US2940972A
(en)
|
1957-06-27 |
1960-06-14 |
Thomae Gmbh Dr K |
Tri-and tetra-substituted pteridine derivatives
|
US4666828A
(en)
|
1984-08-15 |
1987-05-19 |
The General Hospital Corporation |
Test for Huntington's disease
|
US4683202A
(en)
|
1985-03-28 |
1987-07-28 |
Cetus Corporation |
Process for amplifying nucleic acid sequences
|
US4801531A
(en)
|
1985-04-17 |
1989-01-31 |
Biotechnology Research Partners, Ltd. |
Apo AI/CIII genomic polymorphisms predictive of atherosclerosis
|
US5272057A
(en)
|
1988-10-14 |
1993-12-21 |
Georgetown University |
Method of detecting a predisposition to cancer by the use of restriction fragment length polymorphism of the gene for human poly (ADP-ribose) polymerase
|
US5192659A
(en)
|
1989-08-25 |
1993-03-09 |
Genetype Ag |
Intron sequence analysis method for detection of adjacent and remote locus alleles as haplotypes
|
GB9125001D0
(en)
|
1991-11-25 |
1992-01-22 |
Ici Plc |
Heterocyclic compounds
|
US5843941A
(en)
|
1993-05-14 |
1998-12-01 |
Genentech, Inc. |
Ras farnesyl transferase inhibitors
|
US5700823A
(en)
|
1994-01-07 |
1997-12-23 |
Sugen, Inc. |
Treatment of platelet derived growth factor related disorders such as cancers
|
US6331555B1
(en)
|
1995-06-01 |
2001-12-18 |
University Of California |
Treatment of platelet derived growth factor related disorders such as cancers
|
US6218529B1
(en)
|
1995-07-31 |
2001-04-17 |
Urocor, Inc. |
Biomarkers and targets for diagnosis, prognosis and management of prostate, breast and bladder cancer
|
CA2262403C
(en)
|
1995-07-31 |
2011-09-20 |
Urocor, Inc. |
Biomarkers and targets for diagnosis, prognosis and management of prostate disease
|
TW472045B
(en)
|
1996-09-25 |
2002-01-11 |
Astra Ab |
Protein kinase C inhibitor compounds, method for their preparation, pharmaceutical composition thereof and intermediate used for their preparation
|
CZ298521B6
(cs)
|
1997-05-28 |
2007-10-24 |
Aventis Pharmaceuticals Inc. |
Derivát chinolinu a chinoxalinu, farmaceutický prostredek obsahující tuto slouceninu a použití tétoslouceniny
|
UA71555C2
(en)
|
1997-10-06 |
2004-12-15 |
Zentaris Gmbh |
Methods for modulating function of serine/threonine protein kinases by 5-azaquinoline derivatives
|
WO2000042026A1
(en)
|
1999-01-15 |
2000-07-20 |
Novo Nordisk A/S |
Non-peptide glp-1 agonists
|
EP1208231B2
(en)
|
1999-05-05 |
2009-12-30 |
Institut Curie |
Means for detecting and treating pathologies linked to fgfr3
|
US7135311B1
(en)
|
1999-05-05 |
2006-11-14 |
Institut Curie |
Means for detecting and treating pathologies linked to FGFR3
|
MXPA02001108A
(es)
|
1999-09-15 |
2002-08-20 |
Warner Lambert Co |
Pieridinonas como inhibidores de la cinasa.
|
DE10013318A1
(de)
|
2000-03-17 |
2001-09-20 |
Merck Patent Gmbh |
Formulierung enthaltend Chinoxalinderivate
|
WO2002076985A1
(en)
|
2001-03-23 |
2002-10-03 |
Smithkline Beecham Corporation |
Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases
|
US7569592B2
(en)
|
2001-12-18 |
2009-08-04 |
Merck & Co., Inc. |
Heteroaryl substituted pyrazole modulators of metabotropic glutamate receptor-5
|
RU2323215C2
(ru)
|
2001-12-24 |
2008-04-27 |
Астразенека Аб |
Замещенные производные хиназолина как ингибиторы ауроракиназы
|
JP2003213463A
(ja)
|
2002-01-17 |
2003-07-30 |
Sumitomo Chem Co Ltd |
金属腐食防止剤および洗浄液
|
CA2480800C
(en)
|
2002-04-08 |
2008-09-23 |
Mark T. Bilodeau |
Inhibitors of akt activity
|
US7265378B2
(en)
|
2002-07-10 |
2007-09-04 |
E. I. Du Pont De Nemours And Company |
Electronic devices made with electron transport and/or anti-quenching layers
|
US7825132B2
(en)
|
2002-08-23 |
2010-11-02 |
Novartis Vaccines And Diagnostics, Inc. |
Inhibition of FGFR3 and treatment of multiple myeloma
|
KR20110050745A
(ko)
|
2002-10-03 |
2011-05-16 |
탈자진 인코포레이티드 |
혈관항상성 유지제 및 그의 사용 방법
|
AR043059A1
(es)
|
2002-11-12 |
2005-07-13 |
Bayer Pharmaceuticals Corp |
Derivados de indolil pirazinona utiles para el tratamiento de trastornos hiper-proliferativos
|
US7098332B2
(en)
|
2002-12-20 |
2006-08-29 |
Hoffmann-La Roche Inc. |
5,8-Dihydro-6H-pyrido[2,3-d]pyrimidin-7-ones
|
EP1590341B1
(en)
|
2003-01-17 |
2009-06-17 |
Warner-Lambert Company LLC |
2-aminopyridine substituted heterocycles as inhibitors of cellular proliferation
|
EP1620413A2
(en)
|
2003-04-30 |
2006-02-01 |
Cytokinetics, Inc. |
Compounds, compositions, and methods
|
CN102584813B
(zh)
|
2003-05-14 |
2016-07-06 |
Ngc药物公司 |
化合物及其在调节淀粉样蛋白β中的用途
|
PT1636228E
(pt)
|
2003-05-23 |
2009-02-02 |
Aeterna Zentaris Gmbh |
Novas piridopirazinas e sua utilização como moduladores de cinases
|
DE10323345A1
(de)
|
2003-05-23 |
2004-12-16 |
Zentaris Gmbh |
Neue Pyridopyrazine und deren Verwendung als Kinase-Inhibitoren
|
WO2005007099A2
(en)
|
2003-07-10 |
2005-01-27 |
Imclone Systems Incorporated |
Pkb inhibitors as anti-tumor agents
|
EP1646383A4
(en)
|
2003-07-21 |
2009-03-25 |
Bethesda Pharmaceuticals Inc |
DESIGN AND SYNTHESIS OF LIGANDS OPTIMIZED FOR PPAR
|
AU2004261667A1
(en)
|
2003-08-01 |
2005-02-10 |
Genelabs Technologies, Inc. |
Bicyclic imidazol derivatives against Flaviviridae
|
DE602004008312T2
(de)
|
2003-10-17 |
2008-04-17 |
4 Aza Ip Nv |
Heterocyclus-substituierte pteridin-derivate und ihre verwendung in der therapie
|
KR101167573B1
(ko)
|
2003-11-07 |
2012-07-30 |
노바티스 백신즈 앤드 다이아그노스틱스 인코포레이티드 |
개선된 약학적 성질을 갖는 퀴놀리논 화합물의 약학적으로허용가능한 염
|
CA2546300C
(en)
|
2003-11-20 |
2012-10-02 |
Janssen Pharmaceutica N.V. |
6-alkenyl and 6-phenylalkyl substituted 2-quinolinones and 2-quinoxalinones as poly(adp-ribose) polymerase inhibitors
|
MXPA06005735A
(es)
|
2003-11-24 |
2006-08-17 |
Hoffmann La Roche |
Pirazolil e imidazolil pirimidinas.
|
EP2228369A1
(en)
|
2003-12-23 |
2010-09-15 |
Astex Therapeutics Ltd. |
Pyrazole derivatives as protein kinase modulators
|
US7098222B2
(en)
|
2004-05-12 |
2006-08-29 |
Abbott Laboratories |
Bicyclic-substituted amines having cyclic-substituted monocyclic substituents
|
US7205316B2
(en)
|
2004-05-12 |
2007-04-17 |
Abbott Laboratories |
Tri- and bi-cyclic heteroaryl histamine-3 receptor ligands
|
BRPI0514691A
(pt)
|
2004-08-31 |
2008-06-17 |
Astrazeneca Ab |
composto ou um sal farmaceuticamente aceitável do mesmo, processo para preparar o mesmo, composição farmacêutica, e, uso de um composto ou um sal farmaceuticamente aceitável do mesmo
|
MX2007004276A
(es)
|
2004-10-14 |
2007-05-16 |
Hoffmann La Roche |
1,5-naftiridin-azolidinonas que tienen actividad antiproliferativa de cdk-1.
|
EP1659175A1
(en)
|
2004-11-18 |
2006-05-24 |
Institut Curie |
Alterations in seborrheic keratoses and their applications
|
ES2425567T3
(es)
|
2004-12-24 |
2013-10-16 |
Spinifex Pharmaceuticals Pty Ltd |
Método de tratamiento o profilaxis
|
WO2006084338A1
(en)
|
2005-02-14 |
2006-08-17 |
Bionomics Limited |
Novel tubulin polymerisation inhibitors
|
WO2006092430A1
(de)
|
2005-03-03 |
2006-09-08 |
Universität des Saarlandes |
Selektive hemmstoffe humaner corticoidsynthasen
|
NZ563193A
(en)
|
2005-05-09 |
2010-05-28 |
Ono Pharmaceutical Co |
Human monoclonal antibodies to programmed death 1(PD-1) and methods for treating cancer using anti-PD-1 antibodies alone or in combination with other immunotherapeutics
|
US20090156617A1
(en)
|
2005-05-12 |
2009-06-18 |
Northrup Alan B |
Tyrosine kinase inhibitors
|
MX2007014258A
(es)
|
2005-05-18 |
2008-01-22 |
Wyeth Corp |
Inhibidores de 4,6-diamino-[1,7]naftiridin-3-carbonitrilo de la tpl2 cinasa y metodos de fabricacion y uso de los mismos.
|
DK1907424T3
(en)
|
2005-07-01 |
2015-11-09 |
Squibb & Sons Llc |
HUMAN MONOCLONAL ANTIBODIES TO PROGRAMMED death ligand 1 (PD-L1)
|
GB0513692D0
(en)
|
2005-07-04 |
2005-08-10 |
Karobio Ab |
Novel pharmaceutical compositions
|
ZA200801822B
(en)
|
2005-08-26 |
2009-09-30 |
Serono Lab |
Pyrazine derivatives and use as p13k inhibitors
|
EP1790342A1
(de)
|
2005-11-11 |
2007-05-30 |
Zentaris GmbH |
Pyridopyrazin-Derivate und deren Verwendung als Modulatoren der Signaltransduktionswege
|
US8217042B2
(en)
|
2005-11-11 |
2012-07-10 |
Zentaris Gmbh |
Pyridopyrazines and their use as modulators of kinases
|
KR101400905B1
(ko)
|
2005-11-11 |
2014-05-29 |
아에테르나 젠타리스 게엠베하 |
신규한 피리도피라진 및 키나제의 조절제로서의 이의 용도
|
US20090247576A1
(en)
|
2005-11-22 |
2009-10-01 |
Eisai R & D Management Co., Ltd. |
Anti-tumor agent for multiple myeloma
|
BRPI0620292B1
(pt)
|
2005-12-21 |
2021-08-24 |
Janssen Pharmaceutica N. V. |
Compostos de triazolopiridazinas como moduladores da cinase, composição, uso, combinação e processo de preparo do referido composto
|
CA2651072A1
(en)
|
2006-05-01 |
2007-11-08 |
Pfizer Products Inc. |
Substituted 2-amino-fused heterocyclic compounds
|
GB0609621D0
(en)
|
2006-05-16 |
2006-06-21 |
Astrazeneca Ab |
Novel co-crystal
|
ATE549338T1
(de)
|
2006-05-24 |
2012-03-15 |
Boehringer Ingelheim Int |
Substituierte pteridine, die mit einem viergliedrigen heterocyclus substituiert sind
|
CA2654317A1
(en)
|
2006-06-12 |
2007-12-21 |
Trubion Pharmaceuticals, Inc. |
Single-chain multivalent binding proteins with effector function
|
WO2008003702A2
(en)
|
2006-07-03 |
2008-01-10 |
Vereniging Voor Christelijk Hoger Onderwijs, Wetenschappelijk Onderzoek En Patientenzorg |
Fused bicyclic compounds interacting with the histamine h4 receptor
|
WO2008060907A2
(en)
|
2006-11-10 |
2008-05-22 |
Bristol-Myers Squibb Company |
Pyrrolo-pyridine kinase inhibitors
|
JP2008127446A
(ja)
|
2006-11-20 |
2008-06-05 |
Canon Inc |
1,5−ナフチリジン化合物及び有機発光素子
|
NZ578329A
(en)
|
2006-12-13 |
2012-05-25 |
Schering Corp |
Igf1r inhibitors for treating cancer
|
US7872018B2
(en)
|
2006-12-21 |
2011-01-18 |
Plexxikon, Inc. |
Compounds and methods for kinase modulation, and indications therefor
|
WO2008079988A2
(en)
|
2006-12-22 |
2008-07-03 |
Novartis Ag |
Quinazolines for pdk1 inhibition
|
EP2114941B1
(en)
|
2006-12-22 |
2015-03-25 |
Astex Therapeutics Limited |
Bicyclic heterocyclic compounds as fgfr inhibitors
|
KR20080062876A
(ko)
|
2006-12-29 |
2008-07-03 |
주식회사 대웅제약 |
신규한 항진균성 트리아졸 유도체
|
WO2008109369A2
(en)
|
2007-03-02 |
2008-09-12 |
Mdrna, Inc. |
Nucleic acid compounds for inhibiting tnf gene expression and uses thereof
|
US8163923B2
(en)
|
2007-03-14 |
2012-04-24 |
Advenchen Laboratories, Llc |
Spiro substituted compounds as angiogenesis inhibitors
|
EP1990342A1
(en)
|
2007-05-10 |
2008-11-12 |
AEterna Zentaris GmbH |
Pyridopyrazine Derivatives, Process of Manufacturing and Uses thereof
|
TW200902008A
(en)
|
2007-05-10 |
2009-01-16 |
Smithkline Beecham Corp |
Quinoxaline derivatives as PI3 kinase inhibitors
|
JP2010529031A
(ja)
|
2007-05-29 |
2010-08-26 |
グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー |
Pi3キナーゼ阻害剤としてのナフチリジン誘導体
|
AR066879A1
(es)
|
2007-06-08 |
2009-09-16 |
Novartis Ag |
Derivados de quinoxalina como inhibidores de la actividad de cinasa de tirosina de las cinasas janus
|
PL2172450T3
(pl)
|
2007-06-20 |
2014-03-31 |
Mitsubishi Tanabe Pharma Corp |
Nowe pochodne sulfonamidowe kwasu malonowego i ich zastosowanie farmaceutyczne
|
US8629144B2
(en)
|
2007-06-21 |
2014-01-14 |
Janssen Pharmaceutica Nv |
Polymorphic and hydrate forms, salts and process for preparing 6-{difluoro[6-(1-methyl-1H-pyrazol-4-yl)[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}quinoline
|
US20090263397A1
(en)
|
2007-07-06 |
2009-10-22 |
Buck Elizabeth A |
Combination anti-cancer therapy
|
BRPI0814777A2
(pt)
|
2007-08-08 |
2015-03-03 |
Glaxosmithkline Llc |
Composto, composição farmacêutica, método para tratar um neoplasma, uso de um composto, e, composição farmacêutica.
|
WO2009019518A1
(en)
|
2007-08-09 |
2009-02-12 |
Astrazeneca Ab |
Pyrimidine compounds having a fgfr inhibitory effect
|
JP2010535804A
(ja)
|
2007-08-09 |
2010-11-25 |
グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー |
Pi3キナーゼ阻害薬としてのキノキサリン誘導体
|
WO2013173485A1
(en)
|
2012-05-15 |
2013-11-21 |
Predictive Biosciences, Inc. |
Detection of bladder cancers
|
US20090054304A1
(en)
|
2007-08-23 |
2009-02-26 |
Kalypsys, Inc. |
Heterocyclic modulators of tgr5 for treatment of disease
|
MY152948A
(en)
|
2007-11-16 |
2014-12-15 |
Incyte Corp |
4-pyrazolyl-n-arylpyrimidin-2-amines and 4-pyrazolyl-n-heteroarylpyrimidin-2-amines as janus kinase inhibitors
|
MX2010012064A
(es)
|
2008-05-05 |
2010-12-06 |
Schering Corp |
Uso secuencial de agentes quimioterapeuticos citotoxicos para el tratamiento de cancer.
|
JP5351254B2
(ja)
|
2008-05-23 |
2013-11-27 |
ノバルティス アーゲー |
キノキサリン−およびキノリン−カルボキシアミド誘導体
|
JP2012509342A
(ja)
|
2008-11-20 |
2012-04-19 |
オーエスアイ・フアーマスーテイカルズ・インコーポレーテツド |
置換ピロロ[2,3−b]−ピリジンおよび−ピラジン
|
AU2010206161B2
(en)
|
2009-01-21 |
2014-08-07 |
Basilea Pharmaceutica Ag |
Novel bicyclic antibiotics
|
WO2010088177A1
(en)
|
2009-02-02 |
2010-08-05 |
Merck Sharp & Dohme Corp. |
Inhibitors of akt activity
|
TW201041888A
(en)
|
2009-05-06 |
2010-12-01 |
Plexxikon Inc |
Compounds and methods for kinase modulation, and indications therefor
|
RU2567752C2
(ru)
|
2009-06-12 |
2015-11-10 |
Абивакс |
Соединения, пригодные для лечения рака
|
JP5696856B2
(ja)
|
2009-09-03 |
2015-04-08 |
バイオエナジェニックス |
Paskの阻害用複素環式化合物
|
US9340528B2
(en)
|
2009-09-04 |
2016-05-17 |
Bayer Pharma Aktiengesellschaft |
Substituted aminoquinoxalines as tyrosine threonine kinase inhibitors
|
US20110123545A1
(en)
|
2009-11-24 |
2011-05-26 |
Bristol-Myers Squibb Company |
Combination of vegfr2 and igf1r inhibitors for the treatment of proliferative diseases
|
EP2332939A1
(en)
|
2009-11-26 |
2011-06-15 |
Æterna Zentaris GmbH |
Novel Naphthyridine derivatives and the use thereof as kinase inhibitors
|
CA2829790C
(en)
|
2010-03-30 |
2018-06-05 |
Verseon Corporation |
Multisubstituted aromatic compounds as inhibitors of thrombin
|
GB201007286D0
(en)
|
2010-04-30 |
2010-06-16 |
Astex Therapeutics Ltd |
New compounds
|
US8513421B2
(en)
|
2010-05-19 |
2013-08-20 |
Millennium Pharmaceuticals, Inc. |
Substituted hydroxamic acids and uses thereof
|
WO2011149937A1
(en)
|
2010-05-24 |
2011-12-01 |
Intellikine, Inc. |
Heterocyclic compounds and uses thereof
|
GB201020179D0
(en)
*
|
2010-11-29 |
2011-01-12 |
Astex Therapeutics Ltd |
New compounds
|
CN102532141A
(zh)
|
2010-12-08 |
2012-07-04 |
中国科学院上海药物研究所 |
[1,2,4]三唑并[4,3-b][1,2,4]三嗪类化合物、其制备方法和用途
|
KR101928116B1
(ko)
|
2011-01-31 |
2018-12-11 |
노파르티스 아게 |
신규 헤테로시클릭 유도체
|
WO2012106556A2
(en)
|
2011-02-02 |
2012-08-09 |
Amgen Inc. |
Methods and compositons relating to inhibition of igf-1r
|
US9295673B2
(en)
|
2011-02-23 |
2016-03-29 |
Intellikine Llc |
Combination of mTOR inhibitors and P13-kinase inhibitors, and uses thereof
|
WO2012118492A1
(en)
|
2011-03-01 |
2012-09-07 |
Array Biopharma Inc. |
Heterocyclic sulfonamides as raf inhibitors
|
US9896730B2
(en)
|
2011-04-25 |
2018-02-20 |
OSI Pharmaceuticals, LLC |
Use of EMT gene signatures in cancer drug discovery, diagnostics, and treatment
|
PE20190262A1
(es)
|
2011-08-01 |
2019-02-25 |
Genentech Inc |
Metodos para tratar el cancer por el uso de antagonistas de union al eje pd-1 e inhibidores de mek
|
WO2013032951A1
(en)
|
2011-08-26 |
2013-03-07 |
Neupharma, Inc. |
Certain chemical entities, compositions, and methods
|
WO2013040515A1
(en)
|
2011-09-14 |
2013-03-21 |
Neupharma, Inc. |
Certain chemical entities, compositions, and methods
|
US9249110B2
(en)
|
2011-09-21 |
2016-02-02 |
Neupharma, Inc. |
Substituted quinoxalines as B-raf kinase inhibitors
|
EP2761300A4
(en)
|
2011-09-27 |
2015-12-02 |
Univ Michigan |
FUSIONS OF RECURRENT GENES IN BREAST CANCER
|
WO2013052699A2
(en)
|
2011-10-04 |
2013-04-11 |
Gilead Calistoga Llc |
Novel quinoxaline inhibitors of pi3k
|
JO3210B1
(ar)
|
2011-10-28 |
2018-03-08 |
Merck Sharp & Dohme |
مثبط منصهر لبروتين نقل الكوليسترليستير اوكسازوليدينون ثمائي الحلقة
|
GB201118652D0
(en)
|
2011-10-28 |
2011-12-07 |
Astex Therapeutics Ltd |
New compounds
|
GB201118654D0
(en)
|
2011-10-28 |
2011-12-07 |
Astex Therapeutics Ltd |
New compounds
|
GB201118675D0
(en)
|
2011-10-28 |
2011-12-14 |
Astex Therapeutics Ltd |
New compounds
|
CA2853256C
(en)
|
2011-10-28 |
2019-05-14 |
Novartis Ag |
Novel purine derivatives and their use in the treatment of disease
|
GB201118656D0
(en)
|
2011-10-28 |
2011-12-07 |
Astex Therapeutics Ltd |
New compounds
|
AR088941A1
(es)
|
2011-11-23 |
2014-07-16 |
Bayer Ip Gmbh |
Anticuerpos anti-fgfr2 y sus usos
|
WO2013088191A1
(en)
|
2011-12-12 |
2013-06-20 |
Institut National De La Sante Et De La Recherche Medicale (Inserm) |
Antagonist of the fibroblast growth factor receptor 3 (fgfr3) for use in the treatment or the prevention of skeletal disorders linked with abnormal activation of fgfr3
|
GB201203442D0
(en)
|
2012-02-28 |
2012-04-11 |
Univ Birmingham |
Immunotherapeutic molecules and uses
|
ES2702305T3
(es)
|
2012-03-08 |
2019-02-28 |
Astellas Pharma Inc |
Nuevo producto de fusión de FGFR3
|
US20150086584A1
(en)
|
2012-03-22 |
2015-03-26 |
University Of Miami |
Multi-specific binding agents
|
US9254288B2
(en)
|
2012-05-07 |
2016-02-09 |
The Translational Genomics Research Institute |
Susceptibility of tumors to tyrosine kinase inhibitors and treatment thereof
|
GB201209609D0
(en)
|
2012-05-30 |
2012-07-11 |
Astex Therapeutics Ltd |
New compounds
|
GB201209613D0
(en)
|
2012-05-30 |
2012-07-11 |
Astex Therapeutics Ltd |
New compounds
|
JPWO2014007369A1
(ja)
|
2012-07-05 |
2016-06-02 |
国立研究開発法人国立がん研究センター |
Fgfr2融合遺伝子
|
US20150203589A1
(en)
*
|
2012-07-24 |
2015-07-23 |
The Trustees Of Columbia University In The City Of New York |
Fusion proteins and methods thereof
|
CN104797936B
(zh)
|
2012-07-24 |
2017-11-24 |
纽约市哥伦比亚大学理事会 |
融合蛋白及其方法
|
EP2877209A1
(en)
|
2012-07-27 |
2015-06-03 |
Genentech, Inc. |
Methods of treating fgfr3 related conditions
|
JP6320382B2
(ja)
|
2012-08-13 |
2018-05-09 |
ザ ロックフェラー ユニヴァーシティ |
メラノーマの処置および診断
|
MX369550B
(es)
|
2012-09-27 |
2019-11-12 |
Chugai Pharmaceutical Co Ltd |
Gen de fusion del receptor de factor de crecimiento de fibroblastos 3 (fgfr3) y medicamentos farmaceutico para tratar el mismo.
|
EP2914622B1
(en)
|
2012-11-05 |
2023-06-07 |
Foundation Medicine, Inc. |
Novel fusion molecules and uses thereof
|
US10980804B2
(en)
|
2013-01-18 |
2021-04-20 |
Foundation Medicine, Inc. |
Methods of treating cholangiocarcinoma
|
US20160084839A1
(en)
|
2013-04-02 |
2016-03-24 |
Marisa Dolled-Filhart |
Immunohistochemical assay for detecting expression of programmed death ligand 1 (pd-l1) in tumor tissue
|
EP2981621B1
(en)
|
2013-04-05 |
2019-05-22 |
Life Technologies Corporation |
Gene fusions
|
GB201307577D0
(en)
|
2013-04-26 |
2013-06-12 |
Astex Therapeutics Ltd |
New compounds
|
US20160186269A1
(en)
|
2013-05-27 |
2016-06-30 |
Stichting Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis |
Novel translocations in lung cancer
|
WO2015006723A1
(en)
|
2013-07-12 |
2015-01-15 |
The Regents Of The University Of Michigan |
Recurrent gene fusions in cancer
|
WO2015016718A1
(en)
|
2013-08-02 |
2015-02-05 |
Bionovion Holding B.V. |
Combining cd27 agonists and immune checkpoint inhibition for immune stimulation
|
JP2016527274A
(ja)
|
2013-08-02 |
2016-09-08 |
イグナイタ インコーポレイテッド |
AXL/cMET阻害剤を単独または他の薬剤と組み合わせて用いて各種がんを治療する方法
|
US9221804B2
(en)
|
2013-10-15 |
2015-12-29 |
Janssen Pharmaceutica Nv |
Secondary alcohol quinolinyl modulators of RORγt
|
WO2015077717A1
(en)
|
2013-11-25 |
2015-05-28 |
The Broad Institute Inc. |
Compositions and methods for diagnosing, evaluating and treating cancer by means of the dna methylation status
|
US9067998B1
(en)
|
2014-07-15 |
2015-06-30 |
Kymab Limited |
Targeting PD-1 variants for treatment of cancer
|
WO2015100257A1
(en)
|
2013-12-23 |
2015-07-02 |
The General Hospital Corporation |
Methods and assays for determining reduced brca1 pathway function in a cancer cell
|
JOP20200094A1
(ar)
*
|
2014-01-24 |
2017-06-16 |
Dana Farber Cancer Inst Inc |
جزيئات جسم مضاد لـ pd-1 واستخداماتها
|
RU2715893C2
(ru)
|
2014-03-26 |
2020-03-04 |
Астекс Терапьютикс Лтд |
Комбинации ингибитора fgfr и ингибитора igf1r
|
PL3122358T3
(pl)
|
2014-03-26 |
2021-06-14 |
Astex Therapeutics Ltd. |
Połączenia inhibitorów fgfr i cmet w leczeniu nowotworu
|
JO3512B1
(ar)
|
2014-03-26 |
2020-07-05 |
Astex Therapeutics Ltd |
مشتقات كينوكسالين مفيدة كمعدلات لإنزيم fgfr كيناز
|
SG11201609468WA
(en)
|
2014-05-29 |
2016-12-29 |
Medimmune Ltd |
Antagonists of pdl-1 and pd-1 for the treatment of hpv-negative cancers
|
EP3164121A4
(en)
|
2014-07-01 |
2018-06-13 |
Vicus Therapeutics, LLC |
Combination drug therapies for cancer and methods of making and using them
|
CN112546230A
(zh)
|
2014-07-09 |
2021-03-26 |
博笛生物科技有限公司 |
用于治疗癌症的联合治疗组合物和联合治疗方法
|
EP3177321B1
(en)
|
2014-08-08 |
2020-11-25 |
Oncoquest Pharmaceuticals Inc. |
Tumor antigen specific antibodies and tlr3 stimulation to enhance the performance of checkpoint interference therapy of cancer
|
TW201618775A
(zh)
|
2014-08-11 |
2016-06-01 |
艾森塔製藥公司 |
Btk抑制劑、pi3k抑制劑、jak-2抑制劑、pd-1抑制劑及/或pd-l1抑制劑之治療組合物
|
SG11201701710SA
(en)
|
2014-09-08 |
2017-04-27 |
Celgene Corp |
Methods for treating a disease or disorder using oral formulations of cytidine analogs in combination with an anti-pd1 or anti-pdl1 monoclonal antibody
|
JP6681905B2
(ja)
|
2014-09-13 |
2020-04-15 |
ノバルティス アーゲー |
Alk阻害剤の併用療法
|
US20170275705A1
(en)
|
2014-09-15 |
2017-09-28 |
The Johns Hopkins University |
Biomarkers useful for determining response to pd-1 blockade therapy
|
SG11201702381QA
(en)
*
|
2014-09-26 |
2017-04-27 |
Janssen Pharmaceutica Nv |
Use of fgfr mutant gene panels in identifying cancer patients that will be responsive to treatment with an fgfr inhibitor
|
AU2015327868A1
(en)
|
2014-10-03 |
2017-04-20 |
Novartis Ag |
Combination therapies
|
CR20170143A
(es)
|
2014-10-14 |
2017-06-19 |
Dana Farber Cancer Inst Inc |
Moléculas de anticuerpo que se unen a pd-l1 y usos de las mismas
|
CA2965414C
(en)
|
2014-10-29 |
2024-01-09 |
Teva Pharmaceuticals Australia Pty Ltd |
Interferon .alpha.2.beta. variants
|
WO2016094309A1
(en)
|
2014-12-10 |
2016-06-16 |
Myosotis |
Inhibition of tnf signaling in cancer immunotherapy
|
WO2016100882A1
(en)
|
2014-12-19 |
2016-06-23 |
Novartis Ag |
Combination therapies
|
US20170369570A1
(en)
|
2015-01-20 |
2017-12-28 |
Immunexcite, Inc. |
Compositions and methods for cancer immunotherapy
|
JOP20200201A1
(ar)
|
2015-02-10 |
2017-06-16 |
Astex Therapeutics Ltd |
تركيبات صيدلانية تشتمل على n-(3.5- ثنائي ميثوكسي فينيل)-n'-(1-ميثيل إيثيل)-n-[3-(ميثيل-1h-بيرازول-4-يل) كينوكسالين-6-يل]إيثان-1.2-ثنائي الأمين
|
WO2016128912A1
(en)
|
2015-02-12 |
2016-08-18 |
Acerta Pharma B.V. |
Therapeutic combinations of a btk inhibitor, a pi3k inhibitor, a jak-2 inhibitor, a pd-1 inhibitor, and/or a pd-l1 inhibitor
|
WO2016134234A1
(en)
|
2015-02-19 |
2016-08-25 |
Bioclin Therapeutics, Inc. |
Methods, compositions, and kits for treatment of cancer
|
AR103726A1
(es)
|
2015-02-27 |
2017-05-31 |
Merck Sharp & Dohme |
Cristales de anticuerpos monoclonales anti-pd-1 humanos
|
KR20170122810A
(ko)
|
2015-03-04 |
2017-11-06 |
머크 샤프 앤드 돔 코포레이션 |
암을 치료하기 위한 pd-1 길항제 및 에리불린의 조합
|
CA2978226A1
(en)
|
2015-03-04 |
2016-09-09 |
Merck Sharpe & Dohme Corp. |
Combination of a pd-1 antagonist and a vegfr/fgfr/ret tyrosine kinase inhibitor for treating cancer
|
IL254529B2
(en)
|
2015-03-20 |
2024-05-01 |
Syndax Pharmaceuticals Inc |
A combination of a histone deacetylase inhibitor and an antibody against programmed cell death protein 1 for the treatment of cancer
|
WO2016153839A1
(en)
|
2015-03-20 |
2016-09-29 |
Merck Sharp & Dohme Corp. |
Combination of a pd-1 antagonist and vorinostat for treating cancer
|
JP6879996B2
(ja)
|
2015-03-26 |
2021-06-02 |
オンコセック メディカル インコーポレイテッド |
悪性腫瘍の治療方法
|
US10478494B2
(en)
|
2015-04-03 |
2019-11-19 |
Astex Therapeutics Ltd |
FGFR/PD-1 combination therapy for the treatment of cancer
|
AU2016249395B2
(en)
|
2015-04-17 |
2022-04-07 |
Bristol-Myers Squibb Company |
Compositions comprising a combination of an anti-PD-1 antibody and another antibody
|
US20160347836A1
(en)
|
2015-05-28 |
2016-12-01 |
Bristol-Myers Squibb Company |
Treatment of hodgkin's lymphoma using an anti-pd-1 antibody
|
US20180155429A1
(en)
|
2015-05-28 |
2018-06-07 |
Bristol-Myers Squibb Company |
Treatment of pd-l1 positive lung cancer using an anti-pd-1 antibody
|
US11078278B2
(en)
|
2015-05-29 |
2021-08-03 |
Bristol-Myers Squibb Company |
Treatment of renal cell carcinoma
|
MX2017015811A
(es)
|
2015-06-12 |
2018-04-10 |
Squibb Bristol Myers Co |
Tratamiento de cancer por bloqueo combinado de las trayectorias de señalizacion de muerte programada 1 (pd)-1 y receptor 4 de quimiocina c-x-c(cxcr4).
|
EP3313443B9
(en)
|
2015-06-25 |
2023-10-04 |
Immunomedics, Inc. |
Combining anti-hla-dr or anti-trop-2 antibodies with microtubule inhibitors, parp inhibitors, bruton kinase inhibitors or phosphoinositide 3-kinase inhibitors significantly improves therapeutic outcome in cancer
|
CN108289892B
(zh)
|
2015-06-29 |
2021-11-23 |
维瑞斯特姆股份有限公司 |
治疗组合物、组合和使用方法
|
GB201512869D0
(en)
|
2015-07-21 |
2015-09-02 |
Almac Diagnostics Ltd |
Gene signature for minute therapies
|
AU2016297583A1
(en)
|
2015-07-22 |
2018-02-01 |
Hznp Limited |
Combination of immunomodulatory agent with PD-1-or PD-L1 checkpoint inhibitors in the treatment of cancer
|
WO2017046746A1
(en)
|
2015-09-15 |
2017-03-23 |
Acerta Pharma B.V. |
Therapeutic combinations of a btk inhibitor and a gitr binding molecule, a 4-1bb agonist, or an ox40 agonist
|
EP3380523A1
(en)
|
2015-11-23 |
2018-10-03 |
Five Prime Therapeutics, Inc. |
Fgfr2 inhibitors alone or in combination with immune stimulating agents in cancer treatment
|
EP4015537A1
(en)
|
2015-12-01 |
2022-06-22 |
GlaxoSmithKline Intellectual Property Development Limited |
Combination treatments and uses and methods thereof
|