|
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
|
|
US5710158A
(en)
|
1991-05-10 |
1998-01-20 |
Rhone-Poulenc Rorer Pharmaceuticals Inc. |
Aryl and heteroaryl quinazoline compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
|
|
GB9125001D0
(en)
|
1991-11-25 |
1992-01-22 |
Ici Plc |
Heterocyclic compounds
|
|
AU661533B2
(en)
|
1992-01-20 |
1995-07-27 |
Astrazeneca Ab |
Quinazoline derivatives
|
|
AU6909194A
(en)
|
1993-05-14 |
1994-12-12 |
Board Of Regents, The University Of Texas System |
Preparation of n-cyanodithioimino-carbonates and 3-mercapto-5-amino-1h-1,2,4-triazole
|
|
US5700823A
(en)
|
1994-01-07 |
1997-12-23 |
Sugen, Inc. |
Treatment of platelet derived growth factor related disorders such as cancers
|
|
IL115256A0
(en)
|
1994-11-14 |
1995-12-31 |
Warner Lambert Co |
6-Aryl pyrido (2,3-d) pyrimidines and naphthyridines and their use
|
|
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
|
|
US5882864A
(en)
|
1995-07-31 |
1999-03-16 |
Urocor Inc. |
Biomarkers and targets for diagnosis, prognosis and management of prostate disease
|
|
US6060498A
(en)
|
1996-02-26 |
2000-05-09 |
Eisai Co., Ltd. |
Composition containing antitumor agent
|
|
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
|
|
EP1001945B1
(en)
|
1997-05-28 |
2011-03-02 |
Aventis Pharmaceuticals Inc. |
QUINOLINE AND QUINOXALINE COMPOUNDS WHICH INHIBIT PLATELET-DERIVED GROWTH FACTOR AND/OR p56lck TYROSINE KINASES
|
|
US6235740B1
(en)
|
1997-08-25 |
2001-05-22 |
Bristol-Myers Squibb Co. |
Imidazoquinoxaline protein tyrosine kinase inhibitors
|
|
UA71555C2
(en)
|
1997-10-06 |
2004-12-15 |
Zentaris Gmbh |
Methods for modulating function of serine/threonine protein kinases by 5-azaquinoline derivatives
|
|
WO1999042461A1
(en)
|
1998-02-23 |
1999-08-26 |
Warner-Lambert Company |
Substituted quinoxaline derivatives as interleukin-8 receptor antagonists
|
|
AU3033500A
(en)
|
1999-01-15 |
2000-08-01 |
Agouron Pharmaceuticals, Inc. |
Non-peptide glp-1 agonists
|
|
DE60032910T3
(en)
|
1999-05-05 |
2010-07-29 |
Institut Curie |
MEDIUM FOR THE DETECTION AND TREATMENT OF DISEASES RELATED TO FGFR3
|
|
US7135311B1
(en)
|
1999-05-05 |
2006-11-14 |
Institut Curie |
Means for detecting and treating pathologies linked to FGFR3
|
|
SK3542002A3
(en)
|
1999-09-15 |
2003-04-01 |
Warner Lambert Co |
Pteridinones as kinase inhibitors
|
|
DE10013318A1
(en)
|
2000-03-17 |
2001-09-20 |
Merck Patent Gmbh |
Quinoxaline derivatives are used as photo-stable UV filters in cosmetic or pharmaceutical sunscreens for the hair or skin
|
|
WO2002076985A1
(en)
|
2001-03-23 |
2002-10-03 |
Smithkline Beecham Corporation |
Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases
|
|
US20030235628A1
(en)
|
2001-09-19 |
2003-12-25 |
Rajneesh Taneja |
Methods and pharmaceutical formulations for protecting pharmaceutical compounds from acidic environments
|
|
ES2295441T3
(en)
|
2001-12-18 |
2008-04-16 |
MERCK & CO., INC. |
MODULATORS OF PIRAZOL HETEROARIL REPLACED 5 METABOTROPIC RECEIVER OF GLUTAMATE.
|
|
US20030229067A1
(en)
|
2001-12-20 |
2003-12-11 |
Arlindo Castelhano |
Pyrrolopyrimidine A2b selective antagonist compounds, their synthesis and use
|
|
SI1463506T1
(en)
|
2001-12-24 |
2010-01-29 |
Astrazeneca Ab |
Substituted quinazoline derivatives as inhibitors of aurora kinases
|
|
JP2003213463A
(en)
|
2002-01-17 |
2003-07-30 |
Sumitomo Chem Co Ltd |
Metal corrosion inhibitor and cleaning solution
|
|
WO2003086394A1
(en)
|
2002-04-08 |
2003-10-23 |
Merck & Co., Inc. |
Inhibitors of akt activity
|
|
US7074534B2
(en)
|
2002-07-10 |
2006-07-11 |
E. I. Du Pont De Nemours And Company |
Polymeric charge transport compositions and electronic devices made with such compositions
|
|
PA8577501A1
(en)
|
2002-07-25 |
2004-02-07 |
Warner Lambert Co |
KINASE INHIBITORS
|
|
US7825132B2
(en)
|
2002-08-23 |
2010-11-02 |
Novartis Vaccines And Diagnostics, Inc. |
Inhibition of FGFR3 and treatment of multiple myeloma
|
|
JP4560483B2
(en)
|
2002-10-03 |
2010-10-13 |
ターゲジェン インコーポレーティッド |
Angiogenic substances and methods for their use
|
|
CA2502825A1
(en)
|
2002-10-22 |
2004-05-06 |
Dainippon Pharmaceutical Co., Ltd. |
Stabilized composition
|
|
AR043059A1
(en)
|
2002-11-12 |
2005-07-13 |
Bayer Pharmaceuticals Corp |
DERIVATIVES OF INDOLIL PIRAZINONA USEFUL FOR THE TREATMENT OF HYPER-PROLIFERATIVE DISORDERS
|
|
US7098332B2
(en)
|
2002-12-20 |
2006-08-29 |
Hoffmann-La Roche Inc. |
5,8-Dihydro-6H-pyrido[2,3-d]pyrimidin-7-ones
|
|
JP2006516561A
(en)
|
2003-01-17 |
2006-07-06 |
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 |
2-Aminopyridine substituted heterocycles as inhibitors of cell proliferation
|
|
US20040204450A1
(en)
|
2003-03-28 |
2004-10-14 |
Pfizer Inc |
Quinoline and quinoxaline compounds
|
|
WO2004098494A2
(en)
|
2003-04-30 |
2004-11-18 |
Cytokinetics, Inc. |
Compounds, compositions, and methods
|
|
CN102584813B
(en)
|
2003-05-14 |
2016-07-06 |
Ngc药物公司 |
Compound and the purposes in regulating amyloid beta thereof
|
|
DE10323345A1
(en)
|
2003-05-23 |
2004-12-16 |
Zentaris Gmbh |
New pyridopyrazines and their use as kinase inhibitors
|
|
DK1636228T3
(en)
|
2003-05-23 |
2009-02-23 |
Aeterna Zentaris Gmbh |
Novel pyridopyrazines and their use as kinase modulators
|
|
WO2005007099A2
(en)
|
2003-07-10 |
2005-01-27 |
Imclone Systems Incorporated |
Pkb inhibitors as anti-tumor agents
|
|
AU2004259000A1
(en)
|
2003-07-21 |
2005-02-03 |
Bethesda Pharmaceuticals, Inc. |
Design and synthesis of optimized ligands for PPAR
|
|
TW200517381A
(en)
|
2003-08-01 |
2005-06-01 |
Genelabs Tech Inc |
Bicyclic heteroaryl derivatives
|
|
AU2004283479A1
(en)
|
2003-10-17 |
2005-05-06 |
4 Aza Bioscience Nv |
Heterocycle-substituted pteridine derivatives and their use in therapy
|
|
AU2003300692A1
(en)
|
2003-10-30 |
2005-05-19 |
Lupin Ltd. |
Stable formulations of ace inhibitors and methods for preparation thereof
|
|
EP2762475A1
(en)
|
2003-11-07 |
2014-08-06 |
Novartis Vaccines and Diagnostics, Inc. |
Pharmaceutically acceptable salts of quinolinone compounds and their medical use
|
|
SG150533A1
(en)
|
2003-11-20 |
2009-03-30 |
Janssen Pharmaceutica Nv |
6-alkenyl and 6-phenylalkyl substituted 2-quinolinones and 2- quinoxalinones as poly(adp-ribose) polymerase inhibitors
|
|
KR100861515B1
(en)
|
2003-11-24 |
2008-10-02 |
에프. 호프만-라 로슈 아게 |
Pyrazolyl and imidazolyl pyrimidines
|
|
AU2004303602C1
(en)
|
2003-12-23 |
2009-05-28 |
Astex Therapeutics Limited |
Pyrazole derivatives as protein kinase modulators
|
|
US7205316B2
(en)
|
2004-05-12 |
2007-04-17 |
Abbott Laboratories |
Tri- and bi-cyclic heteroaryl histamine-3 receptor ligands
|
|
US7098222B2
(en)
|
2004-05-12 |
2006-08-29 |
Abbott Laboratories |
Bicyclic-substituted amines having cyclic-substituted monocyclic substituents
|
|
US7446196B2
(en)
|
2004-06-03 |
2008-11-04 |
Kosan Biosciences, Incorporated |
Leptomycin compounds
|
|
BRPI0514691A
(en)
|
2004-08-31 |
2008-06-17 |
Astrazeneca Ab |
compound or a pharmaceutically acceptable salt thereof, process for preparing it, pharmaceutical composition, and use of a compound or pharmaceutically acceptable salt thereof
|
|
KR100875408B1
(en)
|
2004-10-14 |
2008-12-23 |
에프. 호프만-라 로슈 아게 |
1,5-naphthyridine azolidinone with CDX1 antiproliferative activity
|
|
MX2007004480A
(en)
|
2004-10-15 |
2007-05-08 |
Astrazeneca Ab |
Quinoxalines as b raf inhibitors.
|
|
EP1659175A1
(en)
|
2004-11-18 |
2006-05-24 |
Institut Curie |
Alterations in seborrheic keratoses and their applications
|
|
US8628796B2
(en)
|
2004-12-09 |
2014-01-14 |
Insys Therapeutics, Inc. |
Room-temperature stable dronabinol formulations
|
|
WO2006066361A1
(en)
|
2004-12-24 |
2006-06-29 |
The University Of Queensland |
Method of treatment or prophylaxis
|
|
US20090208575A1
(en)
|
2005-01-03 |
2009-08-20 |
Lupin Limited |
Pharmaceutical Composition Of Acid Labile Substances
|
|
AU2006212726C1
(en)
|
2005-02-14 |
2013-05-16 |
Bionomics Limited |
Novel tubulin polymerisation inhibitors
|
|
WO2006092430A1
(en)
|
2005-03-03 |
2006-09-08 |
Universität des Saarlandes |
Selective inhibitors of human corticosteroid synthases
|
|
JP2008540535A
(en)
|
2005-05-12 |
2008-11-20 |
メルク エンド カムパニー インコーポレーテッド |
Tyrosine kinase inhibitor
|
|
ES2380887T3
(en)
|
2005-05-13 |
2012-05-21 |
Topotarget Uk Limited |
Pharmaceutical formulations of HDAC inhibitors
|
|
CA2608362A1
(en)
|
2005-05-18 |
2006-11-23 |
Wyeth |
4, 6-diamino-[1,7] naphthyridine-3-carbonitrile inhibitors of tpl2 kinase and methods of making and using the same
|
|
JP5068167B2
(en)
|
2005-06-10 |
2012-11-07 |
中外製薬株式会社 |
Stabilizer for protein preparation containing meglumine and use thereof
|
|
GB0513692D0
(en)
|
2005-07-04 |
2005-08-10 |
Karobio Ab |
Novel pharmaceutical compositions
|
|
WO2007023186A1
(en)
|
2005-08-26 |
2007-03-01 |
Laboratoires Serono S.A. |
Pyrazine derivatives and use as pi3k inhibitors
|
|
EP1931645B1
(en)
|
2005-10-07 |
2014-07-16 |
Exelixis, Inc. |
N- (3-amino-quinoxalin-2-yl) -sulfonamide derivatives and their use as phosphatidylinositol 3-kinase inhibitors
|
|
CA2628039A1
(en)
|
2005-11-11 |
2007-05-18 |
Aeterna Zentaris Gmbh |
Novel pyridopyrazines and their use as modulators of kinases
|
|
US8217042B2
(en)
|
2005-11-11 |
2012-07-10 |
Zentaris Gmbh |
Pyridopyrazines and their use as modulators of kinases
|
|
EP1790342A1
(en)
|
2005-11-11 |
2007-05-30 |
Zentaris GmbH |
Pyridopyrazine derivatives and their use as signal transduction modulators
|
|
CN1966500B
(en)
|
2005-11-17 |
2011-03-30 |
中国科学院上海药物研究所 |
A class of quinoxaline derivatives, preparation method and use
|
|
WO2007061127A1
(en)
|
2005-11-22 |
2007-05-31 |
Eisai R & D Management Co., Ltd. |
Anti-tumor agent for multiple myeloma
|
|
DK1966214T3
(en)
|
2005-12-21 |
2017-02-13 |
Janssen Pharmaceutica Nv |
TRIAZOLPYRIDAZINES AS TYROSINKINASA MODULATORS
|
|
AR060358A1
(en)
|
2006-04-06 |
2008-06-11 |
Novartis Vaccines & Diagnostic |
QUINAZOLINS FOR THE INHIBITION OF PDK 1
|
|
US7998978B2
(en)
|
2006-05-01 |
2011-08-16 |
Pfizer Inc. |
Substituted 2-amino-fused heterocyclic compounds
|
|
GB0609621D0
(en)
|
2006-05-16 |
2006-06-21 |
Astrazeneca Ab |
Novel co-crystal
|
|
ATE549338T1
(en)
|
2006-05-24 |
2012-03-15 |
Boehringer Ingelheim Int |
SUBSTITUTED PTERIDINES SUBSTITUTED WITH A FOUR-MEMBER HETEROCYCLE
|
|
TWI398252B
(en)
|
2006-05-26 |
2013-06-11 |
Novartis Ag |
Pyrrolopyrimidine compounds and their uses
|
|
US20100016293A1
(en)
|
2006-07-03 |
2010-01-21 |
Rogier Adriaan Smits |
Quinazolines and Related Heterocyclic Compounds, and Their Therapeutic Use
|
|
AU2007284562B2
(en)
|
2006-08-16 |
2013-05-02 |
Exelixis, Inc. |
Using PI3K and MEK modulators in treatments of cancer
|
|
CN101600714B
(en)
|
2006-11-10 |
2013-08-21 |
百时美施贵宝公司 |
Novel pyrindole kinase inhibitors
|
|
JP2008127446A
(en)
|
2006-11-20 |
2008-06-05 |
Canon Inc |
1,5-naphthyridine compound and organic light-emitting device
|
|
MX2009006466A
(en)
|
2006-12-13 |
2009-06-26 |
Schering Corp |
Methods of treatment.
|
|
RU2009122670A
(en)
|
2006-12-21 |
2011-01-27 |
Плекссикон, Инк. (Us) |
COMPOUNDS AND METHODS FOR MODULATION OF KINASES AND INDICATIONS FOR THEIR USE
|
|
HRP20150642T1
(en)
|
2006-12-22 |
2015-08-14 |
Astex Therapeutics Limited |
BIKE HETEROCYCLIC SUBSTANCES AS FGFR INHIBITORS
|
|
US20100216767A1
(en)
|
2006-12-22 |
2010-08-26 |
Mina Aikawa |
Quinazolines for pdk1 inhibition
|
|
KR20080062876A
(en)
|
2006-12-29 |
2008-07-03 |
주식회사 대웅제약 |
Novel Antifungal Triazole Derivatives
|
|
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
|
|
EP2150255A4
(en)
|
2007-05-10 |
2011-10-05 |
Glaxosmithkline Llc |
Quinoxaline derivatives as p13 kinase inhibitors
|
|
EP1990342A1
(en)
|
2007-05-10 |
2008-11-12 |
AEterna Zentaris GmbH |
Pyridopyrazine Derivatives, Process of Manufacturing and Uses thereof
|
|
WO2008150827A1
(en)
|
2007-05-29 |
2008-12-11 |
Smithkline Beecham Corporation |
Naphthyridine, derivatives as p13 kinase inhibitors
|
|
AR066879A1
(en)
|
2007-06-08 |
2009-09-16 |
Novartis Ag |
DERIVATIVES OF QUINOXALINE AS INHIBITORS OF THE TYPOSINE CINASA ACTIVITY OF THE JANUS CINASES
|
|
BRPI0813105A2
(en)
|
2007-06-20 |
2015-08-04 |
Mitsubishi Tanabe Pharma Corp |
Sulfonamide derivative of malonic acid and its pharmaceutical use
|
|
WO2008155378A1
(en)
|
2007-06-21 |
2008-12-24 |
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
|
|
CN101827848B
(en)
|
2007-08-08 |
2012-11-07 |
葛兰素史密丝克莱恩有限责任公司 |
2-[(2-{phenylamino}-1H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]benzamide derivatives as IGF-1R inhibitors for the treatment of cancer
|
|
WO2009019518A1
(en)
|
2007-08-09 |
2009-02-12 |
Astrazeneca Ab |
Pyrimidine compounds having a fgfr inhibitory effect
|
|
WO2009021083A1
(en)
|
2007-08-09 |
2009-02-12 |
Smithkline Beecham Corporation |
Quinoxaline derivatives as pi3 kinase inhibitors
|
|
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
|
|
WO2009064835A1
(en)
|
2007-11-16 |
2009-05-22 |
Incyte Corporation |
4-pyrazolyl-n-arylpyrimidin-2-amines and 4-pyrazolyl-n-heteroarylpyrimidin-2-amines as janus kinase inhibitors
|
|
NZ585516A
(en)
|
2007-12-21 |
2012-07-27 |
Hoffmann La Roche |
Anti-cd20 antibody formulation
|
|
US20110129456A1
(en)
|
2008-05-05 |
2011-06-02 |
Yaolin Wang |
Sequential Administration of Chemotherapeutic Agents for Treatment of Cancer
|
|
BRPI0913031A2
(en)
|
2008-05-23 |
2019-11-26 |
Novartis Ag |
quinoline and quinoxaline derivatives as protein tyrosine kinase inhibitors, their uses and manufacturing process, as well as pharmaceutical compositions and combinations comprising them
|
|
MY188453A
(en)
|
2008-11-15 |
2021-12-09 |
Melinta Subsidiary Corp |
Antimicrobial compositions
|
|
US8592448B2
(en)
|
2008-11-20 |
2013-11-26 |
OSI Pharmaceuticals, LLC |
Substituted pyrrolo[2,3-b]-pyridines and -pyrazines
|
|
JP5662346B2
(en)
|
2009-01-21 |
2015-01-28 |
バジリア ファルマスーチカ アーゲーBasilea Pharmaceutica AG |
New bicyclic antibiotics
|
|
CA2750051A1
(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
|
|
FR2945950A1
(en)
|
2009-05-27 |
2010-12-03 |
Elan Pharma Int Ltd |
ANTICANCER NANOPARTICLE COMPOSITIONS AND METHODS FOR PREPARING THE SAME
|
|
DK3517534T3
(en)
|
2009-06-12 |
2024-05-27 |
Abivax |
COMPOUNDS USEFUL IN THE TREATMENT OF CANCER
|
|
BR112012004533B1
(en)
|
2009-09-03 |
2021-11-09 |
Bioenergenix |
COMPOUND, PHARMACEUTICAL COMPOSITION, AND USE OF COMPOUND
|
|
CA2772790C
(en)
|
2009-09-04 |
2017-06-27 |
Benjamin Bader |
Substituted aminoquinoxalines as tyrosine threonine kinase inhibitors
|
|
PL2477611T3
(en)
|
2009-09-18 |
2017-09-29 |
Sanofi |
(z)-2-cyano-3-hydroxy-but-2-enoic acid-(4'-trifluormethylphenyl)-amide tablet formulations with improved stability
|
|
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
|
|
CN110269856A
(en)
|
2010-03-30 |
2019-09-24 |
维颂公司 |
Inhibitor of the polysubstituted aromatic compounds as fibrin ferment
|
|
GB201007286D0
(en)
*
|
2010-04-30 |
2010-06-16 |
Astex Therapeutics Ltd |
New compounds
|
|
WO2011146591A1
(en)
|
2010-05-19 |
2011-11-24 |
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
(en)
|
2010-12-08 |
2012-07-04 |
中国科学院上海药物研究所 |
(1,2,4)-triazolo-(4,3-b) (1,2,4)-triazine compounds, as well as preparation method and use thereof
|
|
PT2670753T
(en)
|
2011-01-31 |
2017-01-10 |
Novartis Ag |
Novel heterocyclic derivatives
|
|
WO2012106556A2
(en)
|
2011-02-02 |
2012-08-09 |
Amgen Inc. |
Methods and compositons relating to inhibition of igf-1r
|
|
JP6130305B2
(en)
|
2011-02-23 |
2017-05-17 |
インテリカイン, エルエルシー |
Combinations of kinase inhibitors and their use
|
|
WO2012118492A1
(en)
|
2011-03-01 |
2012-09-07 |
Array Biopharma Inc. |
Heterocyclic sulfonamides as raf inhibitors
|
|
EP2702173A1
(en)
|
2011-04-25 |
2014-03-05 |
OSI Pharmaceuticals, LLC |
Use of emt gene signatures in cancer drug discovery, diagnostics, and treatment
|
|
CA2846574C
(en)
|
2011-08-26 |
2020-07-07 |
Neupharma, Inc. |
Quinoxaline sulfonamide derivates for use as kinase inhibitors
|
|
CN115403531A
(en)
|
2011-09-14 |
2022-11-29 |
润新生物公司 |
Chemical entities, compositions, and methods as kinase inhibitors
|
|
EP2757885B1
(en)
|
2011-09-21 |
2017-03-15 |
Neupharma, Inc. |
Certain chemical entites, compositions, and methods
|
|
US20130096021A1
(en)
|
2011-09-27 |
2013-04-18 |
Arul M. Chinnaiyan |
Recurrent gene fusions in breast cancer
|
|
WO2013052699A2
(en)
|
2011-10-04 |
2013-04-11 |
Gilead Calistoga Llc |
Novel quinoxaline inhibitors of pi3k
|
|
GB201118652D0
(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
|
|
GB201118656D0
(en)
|
2011-10-28 |
2011-12-07 |
Astex Therapeutics Ltd |
New compounds
|
|
JO3210B1
(en)
|
2011-10-28 |
2018-03-08 |
Merck Sharp & Dohme |
Fusible inhibitor of the cholesterolester transporter oxazolidinone octahedral
|
|
PT2771342T
(en)
|
2011-10-28 |
2016-08-17 |
Novartis Ag |
Purine derivatives and their use in the treatment of disease
|
|
GB201118654D0
(en)
|
2011-10-28 |
2011-12-07 |
Astex Therapeutics Ltd |
New compounds
|
|
AR088941A1
(en)
|
2011-11-23 |
2014-07-16 |
Bayer Ip Gmbh |
ANTI-FGFR2 ANTIBODIES AND THEIR USES
|
|
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
|
|
MX365214B
(en)
|
2012-03-08 |
2019-05-27 |
Astellas Pharma Inc |
Novel fgfr3 fusion product.
|
|
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
|
|
EP2871236A4
(en)
|
2012-07-05 |
2016-03-09 |
Nat Cancer Ct |
HYBRID FGFR2 GENE
|
|
CA2878508A1
(en)
|
2012-07-09 |
2014-01-16 |
Coherus Biosciences, Inc. |
Etanercept formulations exhibiting marked reduction in sub-visible particles
|
|
US20150203589A1
(en)
|
2012-07-24 |
2015-07-23 |
The Trustees Of Columbia University In The City Of New York |
Fusion proteins and methods thereof
|
|
AU2013295805B2
(en)
|
2012-07-24 |
2019-05-02 |
The Trustees Of Columbia University In The City Of New York |
Fusion proteins and methods thereof
|
|
CA2878183A1
(en)
|
2012-07-27 |
2014-01-30 |
Genentech, Inc. |
Methods of treating fgfr3 related conditions
|
|
HK1210500A1
(en)
|
2012-09-27 |
2016-04-22 |
中外制药株式会社 |
Fgfr3 fusion gene and pharmaceutical drug targeting same
|
|
AU2013337264B2
(en)
|
2012-11-05 |
2018-03-08 |
Foundation Medicine, Inc. |
Novel fusion molecules and uses thereof
|
|
HK1215210A1
(en)
|
2012-11-07 |
2016-08-19 |
Teva Pharmaceutical Industries Ltd. |
Amine salts of laquinimod
|
|
EP3939614A1
(en)
|
2013-01-18 |
2022-01-19 |
Foundation Medicine, Inc. |
Methods of treating cholangiocarcinoma
|
|
WO2014165710A2
(en)
|
2013-04-05 |
2014-10-09 |
Life Technologies Corporation |
Gene fusions
|
|
GB201307577D0
(en)
|
2013-04-26 |
2013-06-12 |
Astex Therapeutics Ltd |
New compounds
|
|
WO2014193229A2
(en)
|
2013-05-27 |
2014-12-04 |
Stichting Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis |
Novel translocations in lung cancer
|
|
WO2014198337A1
(en)
|
2013-06-14 |
2014-12-18 |
Synthon B.V. |
Stable and water soluble pharmaceutical compositions comprising pemetrexed
|
|
WO2014201111A1
(en)
|
2013-06-14 |
2014-12-18 |
The Brigham And Women's Hospital, Inc. |
Treatment of mtor hyperactive related diseases and disorders
|
|
EP3019628A4
(en)
|
2013-07-12 |
2017-05-10 |
The Regents Of The University Of Michigan |
Recurrent gene fusions in cancer
|
|
HK1226058A1
(en)
|
2013-08-02 |
2017-09-22 |
亚尼塔公司 |
Methods of treating various cancers using an axl/cmet inhibitor alone or in combination with other agents
|
|
US9221804B2
(en)
|
2013-10-15 |
2015-12-29 |
Janssen Pharmaceutica Nv |
Secondary alcohol quinolinyl modulators of RORγt
|
|
JO3512B1
(en)
*
|
2014-03-26 |
2020-07-05 |
Astex Therapeutics Ltd |
Quinoxaline derivatives useful as fgfr kinase modulators
|
|
HUE053653T2
(en)
|
2014-03-26 |
2021-07-28 |
Astex Therapeutics Ltd |
Combinations of FGFR inhibitor and IGF1R inhibitor
|
|
ES3014202T3
(en)
|
2014-03-26 |
2025-04-21 |
Astex Therapeutics Ltd |
Cmet-inhibitors for use in delaying the emergence in resistance to fgfr inhibitors
|
|
SMT202200177T1
(en)
|
2014-09-26 |
2022-05-12 |
Janssen Pharmaceutica Nv |
Use of fgfr mutant gene panels in identifying cancer patients that will be responsive to treatment with an fgfr inhibitor
|
|
JOP20200201A1
(en)
|
2015-02-10 |
2017-06-16 |
Astex Therapeutics Ltd |
Pharmaceutical compositions comprising n-(3,5-dimethoxyphenyl)-n'-(1-methylethyl)-n-[3-(1-methyl-1h-pyrazol-4-yl)quinoxalin-6-yl]ethane-1,2-diamine
|
|
US20160243228A1
(en)
|
2015-02-19 |
2016-08-25 |
Bioclin Therapeutics, Inc. |
Methods, compositions, and kits for treatment of cancer
|
|
US10478494B2
(en)
|
2015-04-03 |
2019-11-19 |
Astex Therapeutics Ltd |
FGFR/PD-1 combination therapy for the treatment of cancer
|
|
CN105030777B
(en)
|
2015-07-14 |
2017-07-21 |
中国人民解放军第三军医大学第三附属医院 |
Enhancing ALK TKI curative effects, the compound and its preparation for delaying its resistance
|
|
CN105147687A
(en)
|
2015-09-28 |
2015-12-16 |
青岛华之草医药科技有限公司 |
Pharmaceutical dasatinib composition capsules for treating leukemia
|
|
JOP20190280A1
(en)
|
2017-06-02 |
2019-12-02 |
Janssen Pharmaceutica Nv |
FGFR2 inhibitors for treating cholangiocarcinoma
|