|
US5719147A
(en)
*
|
1992-06-29 |
1998-02-17 |
Merck & Co., Inc. |
Morpholine and thiomorpholine tachykinin receptor antagonists
|
|
EP0758329A1
(en)
*
|
1994-05-05 |
1997-02-19 |
MERCK SHARP & DOHME LTD. |
Morpholine derivatives and their use as antagonists of tachikinins
|
|
EP0777659B1
(en)
*
|
1994-08-15 |
2001-06-06 |
MERCK SHARP & DOHME LTD. |
Morpholine derivatives and their use as therapeutic agents
|
|
GB9417956D0
(en)
*
|
1994-09-02 |
1994-10-26 |
Merck Sharp & Dohme |
Therapeutic agents
|
|
GB9426104D0
(en)
*
|
1994-12-23 |
1995-02-22 |
Merck Sharp & Dohme |
Use of surfactants and emulsions
|
|
GB9505491D0
(en)
*
|
1995-03-18 |
1995-05-03 |
Merck Sharp & Dohme |
Therapeutic agents
|
|
GB9513972D0
(en)
*
|
1995-07-08 |
1995-09-06 |
Merck Sharp & Dohme |
Pharmaceutical compositions
|
|
GB9523244D0
(en)
*
|
1995-11-14 |
1996-01-17 |
Merck Sharp & Dohme |
Therapeutic agents
|
|
US5891875A
(en)
*
|
1996-05-20 |
1999-04-06 |
Eli Lilly And Company |
Morpholinyl tachykinin receptor antagonists
|
|
ATE265209T1
(de)
*
|
1996-07-17 |
2004-05-15 |
Merck & Co Inc |
Änderung des zirkadischen rhythmus mit nicht- peptidischen neurokinin-1 rezeptor antagonisten
|
|
US6117855A
(en)
|
1996-10-07 |
2000-09-12 |
Merck Sharp & Dohme Ltd. |
Use of a NK-1 receptor antagonist and an antidepressant and/or an anti-anxiety agent
|
|
US6100256A
(en)
*
|
1996-12-02 |
2000-08-08 |
Merck Sharp & Dohme Ltd. |
Use of NK-1 receptors antagonists for treating schizophrenic disorders
|
|
CA2273809A1
(en)
*
|
1996-12-02 |
1998-06-11 |
Merck Sharp & Dohme Limited |
Use of nk-1 receptor antagonists for treating movement disorders
|
|
DE69732133T2
(de)
*
|
1996-12-02 |
2005-12-22 |
Merck Sharp & Dohme Ltd., Hoddesdon |
Verwendung von NK-1 Rezeptorantagonisten zur Behandlung von schweren Depressionen
|
|
US6613765B1
(en)
|
1996-12-02 |
2003-09-02 |
Merck Sharp & Dohme Limited |
Use of NK-1 receptor antagonists for treating major depressive disorders
|
|
EP0942730A1
(en)
*
|
1996-12-02 |
1999-09-22 |
MERCK SHARP & DOHME LTD. |
Use of nk-1 receptor antagonists for treating bipolar disorders
|
|
DE69733148T2
(de)
*
|
1996-12-02 |
2006-02-02 |
Merck Sharp & Dohme Ltd., Hoddesdon |
Die verwendung von nk-1 rezeptorantagonisten für die behandlung von kognitiven störungen
|
|
AU732633B2
(en)
*
|
1996-12-02 |
2001-04-26 |
Merck Sharp & Dohme Limited |
Use of NK-1 receptor antagonists for treating schizophrenic disorders
|
|
EP0942731B1
(en)
*
|
1996-12-02 |
2004-11-17 |
MERCK SHARP & DOHME LTD. |
Use of nk-1 receptor antagonists for treating substance use disorders
|
|
EP0942729B1
(en)
*
|
1996-12-02 |
2004-09-01 |
MERCK SHARP & DOHME LTD. |
Use of nk-1 receptor antagonists for treating stress disorders
|
|
ATE288756T1
(de)
*
|
1996-12-02 |
2005-02-15 |
Merck Sharp & Dohme |
Verwendung von nk-1 rezeptorantagonisten zur behandlung von schweren depressionen, die von angstzuständen begleitet werden
|
|
EP0942728A1
(en)
*
|
1996-12-02 |
1999-09-22 |
MERCK SHARP & DOHME LTD. |
Use of nk-1 receptor antagonists for treating sexual dysfunction
|
|
US6114315A
(en)
*
|
1996-12-02 |
2000-09-05 |
Merck Sharp & Dohme Ltd. |
Use of NK-1 receptor antagonists for treating major depressive disorders with anxiety
|
|
CA2273785A1
(en)
*
|
1996-12-02 |
1998-06-11 |
Raymond Baker |
Use of nk-1 receptor antagonists for treating severe anxiety disorders
|
|
US5977104A
(en)
*
|
1996-12-02 |
1999-11-02 |
Merck Sharp & Dohme Ltd. |
Use of NK-1 receptor antagonists for treating bipolar disorders
|
|
GB9700555D0
(en)
*
|
1997-01-13 |
1997-03-05 |
Merck Sharp & Dohme |
Therapeutic agents
|
|
JP2001524960A
(ja)
*
|
1997-04-24 |
2001-12-04 |
メルク シヤープ エンド ドーム リミテツド |
摂食障害を治療するためのnk−1受容体拮抗薬の使用
|
|
GB9716463D0
(en)
*
|
1997-08-04 |
1997-10-08 |
Merck Sharp & Dohme |
Therapeutic agents
|
|
CA2298777A1
(en)
*
|
1997-08-04 |
1999-02-18 |
Merck Sharp & Dohme Limited |
Use of nk-1 receptor antagonists for treating mania
|
|
GB9716457D0
(en)
*
|
1997-08-04 |
1997-10-08 |
Merck Sharp & Dohme |
Therapeutic agents
|
|
CA2298779A1
(en)
*
|
1997-08-04 |
1999-02-18 |
Merck Sharp & Dohme Limited |
Use of nk-1 receptor antagonists for treating aggressive behaviour disorders
|
|
US6271230B1
(en)
|
1997-12-01 |
2001-08-07 |
Merck Sharp & Dohme Limited |
Use of NK-1 receptor antagonists for treating cognitive disorders
|
|
US6087348A
(en)
*
|
1997-12-01 |
2000-07-11 |
Merck Sharp & Dohme Ltd. |
Use of NK-1 receptor antagonists for treating stress disorders
|
|
US6156749A
(en)
*
|
1997-12-01 |
2000-12-05 |
Merck Sharp & Dohme Limited |
Use of NK-1 receptor antagonists for treating movement disorders
|
|
US5972938A
(en)
|
1997-12-01 |
1999-10-26 |
Merck & Co., Inc. |
Method for treating or preventing psychoimmunological disorders
|
|
GB9810092D0
(en)
*
|
1998-05-11 |
1998-07-08 |
Merck Sharp & Dohme |
Therapeutic agents
|
|
WO1999064006A1
(en)
*
|
1998-06-11 |
1999-12-16 |
Merck Sharp & Dohme Limited |
Use of a nk-1 receptor antagonist for treating psychiatric disorders
|
|
GB9812617D0
(en)
*
|
1998-06-11 |
1998-08-12 |
Merck Sharp & Dohme |
Therapeutic use
|
|
JP2002517448A
(ja)
*
|
1998-06-11 |
2002-06-18 |
メルク シャープ エンド ドーム リミテッド |
精神障害の治療用nk−1受容体アンタゴニストの使用
|
|
GB9812662D0
(en)
*
|
1998-06-11 |
1998-08-12 |
Merck Sharp & Dohme |
Therapeutic use
|
|
GB9812664D0
(en)
*
|
1998-06-11 |
1998-08-12 |
Merck Sharp & Dohme |
Therapeutic use
|
|
GB9813025D0
(en)
*
|
1998-06-16 |
1998-08-12 |
Merck Sharp & Dohme |
Chemical synthesis
|
|
GB9816897D0
(en)
*
|
1998-08-04 |
1998-09-30 |
Merck Sharp & Dohme |
Therapeutic use
|
|
CA2348526A1
(en)
*
|
1998-10-30 |
2000-05-11 |
Merck & Co., Inc. |
Process for the preparation of 2-(r)-(1- (r)-(3,5-bis (trifluoromethyl) phenyl)ethoxy) -4-((5-dimethylaminomethyl) -1,2,3-triazol -4-yl)methyl) -3-(s)-(4- fluorophenyl) morpholine
|
|
WO2000026214A1
(en)
*
|
1998-10-30 |
2000-05-11 |
Merck & Co., Inc. |
Linear process for the preparation of a morpholine compound
|
|
HUP0200139A3
(en)
|
1999-02-24 |
2003-01-28 |
Hoffmann La Roche |
3-phenylpyridine derivatives and their use as nk-1 receptor antagonists, process for their preparation and pharmaceutical compositions containing them
|
|
PL350427A1
(en)
|
1999-02-24 |
2002-12-16 |
Hoffmann La Roche |
Phenyl− and pyridinyl derivatives as neurokinin 1 antagonists
|
|
ATE277905T1
(de)
|
1999-02-24 |
2004-10-15 |
Hoffmann La Roche |
4-phenylpyridinderivate und deren verwendung als nk-1 rezeptorantagonisten
|
|
US6291465B1
(en)
|
1999-03-09 |
2001-09-18 |
Hoffmann-La Roche Inc. |
Biphenyl derivatives
|
|
JO2308B1
(en)
|
1999-05-31 |
2005-09-12 |
اف. هوفمان- لاروش أيه جي |
Derivatives of phenylpyrmidine
|
|
US6274588B1
(en)
|
1999-05-31 |
2001-08-14 |
Hoffmann-La Roche Inc. |
4-phenyl-pyrimidine derivatives
|
|
EP1228068A1
(en)
|
1999-10-29 |
2002-08-07 |
Merck & Co., Inc. |
Polymorphic form of a tachykinin receptor antagonist
|
|
JP4907818B2
(ja)
|
1999-11-03 |
2012-04-04 |
エーエムアール テクノロジー インコーポレイテッド |
アリールおよびヘテロアリール置換テトラヒドロイソキノリン、ならびにノルエピネフリン、ドーパミンおよびセロトニンの再取り込みを阻止するためのそれらの使用
|
|
US7163949B1
(en)
|
1999-11-03 |
2007-01-16 |
Amr Technology, Inc. |
4-phenyl substituted tetrahydroisoquinolines and use thereof
|
|
PT1103545E
(pt)
*
|
1999-11-29 |
2004-03-31 |
Hoffmann La Roche |
2-(3,5-bis-trifluorometil-fenil)-n-metil-n-(6-morfolin-4-il-4-o-totil-piridin-3-il)-isobutiramida
|
|
US6452001B2
(en)
|
2000-05-25 |
2002-09-17 |
Hoffmann-La Roche Inc. |
Diazapane derivatives useful as antagonists of neurokinin 1 receptor and methods for their formation
|
|
US6482829B2
(en)
|
2000-06-08 |
2002-11-19 |
Hoffmann-La Roche Inc. |
Substituted heterocyclic siprodecane compound active as an antagonist of neurokinin 1 receptor
|
|
AR030284A1
(es)
|
2000-06-08 |
2003-08-20 |
Merck & Co Inc |
Proceso para la sintesis de (2r, 2-alfa-r,3a) -2-[1-(3,5-bis(trifluorometil) fenil) etoxi]-3-(4-fluorofenil)-1,4-oxazina; dicho compuesto y sus formas polimorficas
|
|
WO2001096319A1
(en)
*
|
2000-06-09 |
2001-12-20 |
Merck & Co., Inc. |
Trans-glycosidation process for the synthesis of (2r, 2-alpha-r, 3a)-2-[1-(3,5-bis(trifluoromethyl)phenyl)ethoxy]-3-(4-fluorophenyl)-1,4-oxazine
|
|
CN100430401C
(zh)
|
2000-07-11 |
2008-11-05 |
Amr科技公司 |
新的4-苯基取代的四氢异喹啉类化合物及其治疗用途
|
|
WO2002006236A1
(en)
|
2000-07-14 |
2002-01-24 |
F. Hoffmann-La Roche Ag |
N-oxides as nk1 receptor antagonist prodrugs of 4-phenyl-pyridine derivatives
|
|
TWI287003B
(en)
|
2000-07-24 |
2007-09-21 |
Hoffmann La Roche |
4-phenyl-pyridine derivatives
|
|
TWI259180B
(en)
|
2000-08-08 |
2006-08-01 |
Hoffmann La Roche |
4-Phenyl-pyridine derivatives
|
|
GB0020721D0
(en)
*
|
2000-08-22 |
2000-10-11 |
Merck Sharp & Dohme |
Therapeutic agents
|
|
YU39503A
(sh)
|
2000-11-22 |
2006-05-25 |
F. Hoffmann-La Roche Ag. |
Derivati pirimidina
|
|
US6642226B2
(en)
|
2001-02-06 |
2003-11-04 |
Hoffman-La Roche Inc. |
Substituted phenyl-piperidine methanone compounds
|
|
AU2002354909B2
(en)
*
|
2001-07-16 |
2006-10-05 |
Ortho-Mcneil Pharmaceutical, Inc. |
Carbamate compounds for use in preventing or treating neuropathic pain and cluster and migraine headache-associated pain
|
|
US6849624B2
(en)
|
2001-07-31 |
2005-02-01 |
Hoffmann-La Roche Inc. |
Aromatic and heteroaromatic substituted amides
|
|
US6638981B2
(en)
|
2001-08-17 |
2003-10-28 |
Epicept Corporation |
Topical compositions and methods for treating pain
|
|
AR039625A1
(es)
*
|
2002-04-18 |
2005-03-02 |
Merck & Co Inc |
Proceso para la preparacion de 5-((2(r)--(1(r)- (3,5-bis (trifluormetil) fenil)etoxi-3 (s) - (4-fluorfenil) -4-morfolinil) metil) -1,2-dihidro-3h-1,2,4-triazol-3-ona
|
|
DE602004007486T2
(de)
*
|
2003-01-31 |
2008-04-30 |
F. Hoffmann-La Roche Ag |
Neue kristallmodifikation von 2-(3,5-bis-trifluormethyl-phenyl)-n-6-(1,1-dioxo-1lamda-6-thiomorpholin-4-yl)-4(4-fluor-2-methyl-phenyl)-pyridin-3-yl-n-methyl-isobutyramid
|
|
RU2228752C1
(ru)
*
|
2003-03-21 |
2004-05-20 |
Государственный научный центр - Институт биофизики |
Фармацевтическая композиция, содержащая ондансетрон и бензамид
|
|
CA2530886C
(en)
|
2003-07-03 |
2013-05-28 |
F. Hoffmann-La Roche Ag |
Dual nk1/nk3 antagonists for treating schizophrenia
|
|
TWI280239B
(en)
|
2003-07-15 |
2007-05-01 |
Hoffmann La Roche |
Process for preparation of pyridine derivatives
|
|
ES2246687B2
(es)
|
2004-02-11 |
2006-11-16 |
Miguel Muñoz Saez |
Utilizacion de antagonistas no peptidicos de receptores nk1 para la produccion de apoptosis en celulas tumorales.
|
|
RU2388751C2
(ru)
|
2004-07-15 |
2010-05-10 |
Амр Текнолоджи, Инк. |
Арил- и гетероарилзамещенные тетрагидроизохинолины и их применение для блокирования обратного захвата норэпинефрина, допамина и серотонина
|
|
JP2008525313A
(ja)
|
2004-12-27 |
2008-07-17 |
エーザイ・アール・アンド・ディー・マネジメント株式会社 |
抗痴呆薬の安定化方法
|
|
CA2601935C
(en)
|
2005-02-22 |
2013-04-09 |
F. Hoffmann-La Roche Ag |
Nk1 antagonists
|
|
AU2006226665B2
(en)
|
2005-03-23 |
2011-01-27 |
Helsinn Healthcare S.A. |
Metabolites for NK-I antagonists for emesis
|
|
ES2382814T3
(es)
|
2005-05-17 |
2012-06-13 |
Merck Sharp & Dohme Ltd. |
Ácido cis-4-[(4-clorofenil)sulfonil]-4-(2,5-difluorofenil)ciclohexanopropanoico para el tratamiento del cáncer
|
|
EA019115B1
(ru)
|
2005-07-15 |
2014-01-30 |
Олбани Молекьюлар Рисерч, Инк. |
Арил- и гетероарилзамещенные тетрагидробензазепины и их применение для блокировки обратного захвата норэпинефрина, допамина и серотонина
|
|
AU2006298898B2
(en)
|
2005-09-23 |
2011-06-30 |
F. Hoffmann-La Roche Ag |
Novel dosage formulation
|
|
CN101277960A
(zh)
|
2005-09-29 |
2008-10-01 |
默克公司 |
作为黑皮质素-4受体调节剂的酰化螺哌啶衍生物
|
|
EP2266980A1
(en)
*
|
2005-10-05 |
2010-12-29 |
Ranbaxy Laboratories Limited |
Polymorphic form of aprepitant intermediate
|
|
RU2392277C2
(ru)
*
|
2005-12-28 |
2010-06-20 |
Асино Фарма Аг |
Способ получения рацемического небиволола
|
|
GB0603041D0
(en)
|
2006-02-15 |
2006-03-29 |
Angeletti P Ist Richerche Bio |
Therapeutic compounds
|
|
EP2698157B1
(en)
|
2006-09-22 |
2015-05-20 |
Merck Sharp & Dohme Corp. |
Method of treatment using fatty acid synthesis inhibitors
|
|
US20110218176A1
(en)
|
2006-11-01 |
2011-09-08 |
Barbara Brooke Jennings-Spring |
Compounds, methods, and treatments for abnormal signaling pathways for prenatal and postnatal development
|
|
EP2805945B1
(en)
|
2007-01-10 |
2019-04-03 |
MSD Italia S.r.l. |
Amide substituted indazoles as poly(ADP-ribose)polymerase (PARP) inhibitors
|
|
KR20090112722A
(ko)
|
2007-01-24 |
2009-10-28 |
글락소 그룹 리미티드 |
3,5-디아미노-6-(2,3-디클로로페닐)-1,2,4-트리아진 또는 r(-)-2,4-디아미노-5-(2,3-디클로로페닐)-6-플루오로메틸 피리미딘 및 nk1을 포함하는 제약 조성물
|
|
WO2008120653A1
(ja)
|
2007-04-02 |
2008-10-09 |
Banyu Pharmaceutical Co., Ltd. |
インドールジオン誘導体
|
|
CN101657418B
(zh)
|
2007-04-20 |
2012-05-30 |
弗·哈夫曼-拉罗切有限公司 |
作为nk1/nk3受体双重拮抗剂的吡咯烷衍生物
|
|
US8389553B2
(en)
|
2007-06-27 |
2013-03-05 |
Merck Sharp & Dohme Corp. |
4-carboxybenzylamino derivatives as histone deacetylase inhibitors
|
|
RU2010106974A
(ru)
|
2007-08-07 |
2011-09-20 |
Ф.Хоффманн-Ля Рош Аг (Ch) |
Ариловые эфиры пирролидина в качестве антагонистов рецепторов nk3
|
|
WO2009104080A2
(en)
|
2008-02-20 |
2009-08-27 |
Targia Pharmaceuticals |
Cns pharmaceutical compositions and methods of use
|
|
AU2009222122A1
(en)
|
2008-03-03 |
2009-09-11 |
Tiger Pharmatech |
Tyrosine kinase inhibitors
|
|
US9156812B2
(en)
|
2008-06-04 |
2015-10-13 |
Bristol-Myers Squibb Company |
Crystalline form of 6-[(4S)-2-methyl-4-(2-naphthyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridazin-3-amine
|
|
US8691825B2
(en)
|
2009-04-01 |
2014-04-08 |
Merck Sharp & Dohme Corp. |
Inhibitors of AKT activity
|
|
KR20120034644A
(ko)
|
2009-05-12 |
2012-04-12 |
알바니 몰레큘라 리써치, 인크. |
아릴, 헤테로아릴, 및 헤테로사이클 치환된 테트라하이드로이소퀴놀린 및 이의 용도
|
|
CA2760837C
(en)
|
2009-05-12 |
2018-04-03 |
Albany Molecular Research, Inc. |
7-([1,2,4]triazolo[1,5-.alpha.]pyridin-6-yl)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydroisoquinoline and use thereof
|
|
WO2010132487A1
(en)
|
2009-05-12 |
2010-11-18 |
Bristol-Myers Squibb Company |
CRYSTALLINE FORMS OF (S)-7-([1,2,4]TRIAZOLO[1,5-a]PYRIDIN-6-YL)-4-(3,4-DICHLOROHPHENYL)-1,2,3,4-TETRAHYDROISOQUINOLINE AND USE THEREOF
|
|
BR112012008849A2
(pt)
|
2009-10-14 |
2015-09-22 |
Schering Corp |
composto, composição farmacêutica, e, uso de um composto
|
|
US8487102B2
(en)
|
2010-04-20 |
2013-07-16 |
Hoffmann-La Roche Inc. |
Pyrrazolopyridine compounds as dual NK1/NK3 receptor antagonists
|
|
US8999957B2
(en)
|
2010-06-24 |
2015-04-07 |
Merck Sharp & Dohme Corp. |
Heterocyclic compounds as ERK inhibitors
|
|
US8518907B2
(en)
|
2010-08-02 |
2013-08-27 |
Merck Sharp & Dohme Corp. |
RNA interference mediated inhibition of catenin (cadherin-associated protein), beta 1 (CTNNB1) gene expression using short interfering nucleic acid (siNA)
|
|
ES2376564B1
(es)
|
2010-08-12 |
2013-01-24 |
Manuel Vicente Salinas Martín |
Utilización de anticuerpos contra los receptores nk1, nk2 y/o nk3, para producir apoptosis en las células tumorales y modificar el estroma, la inmunidad y la vascularización intra y peritumorales, como tratamiento del cáncer.
|
|
EP3587574B1
(en)
|
2010-08-17 |
2022-03-16 |
Sirna Therapeutics, Inc. |
Rna interference mediated inhibition of hepatitis b virus (hbv) gene expression using short interfering nucleic acid (sina)
|
|
EP2608669B1
(en)
|
2010-08-23 |
2016-06-22 |
Merck Sharp & Dohme Corp. |
NOVEL PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS
|
|
WO2012030685A2
(en)
|
2010-09-01 |
2012-03-08 |
Schering Corporation |
Indazole derivatives useful as erk inhibitors
|
|
US9242981B2
(en)
|
2010-09-16 |
2016-01-26 |
Merck Sharp & Dohme Corp. |
Fused pyrazole derivatives as novel ERK inhibitors
|
|
ES2663009T3
(es)
|
2010-10-29 |
2018-04-10 |
Sirna Therapeutics, Inc. |
Inhibición de la expresión génica mediada por interferencia por ARN utilizando ácidos nucleicos de interferencia cortos (ANic)
|
|
US9351965B2
(en)
|
2010-12-21 |
2016-05-31 |
Merck Sharp & Dohme Corp. |
Indazole derivatives useful as ERK inhibitors
|
|
EP2699567A1
(en)
|
2011-04-21 |
2014-02-26 |
Merck Sharp & Dohme Corp. |
Insulin-like growth factor-1 receptor inhibitors
|
|
WO2013063214A1
(en)
|
2011-10-27 |
2013-05-02 |
Merck Sharp & Dohme Corp. |
Novel compounds that are erk inhibitors
|
|
WO2013087964A1
(es)
|
2011-12-13 |
2013-06-20 |
Servicio Andaluz De Salud |
Uso de agentes modificadores del ambiente peritumoral para el tratamiento del cáncer
|
|
US20150299696A1
(en)
|
2012-05-02 |
2015-10-22 |
Sirna Therapeutics, Inc. |
SHORT INTERFERING NUCLEIC ACID (siNA) COMPOSITIONS
|
|
BR112015006990A2
(pt)
|
2012-09-28 |
2017-07-04 |
Merck Sharp & Dohme |
composto, composição farmacêutica, e, uso de pelo menos um composto
|
|
PL2925888T3
(pl)
|
2012-11-28 |
2018-03-30 |
Merck Sharp & Dohme Corp. |
Kompozycje i sposoby do stosowania w leczeniu nowotworów
|
|
WO2014100065A1
(en)
|
2012-12-20 |
2014-06-26 |
Merck Sharp & Dohme Corp. |
Substituted imidazopyridines as hdm2 inhibitors
|
|
US9540377B2
(en)
|
2013-01-30 |
2017-01-10 |
Merck Sharp & Dohme Corp. |
2,6,7,8 substituted purines as HDM2 inhibitors
|
|
ES2493693B1
(es)
|
2013-02-11 |
2015-07-07 |
Servicio Andaluz De Salud |
Método para predecir o pronosticar la respuesta de un sujeto humano que padece un cáncer al tratamiento con un antagonista del receptor NK1
|
|
US20160194368A1
(en)
|
2013-09-03 |
2016-07-07 |
Moderna Therapeutics, Inc. |
Circular polynucleotides
|
|
ES2541870B1
(es)
|
2013-12-27 |
2016-05-12 |
Servicio Andaluz De Salud |
Uso de antagonistas no peptídicos de NK1 en una determinada dosis para el tratamiento del cáncer
|
|
WO2015101596A2
(en)
*
|
2013-12-30 |
2015-07-09 |
Oncoprevent Gmbh |
Neurokinin-1 receptor antagonists for use in a method of prevention of cancer
|
|
TW201613888A
(en)
|
2014-09-26 |
2016-04-16 |
Helsinn Healthcare Sa |
Crystalline forms of an NK-1 antagonist
|
|
US10005803B2
(en)
|
2015-10-06 |
2018-06-26 |
Helsinn Healthcare Sa |
Crystalline forms of fosnetupitant
|
|
KR102459416B1
(ko)
|
2016-06-06 |
2022-10-27 |
헬신 헬쓰케어 에스.에이. |
포스네투피탄트의 생리학적으로 균형잡힌 주사가능 제제
|
|
WO2018071283A1
(en)
|
2016-10-12 |
2018-04-19 |
Merck Sharp & Dohme Corp. |
Kdm5 inhibitors
|
|
WO2019094312A1
(en)
|
2017-11-08 |
2019-05-16 |
Merck Sharp & Dohme Corp. |
Prmt5 inhibitors
|
|
EP3706742B1
(en)
|
2017-11-08 |
2023-03-15 |
Merck Sharp & Dohme LLC |
Prmt5 inhibitors
|
|
EP3833668B1
(en)
|
2018-08-07 |
2025-03-19 |
Merck Sharp & Dohme LLC |
Prmt5 inhibitors
|
|
US11981701B2
(en)
|
2018-08-07 |
2024-05-14 |
Merck Sharp & Dohme Llc |
PRMT5 inhibitors
|
|
MX2021001486A
(es)
|
2018-08-07 |
2021-07-15 |
Merck Sharp & Dohme Llc |
Inhibidores prmt5.
|