|
US3707475A
(en)
|
1970-11-16 |
1972-12-26 |
Pfizer |
Antiinflammatory imidazoles
|
|
DE3029376A1
(de)
|
1980-07-31 |
1982-03-18 |
Nepera Chemical Co. Inc., Harriman, N.Y. |
Verfahren zur herstellung von 2,4,5-tris-pyridylimidazolen
|
|
EP0149884B1
(en)
|
1983-09-09 |
1992-12-16 |
Takeda Chemical Industries, Ltd. |
5-pyridyl-1,3-thiazole derivatives, their production and use
|
|
JP2722586B2
(ja)
|
1989-01-13 |
1998-03-04 |
大正製薬株式会社 |
インドリルイミダゾール誘導体
|
|
JP2808460B2
(ja)
|
1989-11-16 |
1998-10-08 |
大正製薬株式会社 |
イミダゾール誘導体
|
|
US6358932B1
(en)
|
1994-05-31 |
2002-03-19 |
Isis Pharmaceticals, Inc. |
Antisense oligonucleotide inhibition of raf gene expression
|
|
US5717100A
(en)
|
1995-10-06 |
1998-02-10 |
Merck & Co., Inc. |
Substituted imidazoles having anti-cancer and cytokine inhibitory activity
|
|
GB2306108A
(en)
|
1995-10-13 |
1997-04-30 |
Merck & Co Inc |
Treatment of Raf-mediated cancers with imidazole derivatives
|
|
EP0923579A1
(en)
|
1996-08-27 |
1999-06-23 |
Novartis AG |
Herbicidal s-substituted 1,2,4,6-thiatriazines
|
|
WO1998038984A2
(en)
|
1997-03-05 |
1998-09-11 |
Sugen, Inc. |
Formulations for hydrophobic pharmaceutical agents
|
|
AR012634A1
(es)
|
1997-05-02 |
2000-11-08 |
Sugen Inc |
Compuesto basado en quinazolina, composicion famaceutica que lo comprende, metodo para sintetizarlo, su uso, metodos de modulacion de la funcion deserina/treonina proteinaquinasa con dicho compuesto y metodo in vitro para identificar compuestos que modulan dicha funcion
|
|
GB9711650D0
(en)
|
1997-06-05 |
1997-07-30 |
Pfizer Ltd |
Compounds useful in therapy
|
|
GB9716557D0
(en)
|
1997-08-06 |
1997-10-08 |
Glaxo Group Ltd |
Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity
|
|
US6022884A
(en)
|
1997-11-07 |
2000-02-08 |
Amgen Inc. |
Substituted pyridine compounds and methods of use
|
|
US6211177B1
(en)
|
1998-11-24 |
2001-04-03 |
Cell Pathways, Inc. |
Method for treating neoplasia by exposure to substituted 2-aryl-benzimidazole derivatives
|
|
WO2000042012A1
(en)
|
1999-01-13 |
2000-07-20 |
Bayer Corporation |
φ-CARBOXYARYL SUBSTITUTED DIPHENYL UREAS AS RAF KINASE INHIBITORS
|
|
US6548529B1
(en)
|
1999-04-05 |
2003-04-15 |
Bristol-Myers Squibb Company |
Heterocyclic containing biphenyl aP2 inhibitors and method
|
|
AU4798000A
(en)
|
1999-04-09 |
2000-11-14 |
Smithkline Beecham Corporation |
Triarylimidazoles
|
|
EP1169038B9
(en)
|
1999-04-15 |
2013-07-10 |
Bristol-Myers Squibb Company |
Cyclic protein tyrosine kinase inhibitors
|
|
JP2000302680A
(ja)
|
1999-04-23 |
2000-10-31 |
Takeda Chem Ind Ltd |
脳保護剤
|
|
ATE339406T1
(de)
|
1999-09-23 |
2006-10-15 |
Astrazeneca Ab |
Chinazoline verbindungen als heilmittel
|
|
DE60015594T2
(de)
|
1999-11-22 |
2005-10-27 |
Smithkline Beecham P.L.C., Brentford |
Imidazolderivate und deren verwendung als raf kinase inhibitoren
|
|
EP1251849A1
(en)
|
2000-01-18 |
2002-10-30 |
Vertex Pharmaceuticals Incorporated |
Gyrase inhibitors and uses thereof
|
|
MXPA02007134A
(es)
|
2000-01-18 |
2003-03-27 |
Vertex Pharma |
Inhibidores de girasa y usos de los mismos.
|
|
AR029803A1
(es)
|
2000-02-21 |
2003-07-16 |
Smithkline Beecham Plc |
Imidazoles sustituidos con piridilo y composiciones farmaceuticas que las comprenden
|
|
GB0005357D0
(en)
|
2000-03-06 |
2000-04-26 |
Smithkline Beecham Plc |
Compounds
|
|
US7235658B2
(en)
|
2000-03-06 |
2007-06-26 |
Smithkline Beecham P.L.C. |
Imidazol derivatives as Raf kinase inhibitors
|
|
GB0007405D0
(en)
|
2000-03-27 |
2000-05-17 |
Smithkline Beecham Corp |
Compounds
|
|
EP1268474A2
(en)
|
2000-03-30 |
2003-01-02 |
Takeda Chemical Industries, Ltd. |
Substituted 1,3-thiazole compounds, their production and use
|
|
US6608053B2
(en)
|
2000-04-27 |
2003-08-19 |
Yamanouchi Pharmaceutical Co., Ltd. |
Fused heteroaryl derivatives
|
|
CN1245386C
(zh)
|
2000-06-12 |
2006-03-15 |
卫材株式会社 |
1,2-二氢吡啶化合物及其制备方法和用途
|
|
AP2001002217A0
(en)
|
2000-07-19 |
2001-09-30 |
Warner Lambert Co |
Oxygenated esters of 4-iodo phenylamino benzhydroxamic acids.
|
|
CA2428191A1
(en)
|
2000-11-07 |
2002-05-30 |
Bristol-Myers Squibb Company |
Acid derivatives useful as serine protease inhibitors
|
|
US20040053943A1
(en)
|
2000-11-20 |
2004-03-18 |
Adams Jerry L. |
Novel compounds
|
|
US7238813B2
(en)
|
2000-11-29 |
2007-07-03 |
Smithkline Beecham Corporation |
Chemical compounds
|
|
ATE341539T1
(de)
|
2001-01-26 |
2006-10-15 |
Chugai Pharmaceutical Co Ltd |
Malonyl coa-decarboxylase inhibitoren als stoffwechselmodulatoren
|
|
WO2002062792A1
(en)
|
2001-02-02 |
2002-08-15 |
Takeda Chemical Industries, Ltd. |
Jnk inhibitor
|
|
WO2002076960A1
(en)
|
2001-03-22 |
2002-10-03 |
Abbott Gmbh & Co. Kg |
Transition metal mediated process
|
|
JP2002338537A
(ja)
|
2001-05-16 |
2002-11-27 |
Mitsubishi Pharma Corp |
アミド化合物およびその医薬用途
|
|
GB0112348D0
(en)
|
2001-05-19 |
2001-07-11 |
Smithkline Beecham Plc |
Compounds
|
|
GB0129260D0
(en)
|
2001-12-06 |
2002-01-23 |
Eisai London Res Lab Ltd |
Pharmaceutical compositions and their uses
|
|
IL164302A0
(en)
|
2002-03-29 |
2005-12-18 |
Chiron Corp |
Substituted benzazoles and use thereof as raf kinase inhibitors
|
|
US8299108B2
(en)
|
2002-03-29 |
2012-10-30 |
Novartis Ag |
Substituted benzazoles and methods of their use as inhibitors of raf kinase
|
|
AR039241A1
(es)
|
2002-04-04 |
2005-02-16 |
Biogen Inc |
Heteroarilos trisustituidos y metodos para su produccion y uso de los mismos
|
|
WO2004016597A2
(en)
|
2002-08-14 |
2004-02-26 |
Vertex Pharmaceuticals Incorporated |
Protein kinase inhibitors and uses thereof
|
|
AP2005003261A0
(en)
|
2002-09-18 |
2005-03-31 |
Pfizer Prod Inc |
Novel oxazole and thiazole compounds as transforming growth factor (TGF) inhibitors.
|
|
DE60328028D1
(de)
|
2002-09-18 |
2009-07-30 |
Pfizer Prod Inc |
Imidazolverbindungen als inhibitoren des transformierenden wachstumsfaktors (twf)
|
|
US7531553B2
(en)
|
2003-03-21 |
2009-05-12 |
Amgen Inc. |
Heterocyclic compounds and methods of use
|
|
AR045944A1
(es)
|
2003-09-24 |
2005-11-16 |
Novartis Ag |
Derivados de isoquinolina 1.4-disustituidas
|
|
AU2004279427B2
(en)
|
2003-10-08 |
2008-07-03 |
Irm Llc |
Compounds and compositions as protein kinase inhibitors
|
|
KR20060118472A
(ko)
|
2003-10-16 |
2006-11-23 |
카이론 코포레이션 |
치환 벤자졸 및 raf 키나아제의 저해제로서 그것의 사용
|
|
CA2545942C
(en)
|
2003-11-14 |
2012-07-10 |
Lorus Therapeutics Inc. |
Aryl imidazoles and their use as anti-cancer agents
|
|
CA2556944C
(en)
|
2004-03-05 |
2012-10-09 |
Taisho Pharmaceutical Co., Ltd. |
Thiazole derivative
|
|
KR100749566B1
(ko)
|
2004-04-21 |
2007-08-16 |
이화여자대학교 산학협력단 |
Alk5 및/또는 alk4 억제제로 유효한 2-피리딜이치환된 이미다졸 유도체
|
|
US20060106020A1
(en)
|
2004-04-28 |
2006-05-18 |
Rodgers James D |
Tetracyclic inhibitors of Janus kinases
|
|
PE20060315A1
(es)
|
2004-05-24 |
2006-05-15 |
Irm Llc |
Compuestos de tiazol como moduladores de ppar
|
|
EP1894932A1
(en)
|
2004-06-11 |
2008-03-05 |
Japan Tobacco, Inc. |
5-amino-2,4,7-trioxo-3,4,7,8-tetrahydro-2H-pyrido[2,3-d]pyrimidine derivatives and related compounds for the treatment of cancer
|
|
US7453002B2
(en)
|
2004-06-15 |
2008-11-18 |
Bristol-Myers Squibb Company |
Five-membered heterocycles useful as serine protease inhibitors
|
|
GB0415365D0
(en)
|
2004-07-09 |
2004-08-11 |
Astrazeneca Ab |
Pyrimidine derivatives
|
|
GB0415364D0
(en)
|
2004-07-09 |
2004-08-11 |
Astrazeneca Ab |
Pyrimidine derivatives
|
|
GB0415367D0
(en)
|
2004-07-09 |
2004-08-11 |
Astrazeneca Ab |
Pyrimidine derivatives
|
|
WO2006026306A1
(en)
|
2004-08-31 |
2006-03-09 |
Biogen Idec Ma Inc. |
Pyrimidinylimidazoles as tgf-beta inhibitors
|
|
WO2006038734A1
(en)
|
2004-10-08 |
2006-04-13 |
Astellas Pharma Inc. |
Pyridazinone derivatives cytokines inhibitors
|
|
WO2006044509A2
(en)
|
2004-10-15 |
2006-04-27 |
Biogen Idec Ma Inc. |
Methods of treating vascular injuries
|
|
JP2007246520A
(ja)
|
2006-02-15 |
2007-09-27 |
Takeda Yuichiro |
Rage阻害剤
|
|
WO2007118149A2
(en)
|
2006-04-07 |
2007-10-18 |
Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical Lollege |
Thiazole and thiophene analogues, and their use in treating autoimmune diseases and cancers
|
|
JP4450857B2
(ja)
|
2006-08-08 |
2010-04-14 |
中外製薬株式会社 |
Pi3k阻害剤としてのピリミジン誘導体およびその用途
|
|
WO2008071605A2
(en)
|
2006-12-15 |
2008-06-19 |
F. Hoffmann-La Roche Ag |
Methods of treating inflammatory diseases
|
|
UA98961C2
(uk)
|
2007-06-27 |
2012-07-10 |
Астразенека Аб |
Похідні піразинону та їх застосування у лікуванні легеневих захворювань
|
|
US7968536B2
(en)
|
2007-06-29 |
2011-06-28 |
Millennium Pharmaceuticals, Inc. |
Heterocyclic compounds useful as RAF kinase inhibitors
|
|
AR067354A1
(es)
|
2007-06-29 |
2009-10-07 |
Sunesis Pharmaceuticals Inc |
Compuestos utiles como inhibidores de la raf quinasa
|
|
CA2692379A1
(en)
|
2007-07-02 |
2009-01-08 |
Boehringer Ingelheim International Gmbh |
Antiproliferative compounds based on 5-membered heterocycles
|
|
EP2178866A2
(en)
|
2007-07-09 |
2010-04-28 |
AstraZeneca AB |
Trisubstituted pyrimidine derivatives for the treatment of proliferative diseases
|
|
JP2010533729A
(ja)
|
2007-07-17 |
2010-10-28 |
プレキシコン,インコーポレーテッド |
キナーゼ調節のための化合物と方法、及びそのための適応
|
|
CA2693967A1
(en)
|
2007-07-19 |
2009-01-29 |
Schering Corporation |
Heterocyclic amide compounds as protein kinase inhibitors
|
|
EP2197876A1
(en)
|
2007-08-29 |
2010-06-23 |
Glaxosmithkline LLC |
Thiazole and oxazole kinase inhibitors
|
|
UY31322A1
(es)
|
2007-09-05 |
2009-04-30 |
|
Amidas heterocíclicas y sus métodos de uso-975
|
|
WO2009047163A1
(en)
|
2007-10-10 |
2009-04-16 |
F. Hoffmann-La Roche Ag |
Methods of treating inflammatory diseases
|
|
TW200940537A
(en)
|
2008-02-26 |
2009-10-01 |
Astrazeneca Ab |
Heterocyclic urea derivatives and methods of use thereof
|
|
KR101408517B1
(ko)
|
2008-03-21 |
2014-06-17 |
노파르티스 아게 |
신규한 헤테로시클릭 화합물 및 그의 용도
|
|
US8865732B2
(en)
|
2008-03-21 |
2014-10-21 |
Novartis Ag |
Heterocyclic compounds and uses thereof
|
|
UA103319C2
(en)
|
2008-05-06 |
2013-10-10 |
Глаксосмитклайн Ллк |
Thiazole- and oxazole-benzene sulfonamide compounds
|
|
BRPI0915205A2
(pt)
|
2008-06-11 |
2017-03-21 |
Dana Farber Cancer Inst Inc |
compostos e composições úteis para o tratamento de malária
|
|
SI2324008T1
(sl)
|
2008-07-24 |
2012-08-31 |
Nerviano Medical Sciences Srl |
3,4-diarilpirazoli kot protein-kinazni inhibitorji
|
|
NZ591176A
(en)
|
2008-08-22 |
2012-11-30 |
Novartis Ag |
Pyrrolopyrimidine compounds as cdk inhibitors
|
|
WO2010048149A2
(en)
|
2008-10-20 |
2010-04-29 |
Kalypsys, Inc. |
Heterocyclic modulators of gpr119 for treatment of disease
|
|
MX2011006503A
(es)
|
2008-12-19 |
2011-09-06 |
Vertex Pharma |
Derivados de pirazina utiles como inhibidores de la cinasa de atr.
|
|
US8242260B2
(en)
|
2009-08-28 |
2012-08-14 |
Novartis Ag |
Compounds and compositions as protein kinase inhibitors
|
|
CA2771563A1
(en)
|
2009-09-04 |
2011-03-10 |
Novartis Ag |
Bipyridines useful for the treatment of proliferative diseases
|
|
EP2498608A4
(en)
|
2009-11-10 |
2013-04-24 |
Glaxosmithkline Llc |
BENZOLSULFONAMIDE THIAZOL AND OXAZOLE COMPOUNDS
|
|
US9315491B2
(en)
|
2009-12-28 |
2016-04-19 |
Development Center For Biotechnology |
Pyrimidine compounds as mTOR and PI3K inhibitors
|
|
EP2520575B1
(en)
|
2009-12-28 |
2016-11-30 |
General Incorporated Association Pharma Valley Project Supporting Organisation |
1,3,4-oxadiazole-2-carboxamide compound
|
|
KR20110123657A
(ko)
|
2010-05-07 |
2011-11-15 |
에스케이케미칼주식회사 |
피콜린아마이드 및 피리미딘-4-카복사미드 화합물, 이의 제조방법 및 이를 함유하는 약제학적 조성물
|
|
KR20130048293A
(ko)
|
2010-06-25 |
2013-05-09 |
노파르티스 아게 |
단백질 키나제 억제제로서의 헤테로아릴 화합물 및 조성물
|
|
WO2012027438A1
(en)
|
2010-08-26 |
2012-03-01 |
Glaxosmithkline Llc |
Pharmaceutical combination of a vegfr inhibitor and a mek inhibitor useful for treating cancer
|
|
CN101993415B
(zh)
|
2010-09-15 |
2013-08-14 |
北京韩美药品有限公司 |
作为Hedgehog通路抑制剂的化合物以及包含该化合物的药物组合物及其应用
|
|
US20120115878A1
(en)
|
2010-11-10 |
2012-05-10 |
John Vincent Calienni |
Salt(s) of 7-cyclopentyl-2-(5-piperazin-1-yl-pyridin-2-ylamino)-7h-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid dimethylamide and processes of making thereof
|
|
TWI505828B
(zh)
|
2010-12-20 |
2015-11-01 |
葛蘭素史克智慧財產(第二)有限公司 |
新穎醫藥組成物
|
|
PT2672967T
(pt)
|
2011-02-07 |
2018-12-07 |
Plexxikon Inc |
Compostos e métodos de modulação da quinase e suas indicações
|
|
WO2012125981A2
(en)
|
2011-03-17 |
2012-09-20 |
Selexagen Therapeutics, Inc. |
Raf kinase inhibitors
|
|
WO2013022766A1
(en)
|
2011-08-05 |
2013-02-14 |
Flynn Gary A |
Preparation and methods of use for ortho-aryl 5- membered heteroaryl-carboxamide containing multi-targeted kinase inhibitors
|
|
BR112014004560A2
(pt)
|
2011-09-01 |
2017-04-04 |
Irm Llc |
compostos e composições como inibidores de c-kit quinase
|
|
BR112014006743A8
(pt)
|
2011-09-21 |
2018-01-09 |
Cellzome Ltd |
composto, uso de um composto, e, método para tratar, controlar, retardar ou impedir uma ou mais condições
|
|
EP2844655A1
(en)
|
2012-05-02 |
2015-03-11 |
Lupin Limited |
Substituted pyridine compounds as crac modulators
|
|
KR20150020169A
(ko)
|
2012-05-15 |
2015-02-25 |
노파르티스 아게 |
Abl1, abl2 및 bcr-abl1의 활성을 억제하기 위한 벤즈아미드 유도체
|
|
AR091654A1
(es)
|
2012-07-02 |
2015-02-18 |
Biogen Idec Inc |
COMPUESTOS QUE CONTIENEN BIARILO COMO AGONISTAS INVERSOS DE RECEPTORES ROR-g
|
|
AR091876A1
(es)
|
2012-07-26 |
2015-03-04 |
Novartis Ag |
Combinaciones farmaceuticas para el tratamiento de enfermedades proliferativas
|
|
TR201904980T4
(tr)
|
2012-08-07 |
2019-05-21 |
Novartis Ag |
Bir B-Raf inhibitörü, bir EGFR inhibitörü ve isteğe bağlı olarak bir PI3K-alfa inhibitörü içeren farmasötik kombinasyonlar.
|
|
EP2892535B1
(en)
*
|
2012-09-04 |
2021-09-22 |
Novartis AG |
Method of adjuvant cancer treatment
|
|
CN105102456B
(zh)
|
2012-09-28 |
2017-11-14 |
癌症研究技术有限公司 |
非典型蛋白激酶c的氮杂喹唑啉抑制剂
|
|
WO2014058691A1
(en)
|
2012-10-08 |
2014-04-17 |
Merck Sharp & Dohme Corp. |
Inhibitors of irak4 activity
|
|
WO2014097125A1
(en)
|
2012-12-20 |
2014-06-26 |
Novartis Ag |
Pharmaceutical combination comprising binimetinib
|
|
US9242969B2
(en)
|
2013-03-14 |
2016-01-26 |
Novartis Ag |
Biaryl amide compounds as kinase inhibitors
|
|
SI2976106T1
(sl)
|
2013-03-21 |
2021-08-31 |
Array Biopharma Inc. |
Kombinacijska terapija, ki vsebuje zaviralec B-Raf in drugi zaviralec
|
|
SG11201601467SA
(en)
|
2013-11-01 |
2016-05-30 |
Novartis Ag |
Aminoheteroaryl benzamides as kinase inhibitors
|
|
AU2014368906B2
(en)
|
2013-12-20 |
2020-04-30 |
Biomed Valley Discoveries, Inc. |
Cancer treatment using combinations of ERK and RAF inhibitors
|
|
UY36294A
(es)
|
2014-09-12 |
2016-04-29 |
Novartis Ag |
Compuestos y composiciones como inhibidores de quinasa
|
|
CN107001329B
(zh)
|
2014-09-12 |
2020-09-01 |
诺华股份有限公司 |
作为激酶抑制剂的化合物和组合物
|
|
US10167279B2
(en)
|
2014-09-12 |
2019-01-01 |
Novartis Ag |
Compounds and compositions as RAF kinase inhibitors
|
|
WO2016115376A1
(en)
|
2015-01-14 |
2016-07-21 |
The Regents Of The University Of California |
Detection and treatment of double drug resistant melanomas
|
|
EP4119559A1
(en)
|
2015-04-15 |
2023-01-18 |
BeiGene, Ltd. |
Maleate salts of a b-raf kinase inhibitor, crystalline forms, methods of preparation, and uses therefore
|
|
KR20180033523A
(ko)
|
2015-07-10 |
2018-04-03 |
젠맵 에이/에스 |
암 치료를 위한 axl-특이적 항체-약물 접합체
|
|
WO2017037575A1
(en)
|
2015-08-28 |
2017-03-09 |
Novartis Ag |
A pharmaceutical combination comprising the pi3k inhibitor alpelisib and the cdk4/6 inhibitor ribociclib, and the use thereof in the treatment/prevention of cancer
|
|
JP2018525425A
(ja)
|
2015-08-28 |
2018-09-06 |
ノバルティス アーゲー |
がんを治療または予防するためのリボシクリブとダブラフェニブの組み合わせ
|
|
KR102439911B1
(ko)
|
2016-06-03 |
2022-09-05 |
어레이 바이오파마 인크. |
제약학적 복합제제
|
|
BR112018075371A2
(pt)
|
2016-06-10 |
2019-03-19 |
Novartis Ag |
usos terapêuticos de um inibidor de c-raf
|
|
US10973829B2
(en)
|
2016-09-19 |
2021-04-13 |
Novartis Ag |
Therapeutic uses of a C-RAF inhibitor
|
|
US11590133B2
(en)
|
2016-12-11 |
2023-02-28 |
Memorial Sloan Kettering Cancer Center |
Methods and compositions for treatment of BRAF mutant cancers
|
|
IL311471A
(en)
|
2017-05-02 |
2024-05-01 |
Novartis Ag |
Combination therapy
|
|
WO2018213302A1
(en)
|
2017-05-16 |
2018-11-22 |
Biomed Valley Discoveries, Inc. |
Compositions and methods for treating cancer with atypical braf mutations
|
|
MX2020002553A
(es)
|
2017-09-08 |
2020-07-22 |
Hoffmann La Roche |
Metodos de diagnostico y terapeuticos para el cancer.
|
|
TW202023556A
(zh)
|
2018-08-27 |
2020-07-01 |
美商庫拉腫瘤技術股份有限公司 |
以mapk路徑抑制劑治療腺癌
|
|
KR20210105388A
(ko)
|
2018-12-20 |
2021-08-26 |
노파르티스 아게 |
암 치료에서 사용하기 위한 raf 저해제와 cdk4/6 저해제를 이용하는 병용요법
|
|
EP4563150A3
(en)
|
2019-05-13 |
2025-07-23 |
Novartis AG |
New crystalline forms of n-(3-(2-(2-hydroxyethoxy)-6-morpholinopyridin-4-yl)-4-methvlphenyl)-2(trifluoromethyl) isonicotinamide as raf inhibitors for the treatment of cancer
|
|
EP4106756A1
(en)
|
2020-02-18 |
2022-12-28 |
Novartis AG |
Therapeutic combinations comprising a raf inhibitor for use in treating braf mutant nsclc
|
|
JP2023525100A
(ja)
|
2020-05-12 |
2023-06-14 |
ノバルティス アーゲー |
Craf阻害剤を含む治療的組み合わせ
|
|
TW202227088A
(zh)
|
2020-08-31 |
2022-07-16 |
瑞士商諾華公司 |
組合療法
|