US6777217B1
(en)
|
1996-03-26 |
2004-08-17 |
President And Fellows Of Harvard College |
Histone deacetylases, and uses related thereto
|
US6822267B1
(en)
*
|
1997-08-20 |
2004-11-23 |
Advantest Corporation |
Signal transmission circuit, CMOS semiconductor device, and circuit board
|
KR20070053362A
(ko)
|
1999-11-23 |
2007-05-23 |
메틸진, 인크. |
히스톤 디아세틸라제의 억제제
|
US20030129724A1
(en)
|
2000-03-03 |
2003-07-10 |
Grozinger Christina M. |
Class II human histone deacetylases, and uses related thereto
|
PE20020354A1
(es)
*
|
2000-09-01 |
2002-06-12 |
Novartis Ag |
Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda)
|
AU2001290134A1
(en)
|
2000-09-29 |
2002-04-08 |
Prolifix Limited |
Carbamic acid compounds comprising an amide linkage as hdac inhibitors
|
US7312247B2
(en)
*
|
2001-03-27 |
2007-12-25 |
Errant Gene Therapeutics, Llc |
Histone deacetylase inhibitors
|
ATE517624T1
(de)
|
2001-10-16 |
2011-08-15 |
Sloan Kettering Inst Cancer |
Behandlung von neurodegenerativen erkrankungen und krebs im gehirn
|
CN100457183C
(zh)
*
|
2001-11-06 |
2009-02-04 |
诺瓦提斯公司 |
环氧酶-2抑制剂/组蛋白脱乙酰酶抑制剂的组合
|
US7456219B2
(en)
|
2002-03-04 |
2008-11-25 |
Merck Hdac Research, Llc |
Polymorphs of suberoylanilide hydroxamic acid
|
US7148257B2
(en)
|
2002-03-04 |
2006-12-12 |
Merck Hdac Research, Llc |
Methods of treating mesothelioma with suberoylanilide hydroxamic acid
|
KR100868813B1
(ko)
|
2002-03-04 |
2008-11-14 |
슬로안-케테링인스티튜트퍼캔서리서치 |
말단 분화의 유도 방법
|
ATE399012T1
(de)
|
2002-04-03 |
2008-07-15 |
Topotarget Uk Ltd |
Carbaminsäurederivate enthaltend eine piperazin verknüpfung als hdac-inhibitoren
|
WO2003087066A1
(en)
*
|
2002-04-11 |
2003-10-23 |
Sk Chemicals, Co., Ltd. |
α,β-UNSATURATED HYDROXAMIC ACID DERIVATIVES AND THEIR USE AS HISTONE DEACETYLASE INHIBITORS
|
US20040018968A1
(en)
*
|
2002-04-15 |
2004-01-29 |
George Sgouros |
Use of histone deacetylase inhibitors in combination with radiation for the treatment of cancer
|
CN1658904A
(zh)
*
|
2002-06-10 |
2005-08-24 |
诺瓦提斯公司 |
包含埃坡霉素的组合及其药学用途
|
AU2003254951A1
(en)
*
|
2002-08-20 |
2004-03-11 |
Yamanouchi Pharmaceutical Co., Ltd. |
Arthrodial cartilage extracellular matrix degradation inhibitor
|
JP2006501267A
(ja)
*
|
2002-09-13 |
2006-01-12 |
バージニア コモンウェルス ユニバーシティー |
白血病の処置のためのa)N−{5−[4−(4−メチル−ピペラジノ−メチル)−ベンゾイルアミド]−2−メチルフェニル}−4−(3−ピリジル)−2−ピリミジン−アミンおよびb)ヒストンデアセチラーゼインヒビターの組合せ剤
|
US7154002B1
(en)
|
2002-10-08 |
2006-12-26 |
Takeda San Diego, Inc. |
Histone deacetylase inhibitors
|
US7250514B1
(en)
|
2002-10-21 |
2007-07-31 |
Takeda San Diego, Inc. |
Histone deacetylase inhibitors
|
AU2003280838A1
(en)
*
|
2002-11-19 |
2004-06-15 |
Takeda Pharmaceutical Company Limited |
Indole derivatives as somatostatin agonists or antagonists
|
WO2004052292A2
(en)
|
2002-12-06 |
2004-06-24 |
University Of South Florida |
Histone deacetylase inhibitor enhancement of trail-induced apoptosis
|
US7135493B2
(en)
|
2003-01-13 |
2006-11-14 |
Astellas Pharma Inc. |
HDAC inhibitor
|
JP4612621B2
(ja)
|
2003-01-17 |
2011-01-12 |
トポターゲット ユーケー リミテッド |
Hdac阻害剤としてのエステル又はケトン結合を含むカルバミン酸化合物
|
AU2003900608A0
(en)
*
|
2003-02-11 |
2003-02-27 |
Fujisawa Pharmaceutical Co., Ltd. |
Hdac inhibitor
|
AU2003900587A0
(en)
*
|
2003-02-11 |
2003-02-27 |
Fujisawa Pharmaceutical Co., Ltd. |
Hdac inhibitor
|
WO2004076386A2
(en)
|
2003-02-25 |
2004-09-10 |
Topotarget Uk Limited |
Carbamic acid compounds comprising a bicyclic heteroaryl group as hdac inhibitors
|
US7169801B2
(en)
|
2003-03-17 |
2007-01-30 |
Takeda San Diego, Inc. |
Histone deacetylase inhibitors
|
BRPI0410648A
(pt)
*
|
2003-05-21 |
2006-07-04 |
Novartis Ag |
combinação de inibidores de histona desacetilase com agentes quimioterápicos
|
WO2005011598A2
(en)
*
|
2003-07-31 |
2005-02-10 |
University Of South Florida |
Leukemia treatment method and composition
|
WO2005013958A1
(en)
*
|
2003-08-07 |
2005-02-17 |
Novartis Ag |
Histone deacetylase inhibitors as immunosuppressants
|
JP2007501774A
(ja)
*
|
2003-08-08 |
2007-02-01 |
ノバルティス アクチエンゲゼルシャフト |
スタウロスポリンを含む組み合わせ
|
AU2004266169B9
(en)
|
2003-08-26 |
2007-05-10 |
Merck Hdac Research, Llc |
Method of treating cancer with HDAC inhibitors
|
CA2535889A1
(en)
|
2003-08-29 |
2005-03-17 |
Aton Pharma, Inc. |
Combination methods of treating cancer
|
CN100455564C
(zh)
*
|
2003-09-12 |
2009-01-28 |
深圳微芯生物科技有限责任公司 |
组蛋白去乙酰化酶抑制剂及其药用制剂的制备和应用
|
AU2004271730A1
(en)
*
|
2003-09-18 |
2005-03-24 |
Novartis Ag |
Combination of a histone deacetylase inhibitor with a death receptor ligand
|
NZ545864A
(en)
*
|
2003-09-22 |
2009-12-24 |
S Bio Pte Ltd |
Benzimidazole derivates: preparation and pharmaceutical applications
|
EP1673349B1
(de)
*
|
2003-09-22 |
2010-06-30 |
S*Bio Pte Ltd |
Benzimidazolderivate: herstellung und pharmazeutische anwendungen
|
BRPI0414698A
(pt)
*
|
2003-09-23 |
2006-11-28 |
Novartis Ag |
combinação de um inibidor receptor de vegf com um agente quimioterapêutico
|
WO2005040161A1
(en)
*
|
2003-10-27 |
2005-05-06 |
S*Bio Pte Ltd |
Biaryl linked hydroxamates: preparation and pharmaceutical applications
|
JP5107579B2
(ja)
*
|
2003-12-02 |
2012-12-26 |
ザ オハイオ ステート ユニバーシティー リサーチ ファウンデーション |
新規の種類のヒストン脱アセチル化酵素阻害剤としてのZn2+キレートモチーフ係留短鎖脂肪酸
|
EP1541549A1
(de)
*
|
2003-12-12 |
2005-06-15 |
Exonhit Therapeutics S.A. |
Tricyclische Hydroxamat- und Benzamid-Derivate, Zusammensetzungen und Methoden
|
US20050137234A1
(en)
*
|
2003-12-19 |
2005-06-23 |
Syrrx, Inc. |
Histone deacetylase inhibitors
|
WO2005065681A1
(en)
*
|
2003-12-19 |
2005-07-21 |
Takeda San Diego, Inc. |
N- hydroxy-3-(3-(1h-imidazol-2-yl)-phenyl)-acrylamide derivatives and related compounds as histone deacetylase (hdac) inhibitors for the treatment of cancer
|
US20050197336A1
(en)
*
|
2004-03-08 |
2005-09-08 |
Miikana Therapeutics Corporation |
Inhibitors of histone deacetylase
|
US7345043B2
(en)
*
|
2004-04-01 |
2008-03-18 |
Miikana Therapeutics |
Inhibitors of histone deacetylase
|
PE20110102A1
(es)
|
2004-04-07 |
2011-02-07 |
Novartis Ag |
Derivados de n-(2-oxo-2-pirrolidinil-1-il)etil-2-amino-acetamida como inhibidores de proteinas de apoptosis (iap)
|
WO2006020004A2
(en)
*
|
2004-07-19 |
2006-02-23 |
Merck & Co., Inc. |
Histone deacetylase inhibitors
|
MX2007001550A
(es)
*
|
2004-08-09 |
2007-04-10 |
Astellas Pharma Inc |
Compuestos de hidroxiamida que tienen actividad como inhibidores de histona desacetilasa (hdac).
|
ITMI20041869A1
(it)
*
|
2004-10-01 |
2005-01-01 |
Dac Srl |
Nuovi inibitori delle istone deacetilasi
|
US8242175B2
(en)
|
2004-10-01 |
2012-08-14 |
Dac S.R.L. |
Class of histone deacetylase inhibitors
|
US7235688B1
(en)
|
2004-11-04 |
2007-06-26 |
University Of Notre Dame Du Lac |
Process for preparing histone deacetylase inhibitors and intermediates thereof
|
US20070021612A1
(en)
*
|
2004-11-04 |
2007-01-25 |
University Of Notre Dame Du Lac |
Processes and compounds for preparing histone deacetylase inhibitors and intermediates thereof
|
WO2006066133A2
(en)
*
|
2004-12-16 |
2006-06-22 |
Takeda San Diego, Inc. |
Histone deacetylase inhibitors
|
EP1851219A1
(de)
|
2005-02-14 |
2007-11-07 |
Miikana Therapeutics, Inc. |
Fusionierte heterocyclische verbindungen als histondeacetylase-hemmer
|
US7666880B2
(en)
*
|
2005-03-21 |
2010-02-23 |
S*Bio Pte Ltd. |
Imidazo[1,2-A]pyridine derivatives: preparation and pharmaceutical applications
|
US8999289B2
(en)
|
2005-03-22 |
2015-04-07 |
President And Fellows Of Harvard College |
Treatment of protein degradation disorders
|
GB0509223D0
(en)
*
|
2005-05-05 |
2005-06-15 |
Chroma Therapeutics Ltd |
Enzyme inhibitors
|
GB0509225D0
(en)
|
2005-05-05 |
2005-06-15 |
Chroma Therapeutics Ltd |
Inhibitors of enzymatic activity
|
US7642253B2
(en)
*
|
2005-05-11 |
2010-01-05 |
Takeda San Diego, Inc. |
Histone deacetylase inhibitors
|
TWI365068B
(en)
|
2005-05-20 |
2012-06-01 |
Merck Sharp & Dohme |
Formulations of suberoylanilide hydroxamic acid and methods for producing same
|
GB0510390D0
(en)
|
2005-05-20 |
2005-06-29 |
Novartis Ag |
Organic compounds
|
CN101263121A
(zh)
|
2005-07-14 |
2008-09-10 |
塔克达圣地亚哥公司 |
组蛋白脱乙酰基酶抑制剂
|
WO2007016532A2
(en)
*
|
2005-08-02 |
2007-02-08 |
Novartis Ag |
Mutations and polymorphisms of hdac4
|
KR101354237B1
(ko)
|
2005-08-03 |
2014-01-22 |
노파르티스 아게 |
골수종 치료를 위한 hdac 저해제의 용도
|
EP1915141A1
(de)
*
|
2005-08-10 |
2008-04-30 |
Novartis AG |
Verfahren zur verwendung von deacetylase-hemmern
|
AU2006279781A1
(en)
*
|
2005-08-11 |
2007-02-22 |
Novartis Ag |
Combination of organic compounds
|
US20070155730A1
(en)
*
|
2005-08-26 |
2007-07-05 |
Methylgene, Inc. |
Benzodiazepine And Benzopiperazine Analog Inhibitors Of Histone Deacetylase
|
EP2275096A3
(de)
|
2005-08-26 |
2011-07-13 |
Braincells, Inc. |
Neurogenese durch modulation des Muscarinrezeptors
|
EP2258359A3
(de)
|
2005-08-26 |
2011-04-06 |
Braincells, Inc. |
Neurogenese durch Modulation des Muscarinrezeptors mit Sabcomelin
|
WO2007030454A2
(en)
*
|
2005-09-07 |
2007-03-15 |
Novartis Ag |
Mutations and polymorphisms of hdac9
|
WO2007030455A2
(en)
*
|
2005-09-07 |
2007-03-15 |
Novartis Ag |
Mutations and polymorphisms of hdac10
|
WO2007038073A2
(en)
*
|
2005-09-22 |
2007-04-05 |
Novartis Ag |
Mutations and polymorphisms of hdac11
|
KR20080054417A
(ko)
|
2005-09-27 |
2008-06-17 |
노파르티스 아게 |
카르복시아민 화합물 및 hdac 의존성 질환의 치료에있어서의 그의 용도
|
WO2007047998A2
(en)
*
|
2005-10-21 |
2007-04-26 |
Novartis Ag |
Mutations and polymorphisms of hdac2
|
CA2625153A1
(en)
|
2005-10-21 |
2007-04-26 |
Braincells, Inc. |
Modulation of neurogenesis by pde inhibition
|
WO2007050655A2
(en)
|
2005-10-24 |
2007-05-03 |
Novartis Ag |
Combination of histone deacetylase inhibitors and radiation
|
US20070112017A1
(en)
|
2005-10-31 |
2007-05-17 |
Braincells, Inc. |
Gaba receptor mediated modulation of neurogenesis
|
WO2007053502A2
(en)
*
|
2005-11-01 |
2007-05-10 |
Novartis Ag |
Mutations and polymorphisms of hdac5
|
WO2007058992A2
(en)
*
|
2005-11-14 |
2007-05-24 |
Novartis Ag |
Mutations and polymorphisms of hdac6
|
SI2275103T1
(sl)
|
2005-11-21 |
2014-07-31 |
Novartis Ag |
mTor inhibitorji pri zdravljenju endokrinih tumorjev
|
US20070207950A1
(en)
*
|
2005-12-21 |
2007-09-06 |
Duke University |
Methods and compositions for regulating HDAC6 activity
|
EP1976835A2
(de)
*
|
2006-01-13 |
2008-10-08 |
Takeda San Diego, Inc. |
Histondeacetylase-inhibitoren
|
PL1981877T3
(pl)
|
2006-02-07 |
2012-12-31 |
Astellas Pharma Inc |
Związki N-hydroksyakryloamidowe
|
WO2008091349A1
(en)
*
|
2006-02-14 |
2008-07-31 |
The President And Fellows Of Harvard College |
Bifunctional histone deacetylase inhibitors
|
US20100216734A1
(en)
|
2006-03-08 |
2010-08-26 |
Braincells, Inc. |
Modulation of neurogenesis by nootropic agents
|
GB0605120D0
(en)
|
2006-03-14 |
2006-04-26 |
Novartis Ag |
Organic Compounds
|
US20090098137A1
(en)
|
2006-04-05 |
2009-04-16 |
Novartis Ag |
Combinations of therapeutic agents for treating cancer
|
EP2314297A1
(de)
|
2006-04-05 |
2011-04-27 |
Novartis AG |
Kombinationen aus bcr-abl/c-kit/pdgf-r tk-Hemmern zu Krebsbehandlung
|
US8168383B2
(en)
|
2006-04-14 |
2012-05-01 |
Cell Signaling Technology, Inc. |
Gene defects and mutant ALK kinase in human solid tumors
|
EP2447360A1
(de)
|
2006-04-14 |
2012-05-02 |
Cell Signaling Technology, Inc. |
Gendefekte und Mutante ALK-Kinase in festen menschlichen Tumoren
|
US20100137239A1
(en)
|
2006-04-24 |
2010-06-03 |
Gloucester Pharmaceuticals |
Gemcitabine combination therapy
|
US20090018142A9
(en)
*
|
2006-05-02 |
2009-01-15 |
Zhengping Zhuang |
Use of phosphatases to treat tumors overexpressing N-CoR
|
EP2026813A2
(de)
|
2006-05-09 |
2009-02-25 |
Braincells, Inc. |
5-ht-rezeptor-vermittelte neurogenese
|
WO2007134136A2
(en)
|
2006-05-09 |
2007-11-22 |
Braincells, Inc. |
Neurogenesis by modulating angiotensin
|
JP2009536180A
(ja)
|
2006-05-09 |
2009-10-08 |
ノバルティス アクチエンゲゼルシャフト |
鉄キレート剤と抗新生物剤を含む組合せ剤およびそれらの使用
|
WO2007146730A2
(en)
|
2006-06-08 |
2007-12-21 |
Gloucester Pharmaceuticals |
Deacetylase inhibitor therapy
|
NZ572744A
(en)
*
|
2006-06-12 |
2011-05-27 |
Novartis Ag |
Process for making salts of n-hydroxy-3-[4-[[[2-(2-methyl-1h-indol-3-yl)ethyl]amino]methyl]phenyl]-2e-2-propenamide
|
CA2654439C
(en)
*
|
2006-06-12 |
2014-08-05 |
Novartis Ag |
Salts of n-hydroxy-3-[4-[[[2-(2-methyl-1h-indol-3-yl)ethyl]amino]methyl]phenyl]-2e-2-propenamide
|
EA017984B1
(ru)
*
|
2006-06-12 |
2013-04-30 |
Новартис Аг |
Кристаллические безводные формы лактата n-гидрокси-3-[4-[[[2-(2-метил-1h-индол-3-ил)этил]амино]метил]фенил]-2e-2-акриламида
|
ES2553255T3
(es)
*
|
2006-06-12 |
2015-12-07 |
Novartis Ag |
Procedimiento para fabricar materiales de partida para N-hidroxi-3-[4-[2-(2-metil-1H-indol-3-il)-etilaminometil]-fenil]-2E-2-propenamida
|
UA95289C2
(en)
*
|
2006-06-12 |
2011-07-25 |
Новартис Аг |
Salts of n-hydroxy-3-[4-[[[2-(2-methyl-1h-indol-3-yl)ethyl]amino]methyl]phenyl]-2e-2-propenamide
|
EP2034978A1
(de)
*
|
2006-06-26 |
2009-03-18 |
Novartis AG |
Organische verbindungen
|
KR20090064418A
(ko)
|
2006-09-08 |
2009-06-18 |
브레인셀즈 인코퍼레이션 |
4-아실아미노피리딘 유도체 포함 조합물
|
US20100184806A1
(en)
|
2006-09-19 |
2010-07-22 |
Braincells, Inc. |
Modulation of neurogenesis by ppar agents
|
WO2008036046A1
(en)
|
2006-09-20 |
2008-03-27 |
S*Bio Pte Ltd |
IMIDAZO[l,2-a]PYRIDINE HYDROXYMATE COMPOUNDS THAT ARE INHIBITORS OF HISTONE DEACETYLASE
|
CN101516191A
(zh)
*
|
2006-09-28 |
2009-08-26 |
默克公司 |
Saha的胺碱盐和其多晶型物
|
US20090286779A1
(en)
|
2006-09-29 |
2009-11-19 |
Novartis Ag |
Pyrazolopyrimidines as lipid kinase inhibitors
|
GB0619753D0
(en)
*
|
2006-10-06 |
2006-11-15 |
Chroma Therapeutics Ltd |
Enzyme inhibitors
|
JP5043120B2
(ja)
|
2006-10-30 |
2012-10-10 |
クロマ セラピューティクス リミテッド |
ヒストンデアセチラーゼの阻害剤としてのヒドロキサメート
|
US20080242648A1
(en)
*
|
2006-11-10 |
2008-10-02 |
Syndax Pharmaceuticals, Inc., A California Corporation |
COMBINATION OF ERa+ LIGANDS AND HISTONE DEACETYLASE INHIBITORS FOR THE TREATMENT OF CANCER
|
BRPI0719746A2
(pt)
|
2006-12-04 |
2013-12-10 |
Novartis Ag |
Combinação
|
KR20090099561A
(ko)
*
|
2006-12-15 |
2009-09-22 |
아스텔라스세이야쿠 가부시키가이샤 |
N-히드록시아크릴아미드 화합물
|
RU2009130457A
(ru)
*
|
2007-01-10 |
2011-02-20 |
Новартис АГ (CH) |
Составы ингибиторов дезацетилазы
|
WO2008097561A1
(en)
|
2007-02-06 |
2008-08-14 |
Lixte Biotechology Holdings, Inc. |
Oxabicycloheptanes and oxabicycloheptenes, their preparation and use
|
EP2491923A3
(de)
|
2007-02-15 |
2012-12-26 |
Novartis AG |
Kombinationen therapeutischer Wirkstoffe zur Krebsbehandlung
|
US20100056522A1
(en)
|
2007-03-28 |
2010-03-04 |
Santen Pharmaceutical Co., Ltd. |
Intraocular pressure-lowering agent comprising compound having histone deacetylase inhibitor effect as active ingredient
|
US9096565B2
(en)
|
2007-04-09 |
2015-08-04 |
Methylgene Inc. |
Inhibitors of histone deacetylase
|
TW200908964A
(en)
*
|
2007-05-04 |
2009-03-01 |
Novartis Ag |
Use of HDAC inhibitors for the treatment of gastrointestinal cancers
|
AU2008251499A1
(en)
*
|
2007-05-11 |
2008-11-20 |
Novartis Ag |
Use of HDAC inhibitors for the treatment of melanoma
|
WO2008150782A1
(en)
*
|
2007-05-30 |
2008-12-11 |
Novartis Ag |
Use of hdac inhibitors for the treatment of bone destruction
|
US7737175B2
(en)
|
2007-06-01 |
2010-06-15 |
Duke University |
Methods and compositions for regulating HDAC4 activity
|
WO2009020565A1
(en)
*
|
2007-08-03 |
2009-02-12 |
Lixte Biotechnology, Inc. |
Use of phosphates to treat neuroblastomas and medullogastomas
|
CL2008002786A1
(es)
*
|
2007-09-20 |
2009-05-15 |
Novartis Ag |
Torta farmceuticamente aceptable, formada por liofilizacion, que comprende: n-hidroxi-3-[4-[[[2-(2-metil-1h-indol-3-il]-etil]-amino]-metil]-fenil]-2e-2-propenamida o una sal, un regulador de ph seleciondo de lactato o acidop lactico, fodfato o acido fosforico o una combinacion y un agente de volumen; proceso de elaboracion.
|
ES2628748T3
(es)
|
2007-10-01 |
2017-08-03 |
Lixte Biotechnology, Inc. |
Inhibidores de la HDAC
|
CA2703231A1
(en)
*
|
2007-10-22 |
2009-04-30 |
Orchid Research Laboratories Limited |
Histone deacetylase inhibitors
|
CN101417967A
(zh)
*
|
2007-10-26 |
2009-04-29 |
浙江海正药业股份有限公司 |
组蛋白去乙酰酶抑制剂、其组合物及其应用
|
WO2009067453A1
(en)
*
|
2007-11-19 |
2009-05-28 |
Syndax Pharmaceuticals, Inc. |
Combinations of hdac inhibitors and proteasome inhibitors
|
CA2706750A1
(en)
*
|
2007-11-27 |
2009-06-04 |
Ottawa Health Research Institute |
Amplification of cancer-specific oncolytic viral infection by histone deacetylase inhibitors
|
CA2708281A1
(en)
|
2007-12-11 |
2009-08-27 |
Viamet Pharmaceuticals, Inc. |
Metalloenzyme inhibitors using metal binding moieties in combination with targeting moieties
|
ITFI20070288A1
(it)
|
2007-12-21 |
2009-06-22 |
A I L Firenze Sezione Autonoma |
Inibitori delle deacetilasi istoniche
|
EP2100879A1
(de)
*
|
2008-03-13 |
2009-09-16 |
4Sc Ag |
Neuartige N-substituierte Tetrahydroisochinolin/Isoindolin-Hydroxamsäure-Verbindungen
|
CN102036953B
(zh)
|
2008-03-24 |
2015-05-06 |
诺华股份有限公司 |
基于芳基磺酰胺的基质金属蛋白酶抑制剂
|
ES2519474T3
(es)
*
|
2008-03-26 |
2014-11-07 |
Novartis Ag |
Inhibidores de las desacetilasas B basados en hidroxamato
|
JP2011528662A
(ja)
*
|
2008-07-18 |
2011-11-24 |
ノバルティス アーゲー |
ホジキン病の治療のためのhdac阻害剤の使用
|
EP2321264B1
(de)
|
2008-07-23 |
2016-05-04 |
President and Fellows of Harvard College |
Deacetylaseinhibitoren und anwendungen davon
|
US8227473B2
(en)
*
|
2008-08-01 |
2012-07-24 |
Lixte Biotechnology, Inc. |
Oxabicycloheptanes and oxabicycloheptenes, their preparation and use
|
EP2309853A4
(de)
*
|
2008-08-01 |
2012-04-25 |
Lixte Biotechnology Inc |
Verfahren zur zellmitoseregulierung durch hemmung der serin/threonin-phosphatase
|
AU2009277086B2
(en)
|
2008-08-01 |
2015-12-10 |
Lixte Biotechnology, Inc. |
Neuroprotective agents for the prevention and treatment of neurodegenerative diseases
|
WO2010147612A1
(en)
|
2009-06-18 |
2010-12-23 |
Lixte Biotechnology, Inc. |
Methods of modulating cell regulation by inhibiting p53
|
WO2010083617A1
(en)
|
2009-01-21 |
2010-07-29 |
Oncalis Ag |
Pyrazolopyrimidines as protein kinase inhibitors
|
DK2391366T3
(da)
|
2009-01-29 |
2013-01-07 |
Novartis Ag |
Substituerede benzimidazoler til behandling af astrocytomer
|
WO2010099217A1
(en)
|
2009-02-25 |
2010-09-02 |
Braincells, Inc. |
Modulation of neurogenesis using d-cycloserine combinations
|
GB0903480D0
(en)
*
|
2009-02-27 |
2009-04-08 |
Chroma Therapeutics Ltd |
Enzyme Inhibitors
|
KR101168801B1
(ko)
|
2009-03-27 |
2012-07-25 |
주식회사종근당 |
신규한 하이드록사메이트 유도체, 이의 제조방법, 및 이를 함유하는 약제학적 조성물
|
EP2236503B1
(de)
|
2009-04-03 |
2014-02-26 |
NatureWise Biotech & Medicals Corporation |
Zimtzusammensetzungen und Derivate davon zur Hemmung von Histon-Deacetylase
|
US7994357B2
(en)
|
2009-04-03 |
2011-08-09 |
Naturewise Biotech & Medicals Corporation |
Cinamic compounds and derivatives therefrom for the inhibition of histone deacetylase
|
WO2011006908A2
(en)
|
2009-07-16 |
2011-01-20 |
Royal College Of Surgeons In Ireland |
Metal complexes having dual histone deacetylase inhibitory and dna-binding activity
|
US8389526B2
(en)
|
2009-08-07 |
2013-03-05 |
Novartis Ag |
3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives
|
WO2011019393A2
(en)
*
|
2009-08-11 |
2011-02-17 |
President And Fellows Of Harvard College |
Class- and isoform-specific hdac inhibitors and uses thereof
|
BR112012003262A8
(pt)
|
2009-08-12 |
2016-05-17 |
Novartis Ag |
compostos de hidrazona heterocíclica e seus usos para tratar câncer e inflamação
|
PE20170003A1
(es)
|
2009-08-17 |
2017-03-15 |
Intellikine Llc |
Compuestos heterociclicos y usos de los mismos
|
EA201200318A1
(ru)
|
2009-08-20 |
2012-09-28 |
Новартис Аг |
Гетероциклические оксимы
|
WO2011023677A1
(en)
|
2009-08-26 |
2011-03-03 |
Novartis Ag |
Tetra-substituted heteroaryl compounds and their use as mdm2 and/or mdm4 modulators
|
JO3002B1
(ar)
|
2009-08-28 |
2016-09-05 |
Irm Llc |
مركبات و تركيبات كمثبطات كيناز بروتين
|
US20110053925A1
(en)
*
|
2009-08-28 |
2011-03-03 |
Novartis Ag |
Hydroxamate-Based Inhibitors of Deacetylases
|
MY156209A
(en)
|
2009-11-04 |
2016-01-29 |
Novartis Ag |
Heterocyclic sulfonamide derivatives useful mek inhibitors
|
BR112012012210B8
(pt)
|
2009-11-23 |
2021-05-25 |
Cerulean Pharma Inc |
conjugado de (cdp)-taxano de polímero contendo ciclodextrina, composição, composição farmacêutica, forma de dosagem, kit e uso de um conjugado de cdp-taxano
|
EP2509964B1
(de)
|
2009-12-08 |
2014-04-30 |
Novartis AG |
Heterocyclische Sulfonamidderivate
|
CU24130B1
(es)
|
2009-12-22 |
2015-09-29 |
Novartis Ag |
Isoquinolinonas y quinazolinonas sustituidas
|
US8440693B2
(en)
|
2009-12-22 |
2013-05-14 |
Novartis Ag |
Substituted isoquinolinones and quinazolinones
|
WO2011084991A2
(en)
*
|
2010-01-08 |
2011-07-14 |
President And Fellows Of Harvard College |
Fluorinated hdac inhibitors and uses thereof
|
WO2011088181A1
(en)
|
2010-01-13 |
2011-07-21 |
Tempero Pharmaceuticals, Inc. |
Compounds and methods
|
EP2523664A4
(de)
|
2010-01-13 |
2013-06-26 |
Tempero Pharmaceuticals Inc |
Verbindungen und verfahren
|
US20110178287A1
(en)
|
2010-01-19 |
2011-07-21 |
Cerulean Pharma Inc. |
Cyclodextrin-based polymers for therapeutic delivery
|
UY33236A
(es)
|
2010-02-25 |
2011-09-30 |
Novartis Ag |
Inhibidores dimericos de las iap
|
US8217079B2
(en)
|
2010-03-26 |
2012-07-10 |
Italfarmaco Spa |
Method for treating Philadelphia-negative myeloproliferative syndromes
|
WO2011119995A2
(en)
|
2010-03-26 |
2011-09-29 |
Cerulean Pharma Inc. |
Formulations and methods of use
|
UA112517C2
(uk)
|
2010-07-06 |
2016-09-26 |
Новартіс Аг |
Тетрагідропіридопіримідинові похідні
|
EP2407164A1
(de)
|
2010-07-14 |
2012-01-18 |
Dublin Institute of Technology Intellectual Property Ltd |
Kupfer-II-Komplexe von Phenanthrolin und deren Verwendung in der Krebsbehandlung
|
WO2012025701A1
(en)
*
|
2010-08-25 |
2012-03-01 |
Chroma Therapeutics Ltd. |
Alpha, alpha - di substituted glycine ester derivatives and their use as hdac inhibitors
|
WO2012025155A1
(en)
*
|
2010-08-26 |
2012-03-01 |
Novartis Ag |
Hydroxamate-based inhibitors of deacetylases
|
KR20140011301A
(ko)
*
|
2010-08-27 |
2014-01-28 |
노파르티스 아게 |
데아세틸라제의 히드록사메이트-기반 억제제
|
US20130266590A1
(en)
|
2010-12-13 |
2013-10-10 |
Novartis Ag |
Dimeric iap inhibitors
|
UY33794A
(es)
|
2010-12-13 |
2012-07-31 |
Novartis Ag |
Inhibidores diméricos de las iap
|
WO2012097013A1
(en)
|
2011-01-10 |
2012-07-19 |
Nimbus Iris, Inc. |
Irak inhibitors and uses thereof
|
TW201245115A
(en)
|
2011-01-24 |
2012-11-16 |
Chdi Foundation Inc |
Histone deacetylase inhibitors and compositions and methods of use thereof
|
US20130324526A1
(en)
|
2011-02-10 |
2013-12-05 |
Novartis Ag |
[1,2,4] triazolo [4,3-b] pyridazine compounds as inhibitors of the c-met tyrosine kinase
|
EP2678018A4
(de)
|
2011-02-23 |
2015-09-30 |
Intellikine Llc |
Kombination von kinasehemmern und verwendungen dafür
|
WO2012116237A2
(en)
|
2011-02-23 |
2012-08-30 |
Intellikine, Llc |
Heterocyclic compounds and uses thereof
|
MX2013010329A
(es)
|
2011-03-09 |
2014-03-12 |
Sverker Jern |
Compuestos y metodos para mejorarfibrinolisis endogena deteriorada usando inhibidores de histona deacetilasa.
|
EA201391820A1
(ru)
|
2011-06-09 |
2014-12-30 |
Новартис Аг |
Гетероциклические сульфонамидные производные
|
ES2595407T3
(es)
|
2011-06-14 |
2016-12-29 |
Novartis Ag |
Combinación de panobinostat y ruxolitinib en el tratamiento de cáncer, tal como una neoplasia mieloproliferativa
|
WO2012175487A1
(en)
|
2011-06-20 |
2012-12-27 |
Novartis Ag |
Cyclohexyl isoquinolinone compounds
|
US8859535B2
(en)
|
2011-06-20 |
2014-10-14 |
Novartis Ag |
Hydroxy substituted isoquinolinone derivatives
|
MX2013015001A
(es)
|
2011-06-27 |
2014-03-31 |
Novartis Ag |
Formas solidas y sales de derivados de tetrahidro-pirido-pirimidin a.
|
EP2758043A4
(de)
|
2011-08-17 |
2016-02-24 |
Dennis M Brown |
Zusammensetzungen und verfahren zur erhöhung des therapeutischen nutzens von suboptimal verabreichten chemischen verbindungen einschliesslich substituierter hexitole wie dibromodulcitol
|
CA2848809A1
(en)
|
2011-09-15 |
2013-03-21 |
Novartis Ag |
6-substituted 3-(quinolin-6-ylthio)-[1,2,4]triazolo[4,3-a]pyradines as c-met tyrosine kinase
|
BR112014011223A8
(pt)
|
2011-11-11 |
2023-01-31 |
Novartis Ag |
Método de tratar uma doença proliferativa
|
MX353446B
(es)
|
2011-11-23 |
2018-01-12 |
Novartis Ag |
Formulaciones farmaceuticas.
|
CN103130673B
(zh)
*
|
2011-11-28 |
2017-05-03 |
重庆医药工业研究院有限责任公司 |
一种阿戈美拉晶型i的制备方法
|
WO2013080141A1
(en)
|
2011-11-29 |
2013-06-06 |
Novartis Ag |
Pyrazolopyrrolidine compounds
|
US9408885B2
(en)
|
2011-12-01 |
2016-08-09 |
Vib Vzw |
Combinations of therapeutic agents for treating melanoma
|
EP2794594A1
(de)
|
2011-12-22 |
2014-10-29 |
Novartis AG |
Chinolinderivate
|
AP4055A
(en)
|
2011-12-22 |
2017-03-07 |
Novartis Ag |
Dihydro-benzo-oxazine and dihydro-pyrido-oxazine derivatives
|
US20130178520A1
(en)
|
2011-12-23 |
2013-07-11 |
Duke University |
Methods of treatment using arylcyclopropylamine compounds
|
EP2794588A1
(de)
|
2011-12-23 |
2014-10-29 |
Novartis AG |
Verbindungen zur hemmung der interaktion von bcl2 mit bindungspartnern
|
EA201491260A1
(ru)
|
2011-12-23 |
2014-11-28 |
Новартис Аг |
Соединения и композиции для ингибирования взаимодействия bcl2 с партнерами по связыванию
|
EA201491265A1
(ru)
|
2011-12-23 |
2014-11-28 |
Новартис Аг |
Соединения для ингибирования взаимодействия bcl-2 с партнерами по связыванию
|
CA2859869A1
(en)
|
2011-12-23 |
2013-06-27 |
Novartis Ag |
Compounds for inhibiting the interaction of bcl2 with binding partners
|
AU2012355615A1
(en)
|
2011-12-23 |
2014-07-10 |
Novartis Ag |
Compounds for inhibiting the interaction of BCL2 with binding partners
|
WO2013101600A1
(en)
*
|
2011-12-29 |
2013-07-04 |
Pharmacyclics, Inc. |
Cinnamic acid hydroxyamides as inhibitors of histone deacetylase 8
|
EP3608317A1
(de)
|
2012-01-12 |
2020-02-12 |
Yale University |
Verbindungen und verfahren für den verstärkten abbau von gezielten proteinen und anderen polypeptiden durch eine e3-ubiquitinligase
|
US8815926B2
(en)
|
2012-01-26 |
2014-08-26 |
Novartis Ag |
Substituted pyrrolo[3,4-D]imidazoles for the treatment of MDM2/4 mediated diseases
|
TWI573792B
(zh)
|
2012-02-01 |
2017-03-11 |
歐陸斯迪公司 |
新穎治療劑
|
JP2015512425A
(ja)
|
2012-04-03 |
2015-04-27 |
ノバルティス アーゲー |
チロシンキナーゼ阻害剤との組合せ製品及びそれらの使用
|
AU2013261130A1
(en)
|
2012-05-15 |
2014-10-23 |
Novartis Ag |
Benzamide derivatives for inhibiting the activity of ABL1, ABL2 and BCR-ABL1
|
DK2861579T5
(da)
|
2012-05-15 |
2022-10-24 |
Novartis Ag |
Benzamidderivater til at hæmme aktiviteten af ABL1, ABL2 og BCR-ABL1
|
BR112014027181A2
(pt)
|
2012-05-15 |
2017-06-27 |
Novartis Ag |
derivados de benzamida para a inibição da atividade de abl1, abl2 e bcr-abl1
|
AU2013261129B2
(en)
|
2012-05-15 |
2016-05-12 |
Novartis Ag |
Compounds and compositions for inhibiting the activity of ABL1, ABL2 and BCR-ABL1
|
CN104321325B
(zh)
|
2012-05-24 |
2016-11-16 |
诺华股份有限公司 |
吡咯并吡咯烷酮化合物
|
US9789193B2
(en)
|
2012-06-15 |
2017-10-17 |
The Brigham And Women's Hospital, Inc. |
Compositions for treating cancer and methods for making the same
|
AR091773A1
(es)
|
2012-07-16 |
2015-02-25 |
Chdi Foundation Inc |
Inhibidores de la histona desacetilasa y composiciones y sus metodos de uso
|
WO2014025395A1
(en)
|
2012-08-06 |
2014-02-13 |
Duke University |
Compounds and methods for targeting hsp90
|
PL2903968T3
(pl)
|
2012-10-02 |
2017-05-31 |
Gilead Sciences, Inc. |
Inhibitory demetylaz histonowych
|
SMT202000168T1
(it)
|
2012-10-30 |
2020-05-08 |
Mei Pharma Inc |
Terapie di combinazione per il trattamento dei tumori chemioresistenti
|
CA2888803A1
(en)
|
2012-11-05 |
2014-05-08 |
Jooeun Bae |
Xbp1, cd138, and cs1 peptides, pharmaceutical compositions that include the peptides, and methods of using such peptides and compositions
|
US20150283136A1
(en)
|
2012-11-08 |
2015-10-08 |
Novartis Ag |
Pharmaceutical combination comprising a b-raf inhibitor and a histone deacetylase inhibitor and their use in the treatment of proliferative diseases
|
TW201422625A
(zh)
|
2012-11-26 |
2014-06-16 |
Novartis Ag |
二氫-吡啶并-□衍生物之固體形式
|
EP2948453B1
(de)
|
2013-01-22 |
2017-08-02 |
Novartis AG |
Pyrazolo[3,4-d]pyrimidinonverbindungen als inhibitoren der p53/mdm2-interaktion
|
US9403827B2
(en)
|
2013-01-22 |
2016-08-02 |
Novartis Ag |
Substituted purinone compounds
|
WO2014128612A1
(en)
|
2013-02-20 |
2014-08-28 |
Novartis Ag |
Quinazolin-4-one derivatives
|
MX2015011097A
(es)
|
2013-02-27 |
2016-03-09 |
Epitherapeutics Aps |
Inhibidores de histona desmetilasas.
|
WO2014151147A1
(en)
|
2013-03-15 |
2014-09-25 |
Intellikine, Llc |
Combination of kinase inhibitors and uses thereof
|
WO2014155268A2
(en)
|
2013-03-25 |
2014-10-02 |
Novartis Ag |
Fgf-r tyrosine kinase activity inhibitors - use in diseases associated with lack of or reduced snf5 activity
|
EP2983674A4
(de)
|
2013-04-08 |
2017-05-10 |
Dennis M. Brown |
Therapeutischer nutzen suboptimal verabreichter chemischer verbindungen
|
US10532050B2
(en)
|
2013-04-09 |
2020-01-14 |
Lixte Biotechnology, Inc. |
Formulations of oxabicycloheptanes and oxabicycloheptenes
|
BR112015027114B1
(pt)
|
2013-04-29 |
2021-12-21 |
Chong Kun Dang Pharmaceutical Corp |
Compostos inibidores seletivos de histona desacetilase e seu uso
|
US20150018376A1
(en)
|
2013-05-17 |
2015-01-15 |
Novartis Ag |
Pyrimidin-4-yl)oxy)-1h-indole-1-carboxamide derivatives and use thereof
|
GB201311891D0
(en)
|
2013-07-03 |
2013-08-14 |
Glaxosmithkline Ip Dev Ltd |
Novel compound
|
GB201311888D0
(en)
|
2013-07-03 |
2013-08-14 |
Glaxosmithkline Ip Dev Ltd |
Novel compounds
|
UY35675A
(es)
|
2013-07-24 |
2015-02-27 |
Novartis Ag |
Derivados sustituidos de quinazolin-4-ona
|
KR20160099081A
(ko)
|
2013-07-26 |
2016-08-19 |
업데이트 파마 인코포레이트 |
비산트렌의 치료 효과 개선용 조합 방법
|
WO2015022663A1
(en)
|
2013-08-14 |
2015-02-19 |
Novartis Ag |
Compounds and compositions as inhibitors of mek
|
US9227969B2
(en)
|
2013-08-14 |
2016-01-05 |
Novartis Ag |
Compounds and compositions as inhibitors of MEK
|
WO2015022664A1
(en)
|
2013-08-14 |
2015-02-19 |
Novartis Ag |
Compounds and compositions as inhibitors of mek
|
MY176421A
(en)
|
2013-09-22 |
2020-08-07 |
Sunshine Lake Pharma Co Ltd |
Substituted aminopyrimidine compounds and methods of use
|
EP3757130A1
(de)
|
2013-09-26 |
2020-12-30 |
Costim Pharmaceuticals Inc. |
Verfahren zur behandlung von blutkrebs
|
CN103467359B
(zh)
*
|
2013-09-27 |
2015-04-22 |
山东大学 |
一种含有吲哚的肉桂酰胺类组蛋白去乙酰化酶抑制剂及其制备方法和应用
|
TW201605450A
(zh)
|
2013-12-03 |
2016-02-16 |
諾華公司 |
Mdm2抑制劑與BRAF抑制劑之組合及其用途
|
CN103664734B
(zh)
*
|
2013-12-10 |
2015-09-23 |
广州康缔安生物科技有限公司 |
杂环羟肟酸类化合物及其药用组合物和应用
|
EP3080125B1
(de)
|
2013-12-12 |
2018-10-10 |
Chong Kun Dang Pharmaceutical Corp. |
Neuartige azaindolderivate als selektive histondeacetylase (hdac)-inhibitoren und pharmazeutische zusammensetzungen damit
|
KR101685639B1
(ko)
|
2014-01-03 |
2016-12-12 |
주식회사 종근당 |
신규한 인돌 유도체 화합물 및 이를 포함하는 약제학적 조성물
|
JOP20200094A1
(ar)
|
2014-01-24 |
2017-06-16 |
Dana Farber Cancer Inst Inc |
جزيئات جسم مضاد لـ pd-1 واستخداماتها
|
JOP20200096A1
(ar)
|
2014-01-31 |
2017-06-16 |
Children’S Medical Center Corp |
جزيئات جسم مضاد لـ tim-3 واستخداماتها
|
CN106661039B
(zh)
|
2014-02-28 |
2019-09-13 |
林伯士拉克许米公司 |
酪氨酸蛋白质激酶2(tyk2)抑制剂和其用途
|
US10000469B2
(en)
|
2014-03-25 |
2018-06-19 |
Duke University |
Heat shock protein 70 (hsp-70) receptor ligands
|
EP3122730B1
(de)
|
2014-03-28 |
2020-03-25 |
Calitor Sciences, LLC |
Substituierte heteroarylverbindungen und verfahren zur verwendung davon
|
CA2943824A1
(en)
|
2014-03-31 |
2015-10-08 |
Gilead Sciences, Inc. |
Inhibitors of histone demethylases
|
RU2016140160A
(ru)
|
2014-04-03 |
2018-05-07 |
Инвиктус Онколоджи Пвт. Лтд. |
Супрамолекулярные комбинаторные лекарственные средства
|
JP6778114B2
(ja)
|
2014-04-14 |
2020-10-28 |
アルビナス・オペレーションズ・インコーポレイテッドArvinas Operations, Inc. |
イミド系タンパク質分解モジュレーター及び関連する使用方法
|
GB201409485D0
(en)
|
2014-05-28 |
2014-07-09 |
Euro Celtique Sa |
Pharmaceutical composition
|
GB201409488D0
(en)
|
2014-05-28 |
2014-07-09 |
Euro Celtique Sa |
Pharmaceutical composition
|
GB201409471D0
(en)
|
2014-05-28 |
2014-07-09 |
Euro Celtique Sa |
Pharmaceutical composition
|
WO2016011658A1
(en)
|
2014-07-25 |
2016-01-28 |
Novartis Ag |
Combination therapy
|
MX2017001461A
(es)
|
2014-07-31 |
2017-05-11 |
Novartis Ag |
Terapia de combinacion.
|
US10071164B2
(en)
|
2014-08-11 |
2018-09-11 |
Yale University |
Estrogen-related receptor alpha based protac compounds and associated methods of use
|
US11311512B2
(en)
|
2014-08-12 |
2022-04-26 |
Monash University |
Lymph directing prodrugs
|
KR20170040805A
(ko)
|
2014-08-27 |
2017-04-13 |
길리애드 사이언시즈, 인코포레이티드 |
히스톤 데메틸라제를 억제하기 위한 화합물 및 방법
|
EP2995630A1
(de)
|
2014-09-09 |
2016-03-16 |
Dublin Institute of Technology |
Aus ionischen Flüssigkeiten hergestellte, hybride Verbindungen und Verwendungen davon in ionenselektiven Elektroden
|
US9993551B2
(en)
|
2014-09-13 |
2018-06-12 |
Novartis Ag |
Combination therapies of EGFR inhibitors
|
US20170209574A1
(en)
|
2014-10-03 |
2017-07-27 |
Novartis Ag |
Combination therapies
|
US20160251376A1
(en)
|
2015-02-27 |
2016-09-01 |
Nimbus Lakshmi, Inc. |
Tyk2 inhibitors and uses thereof
|
JP6692826B2
(ja)
|
2015-03-10 |
2020-05-13 |
アドゥロ バイオテック,インク. |
「インターフェロン遺伝子刺激因子」依存性シグナル伝達の活性化のための組成物及び方法
|
CN107531660A
(zh)
|
2015-03-13 |
2018-01-02 |
福马治疗股份有限公司 |
作为HDAC8抑制剂的α‑肉桂酰胺化合物和组合物
|
MX2017011919A
(es)
|
2015-03-18 |
2018-05-22 |
Arvinas Inc |
Compuestos y metodos para la degradacion mejorada de proteinas especificas.
|
KR101796601B1
(ko)
|
2015-05-22 |
2017-11-10 |
주식회사 종근당 |
선택적 히스톤 탈아세틸화 효소 억제제로서의 헤테로시클릭알킬 유도체 화합물 및 이를 포함하는 약제학적 조성물
|
WO2017004134A1
(en)
|
2015-06-29 |
2017-01-05 |
Nimbus Iris, Inc. |
Irak inhibitors and uses thereof
|
WO2017004133A1
(en)
|
2015-06-29 |
2017-01-05 |
Nimbus Iris, Inc. |
Irak inhibitors and uses thereof
|
EP3331905B1
(de)
|
2015-08-06 |
2022-10-05 |
Dana-Farber Cancer Institute, Inc. |
Gezielte proteindegradierung zur attenuierung adoptiver t-zell-therapie in zusammenhang mit unerwünschten entzündungsreaktionen
|
WO2017032281A1
(zh)
*
|
2015-08-21 |
2017-03-02 |
苏州晶云药物科技有限公司 |
帕比司他乳酸盐的新晶型
|
JP6802263B2
(ja)
|
2015-09-02 |
2020-12-16 |
ニンバス ラクシュミ, インコーポレイテッド |
Tyk2阻害剤およびその使用
|
JP7118888B2
(ja)
|
2015-09-08 |
2022-08-16 |
モナッシュ ユニバーシティ |
リンパ指向性プロドラッグ
|
US9938257B2
(en)
|
2015-09-11 |
2018-04-10 |
Calitor Sciences, Llc |
Substituted heteroaryl compounds and methods of use
|
PT3364958T
(pt)
|
2015-10-23 |
2023-04-10 |
Navitor Pharm Inc |
Moduladores de interação sestrina-gator2 e utilizações dos mesmos
|
AU2016349781A1
(en)
|
2015-11-02 |
2018-05-10 |
Yale University |
Proteolysis targeting chimera compounds and methods of preparing and using same
|
ITUB20155193A1
(it)
|
2015-11-03 |
2017-05-03 |
Italfarmaco Spa |
Sospensioni orali di Givinostat fisicamente e chimicamente stabili
|
WO2017106328A1
(en)
|
2015-12-14 |
2017-06-22 |
X4 Pharmaceuticals, Inc. |
Methods for treating cancer
|
CA3008279A1
(en)
|
2015-12-14 |
2017-06-22 |
X4 Pharmaceuticals, Inc. |
Methods for treating cancer
|
US11370792B2
(en)
|
2015-12-14 |
2022-06-28 |
Raze Therapeutics, Inc. |
Caffeine inhibitors of MTHFD2 and uses thereof
|
JP7055380B2
(ja)
|
2015-12-22 |
2022-04-18 |
エックス4 ファーマシューティカルズ, インコーポレイテッド |
免疫不全疾患を処置するための方法
|
CN105732467A
(zh)
*
|
2016-01-13 |
2016-07-06 |
深圳市康立生生物科技有限公司 |
一种panobinostat(帕比司他)的制备方法
|
EP3426244B1
(de)
|
2016-03-09 |
2023-06-07 |
Raze Therapeutics, Inc. |
3-phosphoglycerat-dehydrogenase-inhibitoren und verwendungen davon
|
EP3426243B1
(de)
|
2016-03-09 |
2021-05-19 |
Raze Therapeutics, Inc. |
3-phosphoglycerat-dehydrogenase-inhibitoren und verwendungen davon
|
WO2017157813A1
(en)
|
2016-03-15 |
2017-09-21 |
F. Hoffmann-La Roche Ag |
Combinations of lsd1 inhibitors for the treatment of hematological malignancies
|
KR102511024B1
(ko)
|
2016-03-15 |
2023-03-16 |
오리존 지노믹스 에스.에이. |
고형 종양의 치료에 사용하기 위한 lsd1 억제제의 조합물
|
CA3019394A1
(en)
|
2016-04-08 |
2017-10-12 |
X4 Pharmaceuticals, Inc. |
Methods for treating cancer
|
WO2017184956A1
(en)
|
2016-04-22 |
2017-10-26 |
Duke University |
Compounds and methods for targeting hsp90
|
AR108257A1
(es)
|
2016-05-02 |
2018-08-01 |
Mei Pharma Inc |
Formas polimórficas de 3-[2-butil-1-(2-dietilamino-etil)-1h-bencimidazol-5-il]-n-hidroxi-acrilamida y usos de las mismas
|
EP3455218A4
(de)
|
2016-05-10 |
2019-12-18 |
C4 Therapeutics, Inc. |
Mit c3-kohlenstoff verknüpfte glutarimiddegronimere zum zielproteinabbau
|
CN109562107A
(zh)
|
2016-05-10 |
2019-04-02 |
C4医药公司 |
用于靶蛋白降解的杂环降解决定子体
|
EP3454862B1
(de)
|
2016-05-10 |
2024-09-11 |
C4 Therapeutics, Inc. |
Spirocyclische degronimere für zielproteinabbau
|
WO2017197051A1
(en)
|
2016-05-10 |
2017-11-16 |
C4 Therapeutics, Inc. |
Amine-linked c3-glutarimide degronimers for target protein degradation
|
ES2870920T3
(es)
|
2016-06-21 |
2021-10-28 |
X4 Pharmaceuticals Inc |
Inhibidores de CXCR4 y usos de los mismos
|
WO2017223229A1
(en)
|
2016-06-21 |
2017-12-28 |
X4 Pharmaceuticals, Inc. |
Cxcr4 inhibitors and uses thereof
|
JP6994767B2
(ja)
|
2016-06-21 |
2022-01-14 |
エックス4 ファーマシューティカルズ, インコーポレイテッド |
Cxcr4阻害剤およびその使用
|
EP3484858A4
(de)
*
|
2016-06-21 |
2020-02-26 |
The University of Melbourne |
Aktivatoren der hiv-latenz
|
WO2018015493A1
(en)
|
2016-07-20 |
2018-01-25 |
Royal College Of Surgeons In Ireland |
Metal complexes having therapeutic applications
|
WO2018039203A1
(en)
|
2016-08-23 |
2018-03-01 |
Oncopep, Inc. |
Peptide vaccines and durvalumab for treating multiple myeloma
|
EP3503914A1
(de)
|
2016-08-23 |
2019-07-03 |
Oncopep, Inc. |
Peptidimpfstoffe und durvalumab zur behandlung von brustkrebs
|
WO2018054960A1
(en)
|
2016-09-21 |
2018-03-29 |
INSERM (Institut National de la Santé et de la Recherche Médicale) |
Methods for predicting and treating resistance to chemotherapy in npm-alk(+) alcl
|
US10207998B2
(en)
|
2016-09-29 |
2019-02-19 |
Duke University |
Substituted benzimidazole and substituted benzothiazole inhibitors of transforming growth factor-β kinase and methods of use thereof
|
US10927083B2
(en)
|
2016-09-29 |
2021-02-23 |
Duke University |
Substituted benzimidazoles as inhibitors of transforming growth factor-β kinase
|
CA3040155C
(en)
|
2016-10-11 |
2024-01-16 |
Euro-Celtique S.A. |
Compound for use in the treatment of hodgkin lymphoma
|
IL265922B2
(en)
|
2016-10-14 |
2025-02-01 |
Nimbus Lakshmi Inc |
TYK2 inhibitors and their uses
|
CN110300590A
(zh)
|
2016-10-21 |
2019-10-01 |
林伯士拉克许米公司 |
Tyk2抑制剂及其用途
|
WO2018089499A1
(en)
|
2016-11-08 |
2018-05-17 |
Navitor Pharmaceuticals, Inc. |
PHENYL AMINO PIPERIDINE mTORC INHIBITORS AND USES THEREOF
|
JP2019535839A
(ja)
|
2016-11-29 |
2019-12-12 |
ピュアテック ヘルス エルエルシー |
治療剤の送達のためのエクソソーム
|
WO2018106636A1
(en)
|
2016-12-05 |
2018-06-14 |
Raze Therapeutics, Inc. |
Shmt inhibitors and uses thereof
|
CA3046515A1
(en)
|
2016-12-08 |
2018-06-14 |
Lixte Biotechnology, Inc. |
Oxabicycloheptanes for modulation of immune response
|
JP2020502238A
(ja)
|
2016-12-23 |
2020-01-23 |
バイスクルアールディー・リミテッド |
新規連結構造を有するペプチド誘導体
|
US10624968B2
(en)
|
2017-01-06 |
2020-04-21 |
Bicyclerd Limited |
Compounds for treating cancer
|
WO2018148440A1
(en)
|
2017-02-08 |
2018-08-16 |
Dana-Farber Cancer Institute, Inc. |
Regulating chimeric antigen receptors
|
AR111233A1
(es)
|
2017-03-08 |
2019-06-19 |
Nimbus Lakshmi Inc |
Inhibidores de tyk2, usos y métodos para la producción de los mismos
|
EP3375778A1
(de)
|
2017-03-14 |
2018-09-19 |
Artax Biopharma Inc. |
Aryl-piperidinderivate
|
EP3375784A1
(de)
|
2017-03-14 |
2018-09-19 |
Artax Biopharma Inc. |
Aza-dihydro-acridonderivate
|
WO2018191146A1
(en)
|
2017-04-10 |
2018-10-18 |
Navitor Pharmaceuticals, Inc. |
Heteroaryl rheb inhibitors and uses thereof
|
JOP20180036A1
(ar)
|
2017-04-18 |
2019-01-30 |
Vifor Int Ag |
أملاح لمثبطات فروبورتين جديدة
|
WO2018197893A1
(en)
|
2017-04-27 |
2018-11-01 |
Bicycletx Limited |
Bicyclic peptide ligands and uses thereof
|
UY37695A
(es)
|
2017-04-28 |
2018-11-30 |
Novartis Ag |
Compuesto dinucleótido cíclico bis 2’-5’-rr-(3’f-a)(3’f-a) y usos del mismo
|
CN107141244B
(zh)
*
|
2017-05-08 |
2019-11-19 |
潍坊医学院 |
吲哚丁酸类组蛋白去乙酰酶抑制剂及其制备方法和应用
|
GB201709405D0
(en)
|
2017-06-13 |
2017-07-26 |
Euro Celtique Sa |
Compounds for treating ovarian cancer
|
GB201709402D0
(en)
|
2017-06-13 |
2017-07-26 |
Euro Celtique Sa |
Compounds for treating t-pll
|
GB201709406D0
(en)
|
2017-06-13 |
2017-07-26 |
Euro-Cletique S A |
Compounds for treating TNBC
|
GB201709403D0
(en)
|
2017-06-13 |
2017-07-26 |
Euro Celtique Sa |
Compounds for treating sarcoma
|
WO2019002842A1
(en)
|
2017-06-26 |
2019-01-03 |
Bicyclerd Limited |
BICYCLIC PEPTIDE LIGANDS WITH DETECTABLE FRACTIONS AND USES THEREOF
|
KR102717819B1
(ko)
|
2017-07-28 |
2024-10-14 |
다케다 야쿠힌 고교 가부시키가이샤 |
Tyk2 억제제 및 이의 용도
|
KR101977970B1
(ko)
|
2017-08-04 |
2019-05-14 |
중원대학교 산학협력단 |
신규한 벤즈아미드계 유도체, 이의 제조방법 및 이를 유효성분으로 함유하는 암 예방 또는 치료용 약학 조성물
|
US11261214B2
(en)
|
2017-08-04 |
2022-03-01 |
Bicycletx Limited |
Bicyclic peptide ligand specific for CD137
|
WO2019034868A1
(en)
|
2017-08-14 |
2019-02-21 |
Bicyclerd Limited |
CONJUGATES PEPTIDE BICYCLIC-LIGAND PPR-A AND USES THEREOF
|
US20200291096A1
(en)
|
2017-08-14 |
2020-09-17 |
Bicyclerd Limited |
Bicyclic peptide ligand sting conjugates and uses thereof
|
US11883497B2
(en)
|
2017-08-29 |
2024-01-30 |
Puretech Lyt, Inc. |
Lymphatic system-directing lipid prodrugs
|
WO2019046491A1
(en)
|
2017-08-29 |
2019-03-07 |
Ariya Therapeutics, Inc. |
LIPIDIC PRODRUGS DIRECTING TO THE LYMPHATIC SYSTEM
|
IL273432B
(en)
|
2017-09-22 |
2022-09-01 |
Kymera Therapeutics Inc |
Protein degraders and uses thereof
|
WO2019060693A1
(en)
|
2017-09-22 |
2019-03-28 |
Kymera Therapeutics, Inc. |
CRBN LIGANDS AND USES THEREOF
|
EP3461480A1
(de)
|
2017-09-27 |
2019-04-03 |
Onxeo |
Kombination von checkpoint-hemmern des dna-schädigungsantwort-zellzyklus und belinostat zur behandlung von krebs
|
EP3461488A1
(de)
|
2017-09-27 |
2019-04-03 |
Onxeo |
Kombination aus einem dbait-molekül und einem hdac-inhibitor zur behandlung von krebs
|
WO2019083960A1
(en)
|
2017-10-24 |
2019-05-02 |
Oncopep, Inc. |
PEPTIDE VACCINES AND HDAC INHIBITORS FOR THE TREATMENT OF MULTIPLE MYELOMA
|
WO2019084030A1
(en)
|
2017-10-24 |
2019-05-02 |
Genentech, Inc. |
(4-HYDROXYPYRROLIDIN-2-YL) -HYDROXAMATE COMPOUNDS AND METHODS OF USE
|
JP2021500409A
(ja)
|
2017-10-24 |
2021-01-07 |
オンコペップ, インコーポレイテッド |
乳がんを処置するためのペプチドワクチンおよびペムブロリズマブ
|
WO2019084026A1
(en)
|
2017-10-24 |
2019-05-02 |
Genentech, Inc. |
(4-HYDROXYPYRROLIDIN-2-YL) -HETEROCYCLIC COMPOUNDS AND METHODS OF USE
|
JP7254076B2
(ja)
|
2017-11-19 |
2023-04-07 |
サンシャイン・レイク・ファーマ・カンパニー・リミテッド |
置換ヘテロアリール化合物及び使用方法
|
US10537585B2
(en)
|
2017-12-18 |
2020-01-21 |
Dexcel Pharma Technologies Ltd. |
Compositions comprising dexamethasone
|
US11608345B1
(en)
|
2017-12-19 |
2023-03-21 |
Puretech Lyt, Inc. |
Lipid prodrugs of rapamycin and its analogs and uses thereof
|
US11304954B2
(en)
|
2017-12-19 |
2022-04-19 |
Puretech Lyt, Inc. |
Lipid prodrugs of mycophenolic acid and uses thereof
|
AU2017444054B2
(en)
|
2017-12-21 |
2021-10-07 |
Hefei Institutes Of Physical Science, Chinese Academy Of Sciences |
Class of pyrimidine derivative kinase inhibitors
|
IL315310A
(en)
|
2017-12-26 |
2024-10-01 |
Kymera Therapeutics Inc |
Irak degraders and uses thereof
|
US11485743B2
(en)
|
2018-01-12 |
2022-11-01 |
Kymera Therapeutics, Inc. |
Protein degraders and uses thereof
|
WO2019140387A1
(en)
|
2018-01-12 |
2019-07-18 |
Kymera Therapeutics, Inc. |
Crbn ligands and uses thereof
|
CA3083040A1
(en)
|
2018-01-20 |
2019-07-25 |
Sunshine Lake Pharma Co., Ltd. |
Substituted aminopyrimidine compounds and methods of use
|
EP3746075A4
(de)
|
2018-01-29 |
2021-09-08 |
Merck Patent GmbH |
Gcn2-inhibitoren und verwendungen davon
|
WO2019148136A1
(en)
|
2018-01-29 |
2019-08-01 |
Merck Patent Gmbh |
Gcn2 inhibitors and uses thereof
|
CA3090271A1
(en)
|
2018-02-12 |
2019-08-15 |
Inimmune Corporation |
Toll-like receptor ligands
|
MX2020008814A
(es)
|
2018-02-27 |
2020-12-11 |
Artax Biopharma Inc |
Derivados de cromeno como inhibidores de la interaccion receptor de antigeno de celula t (tcr) - region no catalitica de la proteina citosolica de la proteina tirosina cinasa (nck).
|
WO2019183523A1
(en)
|
2018-03-23 |
2019-09-26 |
Genentech, Inc. |
Hetero-bifunctional degrader compounds and their use as modulators of targeted ubiquination (vhl)
|
CA3095912A1
(en)
|
2018-04-13 |
2019-10-17 |
Arvinas Operations, Inc. |
Cereblon ligands and bifunctional compounds comprising the same
|
ES2969982T3
(es)
|
2018-04-24 |
2024-05-23 |
Vertex Pharma |
Compuestos de pteridinona y usos de los mismos
|
KR20210005151A
(ko)
|
2018-04-24 |
2021-01-13 |
메르크 파텐트 게엠베하 |
항증식 화합물 및 이의 용도
|
US11925690B2
(en)
|
2018-06-13 |
2024-03-12 |
Amphista Therapeutics Limited |
Bifunctional molecules for targeting Rpn11
|
CN112585127A
(zh)
|
2018-06-13 |
2021-03-30 |
安菲斯塔治疗有限责任公司 |
用于靶向UchL5的双功能分子
|
WO2019238886A1
(en)
|
2018-06-13 |
2019-12-19 |
University Of Dundee |
Bifunctional molecules for targeting usp14
|
JP7382353B2
(ja)
|
2018-06-15 |
2023-11-16 |
ヤンセン ファーマシューティカ エヌ.ベー. |
ラパマイシン類似体およびその使用
|
US11180531B2
(en)
|
2018-06-22 |
2021-11-23 |
Bicycletx Limited |
Bicyclic peptide ligands specific for Nectin-4
|
WO2020010177A1
(en)
|
2018-07-06 |
2020-01-09 |
Kymera Therapeutics, Inc. |
Tricyclic crbn ligands and uses thereof
|
CN108752255A
(zh)
*
|
2018-07-19 |
2018-11-06 |
重庆医科大学 |
一种帕比司他及其关键中间体的制备方法
|
EP3826988A4
(de)
|
2018-07-24 |
2023-03-22 |
Hygia Pharmaceuticals, LLC |
Verbindungen, derivate und analoga für krebs
|
US10548889B1
(en)
|
2018-08-31 |
2020-02-04 |
X4 Pharmaceuticals, Inc. |
Compositions of CXCR4 inhibitors and methods of preparation and use
|
EP3846793B1
(de)
|
2018-09-07 |
2024-01-24 |
PIC Therapeutics, Inc. |
Eif4e-inhibitoren und verwendungen davon
|
CA3115088A1
(en)
|
2018-10-15 |
2020-04-23 |
Nimbus Lakshmi, Inc. |
Tyk2 inhibitors and uses thereof
|
EP3870597A1
(de)
|
2018-10-23 |
2021-09-01 |
BicycleTx Limited |
Bicyclische peptidliganden und ihre verwendungen
|
CN109574936B
(zh)
*
|
2018-11-23 |
2022-02-22 |
沈阳药科大学 |
一种具有hdac6抑制活性的异羟肟酸类化合物及其应用
|
BR112021010484A2
(pt)
|
2018-11-30 |
2021-08-24 |
Kymera Therapeutics, Inc. |
Degradadores de irak e usos dos mesmos
|
EP3886843A4
(de)
|
2018-11-30 |
2022-08-31 |
Nimbus Lakshmi, Inc. |
Tyk2-inhibitoren und verwendungen davon
|
EP3670659A1
(de)
|
2018-12-20 |
2020-06-24 |
Abivax |
Biomarker und verwendungen bei der behandlung von viralen infektionen, entzündlichen oder krebserkrankungen
|
EP3897631A4
(de)
|
2018-12-20 |
2022-11-23 |
C4 Therapeutics, Inc. |
Gezielter proteinabbau
|
EP3914357A4
(de)
|
2019-01-23 |
2022-10-12 |
Nimbus Lakshmi, Inc. |
Tyk2-inhibitoren und verwendungen davon
|
WO2020165600A1
(en)
|
2019-02-14 |
2020-08-20 |
Bicycletx Limited |
Bicyclic peptide ligand sting conjugates and uses thereof
|
AU2020253990A1
(en)
|
2019-04-02 |
2021-10-28 |
Bicycletx Limited |
Bicycle toxin conjugates and uses thereof
|
BR112021019748A2
(pt)
|
2019-04-05 |
2021-12-07 |
Kymera Therapeutics Inc |
Degradadores de stat e usos dos mesmos
|
JP2022534425A
(ja)
|
2019-05-31 |
2022-07-29 |
イケナ オンコロジー, インコーポレイテッド |
Tead阻害剤およびその使用
|
GB201913124D0
(en)
|
2019-09-11 |
2019-10-23 |
Seald As |
Compositions and methods for treatment of cholangiocarcinoma
|
GB201913123D0
(en)
|
2019-09-11 |
2019-10-23 |
Seald As |
Compositions and methods for treatment of cholangiocarcinoma
|
GB201913122D0
(en)
|
2019-09-11 |
2019-10-23 |
Seald As |
Compositions and methods for treatment of cholangiocarcinoma
|
CN115038688A
(zh)
|
2019-09-11 |
2022-09-09 |
文森雷生物科学股份有限公司 |
Usp30抑制剂及其用途
|
GB201913121D0
(en)
|
2019-09-11 |
2019-10-23 |
Seald As |
Compositions and methods for treatment of cholangiocarcinoma
|
EP3798250A1
(de)
|
2019-09-25 |
2021-03-31 |
University College Dublin |
Hyperverzweigte kationische polymere, die als nukleinsäureabgabevektoren für die transfektion geeignet sind
|
EP4034152A1
(de)
|
2019-09-25 |
2022-08-03 |
University College Dublin |
Nanopartikelzusammensetzungen zur gentherapie
|
CA3152582A1
(en)
*
|
2019-11-06 |
2021-05-14 |
Dana-Farber Cancer Institute, Inc. |
Selective histone deacetylase (hdac) degraders and methods of use thereof
|
US11819476B2
(en)
|
2019-12-05 |
2023-11-21 |
Janssen Pharmaceutica Nv |
Rapamycin analogs and uses thereof
|
PH12022551524A1
(en)
|
2019-12-17 |
2024-01-29 |
Kymera Therapeutics Inc |
Irak degraders and uses thereof
|
WO2021127283A2
(en)
|
2019-12-17 |
2021-06-24 |
Kymera Therapeutics, Inc. |
Irak degraders and uses thereof
|
PH12022551486A1
(en)
|
2019-12-19 |
2023-11-13 |
Arvinas Operations Inc |
Compounds and methods for the targeted degradation of androgen receptor
|
KR20220151160A
(ko)
|
2019-12-23 |
2022-11-14 |
카이메라 쎄라퓨틱스 인코포레이티드 |
Smarca 분해제 및 이의 용도
|
WO2021148581A1
(en)
|
2020-01-22 |
2021-07-29 |
Onxeo |
Novel dbait molecule and its use
|
EP4100017A4
(de)
|
2020-02-05 |
2024-04-10 |
PureTech LYT, Inc. |
Lipidprodrugs von neurosteroiden
|
IT202000004075A1
(it)
|
2020-02-27 |
2021-08-27 |
Flamma Spa |
Processo per la preparazione di panobinostat
|
JP2023515888A
(ja)
|
2020-03-03 |
2023-04-14 |
ピク セラピューティクス, インコーポレイテッド |
eIF4E阻害剤及びその使用
|
WO2021185844A1
(en)
|
2020-03-16 |
2021-09-23 |
Pvac Medical Technologies Ltd |
Use of substance and pharmaceutical composition thereof, and medical treatments or uses thereof
|
WO2021233534A1
(en)
|
2020-05-20 |
2021-11-25 |
Pvac Medical Technologies Ltd |
Use of substance and pharmaceutical composition thereof, and medical treatments or uses thereof
|
CA3171258A1
(en)
|
2020-03-19 |
2021-09-23 |
Nan JI |
Mdm2 degraders and uses thereof
|
TW202210483A
(zh)
|
2020-06-03 |
2022-03-16 |
美商凱麥拉醫療公司 |
Irak降解劑之結晶型
|
EP4161521A4
(de)
|
2020-06-03 |
2024-07-10 |
Kymera Therapeutics, Inc. |
Deuterierte irak-abbauer und verwendungen davon
|
EP4192509A1
(de)
|
2020-08-05 |
2023-06-14 |
Ellipses Pharma Ltd |
Behandlung von krebs mit einem cyclodextrinhaltigen polymer-topoisomerase-inhibitor-konjugat und einem parp-inhibitor
|
IL300450A
(en)
|
2020-08-17 |
2023-04-01 |
Bicycletx Ltd |
Bicyclic conjugates specific to nectin-4 and uses thereof
|
US11999964B2
(en)
|
2020-08-28 |
2024-06-04 |
California Institute Of Technology |
Synthetic mammalian signaling circuits for robust cell population control
|
AU2021392040A1
(en)
|
2020-12-02 |
2023-06-29 |
Ikena Oncology, Inc. |
Tead inhibitors and uses thereof
|
WO2022120353A1
(en)
|
2020-12-02 |
2022-06-09 |
Ikena Oncology, Inc. |
Tead inhibitors and uses thereof
|
CA3201962A1
(en)
|
2020-12-18 |
2022-06-23 |
Andrea TESTA |
Novel bifunctional molecules for targeted protein degradation
|
GB202020359D0
(en)
|
2020-12-22 |
2021-02-03 |
Midatech Pharma Wales Ltd |
Pharmaceutical compositions and use thereof in combination therapy for brain cancer
|
EP4271664A1
(de)
|
2020-12-30 |
2023-11-08 |
Kymera Therapeutics, Inc. |
Irak-abbauer und verwendungen davon
|
MX2023009060A
(es)
|
2021-02-02 |
2023-09-29 |
Liminal Biosciences Ltd |
Antagonistas de gpr84 y usos de estos.
|
KR20230152692A
(ko)
|
2021-02-02 |
2023-11-03 |
리미널 바이오사이언시스 리미티드 |
Gpr84 길항제 및 이의 용도
|
AU2022220043A1
(en)
|
2021-02-15 |
2023-08-31 |
Kymera Therapeutics, Inc. |
Irak4 degraders and uses thereof
|
KR20230172548A
(ko)
|
2021-04-16 |
2023-12-22 |
이케나 온콜로지, 인코포레이티드 |
Mek 억제제 및 이의 용도
|
BR112023023223A2
(pt)
|
2021-05-07 |
2024-01-30 |
Kymera Therapeutics Inc |
Degradadores de cdk2 e usos dos mesmos
|
CN118103368A
(zh)
|
2021-08-25 |
2024-05-28 |
皮克医疗公司 |
Eif4e抑制剂及其用途
|
JP2024532276A
(ja)
|
2021-08-25 |
2024-09-05 |
ピク セラピューティクス, インコーポレイテッド |
eIF4E阻害剤及びその使用
|
EP4405680A1
(de)
|
2021-09-20 |
2024-07-31 |
Institut National de la Santé et de la Recherche Médicale (INSERM) |
Verfahren zur verbesserung der wirksamkeit einer hdac-hemmertherapie und vorhersage der reaktion auf die behandlung mit hdac-hemmer
|
GB2611043A
(en)
|
2021-09-22 |
2023-03-29 |
Univ Dublin City |
A cis-platinum(II)-oligomer hybrid
|
AU2022378630A1
(en)
|
2021-10-29 |
2024-05-09 |
Kymera Therapeutics, Inc. |
Irak4 degraders and synthesis thereof
|
EP4433031A1
(de)
|
2021-11-19 |
2024-09-25 |
Branca Bunus Limited |
Zusammensetzung mit einem in einem arzneimittelabgabevehikel verpackten therapeutischen wirkstoff
|
WO2023114984A1
(en)
|
2021-12-17 |
2023-06-22 |
Ikena Oncology, Inc. |
Tead inhibitors and uses thereof
|
US12091411B2
(en)
|
2022-01-31 |
2024-09-17 |
Kymera Therapeutics, Inc. |
IRAK degraders and uses thereof
|
WO2023173057A1
(en)
|
2022-03-10 |
2023-09-14 |
Ikena Oncology, Inc. |
Mek inhibitors and uses thereof
|
WO2023173053A1
(en)
|
2022-03-10 |
2023-09-14 |
Ikena Oncology, Inc. |
Mek inhibitors and uses thereof
|
EP4504165A1
(de)
|
2022-04-05 |
2025-02-12 |
Istituto Nazionale Tumori IRCCS - Fondazione G. Pascale |
Kombination von hdac-hemmern und statinen zur verwendung bei der behandlung von bauchspeicheldrüsenkrebs
|
WO2023211889A1
(en)
|
2022-04-25 |
2023-11-02 |
Ikena Oncology, Inc. |
Polymorphic compounds and uses thereof
|
GB2617409B
(en)
|
2022-04-27 |
2024-06-26 |
Cancertain Ltd |
Method for predicting responsiveness to therapy
|
WO2023230205A1
(en)
|
2022-05-25 |
2023-11-30 |
Ikena Oncology, Inc. |
Mek inhibitors and uses thereof
|
WO2023242597A1
(en)
|
2022-06-16 |
2023-12-21 |
Amphista Therapeutics Limited |
Bifunctional molecules for targeted protein degradation
|
AU2023317584A1
(en)
|
2022-08-02 |
2025-02-13 |
Luca Science Inc. |
Methods of improving cellular therapy with organelle complexes
|
WO2024028363A1
(en)
|
2022-08-02 |
2024-02-08 |
Liminal Biosciences Limited |
Heteroaryl carboxamide and related gpr84 antagonists and uses thereof
|
TW202415650A
(zh)
|
2022-08-02 |
2024-04-16 |
英商利米那生物科技有限公司 |
芳基-三唑基及相關gpr84拮抗劑及其用途
|
WO2024028365A1
(en)
|
2022-08-02 |
2024-02-08 |
Liminal Biosciences Limited |
Substituted pyridone gpr84 antagonists and uses thereof
|
WO2024041744A1
(en)
|
2022-08-26 |
2024-02-29 |
Biodexa Ltd. |
Combination therapy for brain cancer
|
WO2024112894A1
(en)
|
2022-11-22 |
2024-05-30 |
PIC Therapeutics, Inc. |
Eif4e inhibitors and uses thereof
|
WO2024184266A1
(en)
|
2023-03-03 |
2024-09-12 |
Ionctura Sa |
Combination of roginolisib and hdac inhibitor in the treatment of haematological malignancy
|
WO2025026925A1
(en)
|
2023-07-28 |
2025-02-06 |
Ospedale San Raffaele S.R.L. |
Gtf2i inhibitors and uses thereof
|