|
BE792533A
(fr)
|
1971-12-09 |
1973-06-08 |
Int Chem & Nuclear Corp |
Nouvelles pyrazolo (1,5a) pyrimidines et leur procede de preparation
|
|
JPS5868521A
(ja)
|
1981-10-16 |
1983-04-23 |
Hitachi Ltd |
流体継手の羽根車
|
|
AU600575B2
(en)
|
1987-03-18 |
1990-08-16 |
Sb2, Inc. |
Altered antibodies
|
|
US5859205A
(en)
|
1989-12-21 |
1999-01-12 |
Celltech Limited |
Humanised antibodies
|
|
US5994514A
(en)
|
1991-08-14 |
1999-11-30 |
Genentech, Inc. |
Immunoglobulin variants
|
|
AU4116793A
(en)
|
1992-04-24 |
1993-11-29 |
Board Of Regents, The University Of Texas System |
Recombinant production of immunoglobulin-like domains in prokaryotic cells
|
|
WO1994029351A2
(en)
|
1993-06-16 |
1994-12-22 |
Celltech Limited |
Antibodies
|
|
CA2143491C
(en)
|
1994-03-01 |
2011-02-22 |
Yasumasa Ishida |
A novel peptide related to human programmed cell death and dna encoding it
|
|
JP2778921B2
(ja)
|
1994-11-18 |
1998-07-23 |
三共株式会社 |
イミダゾピラゾール誘導体
|
|
US6194551B1
(en)
|
1998-04-02 |
2001-02-27 |
Genentech, Inc. |
Polypeptide variants
|
|
US6528624B1
(en)
|
1998-04-02 |
2003-03-04 |
Genentech, Inc. |
Polypeptide variants
|
|
GB9809951D0
(en)
|
1998-05-08 |
1998-07-08 |
Univ Cambridge Tech |
Binding molecules
|
|
US6737056B1
(en)
|
1999-01-15 |
2004-05-18 |
Genentech, Inc. |
Polypeptide variants with altered effector function
|
|
HUP0104865A3
(en)
|
1999-01-15 |
2004-07-28 |
Genentech Inc |
Polypeptide variants with altered effector function
|
|
NZ530583A
(en)
|
1999-08-23 |
2005-10-28 |
Dana Farber Cancer Inst Inc |
Novel B7-4 molecules and uses therefor
|
|
MXPA02001877A
(es)
|
1999-08-23 |
2002-08-20 |
Dana Farber Cancer Inst Inc |
Pd-1, un receptor para b7-4, y usos del mismo.
|
|
EP1206474B1
(en)
|
1999-08-27 |
2004-05-26 |
Abbott Laboratories |
Sulfonylphenylpyrazole compounds useful as cox-2 inhibitors
|
|
TR200201505T2
(tr)
|
1999-09-17 |
2003-01-21 |
Abbott Gmbh & Co.Kg |
Terapötik maddeler olarak pirazolopirimidinler
|
|
CZ20023203A3
(cs)
|
2000-03-24 |
2003-08-13 |
Micromet Ag |
Multifunkční polypeptidy obsahující vazebné místo k epitopu receptorového komplexu NKG2D
|
|
EP2264072A1
(en)
|
2000-04-13 |
2010-12-22 |
The Rockefeller University |
Enhancement of antibody-mediated cytotoxicity.
|
|
US20020094989A1
(en)
|
2000-10-11 |
2002-07-18 |
Hale Jeffrey J. |
Pyrrolidine modulators of CCR5 chemokine receptor activity
|
|
WO2002039813A1
(en)
|
2000-11-15 |
2002-05-23 |
Ono Pharmaceutical Co., Ltd. |
Pd-1-lacking mouse and use thereof
|
|
PT1355919E
(pt)
|
2000-12-12 |
2011-03-02 |
Medimmune Llc |
Moléculas com semivida longa, composições que as contêm e suas utilizações
|
|
ES2257461T3
(es)
|
2000-12-21 |
2006-08-01 |
Bristol-Myers Squibb Company |
Inhibidores de tiazolilo de tirosina quinasas de la familia tec.
|
|
US20030133939A1
(en)
|
2001-01-17 |
2003-07-17 |
Genecraft, Inc. |
Binding domain-immunoglobulin fusion proteins
|
|
CA2440221C
(en)
|
2001-03-07 |
2013-02-05 |
Merck Patent Gesellschaft Mit Beschraenkter Haftung |
Expression technology for proteins containing a hybrid isotype antibody moiety
|
|
WO2002072576A1
(en)
|
2001-03-09 |
2002-09-19 |
Pfizer Products Inc. |
Benzimidazole anti-inflammatory compounds
|
|
AR036993A1
(es)
|
2001-04-02 |
2004-10-20 |
Wyeth Corp |
Uso de agentes que modulan la interaccion entre pd-1 y sus ligandos en la submodulacion de respuestas inmunologicas
|
|
WO2003004497A1
(en)
|
2001-07-05 |
2003-01-16 |
Sumitomo Pharmaceuticals Company, Limited |
Novel heterocyclic compound
|
|
US7317091B2
(en)
|
2002-03-01 |
2008-01-08 |
Xencor, Inc. |
Optimized Fc variants
|
|
US7662925B2
(en)
|
2002-03-01 |
2010-02-16 |
Xencor, Inc. |
Optimized Fc variants and methods for their generation
|
|
WO2004004771A1
(ja)
|
2002-07-03 |
2004-01-15 |
Ono Pharmaceutical Co., Ltd. |
免疫賦活組成物
|
|
PL382706A1
(pl)
|
2002-08-26 |
2007-11-26 |
Takeda Pharmaceutical Company Limited |
Związek modulujący receptor wapnia i jego zastosowanie
|
|
CN1771231B
(zh)
|
2002-08-26 |
2011-05-25 |
武田药品工业株式会社 |
钙受体调节性化合物及其用途
|
|
EP1578447A4
(en)
|
2002-10-31 |
2009-06-03 |
Genentech Inc |
METHODS AND COMPOSITIONS THAT CAN INCREASE ANTIBODY PRODUCTION
|
|
MXPA05006828A
(es)
|
2002-12-23 |
2005-09-08 |
Wyeth Corp |
Anticuerpos contra pd-1, y sus usos.
|
|
US7960512B2
(en)
|
2003-01-09 |
2011-06-14 |
Macrogenics, Inc. |
Identification and engineering of antibodies with variant Fc regions and methods of using same
|
|
AU2004204494B2
(en)
|
2003-01-09 |
2011-09-29 |
Macrogenics, Inc. |
Identification and engineering of antibodies with variant Fc regions and methods of using same
|
|
EP2270051B1
(en)
|
2003-01-23 |
2019-05-15 |
Ono Pharmaceutical Co., Ltd. |
Antibody specific for human PD-1 and CD3
|
|
US8084582B2
(en)
|
2003-03-03 |
2011-12-27 |
Xencor, Inc. |
Optimized anti-CD20 monoclonal antibodies having Fc variants
|
|
US7405295B2
(en)
|
2003-06-04 |
2008-07-29 |
Cgi Pharmaceuticals, Inc. |
Certain imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of Bruton's tyrosine kinase by such compounds
|
|
US20060183746A1
(en)
|
2003-06-04 |
2006-08-17 |
Currie Kevin S |
Certain imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of Bruton's tyrosine kinase by such compounds
|
|
WO2005005429A1
(en)
|
2003-06-30 |
2005-01-20 |
Cellular Genomics, Inc. |
Certain heterocyclic substituted imidazo[1,2-a]pyrazin-8-ylamines and methods of inhibition of bruton’s tyrosine kinase by such compounds
|
|
CA2533774A1
(en)
|
2003-07-29 |
2005-02-10 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
|
NZ545776A
(en)
|
2003-08-22 |
2009-05-31 |
Biogen Idec Inc |
Improved antibodies having altered effector function and methods for making the same
|
|
US20060134105A1
(en)
|
2004-10-21 |
2006-06-22 |
Xencor, Inc. |
IgG immunoglobulin variants with optimized effector function
|
|
US20050288295A1
(en)
|
2003-11-11 |
2005-12-29 |
Currie Kevin S |
Certain imidazo[1,2-a]pyrazin-8-ylamines, method of making, and method of use thereof
|
|
WO2005077981A2
(en)
|
2003-12-22 |
2005-08-25 |
Xencor, Inc. |
Fc POLYPEPTIDES WITH NOVEL Fc LIGAND BINDING SITES
|
|
GB0400440D0
(en)
|
2004-01-09 |
2004-02-11 |
Isis Innovation |
Receptor modulators
|
|
WO2006033386A1
(ja)
|
2004-09-22 |
2006-03-30 |
Kirin Beer Kabushiki Kaisha |
安定化されたヒトIgG4抗体
|
|
AU2005304473A1
(en)
|
2004-11-10 |
2006-05-18 |
Cgi Pharmaceuticals, Inc. |
Imidazo[1 , 2-a] pyrazin-8-ylamines useful as modulators of kinase activity
|
|
US7767687B2
(en)
|
2004-12-13 |
2010-08-03 |
Biogen Idec Ma Inc. |
Pyrido pyrimidinones, dihydro pyrimido pyrimidinones and pteridinones useful as RAF kinase inhibitors
|
|
WO2006065946A1
(en)
|
2004-12-16 |
2006-06-22 |
Vertex Pharmaceuticals Incorporated |
Pyrid-2-ones useful as inhibitors of tec family protein kinases for the treatment of inflammatory, proliferative and immunologically-mediated diseases
|
|
TW200639163A
(en)
|
2005-02-04 |
2006-11-16 |
Genentech Inc |
RAF inhibitor compounds and methods
|
|
CN101223141A
(zh)
|
2005-03-10 |
2008-07-16 |
Cgi药品股份有限公司 |
特定取代的酰胺,其制备方法和使用方法
|
|
JP4361545B2
(ja)
|
2005-05-09 |
2009-11-11 |
小野薬品工業株式会社 |
ProgrammedDeath1(PD−1)に対するヒトモノクローナル抗体および抗PD−1抗体単独または他の免疫療法と併用した癌治療方法
|
|
KR101804078B1
(ko)
|
2005-06-08 |
2017-12-01 |
다나-파버 캔서 인스티튜트 인크. |
예정 세포사 1(pd-1) 경로를 억제함으로써 지속 감염 및 암을 치료하기 위한 방법 및 조성물
|
|
HRP20151102T1
(xx)
|
2005-07-01 |
2015-11-20 |
E. R. Squibb & Sons, L.L.C. |
Humana monoklonska antitijela za ligand programirane smrti 1 (pd-l1)
|
|
WO2007027729A1
(en)
|
2005-08-29 |
2007-03-08 |
Vertex Pharmaceuticals Incorporated |
3, 5-disubstituted pyrid-2-ones useful as inhibitors of tec family of non-receptor tyrosine kinases
|
|
ATE548363T1
(de)
|
2005-08-29 |
2012-03-15 |
Vertex Pharma |
3,5-disubstituierte pyrid-2-one, die sich als inhibitoren der tec-familie von nicht-rezeptor- tyrosinkinasen eignen
|
|
WO2007026720A1
(ja)
|
2005-08-31 |
2007-03-08 |
Taisho Pharmaceutical Co., Ltd. |
縮環ピラゾール誘導体
|
|
TW200745034A
(en)
|
2005-09-01 |
2007-12-16 |
Astellas Pharma Inc |
New compounds
|
|
CN101365682A
(zh)
|
2005-12-08 |
2009-02-11 |
千禧药品公司 |
具有激酶抑制活性的双环化合物
|
|
KR20080098490A
(ko)
|
2006-01-13 |
2008-11-10 |
파마시클릭스, 인코포레이티드 |
티로신 키나제 억제제 및 이의 용도
|
|
NO347079B1
(no)
|
2006-03-23 |
2023-05-08 |
Bioarctic Neuroscience Ab |
Forbedrede protofibrilselektive antistoffer og anvendelse derav
|
|
WO2007136573A2
(en)
|
2006-05-15 |
2007-11-29 |
Merck & Co., Inc. |
Antidiabetic bicyclic compounds
|
|
WO2007136790A2
(en)
|
2006-05-18 |
2007-11-29 |
Mannkind Corporation |
Intracellular kinase inhibitors
|
|
TWI398252B
(zh)
|
2006-05-26 |
2013-06-11 |
Novartis Ag |
吡咯并嘧啶化合物及其用途
|
|
CN101104640A
(zh)
|
2006-07-10 |
2008-01-16 |
苏州大学 |
抗人pd-l1单克隆抗体制备及应用
|
|
ES2373587T3
(es)
|
2006-08-23 |
2012-02-06 |
Pfizer Products Inc. |
Compuestos de pirimidona como inhibidores de gsk-3.
|
|
EP2061761A1
(en)
|
2006-09-07 |
2009-05-27 |
Millennium Pharmaceuticals, Inc. |
Phenethylamide derivatives with kinase inhibitory activity
|
|
AR063946A1
(es)
|
2006-09-11 |
2009-03-04 |
Cgi Pharmaceuticals Inc |
Determinadas pirimidinas sustituidas, el uso de las mismas para el tratamiento de enfermedades mediadas por la inhibicion de la actividad de btk y composiciones farmaceuticas que las comprenden.
|
|
US20100160292A1
(en)
|
2006-09-11 |
2010-06-24 |
Cgi Pharmaceuticals, Inc |
Kinase Inhibitors, and Methods of Using and Identifying Kinase Inhibitors
|
|
AR063706A1
(es)
|
2006-09-11 |
2009-02-11 |
Cgi Pharmaceuticals Inc |
Determinadas amidas sustituidas, el uso de las mismas para el tratamiento de enfermedades mediadas por la inhibicion de la actividad de btk y composiciones farmaceuticas que las comprenden.
|
|
AR063707A1
(es)
|
2006-09-11 |
2009-02-11 |
Cgi Pharmaceuticals Inc |
Determinadas amidas sustituidas, el uso de las mismas para el tratamiento de enfermedades mediadas por la inhibicion de la actividad de btk y composiciones farmacéuticas que las comprenden.
|
|
SG166093A1
(en)
|
2006-09-22 |
2010-11-29 |
Pharmacyclics Inc |
Inhibitors of brutonæs tyrosine kinase
|
|
AU2007308045A1
(en)
|
2006-10-06 |
2008-04-17 |
Irm Llc |
Protein kinase inhibitors and methods for using thereof
|
|
US8987233B2
(en)
|
2006-11-03 |
2015-03-24 |
Pharmacyclics, Inc. |
Bruton's tyrosine kinase activity probe and method of using
|
|
CN101730699A
(zh)
|
2007-03-21 |
2010-06-09 |
百时美施贵宝公司 |
可用于治疗增殖性、变应性、自身免疫性和炎症性疾病的稠合杂环化合物
|
|
AU2008247500A1
(en)
|
2007-05-04 |
2008-11-13 |
Irm Llc |
Compounds and compositions as c-kit and PDGFR kinase inhibitors
|
|
WO2008144253A1
(en)
|
2007-05-14 |
2008-11-27 |
Irm Llc |
Protein kinase inhibitors and methods for using thereof
|
|
EP2666787B1
(en)
|
2007-05-31 |
2022-02-09 |
Genmab A/S |
STABLE IgG4 ANTIBODIES
|
|
NZ582150A
(en)
|
2007-06-18 |
2012-08-31 |
Msd Oss Bv |
Antibodies to human programmed death receptor pd-1
|
|
EP2195347A1
(en)
|
2007-08-17 |
2010-06-16 |
INSERM (Institut National de la Santé et de la Recherche Médicale) |
Method for treating and diagnosing hematologic malignancies
|
|
CL2008002793A1
(es)
|
2007-09-20 |
2009-09-04 |
Cgi Pharmaceuticals Inc |
Compuestos derivados de amidas sustituidas, inhibidores de la actividad de btk; composicion farmaceutica que los comprende; utiles en el tratamiento del cancer, trastornos oseos, enfermedades autoinmunes, entre otras
|
|
JO3076B1
(ar)
|
2007-10-17 |
2017-03-15 |
Janssen Alzheimer Immunotherap |
نظم العلاج المناعي المعتمد على حالة apoe
|
|
US7982036B2
(en)
|
2007-10-19 |
2011-07-19 |
Avila Therapeutics, Inc. |
4,6-disubstitued pyrimidines useful as kinase inhibitors
|
|
US7989465B2
(en)
|
2007-10-19 |
2011-08-02 |
Avila Therapeutics, Inc. |
4,6-disubstituted pyrimidines useful as kinase inhibitors
|
|
JP5587193B2
(ja)
|
2007-10-23 |
2014-09-10 |
エフ.ホフマン−ラ ロシュ アーゲー |
新規なキナーゼ阻害剤
|
|
WO2009077334A1
(en)
|
2007-12-14 |
2009-06-25 |
F. Hoffmann-La Roche Ag |
Novel imidazo[1,2-a]pyridine and imidazo[1,2-b]pyridazine derivatives
|
|
WO2009098144A1
(en)
|
2008-02-05 |
2009-08-13 |
F. Hoffmann-La Roche Ag |
Novel pyridinones and pyridazinones
|
|
WO2009114335A2
(en)
|
2008-03-12 |
2009-09-17 |
Merck & Co., Inc. |
Pd-1 binding proteins
|
|
US8426424B2
(en)
|
2008-05-06 |
2013-04-23 |
Cgi Pharmaceuticals, Inc. |
Certain substituted amides, method of making, and method of use thereof
|
|
US8338439B2
(en)
|
2008-06-27 |
2012-12-25 |
Celgene Avilomics Research, Inc. |
2,4-disubstituted pyrimidines useful as kinase inhibitors
|
|
NZ624345A
(en)
|
2008-06-27 |
2016-07-29 |
Celgene Avilomics Res Inc |
2,4-disubstituted pyrimidines useful as kinase inhibitors
|
|
MX2010013478A
(es)
|
2008-07-02 |
2010-12-20 |
Hoffmann La Roche |
Nuevas fenilpirazinonas como inhibidores de cinasa.
|
|
CA2726460C
(en)
|
2008-07-15 |
2017-02-21 |
F. Hoffmann-La Roche Ag |
Novel phenyl-imidazopyridines and pyridazines
|
|
CA2730930C
(en)
|
2008-07-16 |
2015-01-13 |
Pharmacyclics, Inc. |
Inhibitors of bruton's tyrosine kinase for the treatment of solid tumors
|
|
WO2010006970A1
(en)
|
2008-07-18 |
2010-01-21 |
F. Hoffmann-La Roche Ag |
Novel phenylimidazopyrazines
|
|
US8476430B2
(en)
|
2008-07-24 |
2013-07-02 |
Bristol-Myers Squibb Company |
Fused heterocyclic compounds useful as kinase modulators
|
|
JP2012510429A
(ja)
|
2008-08-25 |
2012-05-10 |
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その使用方法
|
|
NZ603495A
(en)
|
2008-09-05 |
2014-05-30 |
Celgene Avilomics Res Inc |
Algorithm for designing irreversible inhibitors
|
|
EP2342229A1
(en)
|
2008-09-12 |
2011-07-13 |
ISIS Innovation Limited |
Pd-1 specific antibodies and uses thereof
|
|
EP2342228B1
(en)
|
2008-09-12 |
2017-09-06 |
Oxford University Innovation Limited |
Pd-1 specific antibodies and uses thereof
|
|
AU2009296392B2
(en)
|
2008-09-26 |
2016-06-02 |
Dana-Farber Cancer Institute, Inc. |
Human anti-PD-1, PD-L1, and PD-L2 antibodies and uses therefor
|
|
KR101050829B1
(ko)
|
2008-10-02 |
2011-07-20 |
서울대학교산학협력단 |
항 pd-1 항체 또는 항 pd-l1 항체를 포함하는 항암제
|
|
JP5769199B2
(ja)
|
2008-10-31 |
2015-08-26 |
ジェネンテック, インコーポレイテッド |
ピラゾロピリミジンjak阻害剤化合物と方法
|
|
US20120028981A1
(en)
|
2008-11-05 |
2012-02-02 |
Principia Biopharma Inc. |
Kinase Knockdown Via Electrophilically Enhanced Inhibitors
|
|
EP2365970B1
(en)
|
2008-11-12 |
2018-03-21 |
Gilead Connecticut, Inc. |
Pyridazinones and their use as btk inhibitors
|
|
HUE028582T2
(en)
|
2008-11-28 |
2016-12-28 |
Univ Emory |
Method for determining the efficacy of PD-1 antagonists
|
|
US8426428B2
(en)
|
2008-12-05 |
2013-04-23 |
Principia Biopharma, Inc. |
EGFR kinase knockdown via electrophilically enhanced inhibitors
|
|
KR20250091300A
(ko)
|
2008-12-09 |
2025-06-20 |
제넨테크, 인크. |
항-pd-l1 항체 및 t 세포 기능을 향상시키기 위한 그의 용도
|
|
WO2010068806A1
(en)
|
2008-12-10 |
2010-06-17 |
Cgi Pharmaceuticals, Inc. |
Amide derivatives as btk inhibitors in the treatment of allergic, autoimmune and inflammatory disorders as well as cancer
|
|
WO2010068810A2
(en)
|
2008-12-10 |
2010-06-17 |
Cgi Pharmaceuticals, Inc. |
Certain substituted amides, method of making, and method of use thereof
|
|
WO2010068788A1
(en)
|
2008-12-10 |
2010-06-17 |
Cgi Pharmaceuticals, Inc. |
Heterocyclic amides as btk inhibitors
|
|
US8084620B2
(en)
|
2008-12-19 |
2011-12-27 |
Bristol-Myers Squibb Company |
Carbazole carboxamide compounds useful as kinase inhibitors
|
|
US20100197924A1
(en)
*
|
2008-12-22 |
2010-08-05 |
Millennium Pharmaceuticals, Inc. |
Preparation of aminotetralin compounds
|
|
EP2379559B1
(en)
|
2009-01-06 |
2017-10-25 |
Dana-Farber Cancer Institute, Inc. |
Pyrimido-diazepinone kinase scaffold compounds and methods of treating disorders
|
|
JP5844159B2
(ja)
|
2009-02-09 |
2016-01-13 |
ユニヴェルシテ デクス−マルセイユUniversite D’Aix−Marseille |
Pd−1抗体およびpd−l1抗体ならびにその使用
|
|
US8299077B2
(en)
|
2009-03-02 |
2012-10-30 |
Roche Palo Alto Llc |
Inhibitors of Bruton's tyrosine kinase
|
|
EP2421854B1
(en)
|
2009-04-24 |
2014-07-23 |
F.Hoffmann-La Roche Ag |
Inhibitors of bruton's tyrosine kinase
|
|
EP2424368B1
(en)
|
2009-04-29 |
2014-12-31 |
Locus Pharmaceuticals, Inc. |
Pyrrolotriazine compounds
|
|
CN102458402B
(zh)
|
2009-06-12 |
2013-10-02 |
百时美施贵宝公司 |
用作激酶调节剂的烟酰胺化合物
|
|
AR077468A1
(es)
|
2009-07-09 |
2011-08-31 |
Array Biopharma Inc |
Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa
|
|
EP2464647B1
(en)
|
2009-08-11 |
2016-09-21 |
Bristol-Myers Squibb Company |
Azaindazoles as btk kinase modulators and use thereof
|
|
US9493578B2
(en)
|
2009-09-02 |
2016-11-15 |
Xencor, Inc. |
Compositions and methods for simultaneous bivalent and monovalent co-engagement of antigens
|
|
US9029359B2
(en)
|
2009-09-04 |
2015-05-12 |
Biogen Idec Ma, Inc. |
Heteroaryl Btk inhibitors
|
|
HUE043522T2
(hu)
|
2009-09-04 |
2019-08-28 |
Biogen Ma Inc |
Bruton tirozinkináz inhibitorok
|
|
US7741330B1
(en)
|
2009-10-12 |
2010-06-22 |
Pharmacyclics, Inc. |
Pyrazolo-pyrimidine inhibitors of Bruton's tyrosine kinase
|
|
US8389689B2
(en)
|
2009-10-28 |
2013-03-05 |
Janssen Biotech, Inc. |
Anti-GLP-1R antibodies and their uses
|
|
US10053513B2
(en)
|
2009-11-30 |
2018-08-21 |
Janssen Biotech, Inc. |
Antibody Fc mutants with ablated effector functions
|
|
RS61136B1
(sr)
|
2010-02-19 |
2020-12-31 |
Xencor Inc |
Novi ctla4-ig imunoadhezini
|
|
WO2011120134A1
(en)
|
2010-03-29 |
2011-10-06 |
Zymeworks, Inc. |
Antibodies with enhanced or suppressed effector function
|
|
SG185462A1
(en)
|
2010-05-07 |
2012-12-28 |
Gilead Connecticut Inc |
Pyridone and aza-pyridone compounds and methods of use
|
|
SG185617A1
(en)
|
2010-05-31 |
2012-12-28 |
Ono Pharmaceutical Co |
Purinone derivative
|
|
NZ717373A
(en)
|
2010-06-03 |
2017-11-24 |
Pharmacyclics Llc |
The use of inhibitors of bruton’s tyrosine kinase (btk)
|
|
EP2582668B1
(en)
|
2010-06-16 |
2016-01-13 |
Bristol-Myers Squibb Company |
Carboline carboxamide compounds useful as kinase inhibitors
|
|
WO2011162515A2
(en)
|
2010-06-23 |
2011-12-29 |
Hanmi Holdings Co. , Ltd. |
Novel fused pyrimidine derivatives for inhd3ition of tyrosine kinase activity
|
|
US20120053189A1
(en)
|
2010-06-28 |
2012-03-01 |
Pharmacyclics, Inc. |
Btk inhibitors for the treatment of immune mediated conditions
|
|
US20120100166A1
(en)
|
2010-07-15 |
2012-04-26 |
Zyngenia, Inc. |
Ang-2 Binding Complexes and Uses Thereof
|
|
EP3144298A1
(en)
|
2010-08-10 |
2017-03-22 |
Celgene Avilomics Research, Inc. |
Besylate salt of a btk inhibitor
|
|
AR082590A1
(es)
|
2010-08-12 |
2012-12-19 |
Hoffmann La Roche |
Inhibidores de la tirosina-quinasa de bruton
|
|
KR101864908B1
(ko)
|
2010-09-01 |
2018-06-05 |
질레드 코네티컷 인코포레이티드 |
피리다지논, 그의 제조 방법 및 사용 방법
|
|
CN106220614B
(zh)
|
2010-09-01 |
2019-07-16 |
吉利德康涅狄格有限公司 |
吡啶酮/吡嗪酮、其制备方法及使用方法
|
|
ES2720136T3
(es)
|
2010-12-22 |
2019-07-18 |
Teva Pharmaceuticals Australia Pty Ltd |
Anticuerpo modificado con semivida mejorada
|
|
WO2012130831A1
(en)
|
2011-03-29 |
2012-10-04 |
Roche Glycart Ag |
Antibody fc variants
|
|
PT2691112T
(pt)
|
2011-03-31 |
2018-07-10 |
Merck Sharp & Dohme |
Formulações estáveis de anticorpos para o recetor pd-1 humano de morte programada e tratamentos relacionados
|
|
JP6147727B2
(ja)
|
2011-04-01 |
2017-06-14 |
ユニヴァーシティー オブ ユタ リサーチ ファウンデーション |
チロシン受容体キナーゼbtk阻害剤としての置換n−(3−(ピリミジン−4−イル)フェニル)アクリルアミド類似体
|
|
CA2760174A1
(en)
|
2011-12-01 |
2013-06-01 |
Pharmascience Inc. |
Protein kinase inhibitors and uses thereof
|
|
MX338353B
(es)
|
2011-04-20 |
2016-04-13 |
Medimmune Llc |
Anticuerpos y otras moleculas que se unen a b7 - h1 y pd - 1.
|
|
EA201391558A1
(ru)
|
2011-04-20 |
2014-05-30 |
Глэксо Груп Лимитед |
Тетрагидропиразоло[1,5-а]пиримидины как противотуберкулезные соединения
|
|
WO2012158795A1
(en)
|
2011-05-17 |
2012-11-22 |
Principia Biopharma Inc. |
Pyrazolopyrimidine derivatives as tyrosine kinase inhibitors
|
|
US20140107151A1
(en)
|
2011-05-17 |
2014-04-17 |
Principia Biophama Inc. |
Tyrosine kinase inhibitors
|
|
KR102027598B1
(ko)
|
2011-05-17 |
2019-10-01 |
프린시피아 바이오파마, 인코퍼레이티드 |
타이로신 키나아제 저해제
|
|
CN103582637B
(zh)
|
2011-05-17 |
2015-08-12 |
弗·哈夫曼-拉罗切有限公司 |
酪氨酸激酶抑制剂
|
|
EP2718322B1
(en)
|
2011-06-06 |
2018-08-08 |
Novo Nordisk A/S |
Therapeutic antibodies
|
|
SG10201604682VA
(en)
|
2011-06-10 |
2016-07-28 |
Merck Patent Gmbh |
Compositions and methods for the production of pyrimidine and pyridine compounds with btk inhibitory activity
|
|
EP2723377B1
(en)
|
2011-06-22 |
2018-06-13 |
INSERM (Institut National de la Santé et de la Recherche Médicale) |
Anti-axl antibodies and uses thereof
|
|
CA2841111A1
(en)
|
2011-07-08 |
2013-01-17 |
Novartis Ag |
Novel pyrrolo pyrimidine derivatives
|
|
AR087405A1
(es)
|
2011-08-01 |
2014-03-19 |
Genentech Inc |
Metodos para tratar el cancer por el uso de antagonistas de union al eje pd-1 e inhibidores de mek
|
|
SMT202000561T1
(it)
|
2011-11-28 |
2021-01-05 |
Merck Patent Gmbh |
Anticorpi anti-pd-l1 e usi relativi
|
|
HRP20160641T1
(hr)
|
2011-12-31 |
2016-09-23 |
Beigene, Ltd. |
Fuzionirani triciklički spojevi kao inhibitori raf kinaze
|
|
JP6226752B2
(ja)
|
2012-02-09 |
2017-11-08 |
中外製薬株式会社 |
抗体のFc領域改変体
|
|
WO2013165690A1
(en)
|
2012-04-30 |
2013-11-07 |
Medimmune, Llc |
Molecules with reduced effector function and extended half-lives, compositions, and uses thereof
|
|
SG10201700698WA
(en)
|
2012-05-15 |
2017-02-27 |
Bristol Myers Squibb Co |
Cancer immunotherapy by disrupting pd-1/pd-l1 signaling
|
|
WO2013181634A2
(en)
|
2012-05-31 |
2013-12-05 |
Sorrento Therapeutics Inc. |
Antigen binding proteins that bind pd-l1
|
|
BR112014033066A2
(pt)
|
2012-07-03 |
2017-08-01 |
Janssen Alzheimer Immunotherap |
método para tratamento de um paciente diagnosticado com doença de alzheimer, forma humanizada, quimérica ou revestida de um anticorpo, e, anticorpo.
|
|
US9828434B2
(en)
|
2012-10-04 |
2017-11-28 |
Dana-Farber Cancer Institute, Inc. |
Human monoclonal anti-PD-L1 antibodies and methods of use
|
|
EP2934577A1
(en)
|
2012-12-19 |
2015-10-28 |
Adimab, LLC |
Multivalent antibody analogs, and methods of their preparation and use
|
|
AR093984A1
(es)
|
2012-12-21 |
2015-07-01 |
Merck Sharp & Dohme |
Anticuerpos que se unen a ligando 1 de muerte programada (pd-l1) humano
|
|
TWI635098B
(zh)
|
2013-02-01 |
2018-09-11 |
再生元醫藥公司 |
含嵌合恆定區之抗體
|
|
LT2840892T
(lt)
|
2013-02-20 |
2018-07-25 |
Regeneron Pharmaceuticals, Inc. |
Nežmogaus tipo gyvūnai su modifikuotomis imunoglobulino sunkiųjų grandinių sekomis
|
|
MX364591B
(es)
|
2013-03-15 |
2019-05-02 |
Regeneron Pharma |
Antagonistas de il-33 y usos de estos.
|
|
BR112015025260B1
(pt)
|
2013-04-25 |
2021-11-03 |
Beigene, Ltd |
Compostos heterocíclicos fundidos como inibidores da proteína quinase, sua composição, combinação e uso
|
|
CA2913977C
(en)
|
2013-05-31 |
2022-11-29 |
Sorrento Therapeutics, Inc. |
Antigen binding proteins that bind pd-1
|
|
WO2014193898A1
(en)
*
|
2013-05-31 |
2014-12-04 |
Merck Sharp & Dohme Corp. |
Combination therapies for cancer
|
|
HRP20221262T1
(hr)
*
|
2013-09-13 |
2022-12-09 |
Beigene Switzerland Gmbh |
Protutijela anti-pd1 i njihova uporaba kao terapeutskih i dijagnostičkih sredstava
|
|
CN105848680A
(zh)
|
2013-10-25 |
2016-08-10 |
药品循环有限责任公司 |
使用布鲁顿酪氨酸激酶抑制剂和免疫疗法的治疗
|
|
JOP20200094A1
(ar)
|
2014-01-24 |
2017-06-16 |
Dana Farber Cancer Inst Inc |
جزيئات جسم مضاد لـ pd-1 واستخداماتها
|
|
CN110156892B
(zh)
|
2014-07-03 |
2023-05-16 |
百济神州有限公司 |
抗pd-l1抗体及其作为治疗剂及诊断剂的用途
|
|
WO2016008411A1
(en)
|
2014-07-18 |
2016-01-21 |
Beigene, Ltd. |
5-amino-4-carbamoyl-pyrazole compounds as selective and irreversible t790m over wt-egfr kinase inhibitors and use thereof
|
|
EP3179992B1
(en)
|
2014-08-11 |
2022-05-11 |
Acerta Pharma B.V. |
Therapeutic combinations of a btk inhibitor, a pd-1 inhibitor and/or a pd-l1 inhibitor
|
|
CA2958139A1
(en)
|
2014-08-14 |
2016-02-18 |
Assia Chemical Industries Ltd. |
Solid state forms of ibrutinib
|
|
TW201625304A
(zh)
|
2014-10-24 |
2016-07-16 |
美國禮來大藥廠 |
泌尿上皮癌之療法
|
|
WO2016087994A1
(en)
|
2014-12-05 |
2016-06-09 |
Acerta Pharma B.V. |
Btk inhibitors to treat solid tumors through modulation of the tumor microenvironment
|
|
EP3233103B1
(en)
|
2014-12-18 |
2020-10-14 |
Principia Biopharma Inc. |
Treatment of pemphigus
|
|
HUE061809T2
(hu)
|
2014-12-24 |
2023-08-28 |
Principia Biopharma Inc |
Készítmények csípõbél-éhbél szakaszba történõ hatóanyag beadáshoz
|
|
US9139653B1
(en)
|
2015-04-30 |
2015-09-22 |
Kymab Limited |
Anti-human OX40L antibodies and methods of treatment
|
|
CN107531682B
(zh)
|
2015-04-15 |
2021-05-04 |
百济神州有限公司 |
B-raf激酶抑制剂的马来酸盐、其结晶形式、制备方法和用途
|
|
KR20250151554A
(ko)
|
2015-05-29 |
2025-10-21 |
제넨테크, 인크. |
암에 대한 치료 및 진단 방법
|
|
WO2017024465A1
(en)
|
2015-08-10 |
2017-02-16 |
Innovent Biologics (Suzhou) Co., Ltd. |
Pd-1 antibodies
|
|
US20190022092A1
(en)
|
2015-09-15 |
2019-01-24 |
Acerta Pharma B.V. |
Therapeutic Combinations of a BTK Inhibitor and a GITR Binding Molecule, a 4-1BB Agonist, or an OX40 Agonist
|
|
EP3355875B1
(en)
|
2015-10-01 |
2021-09-29 |
Gilead Sciences, Inc. |
Combination of a btk inhibitor and a checkpoint inhibitor for treating cancers
|
|
WO2017165491A1
(en)
*
|
2016-03-24 |
2017-09-28 |
Millennium Pharmaceuticals, Inc. |
Use of a pd-1 antagonist and a raf inhibitor in the treatment of cancer
|
|
NZ749997A
(en)
|
2016-07-05 |
2022-11-25 |
Beigene Ltd |
Combination of a pd-l antagonist and a raf inhibitor for treating cancer
|
|
WO2018033853A2
(en)
|
2016-08-16 |
2018-02-22 |
Beigene, Ltd. |
Crystalline form of (s)-7-(1-acryloylpiperidin-4-yl)-2-(4-phenoxyphenyl)-4,5,6,7-tetra-hydropyrazolo[1,5-a]pyrimidine-3-carboxamide, preparation, and uses thereof
|
|
TWI739887B
(zh)
|
2016-08-19 |
2021-09-21 |
英屬開曼群島商百濟神州有限公司 |
使用包含btk抑制劑的組合產品治療癌症
|
|
NZ751246A
(en)
|
2016-08-26 |
2023-04-28 |
Beigene Ltd |
Anti-tim-3 antibodies and use thereof
|
|
US10793632B2
(en)
|
2016-08-30 |
2020-10-06 |
Xencor, Inc. |
Bispecific immunomodulatory antibodies that bind costimulatory and checkpoint receptors
|
|
TWI806840B
(zh)
|
2016-09-27 |
2023-07-01 |
英屬開曼群島商百濟神州有限公司 |
使用包含parp抑制劑的組合產品治療癌症
|
|
US10501543B2
(en)
|
2016-10-14 |
2019-12-10 |
Xencor, Inc. |
IL15/IL15Rα heterodimeric Fc-fusion proteins
|
|
EP3573989A4
(en)
|
2017-01-25 |
2020-11-18 |
Beigene, Ltd. |
CRYSTALLINE FORMS OF (S) -7- (1- (BUT-2-YNOYL) PIPERIDIN-4-YL) -2- (4-PHENOXYPHENYL) -4, 5, 6, 7-TETRAHY DROPYRAZOLO [1, 5-A ] PYRIMIDINE-3-CARBOXAMIDE, PREPARATION AND ASSOCIATED USES
|
|
KR20190137151A
(ko)
|
2017-04-20 |
2019-12-10 |
에이디씨 테라퓨틱스 에스에이 |
병용 요법
|
|
TWI877099B
(zh)
|
2017-06-26 |
2025-03-21 |
英屬開曼群島商百濟神州有限公司 |
抗pd-1抗體或其抗原結合片段在製備治療用於患有肝細胞癌(hcc)之藥物的用途
|
|
WO2019034009A1
(en)
|
2017-08-12 |
2019-02-21 |
Beigene, Ltd. |
BTK INHIBITOR WITH ENHANCED DOUBLE SELECTIVITY
|
|
US11786529B2
(en)
|
2017-11-29 |
2023-10-17 |
Beigene Switzerland Gmbh |
Treatment of indolent or aggressive B-cell lymphomas using a combination comprising BTK inhibitors
|
|
CN120459291A
(zh)
|
2018-02-09 |
2025-08-12 |
百济神州有限公司 |
用于尿路上皮癌的免疫治疗方法
|
|
GB201803746D0
(en)
|
2018-03-08 |
2018-04-25 |
Ultrahuman Eight Ltd |
PD1 binding agents
|