AU2299099A
(en)
*
|
1998-02-04 |
1999-08-23 |
Kyowa Hakko Kogyo Co. Ltd. |
Antibodies against human vegf receptor kdr
|
DE19813774A1
(de)
*
|
1998-03-27 |
1999-09-30 |
Max Planck Gesellschaft |
Parapockenvirus-kodierter vaskulärer Endothelzell Wachstumsfaktor (PPV-VEGF)
|
NO983911D0
(no)
*
|
1998-08-26 |
1998-08-26 |
Norsk Hydro As |
Alginatkapsler til bruk ved behandling av hjernesvulst
|
JP2002529421A
(ja)
*
|
1998-11-06 |
2002-09-10 |
ビーエーエスエフ アクチェンゲゼルシャフト |
血管過浸透性の阻害方法
|
CA2361553A1
(fr)
*
|
1999-01-29 |
2000-08-03 |
Zhenping Zhu |
Anticorps specifiques au kdr et leurs utilisations
|
EP1130032A1
(fr)
*
|
2000-02-28 |
2001-09-05 |
Gesellschaft für biotechnologische Forschung mbH (GBF) |
Anticorps monochaines reconnaissant le récepteur humain de type 2 du facteur de croissance vasculaire endothéliale (VEGFR-2/KDR)
|
PL414997A1
(pl)
|
2001-02-19 |
2016-02-29 |
Novartis Ag |
Zastosowanie 40-O-(2-hydroksyetylo)-rapamycyny do leczenia guzów litych nerki
|
DE60219617T2
(de)
|
2001-05-16 |
2008-01-03 |
Novartis Ag |
Kombination von n- 5- 4-(4-methyl-piperazino-methyl)-benzoylamido -2-methylphenyl -4-(3-pyridil)-2pyrimidine-amin mit einem biphosphonat
|
TWI315982B
(en)
|
2001-07-19 |
2009-10-21 |
Novartis Ag |
Combinations comprising epothilones and pharmaceutical uses thereof
|
GB0124317D0
(en)
|
2001-10-10 |
2001-11-28 |
Celltech R&D Ltd |
Biological products
|
GB0206215D0
(en)
|
2002-03-15 |
2002-05-01 |
Novartis Ag |
Organic compounds
|
KR20120125398A
(ko)
|
2002-05-16 |
2012-11-14 |
노파르티스 아게 |
암에서 edg 수용체 결합제의 용도
|
EP2014678B1
(fr)
|
2002-09-12 |
2011-11-02 |
Oncotherapy Science, Inc. |
Peptides KDR et vaccins les comportant
|
US7250289B2
(en)
*
|
2002-11-20 |
2007-07-31 |
Affymetrix, Inc. |
Methods of genetic analysis of mouse
|
CA2524048C
(fr)
|
2003-05-19 |
2013-06-25 |
Irm Llc |
Composes immunosuppresseurs et compositions
|
MY150088A
(en)
|
2003-05-19 |
2013-11-29 |
Irm Llc |
Immunosuppressant compounds and compositions
|
GB0400122D0
(en)
*
|
2004-01-06 |
2004-02-11 |
Badrilla Ltd |
Method of quantifying binding
|
GB0512324D0
(en)
|
2005-06-16 |
2005-07-27 |
Novartis Ag |
Organic compounds
|
EP2377555A3
(fr)
|
2004-11-18 |
2011-11-23 |
Imclone LLC |
Anticorps contre le récepteur 1 du facteur de croissance endothéliale vasculaire
|
US20060222595A1
(en)
*
|
2005-03-31 |
2006-10-05 |
Priyabrata Mukherjee |
Nanoparticles for therapeutic and diagnostic applications
|
GB0510390D0
(en)
|
2005-05-20 |
2005-06-29 |
Novartis Ag |
Organic compounds
|
JP2009510073A
(ja)
|
2005-09-27 |
2009-03-12 |
ノバルティス アクチエンゲゼルシャフト |
カルボキシアミン化合物およびその使用方法
|
ES2481671T3
(es)
|
2005-11-21 |
2014-07-31 |
Novartis Ag |
Inhibidores de mTOR en el tratamiento de tumores endocrinos
|
CN1987468B
(zh)
*
|
2005-12-23 |
2012-01-11 |
上海交通大学医学院附属仁济医院 |
血管内皮生长因子时间分辨荧光免疫分析方法及试剂盒
|
RU2447891C2
(ru)
|
2006-04-05 |
2012-04-20 |
Новартис Аг |
Комбинации терапевтических средств, предназначенные для лечения рака
|
CA2649792A1
(fr)
|
2006-05-09 |
2007-11-15 |
Novartis Ag |
Combinaison comprenant un chelatant du fer et un agent antineoplasique et ses applications
|
GB0612721D0
(en)
|
2006-06-27 |
2006-08-09 |
Novartis Ag |
Organic compounds
|
ATE502943T1
(de)
|
2006-09-29 |
2011-04-15 |
Novartis Ag |
Pyrazolopyrimidine als pi3k-lipidkinasehemmer
|
CA2668235A1
(fr)
|
2006-11-02 |
2008-06-05 |
Yale University |
Estimation de la competence d'ovocytes
|
EP2125895B1
(fr)
*
|
2007-02-02 |
2015-04-08 |
Vegenics Pty Ltd |
Antagoniste du recepteur de facteurs de croissance pour l'allo-immunite de greffe d'organe et l'arteriosclerose
|
AU2008216327A1
(en)
|
2007-02-15 |
2008-08-21 |
Novartis Ag |
Combination of LBH589 with other therapeutic agents for treating cancer
|
TWI436775B
(zh)
|
2007-08-24 |
2014-05-11 |
Oncotherapy Science Inc |
以抗原胜肽合併化療藥劑治療胰臟癌
|
WO2009118305A1
(fr)
|
2008-03-26 |
2009-10-01 |
Novartis Ag |
Inhibiteurs de désacétylases b à base d'hydroxamate
|
US20110200612A1
(en)
|
2008-06-30 |
2011-08-18 |
Michael Schuster |
Treatment of eye diseases and excessive neovascularization using combined therapy
|
EP2344161B1
(fr)
|
2008-10-16 |
2018-12-19 |
Celator Pharmaceuticals, Inc. |
Combinaisons d'une camptothécine de liposome soluble dans l'eau avec du cetuximab ou du bevacizumab
|
JP5805538B2
(ja)
*
|
2008-11-07 |
2015-11-04 |
リサーチ ディベロップメント ファウンデーション |
Cripto/GSP78複合体形成およびシグナル伝達を阻害するための組成物および方法
|
MX2011006610A
(es)
|
2008-12-18 |
2011-06-30 |
Novartis Ag |
Nueva forma polimorfica de acido 1-(4-{l-[(e)-4-ciclohexil-3 -trifluorometil-benciloxi-imino]-etil)-2-etil-bencil)-azetidin-3 carboxilico.
|
WO2010080455A1
(fr)
|
2008-12-18 |
2010-07-15 |
Novartis Ag |
Nouveaux sels
|
KR20170062554A
(ko)
|
2008-12-18 |
2017-06-07 |
노파르티스 아게 |
1-[4-[1-(4-시클로헥실-3-트리플루오로메틸-벤질옥시이미노)-에틸]-2-에틸-벤질]-아제티딘-3-카르복실산의 헤미푸마레이트 염
|
US20110281917A1
(en)
|
2009-01-29 |
2011-11-17 |
Darrin Stuart |
Substituted Benzimidazoles for the Treatment of Astrocytomas
|
TW201109029A
(en)
|
2009-06-11 |
2011-03-16 |
Oncotherapy Science Inc |
Vaccine therapy for choroidal neovascularization
|
MY155570A
(en)
|
2009-06-26 |
2015-10-30 |
Novartis Ag |
1, 3-disubstituted imidazolidin-2-one derivatives as inhibitors of cyp 17
|
US8389526B2
(en)
|
2009-08-07 |
2013-03-05 |
Novartis Ag |
3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives
|
EA201200260A1
(ru)
|
2009-08-12 |
2012-09-28 |
Новартис Аг |
Гетероциклические гидразоны и их применение для лечения рака и воспаления
|
MX2012002066A
(es)
|
2009-08-17 |
2012-03-29 |
Intellikine Inc |
Compuestos heterociclicos y usos de los mismos.
|
EA201200318A1
(ru)
|
2009-08-20 |
2012-09-28 |
Новартис Аг |
Гетероциклические оксимы
|
US20120149661A1
(en)
|
2009-08-26 |
2012-06-14 |
Novartis Ag |
Tetra-substituted heteroaryl compounds and their use as mdm2 and/or mdm4 modulators
|
BR112012005400A2
(pt)
|
2009-09-10 |
2016-04-05 |
Irm Llc |
derivados do tipo éter de heteroarilas bicíclicas
|
CN102596951B
(zh)
|
2009-11-04 |
2015-04-15 |
诺华股份有限公司 |
用作mek抑制剂的杂环磺酰胺衍生物
|
JP2013512215A
(ja)
|
2009-11-25 |
2013-04-11 |
ノバルティス アーゲー |
二環式ヘテロアリールのベンゼン縮合6員酸素含有ヘテロ環誘導体
|
GEP20135998B
(en)
|
2009-12-08 |
2013-12-25 |
Novartis Ag |
Heterocyclic sulfonamide derivatives
|
US8440693B2
(en)
|
2009-12-22 |
2013-05-14 |
Novartis Ag |
Substituted isoquinolinones and quinazolinones
|
CU24130B1
(es)
|
2009-12-22 |
2015-09-29 |
Novartis Ag |
Isoquinolinonas y quinazolinonas sustituidas
|
CN102947274A
(zh)
|
2010-06-17 |
2013-02-27 |
诺瓦提斯公司 |
联苯基取代的1,3-二氢-苯并咪唑-2-亚基胺衍生物
|
JP2013532149A
(ja)
|
2010-06-17 |
2013-08-15 |
ノバルティス アーゲー |
ピペリジニル置換1,3−ジヒドロ−ベンゾイミダゾール−2−イリデンアミン誘導体
|
WO2012035078A1
(fr)
|
2010-09-16 |
2012-03-22 |
Novartis Ag |
Inhibiteurs de la 17α-hydroxylase/c17,20-lyase
|
WO2012107500A1
(fr)
|
2011-02-10 |
2012-08-16 |
Novartis Ag |
Composés de [1, 2, 4] triazolo [4, 3 -b] pyridazine en tant qu'inhibiteurs de la tyrosine kinase c-met
|
US9127000B2
(en)
|
2011-02-23 |
2015-09-08 |
Intellikine, LLC. |
Heterocyclic compounds and uses thereof
|
JP2014507465A
(ja)
|
2011-03-08 |
2014-03-27 |
ノバルティス アーゲー |
フルオロフェニル二環式ヘテロアリール化合物
|
EP2702052B1
(fr)
|
2011-04-28 |
2017-10-18 |
Novartis AG |
Inhibiteurs de 17a-hydroxylase/c17,20-lyase
|
CA2838029A1
(fr)
|
2011-06-09 |
2012-12-13 |
Novartis Ag |
Derives de sulfonamide heterocyclique
|
WO2012175487A1
(fr)
|
2011-06-20 |
2012-12-27 |
Novartis Ag |
Composés de cyclohexyl-isoquinolinone
|
WO2012175520A1
(fr)
|
2011-06-20 |
2012-12-27 |
Novartis Ag |
Dérivés d'isoquinolinone substitués par un hydroxy
|
MX2014002289A
(es)
|
2011-08-26 |
2015-03-20 |
Merrimack Pharmaceuticals Inc |
Anticuerpos fc especificos en tandem.
|
MX339302B
(es)
|
2011-09-15 |
2016-05-19 |
Novartis Ag |
3-(quinolin-6-il-tio)-[1,2,4]-triazolo-[4,3-a]-piridinas 6-sustituidas como cinasas de tirosina.
|
US8969341B2
(en)
|
2011-11-29 |
2015-03-03 |
Novartis Ag |
Pyrazolopyrrolidine compounds
|
EP2794592A1
(fr)
|
2011-12-23 |
2014-10-29 |
Novartis AG |
Composés inhibiteurs de l'interaction entre bcl2 et des partenaires de liaison
|
JP2015503516A
(ja)
|
2011-12-23 |
2015-02-02 |
ノバルティス アーゲー |
Bcl2と結合相手の相互作用を阻害するための化合物
|
AU2012355613A1
(en)
|
2011-12-23 |
2014-07-17 |
Novartis Ag |
Compounds for inhibiting the interaction of BCL2 with binding partners
|
EP2794591A1
(fr)
|
2011-12-23 |
2014-10-29 |
Novartis AG |
Composés inhibiteurs de l'interaction entre bcl2 et des partenaires de liaison
|
JP2015503517A
(ja)
|
2011-12-23 |
2015-02-02 |
ノバルティス アーゲー |
Bcl2と結合相手の相互作用を阻害するための化合物
|
UY34591A
(es)
|
2012-01-26 |
2013-09-02 |
Novartis Ag |
Compuestos de imidazopirrolidinona
|
WO2013149581A1
(fr)
|
2012-04-03 |
2013-10-10 |
Novartis Ag |
Produits combinés comprenant des inhibiteurs de tyrosine kinase et leur utilisation
|
US9365576B2
(en)
|
2012-05-24 |
2016-06-14 |
Novartis Ag |
Pyrrolopyrrolidinone compounds
|
US9556180B2
(en)
|
2013-01-22 |
2017-01-31 |
Novartis Ag |
Pyrazolo[3,4-d]pyrimidinone compounds as inhibitors of the P53/MDM2 interaction
|
WO2014115077A1
(fr)
|
2013-01-22 |
2014-07-31 |
Novartis Ag |
Composés de purinone substitués
|
KR20150143458A
(ko)
|
2013-03-06 |
2015-12-23 |
메리맥 파마슈티컬즈, 인크. |
항-C-MET 탠덤 Fc 이중특이적 항체
|
WO2014151147A1
(fr)
|
2013-03-15 |
2014-09-25 |
Intellikine, Llc |
Combinaison d'inhibiteurs de kinase et ses utilisations
|
WO2014155268A2
(fr)
|
2013-03-25 |
2014-10-02 |
Novartis Ag |
Inhibiteurs de kinase tyrosine fgf-r et leur utilisation dans le traitement de maladies associées à un manque ou à une absence d'activité snf5
|
US10274503B2
(en)
|
2013-05-08 |
2019-04-30 |
Vegenics Pty Limited |
Methods of using VEGF-C biomarkers for age-related macular degeneration (AMD) diagnosis
|
WO2015022663A1
(fr)
|
2013-08-14 |
2015-02-19 |
Novartis Ag |
Composés et compositions utiles comme inhibiteurs de mek
|
WO2015022664A1
(fr)
|
2013-08-14 |
2015-02-19 |
Novartis Ag |
Composés et compositions utiles comme inhibiteurs de mek
|
US9227969B2
(en)
|
2013-08-14 |
2016-01-05 |
Novartis Ag |
Compounds and compositions as inhibitors of MEK
|
WO2015084804A1
(fr)
|
2013-12-03 |
2015-06-11 |
Novartis Ag |
Combinaison d'un inhibiteur de mdm2 et d'un inhibiteur de braf, et leur utilisation
|
WO2015191602A2
(fr)
*
|
2014-06-09 |
2015-12-17 |
Biomed Valley Discoveries, Inc. |
Polythérapies ciblant un stroma associé à une tumeur ou des cellules tumorales
|
RU2695230C2
(ru)
|
2014-07-31 |
2019-07-22 |
Новартис Аг |
Сочетанная терапия
|
KR20240056629A
(ko)
|
2014-09-28 |
2024-04-30 |
더 리전트 오브 더 유니버시티 오브 캘리포니아 |
자극성 및 비자극성 골수성 세포의 조절
|
AU2017217677A1
(en)
|
2016-02-08 |
2018-07-26 |
Vitrisa Therapeutics, Inc. |
Compositions with improved intravitreal half-life and uses thereof
|
US10543231B2
(en)
|
2017-05-19 |
2020-01-28 |
Mayo Foundation For Medical Education And Research |
Methods and materials for treating cancer
|
JP2020525470A
(ja)
*
|
2017-07-03 |
2020-08-27 |
ディヴェロップメント センター フォー バイオテクノロジー |
抗vegfr抗体及びその使用
|
EP3697425A1
(fr)
|
2017-10-18 |
2020-08-26 |
Chemotherapeutisches Forschungsinstitut Georg-Speyer-Haus |
Procédés et composés pour une thérapie par cellules immunitaires améliorées
|
CA3083660A1
(fr)
|
2017-12-12 |
2019-06-20 |
Pionyr Immunotherapeutics, Inc. |
Anticorps anti-trem2 et methodes associees
|
EP3730483B1
(fr)
|
2017-12-21 |
2023-08-30 |
Hefei Institutes of Physical Science, Chinese Academy of Sciences |
Classe d'inhibiteurs de kinase dérivés de pyrimidine
|
WO2021097256A1
(fr)
|
2019-11-14 |
2021-05-20 |
Cohbar, Inc. |
Peptides antagonistes de cxcr4
|