US9808531B2
(en)
|
2015-09-22 |
2017-11-07 |
Graybug Vision, Inc. |
Compounds and compositions for the treatment of ocular disorders
|
GB2543550A
(en)
|
2015-10-21 |
2017-04-26 |
Hox Therapeutics Ltd |
Peptides
|
KR20180073674A
(ko)
|
2015-11-02 |
2018-07-02 |
노파르티스 아게 |
포스파티딜이노시톨 3-키나제 억제제에 대한 투여 요법
|
CN108367079B
(zh)
|
2015-11-12 |
2022-11-22 |
灰色视觉公司 |
用于治疗的聚集性微粒
|
SG11201806419RA
(en)
|
2016-01-27 |
2018-08-30 |
Sutro Biopharma Inc |
Anti-cd74 antibody conjugates, compositions comprising anti-cd74 antibody conjugates and methods of using anti-cd74 antibody conjugates
|
WO2017139417A1
(fr)
|
2016-02-08 |
2017-08-17 |
Vitrisa Therapeutics, Inc. |
Compositions à demi-vie intravitréenne améliorée et leurs utilisations
|
EP3228630A1
(fr)
|
2016-04-07 |
2017-10-11 |
IMBA-Institut für Molekulare Biotechnologie GmbH |
Combinaison d'un antagoniste d'apeline et inhibiteur de l'angiogenèse pour le traitement du cancer
|
CN107459519A
(zh)
|
2016-06-06 |
2017-12-12 |
上海艾力斯医药科技有限公司 |
稠合嘧啶哌啶环衍生物及其制备方法和应用
|
CA3035081A1
(fr)
|
2016-09-02 |
2018-03-08 |
Dana-Farber Cancer Institute, Inc. |
Composition et methodes de traitement des dereglements des lymphocytes b
|
WO2018060833A1
(fr)
|
2016-09-27 |
2018-04-05 |
Novartis Ag |
Schéma posologique pour l'alpelisib, un inhibiteur de la phosphatidylinositol 3-kinase spécifique de l'isoforme alpha
|
KR20190084063A
(ko)
|
2016-10-28 |
2019-07-15 |
이칸 스쿨 오브 메디슨 엣 마운트 시나이 |
Ezh2-매개성 암 치료용 조성물 및 방법
|
US11279694B2
(en)
|
2016-11-18 |
2022-03-22 |
Sumitomo Dainippon Pharma Oncology, Inc. |
Alvocidib prodrugs and their use as protein kinase inhibitors
|
WO2018106606A1
(fr)
|
2016-12-05 |
2018-06-14 |
Apros Therapeutics, Inc. |
Composés de pyrimidine contenant des groupes acides
|
US10786502B2
(en)
|
2016-12-05 |
2020-09-29 |
Apros Therapeutics, Inc. |
Substituted pyrimidines containing acidic groups as TLR7 modulators
|
AU2017370694A1
(en)
|
2016-12-08 |
2019-07-25 |
Icahn School Of Medicine At Mount Sinai |
Compositions and methods for treating CDK4/6-mediated cancer
|
EP3362471B1
(fr)
|
2016-12-19 |
2021-11-17 |
Sumitomo Dainippon Pharma Oncology, Inc. |
Peptides profilants et procédés de profilage de sensibilité
|
CN106916143B
(zh)
*
|
2017-03-14 |
2019-09-27 |
哈尔滨医科大学 |
一种预防和治疗冠心病的药物及其应用
|
CA3056923A1
(fr)
|
2017-03-23 |
2018-09-27 |
Graybug Vision, Inc. |
Composes et compositions pour le traitement de troubles oculaires
|
EP3621654A4
(fr)
|
2017-05-10 |
2021-02-17 |
Graybug Vision, Inc. |
Microparticules à libération prolongée et suspensions de celles-ci destinées à une thérapie médicale
|
WO2019023316A1
(fr)
|
2017-07-26 |
2019-01-31 |
Sutro Biopharma, Inc. |
Méthodes d'utilisation d'anticorps anti-cd74 et de conjugués d'anticorps dans le traitement d'un lymphome à cellules t
|
WO2019055579A1
(fr)
|
2017-09-12 |
2019-03-21 |
Tolero Pharmaceuticals, Inc. |
Régime de traitement pour des cancers qui sont insensibles aux inhibiteurs de bcl-2 à l'aide de l'inhibiteur de mcl-1 alvocidib
|
EP3684814A1
(fr)
|
2017-09-18 |
2020-07-29 |
Sutro Biopharma, Inc. |
Conjugués anticorps-récepteur alpha anti-folate et leurs utilisations
|
US20200237766A1
(en)
|
2017-10-13 |
2020-07-30 |
Tolero Pharmaceuticals, Inc. |
Pkm2 activators in combination with reactive oxygen species for treatment of cancer
|
NL2019801B1
(en)
|
2017-10-25 |
2019-05-02 |
Univ Leiden |
Delivery vectors
|
US11472799B2
(en)
|
2018-03-06 |
2022-10-18 |
Icahn School Of Medicine At Mount Sinai |
Serine threonine kinase (AKT) degradation / disruption compounds and methods of use
|
EP3539536A1
(fr)
|
2018-03-15 |
2019-09-18 |
MH10 Spolka z ograniczona odpowiedzialnoscia |
Composition pharmaceutique de sunitinib ou de son sel dans sa forme polymorphe i
|
US10857153B2
(en)
|
2018-06-04 |
2020-12-08 |
Apros Therapeutics, Inc. |
Pyrimidine compounds containing acidic groups
|
GB201810092D0
(en)
|
2018-06-20 |
2018-08-08 |
Ctxt Pty Ltd |
Compounds
|
WO2019246570A1
(fr)
|
2018-06-21 |
2019-12-26 |
Icahn School Of Medicine At Mount Sinai |
Composés de dégradation/désintégration de la protéine 5 à domaine de répétition wd40 (wdr5) et méthodes d'utilisation
|
GB201810581D0
(en)
|
2018-06-28 |
2018-08-15 |
Ctxt Pty Ltd |
Compounds
|
US11040038B2
(en)
|
2018-07-26 |
2021-06-22 |
Sumitomo Dainippon Pharma Oncology, Inc. |
Methods for treating diseases associated with abnormal ACVR1 expression and ACVR1 inhibitors for use in the same
|
US20220047716A1
(en)
|
2018-09-17 |
2022-02-17 |
Sutro Biopharma, Inc. |
Combination therapies with anti-folate receptor antibody conjugates
|
KR20210099066A
(ko)
|
2018-12-04 |
2021-08-11 |
스미토모 다이니폰 파마 온콜로지, 인크. |
암의 치료를 위한 작용제로서 사용하기 위한 cdk9 억제제 및 그의 다형체
|
JPWO2020130125A1
(ja)
|
2018-12-21 |
2021-11-04 |
第一三共株式会社 |
抗体−薬物コンジュゲートとキナーゼ阻害剤の組み合わせ
|
MX2021009371A
(es)
|
2019-02-12 |
2021-09-10 |
Sumitomo Pharma Oncology Inc |
Formulaciones que comprenden inhibidores de proteina cinasa heterociclicos.
|
JP2022525149A
(ja)
|
2019-03-20 |
2022-05-11 |
スミトモ ダイニッポン ファーマ オンコロジー, インコーポレイテッド |
ベネトクラクスが失敗した急性骨髄性白血病(aml)の処置
|
CN114364798A
(zh)
|
2019-03-21 |
2022-04-15 |
欧恩科斯欧公司 |
用于治疗癌症的Dbait分子与激酶抑制剂的组合
|
CA3133460A1
(fr)
|
2019-03-22 |
2020-10-01 |
Sumitomo Dainippon Pharma Oncology, Inc. |
Compositions comprenant des modulateurs de pkm2 et methodes de traitement les utilisant
|
EP3958845A1
(fr)
|
2019-04-25 |
2022-03-02 |
Synthon B.V. |
Composition pharmaceutique comprenant du sunitinib amorphe
|
US20220362394A1
(en)
|
2019-05-03 |
2022-11-17 |
Sutro Biopharma, Inc. |
Anti-bcma antibody conjugates
|
CA3137916A1
(fr)
|
2019-05-06 |
2020-11-12 |
Ichan School Of Medicine At Mount Sinai |
Composes heterobifonctionnels en tant qu'agents de degradation de hpk1
|
CN114728910B
(zh)
|
2019-08-31 |
2024-05-14 |
上海奕拓医药科技有限责任公司 |
用于fgfr抑制剂的吡唑类衍生物及其制备方法
|
KR20220098759A
(ko)
|
2019-11-08 |
2022-07-12 |
인쎄름 (엥스띠뛰 나씨오날 드 라 쌍떼 에 드 라 흐쉐르슈 메디깔) |
키나제 억제제에 대해 내성을 획득한 암의 치료 방법
|
WO2021148581A1
(fr)
|
2020-01-22 |
2021-07-29 |
Onxeo |
Nouvelle molécule dbait et son utilisation
|
WO2021178597A1
(fr)
|
2020-03-03 |
2021-09-10 |
Sutro Biopharma, Inc. |
Anticorps comprenant des étiquettes de glutamine spécifiques à un site, leurs procédés de préparation et d'utilisation
|
CN111233841A
(zh)
*
|
2020-03-17 |
2020-06-05 |
湖北扬信医药科技有限公司 |
一种舒尼替尼有关物质及其制备方法和用途
|
US12103924B2
(en)
|
2020-06-01 |
2024-10-01 |
Icahn School Of Medicine At Mount Sinai |
Mitogen-activated protein kinase kinase (MEK) degradation compounds and methods of use
|
US20240293365A1
(en)
*
|
2021-06-28 |
2024-09-05 |
The Regents Of The University Of California |
Methods for treating and ameliorating t cell related diseases
|
CN113717159A
(zh)
*
|
2021-09-16 |
2021-11-30 |
中国药科大学 |
吲哚酮类化合物及其药物组合物、制备方法及用途
|
CA3237696A1
(fr)
|
2021-11-08 |
2023-05-11 |
Progentos Therapeutics, Inc. |
Inhibiteurs du recepteur du facteur de croissance derive des plaquettes (pdgfr) alpha et leurs utilisations
|
WO2023228095A1
(fr)
|
2022-05-24 |
2023-11-30 |
Daiichi Sankyo Company, Limited |
Schéma posologique d'un conjugué anticorps anti-cdh6-médicament
|
US20240058465A1
(en)
|
2022-06-30 |
2024-02-22 |
Sutro Biopharma, Inc. |
Anti-ror1 antibody conjugates, compositions comprising anti ror1 antibody conjugates, and methods of making and using anti-ror1 antibody conjugates
|
WO2024017372A1
(fr)
*
|
2022-07-22 |
2024-01-25 |
成都百裕制药股份有限公司 |
Dérivé d'indolone et son utilisation
|
CN118221652A
(zh)
*
|
2022-12-19 |
2024-06-21 |
沈阳药科大学 |
一种吲哚-2-酮衍生物及其制备方法和用途
|
WO2024188282A1
(fr)
*
|
2023-03-14 |
2024-09-19 |
康百达(四川)生物医药科技有限公司 |
Dérivé d'indolone et son utilisation en médecine
|