US4526988A
(en)
*
|
1983-03-10 |
1985-07-02 |
Eli Lilly And Company |
Difluoro antivirals and intermediate therefor
|
ZA859008B
(en)
*
|
1984-12-04 |
1987-07-29 |
Lilly Co Eli |
The treatment of tumors in mammals
|
EP0184365B1
(fr)
*
|
1984-12-04 |
1993-08-04 |
Eli Lilly And Company |
Traitement de tumeurs chez les mammifères
|
US4681873A
(en)
*
|
1985-07-29 |
1987-07-21 |
Warner-Lambert Company |
4-amino-3-halo-2-pyridinone nucleoside and nucleotide compounds
|
CA1295998C
(fr)
*
|
1985-07-29 |
1992-02-18 |
Sai P. Sunkara |
Nucleosides et leur utilisation en tant qu'agents antineoplasiques
|
US4814438A
(en)
*
|
1986-12-24 |
1989-03-21 |
Eli Lilly And Company |
Immunoglobulin conjugates of 2',2'-difluronucleosides
|
US4994558A
(en)
*
|
1986-12-24 |
1991-02-19 |
Eli Lilly And Company |
Immunoglobulin conjugates
|
IL84842A0
(en)
*
|
1986-12-24 |
1988-06-30 |
Lilly Co Eli |
Immunoglobulin conjugates
|
EP0277599A3
(fr)
*
|
1987-01-30 |
1990-05-09 |
Asahi Glass Company Ltd. |
Dérivés de cyclopentane contenant du fluor et procédés pour leur préparation
|
CA1340645C
(fr)
*
|
1987-04-17 |
1999-07-13 |
Victor E. Marquez |
Didesoxynucleosides stables en milieu acide, actifs contre les effets cytopathiques du virus de l'immunoeficience humaine
|
DE3856527T2
(de)
*
|
1987-08-28 |
2002-10-31 |
Eli Lilly And Co., Indianapolis |
Stereoselektives Verfahren zur Herstellung von geschützten 2',2'-difluorlactonen
|
US5223608A
(en)
*
|
1987-08-28 |
1993-06-29 |
Eli Lilly And Company |
Process for and intermediates of 2',2'-difluoronucleosides
|
US4965374A
(en)
*
|
1987-08-28 |
1990-10-23 |
Eli Lilly And Company |
Process for and intermediates of 2',2'-difluoronucleosides
|
US4914028A
(en)
*
|
1988-02-10 |
1990-04-03 |
Eli Lilly And Company |
Method of preparing beta-2',2'-difluoronucleosides
|
US4983724A
(en)
*
|
1988-02-16 |
1991-01-08 |
Eli Lilly And Company |
Inversion of 2,2-difluororibose to a 2,2-difluoroxylose and intermediates therefor
|
IL89258A0
(en)
*
|
1988-02-16 |
1989-09-10 |
Lilly Co Eli |
2',3'-dideoxy-2',2'-difluoro-nucleosides
|
US5644043A
(en)
*
|
1988-02-16 |
1997-07-01 |
Eli Lilly And Company |
2',3'-dideoxy-2',2'-difluoronucleosides and intermediates
|
ATE128141T1
(de)
*
|
1988-03-16 |
1995-10-15 |
Scripps Research Inst |
Als therapeutische mittel verwendbare substituierte adeninderivate.
|
US5057301A
(en)
*
|
1988-04-06 |
1991-10-15 |
Neorx Corporation |
Modified cellular substrates used as linkers for increased cell retention of diagnostic and therapeutic agents
|
JPH0232093A
(ja)
*
|
1988-06-08 |
1990-02-01 |
Merrell Dow Pharmaceut Inc |
抗レトロウィルスジフルオロ化ヌクレオシド類
|
US4987224A
(en)
*
|
1988-08-02 |
1991-01-22 |
University Of Georgia Research Foundation, Inc. |
Method of preparation of 2',3'-dideoxynucleosides
|
US5157114A
(en)
*
|
1988-08-19 |
1992-10-20 |
Burroughs Wellcome Co. |
2',3'-dideoxy-3'-fluoro-5-ethyngluridine
|
US4954623A
(en)
*
|
1989-03-20 |
1990-09-04 |
Eli Lilly And Company |
Recovery of difluoro sugar
|
CA2012129A1
(fr)
*
|
1989-03-20 |
1990-09-20 |
Ramakrishnan Nagarajan |
Recuperation de sucre difluore
|
FI932871A
(fi)
*
|
1992-06-22 |
1993-12-23 |
Lilly Co Eli |
Stereoselektiv anjonglykosylationsprocess
|
US5594124A
(en)
*
|
1992-06-22 |
1997-01-14 |
Eli Lilly And Company |
Stereoselective glycosylation process for preparing 2'-Deoxy-2',2'-difluoropyrimidine nucleosides and 2'-deoxy-2'-fluoropyrimidine nucleosides and intermediates thereof
|
US5401838A
(en)
*
|
1992-06-22 |
1995-03-28 |
Eli Lilly And Company |
Stereoselective fusion glycosylation process for preparing 2'-deoxy-2',2'-difluoronucleosides and 2'-deoxy-2'-fluoronucleosides
|
US5821357A
(en)
*
|
1992-06-22 |
1998-10-13 |
Eli Lilly And Company |
Stereoselective glycosylation process for preparing 2'-deoxy-2',2'-difluoropurine and triazole nucleosides
|
US5606048A
(en)
*
|
1992-06-22 |
1997-02-25 |
Eli Lilly And Company |
Stereoselective glycosylation process for preparing 2'-Deoxy-2', 2'-difluoronucleosides and 2'-deoxy-2'-fluoronucleosides
|
US5371210A
(en)
*
|
1992-06-22 |
1994-12-06 |
Eli Lilly And Company |
Stereoselective fusion glycosylation process for preparing 2'-deoxy-2',2'-difluoronucleosides and 2'-deoxy-2'-fluoronucleosides
|
US5401861A
(en)
*
|
1992-06-22 |
1995-03-28 |
Eli Lilly And Company |
Low temperature process for preparing alpha-anomer enriched 2-deoxy-2,2-difluoro-D-ribofuranosyl sulfonates
|
YU43193A
(sh)
*
|
1992-06-22 |
1997-01-08 |
Eli Lilly And Company |
2'-deoksi-2',2'-difluoro(4-supstituisani)pirimidinski nukleozidi antivirusnog i antikancerogenog dejstva i međuproizvodi
|
US5256798A
(en)
*
|
1992-06-22 |
1993-10-26 |
Eli Lilly And Company |
Process for preparing alpha-anomer enriched 2-deoxy-2,2-difluoro-D-ribofuranosyl sulfonates
|
HU214030B
(en)
*
|
1992-06-22 |
1997-12-29 |
Lilly Co Eli |
Process for preparing alpha-anomer enriched 1-halogen-2-deoxy-2,2-difluoro-d-ribofuranosyl derivatives
|
US5426183A
(en)
*
|
1992-06-22 |
1995-06-20 |
Eli Lilly And Company |
Catalytic stereoselective glycosylation process for preparing 2'-deoxy-2',2'-difluoronucleosides and 2'-deoxy-2'-fluoronucleosides
|
US5252756A
(en)
*
|
1992-06-22 |
1993-10-12 |
Eli Lilly And Company |
Process for preparing beta-anomer enriched 2-deoxy-2,2-difluoro-D-ribofuranosyl-arylsulfonates
|
US5256797A
(en)
|
1992-06-22 |
1993-10-26 |
Eli Lilly And Company |
Process for separating 2-deoxy-2,2-difluoro-D-ribofuranosyl alkylsulfonate anomers
|
US5424416A
(en)
*
|
1993-08-25 |
1995-06-13 |
Eli Lilly And Company |
Process for preparation of 2-deoxy-2,2-difluoro-D-ribofuranosyl-3,5-hydroxy protected-1-alkyl and aryl sulfonates and their use in preparation of 2',2'-difluoro-2'-deoxy nucleosides
|
US5480992A
(en)
*
|
1993-09-16 |
1996-01-02 |
Eli Lilly And Company |
Anomeric fluororibosyl amines
|
US5428176A
(en)
*
|
1994-04-14 |
1995-06-27 |
Eli Lilly And Company |
Process for preparing 2,2-difluoroketene silyl O,S-acetals and α,α-difluoro-β-silyloxy-1,3-dioxolane-4-propanoic acid O,S-esters
|
US5637688A
(en)
|
1994-12-13 |
1997-06-10 |
Eli Lilly And Company |
Process for preparing 1-(2'-deoxy-2'-difluoro-d-ribofuranosyl)-4-aminopyrimidin-2-one hydrochloride
|
US5521294A
(en)
*
|
1995-01-18 |
1996-05-28 |
Eli Lilly And Company |
2,2-difluoro-3-carbamoyl ribose sulfonate compounds and process for the preparation of beta nucleosides
|
US5559222A
(en)
*
|
1995-02-03 |
1996-09-24 |
Eli Lilly And Company |
Preparation of 1-(2'-deoxy-2',2'-difluoro-D-ribo-pentofuranosyl)-cytosine from 2-deoxy-2,2-difluoro-β-D-ribo-pentopyranose
|
US5633367A
(en)
*
|
1995-03-24 |
1997-05-27 |
Eli Lilly And Company |
Process for the preparation of a 2-substituted 3,3-difluorofuran
|
CA2171518A1
(fr)
*
|
1995-03-24 |
1996-09-25 |
Douglas Patton Kjell |
Methode de preparation de 2,2'-anhydro- et 2' -ceto-1-(3',5'-di-o-protege-.beta.-d-arabinofuranosyl)nucleosides
|
US5756775A
(en)
*
|
1995-12-13 |
1998-05-26 |
Eli Lilly And Company |
Process to make α,α-difluoro-β-hydroxyl thiol esters
|
US6001994A
(en)
*
|
1995-12-13 |
1999-12-14 |
Eli Lilly And Company |
Process for making gemcitabine hydrochloride
|
AU1289697A
(en)
|
1995-12-13 |
1997-07-03 |
Eli Lilly And Company |
Alpha, alpha-difluoro-beta-hydroxy thiol esters and their synthesis
|
US5808020A
(en)
*
|
1996-08-12 |
1998-09-15 |
Associated Universities, Inc. |
Optical reaction cell and light source for 18F! fluoride radiotracer synthesis
|
US6013790A
(en)
*
|
1996-09-25 |
2000-01-11 |
Board Of Regents University Of Nebraska-Lincoln |
Heavily fluorinated sugar analogs
|
JP2001518931A
(ja)
*
|
1997-03-24 |
2001-10-16 |
イーライ・リリー・アンド・カンパニー |
ジフルオロヌクレオシドホスホン酸とその誘導体
|
ES2276515T3
(es)
*
|
1998-02-25 |
2007-06-16 |
Emory University |
2'-fluoronucleosidos.
|
TW466112B
(en)
*
|
1998-04-14 |
2001-12-01 |
Lilly Co Eli |
Novel use of 2'-deoxy-2',2'-difluorocytidine for immunosuppressive therapy and pharmaceutical composition comprising the same
|
US6326507B1
(en)
*
|
1998-06-19 |
2001-12-04 |
Trustees Of Dartmouth College |
Therapeutic compounds and methods of use
|
US20030008841A1
(en)
*
|
2000-08-30 |
2003-01-09 |
Rene Devos |
Anti-HCV nucleoside derivatives
|
KR100600550B1
(ko)
*
|
2000-10-20 |
2006-07-13 |
에자이 가부시키가이샤 |
질소 함유 방향환 유도체
|
US7435755B2
(en)
*
|
2000-11-28 |
2008-10-14 |
The Trustees Of Dartmouth College |
CDDO-compounds and combination therapies thereof
|
US8481712B2
(en)
|
2001-01-22 |
2013-07-09 |
Merck Sharp & Dohme Corp. |
Nucleoside derivatives as inhibitors of RNA-dependent RNA viral polymerase
|
WO2003059334A2
(fr)
*
|
2001-10-25 |
2003-07-24 |
Eli Lilly And Company |
Gemcitabine pour traiter la variole
|
CA2472581C
(fr)
*
|
2002-01-15 |
2012-06-26 |
Trustees Of Dartmouth College |
Derives de bis-enone tricyclique et methodes d'utilisation
|
KR20040094692A
(ko)
*
|
2002-02-14 |
2004-11-10 |
파마셋, 리미티드 |
변형된 불소화 뉴클레오사이드 유사체
|
EP1604665B1
(fr)
*
|
2003-03-10 |
2011-05-11 |
Eisai R&D Management Co., Ltd. |
Inhibiteur de kinase c-kit
|
WO2004105747A1
(fr)
*
|
2003-05-20 |
2004-12-09 |
Aronex Pharmaceuticals, Inc |
Chimiotherapie combinee comprenant capecitabine et un complexe a base de platine liposomique
|
AU2003239510A1
(en)
*
|
2003-05-20 |
2005-01-21 |
Aronex Pharmaceuticals, Inc. |
Combination chemotherapy comprising gemcitabine and a liposomal platinum complex
|
WO2005003147A2
(fr)
*
|
2003-05-30 |
2005-01-13 |
Pharmasset, Inc. |
Analogues de nucleosides fluores modifies
|
US20060034943A1
(en)
*
|
2003-10-31 |
2006-02-16 |
Technology Innovations Llc |
Process for treating a biological organism
|
US7683172B2
(en)
*
|
2003-11-11 |
2010-03-23 |
Eisai R&D Management Co., Ltd. |
Urea derivative and process for preparing the same
|
WO2005076888A2
(fr)
|
2004-02-06 |
2005-08-25 |
Threshold Pharmaceuticals, Inc. |
Therapies anticancereuses
|
ATE507240T1
(de)
*
|
2004-03-05 |
2011-05-15 |
Vegenics Pty Ltd |
Materialien und verfahren für wachstumsfaktorbindende konstrukte
|
US20050249667A1
(en)
*
|
2004-03-24 |
2005-11-10 |
Tuszynski Jack A |
Process for treating a biological organism
|
EP2348029A1
(fr)
*
|
2004-07-21 |
2011-07-27 |
Pharmasset, Inc. |
Preparation de pyrimidines et purines 2-desoxy-2-fluoro-d-ribofuranosyl substitues en alkyle et leurs dérives
|
CN101023094B
(zh)
*
|
2004-07-21 |
2011-05-18 |
法莫赛特股份有限公司 |
烷基取代的2-脱氧-2-氟代-d-呋喃核糖基嘧啶和嘌呤及其衍生物的制备
|
KR100578616B1
(ko)
*
|
2004-07-23 |
2006-05-10 |
한미약품 주식회사 |
D-에리트로-2,2-다이플루오로-2-데옥시-1-옥소라이보스화합물의 제조방법
|
BRPI0513783A
(pt)
*
|
2004-07-29 |
2008-05-13 |
Hanmi Pharm Ind Co Ltd |
derivados 1-(alfa)-halo-2, 2-diflúor-2-desóxi-d-ribofuranose e processo para a sua preparação
|
EP1812457A1
(fr)
*
|
2004-07-30 |
2007-08-01 |
Pharmaessentia Corp. |
SYNTHÈSE STÉRÉOSÉLECTIVE DE ß-NUCLÉOSIDES
|
SI3109244T1
(sl)
|
2004-09-14 |
2019-06-28 |
Gilead Pharmasset Llc |
Priprava 2'fluoro-2'-alkil-substituiranih ali drugih neobvezno substituiranih ribofuranozil pirimidinov in purinov in njihovih derivatov
|
WO2006030826A1
(fr)
*
|
2004-09-17 |
2006-03-23 |
Eisai R & D Management Co., Ltd. |
Composition medicamenteuse
|
US20060089328A1
(en)
*
|
2004-10-22 |
2006-04-27 |
Edgar Schridde |
Ready-to-use gemcitabine solutions
|
US7563570B2
(en)
*
|
2004-10-29 |
2009-07-21 |
Pangaea Biotech |
Method of determining a chemotherapeutic regimen for non small cell lung cancer based on BRCA1 expression
|
JP2007522151A
(ja)
*
|
2004-12-08 |
2007-08-09 |
シコール インコーポレイティド |
ジフルオロヌクレオシド及びその調製方法
|
ATE405573T1
(de)
*
|
2004-12-17 |
2008-09-15 |
Lilly Co Eli |
Amid-prodrug von gemcitabin, zusammensetzungen und verwendung damit
|
WO2006077424A1
(fr)
|
2005-01-21 |
2006-07-27 |
Astex Therapeutics Limited |
Composes pharmaceutiques
|
KR20070112774A
(ko)
*
|
2005-03-04 |
2007-11-27 |
다브르 파마 리미티드 |
베타―아노머가 많은21데옥시,21,21-디플루오로-d-리보푸라노실뉴클레오시드의 제조를 위한 중간체 및 제조 방법
|
US7485716B2
(en)
*
|
2005-05-02 |
2009-02-03 |
Pharmaessentia Corp. |
Stereoselective synthesis of β-nucleosides
|
AU2011202539B2
(en)
*
|
2005-06-03 |
2012-07-05 |
Scinopharm Taiwan, Ltd. |
Process of making an alpha-anomer enriched 2-deoxy-2,2-difluoro-d-ribofuranosyl sulfonate and use thereof for making a beta nucleoside
|
NZ563995A
(en)
*
|
2005-06-03 |
2010-01-29 |
Scinopharm Taiwan Ltd |
Process of making an alpha-anomer enriched 2-deoxy-2,2-difluoro-d-ribofuranosyl sulfonate and use thereof for making a beta nucleoside
|
SG164368A1
(en)
|
2005-07-18 |
2010-09-29 |
Bipar Sciences Inc |
Treatment of cancer
|
AT502221A1
(de)
*
|
2005-07-20 |
2007-02-15 |
Pharmacon Forschung & Beratung Gmbh |
Homogemcitabine, verfahren zu ihrer herstellung sowie deren verwendung
|
WO2007015569A1
(fr)
*
|
2005-08-01 |
2007-02-08 |
Eisai R & D Management Co., Ltd. |
Procédé de prédiction de l’efficacité d’un inhibiteur de vascularisation
|
EP1925676A4
(fr)
|
2005-08-02 |
2010-11-10 |
Eisai R&D Man Co Ltd |
Procédé d'analyse de l' effet d 'un inhibiteur de vascularisation
|
WO2007015257A2
(fr)
*
|
2005-08-04 |
2007-02-08 |
Hetero Drugs Limited |
Procede de preparation de gemcitabine utilisant de nouveaux intermediaires
|
CN102716490A
(zh)
*
|
2005-09-01 |
2012-10-10 |
卫材R&D管理有限公司 |
药物组合物的崩解性的改善方法
|
EP1940859A1
(fr)
|
2005-10-28 |
2008-07-09 |
Arch Pharmalabs Limited |
Procede ameliore de preparation de gemcitabine hydrochlorure
|
JPWO2007052849A1
(ja)
|
2005-11-07 |
2009-04-30 |
エーザイ・アール・アンド・ディー・マネジメント株式会社 |
血管新生阻害物質とc−kitキナーゼ阻害物質との併用
|
US20090247576A1
(en)
*
|
2005-11-22 |
2009-10-01 |
Eisai R & D Management Co., Ltd. |
Anti-tumor agent for multiple myeloma
|
JP2009519325A
(ja)
*
|
2005-12-14 |
2009-05-14 |
ドン−エー ファーム.カンパニー リミテッド |
2’、2’−ジフルオロヌクレオシドと中間体の製造プロセス
|
CA2640463A1
(fr)
*
|
2006-02-06 |
2007-10-18 |
Dr. Reddy's Laboratories Ltd. |
Preparation de gemcitabine
|
KR20080099263A
(ko)
*
|
2006-02-07 |
2008-11-12 |
케마지스 리미티드 |
젬시타빈 및 관련된 중간체의 제조 방법
|
US20070249823A1
(en)
*
|
2006-04-20 |
2007-10-25 |
Chemagis Ltd. |
Process for preparing gemcitabine and associated intermediates
|
WO2007136103A1
(fr)
*
|
2006-05-18 |
2007-11-29 |
Eisai R & D Management Co., Ltd. |
Agent antitumoral destiné au cancer de la thyroïde
|
EP2044939A1
(fr)
*
|
2006-06-29 |
2009-04-08 |
Eisai R&D Management Co., Ltd. |
Agent thérapeutique contre la fibrose hépatique
|
US20100160442A1
(en)
*
|
2006-07-18 |
2010-06-24 |
Ossovskaya Valeria S |
Formulations for cancer treatment
|
KR100741310B1
(ko)
*
|
2006-08-01 |
2007-08-01 |
(주) 유일팜테크 |
젬시타빈의 합성에 유용한 신규한나프탈렌-2-카르복실레이트 유도체와 그의 제조방법
|
WO2008026748A1
(fr)
*
|
2006-08-28 |
2008-03-06 |
Eisai R & D Management Co., Ltd. |
Agent antitumoral pour cancer gastrique non différencié
|
WO2008033466A2
(fr)
*
|
2006-09-14 |
2008-03-20 |
Combinatorx (Singapore) Pre. Ltd. |
Compositions et procédés pour le traitement de maladies virales
|
WO2008044045A1
(fr)
|
2006-10-12 |
2008-04-17 |
Astex Therapeutics Limited |
Combinaisons pharmaceutiques
|
US8916552B2
(en)
|
2006-10-12 |
2014-12-23 |
Astex Therapeutics Limited |
Pharmaceutical combinations
|
RU2639543C9
(ru)
|
2006-10-27 |
2018-06-14 |
Дженентек, Инк. |
Антитела и иммуноконъюгаты и их применения
|
CA2670099A1
(fr)
*
|
2006-11-17 |
2008-05-29 |
Trustees Of Dartmouth College |
Synthese et activites biologiques de nouveaux composes tricycliques-bis-enones (tbe)
|
WO2008064132A2
(fr)
*
|
2006-11-17 |
2008-05-29 |
Trustees Of Dartmouth College |
Triterpénoïdes synthétiques et bis-énones tricycliques pour une utilisation dans la stimulation de croissance osseuse et cartilagineuse
|
US8921340B2
(en)
|
2006-11-17 |
2014-12-30 |
Trustees Of Dartmouth College |
Methods for using synthetic triterpenoids in the treatment of bone or cartilage diseases or conditions
|
AU2008205847A1
(en)
|
2007-01-19 |
2008-07-24 |
Eisai R & D Management Co., Ltd. |
Composition for treatment of pancreatic cancer
|
CN101600694A
(zh)
*
|
2007-01-29 |
2009-12-09 |
卫材R&D管理有限公司 |
未分化型胃癌治疗用组合物
|
US7994310B2
(en)
*
|
2007-03-23 |
2011-08-09 |
Dongwoo Syntech Co., Ltd. |
Process for preparing 2′-deoxy-2′, 2′-difluorocytidine
|
US7964580B2
(en)
|
2007-03-30 |
2011-06-21 |
Pharmasset, Inc. |
Nucleoside phosphoramidate prodrugs
|
CN101024667B
(zh)
*
|
2007-03-30 |
2011-01-26 |
湖北益泰药业有限公司 |
盐酸吉西他宾的合成方法
|
US8765690B2
(en)
*
|
2007-04-05 |
2014-07-01 |
Threshold Pharmaceuticals, Inc. |
Treatment of cancer with glufosfamide in patients not receiving insulin therapy
|
US20080262215A1
(en)
*
|
2007-04-23 |
2008-10-23 |
Chemagis Ltd. |
Gemcitabine production process
|
CN100475832C
(zh)
*
|
2007-05-31 |
2009-04-08 |
南京卡文迪许生物工程技术有限公司 |
一种新颖的高立体选择性合成吉西他滨工艺及中间体
|
EP2202297B1
(fr)
*
|
2007-07-18 |
2014-05-14 |
Genelux Corporation |
Utilisation d'un agent chemothérapeutique dans la préparation d'un médicament pour le traitement ou l'amélioration d'effets collatéraux des thérapies avec virus oncolytique
|
US20090048205A1
(en)
*
|
2007-08-15 |
2009-02-19 |
Colin Meyer |
Combination therapy with synthetic triterpenoids and gemcitabine
|
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
|
US20090069354A1
(en)
*
|
2007-09-12 |
2009-03-12 |
Protia, Llc |
Deuterium-enriched gemcitabine
|
WO2009042064A2
(fr)
|
2007-09-21 |
2009-04-02 |
Nektar Therapeutics Al, Corporation |
Conjugués nucléoside phosphate oligomères
|
JP4253357B1
(ja)
|
2007-09-27 |
2009-04-08 |
株式会社湯山製作所 |
手撒き薬剤供給装置、薬剤の手撒き方法、及び、薬剤分包装置
|
JO2778B1
(en)
|
2007-10-16 |
2014-03-15 |
ايساي انك |
Certain vehicles, installations and methods
|
CN101883570B
(zh)
*
|
2007-11-06 |
2013-06-19 |
药华医药股份有限公司 |
β-核苷的新颖合成
|
KR101502267B1
(ko)
|
2007-11-09 |
2015-03-18 |
페레그린 파마수티컬즈, 인크 |
항-vegf 항체 조성물 및 방법
|
CA2704000C
(fr)
|
2007-11-09 |
2016-12-13 |
Eisai R&D Management Co., Ltd. |
Combinaison d'une substance antiangiogenique et d'un complexe de platine antitumoral
|
CN101918003A
(zh)
*
|
2007-11-12 |
2010-12-15 |
彼帕科学公司 |
单独使用parp抑制剂或与抗肿瘤剂组合治疗子宫癌和卵巢癌
|
TW200942231A
(en)
|
2008-01-11 |
2009-10-16 |
Reata Pharmaceuticals Inc |
Synthetic triterpenoids and methods of use in the treatment of disease
|
CA2713930A1
(fr)
*
|
2008-01-29 |
2009-08-06 |
Eisai R & D Management Co., Ltd. |
Utilisation combinee d'un inhibiteur de l'angiogenese et d'un taxane
|
NZ588710A
(en)
|
2008-04-18 |
2012-12-21 |
Reata Pharmaceuticals Inc |
Antioxidant inflammation modulators: oleanolic acid derivatives with amino and other modifications at C-17
|
CN104250280A
(zh)
*
|
2008-04-18 |
2014-12-31 |
里亚塔医药公司 |
抗氧化剂炎症调节剂:c-17同系化齐墩果酸衍生物
|
WO2009129545A1
(fr)
|
2008-04-18 |
2009-10-22 |
Reata Pharmaceuticals, Inc. |
Modulateurs d'inflammation antioxydants: dérivés d'acide oléanolique présentant une saturation dans l'anneau c
|
TW201004627A
(en)
*
|
2008-04-18 |
2010-02-01 |
Reata Pharmaceuticals Inc |
Antioxidant inflammation modulators: novel derivatives of oleanolic acid
|
JP5564490B2
(ja)
|
2008-04-18 |
2014-07-30 |
リアタ ファーマシューティカルズ インコーポレイテッド |
抗炎症性ファルマコアを含む化合物および使用法
|
US8173621B2
(en)
|
2008-06-11 |
2012-05-08 |
Gilead Pharmasset Llc |
Nucleoside cyclicphosphates
|
CA2727813A1
(fr)
*
|
2008-06-12 |
2009-12-17 |
Scinopharm Taiwan, Ltd. |
Polymorphes cristallins de la base gemcitabine
|
JP5758801B2
(ja)
|
2008-07-22 |
2015-08-05 |
トラスティーズ・オブ・ダートマス・カレッジTrustees of Dartmouth College |
単環式シアノエノンおよびその使用方法説明
|
US20110207680A1
(en)
*
|
2008-08-13 |
2011-08-25 |
Curd John G |
Administration of Glufosfamide For The Treatment of Cancer
|
WO2010049947A2
(fr)
*
|
2008-10-28 |
2010-05-06 |
Accrete Pharmaceutical Private Limited |
Préparation de gemcitabine et de ses intermédiaires
|
WO2010075517A2
(fr)
|
2008-12-23 |
2010-07-01 |
Pharmasset, Inc. |
Analogues de nucléoside
|
CL2009002207A1
(es)
|
2008-12-23 |
2011-02-18 |
Gilead Pharmasset Llc |
Compuestos derivados de 3-hidroxi-5-(9h-purin-9-il)tetrahidrofuran-2-il, inhibidor de la replicacion de arn viral dependiente de arn; composicion farmaceutica; uso para el tratamiento de hepatitis c.
|
SG172363A1
(en)
|
2008-12-23 |
2011-07-28 |
Pharmasset Inc |
Synthesis of purine nucleosides
|
US8329666B2
(en)
*
|
2009-04-06 |
2012-12-11 |
Eisai Inc. |
Compositions and methods for treating cancer
|
CA2757743C
(fr)
*
|
2009-04-06 |
2017-10-10 |
Eisai Inc. |
Derives de (2'-desoxy-ribofuranosyl)-1,3,4,7-tetrahydro-(1,3) diazepine-2-0ne pour le traitement du cancer
|
CA2757745C
(fr)
*
|
2009-04-06 |
2018-02-13 |
Eisai Inc. |
Association comprenant des medicaments antineoplasiques a base de cytidine et un inhibiteur de la cytidine desaminase et utilisation de cette association dans le traitement du cancer
|
US8609631B2
(en)
|
2009-04-06 |
2013-12-17 |
Eisai Inc. |
Compositions and methods for treating cancer
|
US20100273730A1
(en)
*
|
2009-04-27 |
2010-10-28 |
Innopharmax, Inc. |
Self-emulsifying pharmaceutical compositions of hydrophilic drugs and preparation thereof
|
GB0907551D0
(en)
|
2009-05-01 |
2009-06-10 |
Univ Dundee |
Treatment or prophylaxis of proliferative conditions
|
TWI583692B
(zh)
|
2009-05-20 |
2017-05-21 |
基利法瑪席特有限責任公司 |
核苷磷醯胺
|
US8618076B2
(en)
|
2009-05-20 |
2013-12-31 |
Gilead Pharmasset Llc |
Nucleoside phosphoramidates
|
EP2459170A2
(fr)
|
2009-07-31 |
2012-06-06 |
Astron Research Limited |
Composition stable pour injection de gemcitabine prête à l'emploi
|
WO2011028638A1
(fr)
|
2009-09-04 |
2011-03-10 |
Schering Corporation |
Modulateurs de points de contrôle du cycle cellulaire et leur utilisation en combinaison avec des inhibiteurs de kinase de point de contrôle
|
EP2536720A1
(fr)
|
2010-02-18 |
2012-12-26 |
Centro Nacional de Investigaciones Oncológicas (CNIO) |
Composés bicycliques destinés à être utilisés en tant qu'inhibiteurs de kinases
|
ES2575160T3
(es)
|
2010-03-15 |
2016-06-24 |
The Board Of Trustees Of The University Of Illinois |
Inhibidores de las interacciones que unen la subunidad alfa de la beta integrina-proteína G
|
US8563530B2
(en)
|
2010-03-31 |
2013-10-22 |
Gilead Pharmassel LLC |
Purine nucleoside phosphoramidate
|
AP3515A
(en)
|
2010-03-31 |
2016-01-11 |
Gilead Pharmasset Llc |
Nucleoside phosphoramidates
|
WO2011143593A1
(fr)
|
2010-05-14 |
2011-11-17 |
Cornerstone Pharmaceuticals, Inc. |
Conjugués de dérivé d'acide lipoïque et d'agent antiprolifératif et leurs utilisations médicales
|
WO2011143590A1
(fr)
|
2010-05-14 |
2011-11-17 |
Cornerstone Pharmaceuticals, Inc. |
Compositions et méthodes de polythérapie utilisant dérivés d'acide lipoïque et agent antiprolifératif
|
MX2012014776A
(es)
|
2010-06-25 |
2013-01-29 |
Eisai R&D Man Co Ltd |
Agente antitumoral que emplea compuestos con efecto inhibidor de cinasas combinados.
|
CN103209987B
(zh)
|
2010-09-22 |
2017-06-06 |
艾丽奥斯生物制药有限公司 |
取代的核苷酸类似物
|
WO2012069972A1
(fr)
|
2010-11-19 |
2012-05-31 |
Piramal Life Sciences Limited |
Combinaison pharmaceutique pour le traitement du cancer du sein
|
JP6069215B2
(ja)
|
2010-11-30 |
2017-02-01 |
ギリアド ファーマセット エルエルシー |
化合物
|
WO2012087943A2
(fr)
|
2010-12-20 |
2012-06-28 |
The Regents Of The University Of Michigan |
Inhibiteurs de l'interaction de liaison entre le récepteur du facteur de croissance épidermique et la protéine de choc thermique 90
|
CN102153602B
(zh)
*
|
2011-02-24 |
2013-11-06 |
中国农业大学 |
呋喃糖基修饰的1,3,4-噻二唑衍生物及其制备方法与作为杀菌剂的应用
|
CN102153601A
(zh)
*
|
2011-02-26 |
2011-08-17 |
湖南欧亚生物有限公司 |
一种高选择性的制备盐酸吉西他滨以及其中间体的方法
|
TW201242597A
(en)
|
2011-03-14 |
2012-11-01 |
Piramal Life Sciences Ltd |
A synergistic pharmaceutical combination for the treatment of pancreatic cancer
|
SG194045A1
(en)
|
2011-04-01 |
2013-11-29 |
Genentech Inc |
Combinations of akt inhibitor compounds and abiraterone, and methods of use
|
US8765933B2
(en)
|
2011-04-07 |
2014-07-01 |
Pharmaessentia Corp. |
Asynthesis of β-nucleosides
|
KR20130138840A
(ko)
|
2011-04-13 |
2013-12-19 |
머크 샤프 앤드 돔 코포레이션 |
2''-치환된 뉴클레오시드 유도체 및 바이러스성 질환의 치료를 위한 그의 사용 방법
|
JP2014511875A
(ja)
|
2011-04-13 |
2014-05-19 |
メルク・シャープ・アンド・ドーム・コーポレーション |
2’−シアノ置換ヌクレオシド誘導体およびウイルス疾患の治療のためのその使用方法
|
EP2697242B1
(fr)
|
2011-04-13 |
2018-10-03 |
Merck Sharp & Dohme Corp. |
Dérivés de nucléosides à substitution 2'-azido et leurs procédés d'utilisation pour le traitement de maladies virales
|
AU2012246490B2
(en)
|
2011-04-18 |
2016-08-04 |
Eisai R&D Management Co., Ltd. |
Therapeutic agent for tumor
|
EP2714937B1
(fr)
|
2011-06-03 |
2018-11-14 |
Eisai R&D Management Co., Ltd. |
Biomarqueurs pour la prédiction et l'estimation de la sensibilité de sujets atteints d'un cancer de la thyroïde et du rein vis-à-vis de composés lenvatinib
|
CN102453064B
(zh)
*
|
2011-06-30 |
2014-07-09 |
江苏豪森药业股份有限公司 |
制备吉西他滨盐酸盐的方法
|
US9408863B2
(en)
|
2011-07-13 |
2016-08-09 |
Merck Sharp & Dohme Corp. |
5′-substituted nucleoside analogs and methods of use thereof for the treatment of viral diseases
|
US9416154B2
(en)
|
2011-07-13 |
2016-08-16 |
Merck Sharp & Dohme Corp. |
5′-substituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases
|
PL2750683T3
(pl)
|
2011-10-03 |
2018-10-31 |
Mx Adjuvac Ab |
Nanocząsteczki, sposób ich otrzymywania i ich zastosowanie jako nośnik dla związków amfipatycznych cząsteczek hydrofobowych w dziedzinach medycyny włączając leczenie raka i związki powiązane z żywnością
|
CN102417533A
(zh)
*
|
2011-10-28 |
2012-04-18 |
江苏正大清江制药有限公司 |
盐酸吉西他滨的合成方法
|
US8889159B2
(en)
|
2011-11-29 |
2014-11-18 |
Gilead Pharmasset Llc |
Compositions and methods for treating hepatitis C virus
|
NO2755614T3
(fr)
|
2012-01-03 |
2018-03-31 |
|
|
WO2013142124A1
(fr)
|
2012-03-21 |
2013-09-26 |
Vertex Pharmaceuticals Incorporated |
Formes solides d'un promédicament nucléotidique thiophosphoramidate
|
US9012427B2
(en)
|
2012-03-22 |
2015-04-21 |
Alios Biopharma, Inc. |
Pharmaceutical combinations comprising a thionucleotide analog
|
JP6042527B2
(ja)
|
2012-04-04 |
2016-12-14 |
ハロザイム インコーポレイテッド |
抗ヒアルロナン剤と腫瘍標的タキサンの組み合わせ治療
|
US8921419B2
(en)
|
2012-05-08 |
2014-12-30 |
Trustees Of Dartmouth College |
Triterpenoids and compositions containing the same
|
AU2013266393B2
(en)
|
2012-05-22 |
2017-09-28 |
Idenix Pharmaceuticals Llc |
D-amino acid compounds for liver disease
|
NZ702244A
(en)
|
2012-06-08 |
2017-06-30 |
Hoffmann La Roche |
Mutant selectivity and combinations of a phosphoinositide 3 kinase inhibitor compound and chemotherapeutic agents for the treatment of cancer
|
WO2014006124A1
(fr)
|
2012-07-04 |
2014-01-09 |
F. Hoffmann-La Roche Ag |
Conjugués anticorps-antigène liés par covalence
|
EP2711008A1
(fr)
|
2012-09-19 |
2014-03-26 |
Institut Univ. de Ciència i Tecnologia, S.A. |
N6,N6-dimethyladenosine destiné à être utilisé dans le traitement ou la prévention du cancer du sein primitif et métastatique
|
EP2711009A1
(fr)
|
2012-09-19 |
2014-03-26 |
Institut Univ. de Ciència i Tecnologia, S.A. |
Composés destinés à être utilisés dans le traitement ou la prévention du cancer primitif et métastatique du sein et de la prostate
|
EP2711007A1
(fr)
|
2012-09-19 |
2014-03-26 |
Institut Univ. de Ciència i Tecnologia, S.A. |
4-Aminopyrazolo[3,4-d]pyrimidine destiné à être utilisé dans le traitement ou la prévention du cancer du sein et de la prostate primitif et métastatique
|
US10513534B2
(en)
|
2012-10-08 |
2019-12-24 |
Idenix Pharmaceuticals Llc |
2′-chloro nucleoside analogs for HCV infection
|
US9757432B2
(en)
|
2012-11-14 |
2017-09-12 |
Ohio State Innovation Foundation |
Materials and methods useful for treating glioblastorna
|
KR20150098605A
(ko)
|
2012-12-21 |
2015-08-28 |
에자이 알앤드디 매니지먼트 가부시키가이샤 |
퀴놀린 유도체의 비정질 형태 및 그의 제조방법
|
WO2014163558A1
(fr)
|
2013-04-01 |
2014-10-09 |
Moreinx Ab |
Nanoparticules, constituées de stérol et de saponine de quillaja saponaria molina, leur procédé de préparation et leur utilisation comme support pour des molécules amphipathiques ou hydrophobes dans le domaine médical, notamment pour le traitement du cancer, et composés alimentaires
|
JP6411379B2
(ja)
|
2013-05-14 |
2018-10-24 |
エーザイ・アール・アンド・ディー・マネジメント株式会社 |
レンバチニブ化合物に対する子宮内膜がん対象の応答性を予測及び評価するためのバイオマーカー
|
JP6476591B2
(ja)
*
|
2013-06-05 |
2019-03-06 |
セントラル硝子株式会社 |
(2R)−2−フルオロ−2−C−メチル−D−リボノ−γ−ラクトン類の製造方法
|
ES2582339T3
(es)
*
|
2013-07-10 |
2016-09-12 |
Asteriapharma Gmbh |
Composiciones que comprenden oligómeros de gemcitabina para su uso en terapia
|
US20160158253A1
(en)
*
|
2013-07-26 |
2016-06-09 |
Threshold Pharmaceuticals, Inc. |
Treatment of pancreatic cancer with a combination of a hypoxia-activated prodrug and a taxane
|
ES2900570T3
(es)
|
2013-08-27 |
2022-03-17 |
Gilead Pharmasset Llc |
Formulación de combinación de dos compuestos antivirales
|
MY176465A
(en)
|
2013-10-29 |
2020-08-11 |
Otsuka Pharma Co Ltd |
Synthetic route to 2?-deoxy-2?,2?-difluorotetrahydrouridines
|
US10080807B2
(en)
|
2014-06-09 |
2018-09-25 |
Lipomedix Pharmaceuticals Ltd. |
Combination chemotherapy comprising a liposomal prodrug of mitomycin C
|
BR112016029935A2
(pt)
|
2014-06-26 |
2017-10-31 |
Hoffmann La Roche |
?anticorpos anti-brdu, complexo, formulação farmacêutica e uso de anticorpo?
|
ES2926687T3
(es)
|
2014-08-28 |
2022-10-27 |
Eisai R&D Man Co Ltd |
Derivado de quinolina muy puro y método para su producción
|
WO2016123143A1
(fr)
|
2015-01-26 |
2016-08-04 |
The University Of Chicago |
Lymphocytes t à récepteur d'antigène chimérique (car) reconnaissant le récepteur il 13rα2 spécifique au cancer
|
US10308719B2
(en)
|
2015-01-26 |
2019-06-04 |
The University Of Chicago |
IL13Rα2 binding agents and use thereof in cancer treatment
|
US20180028662A1
(en)
|
2015-02-25 |
2018-02-01 |
Eisai R&D Management Co., Ltd. |
Method for Suppressing Bitterness of Quinoline Derivative
|
US20180044368A1
(en)
*
|
2015-02-25 |
2018-02-15 |
Ligand Pharmaceuticals, Inc. |
Gemcitabine derivatives
|
CA2978226A1
(fr)
|
2015-03-04 |
2016-09-09 |
Merck Sharpe & Dohme Corp. |
Association d'un antagoniste de pd-1 et d'un inhibiteur des tyrosines kinases vegfr/fgfr/ret pour traiter le cancer
|
CA2988707C
(fr)
|
2015-06-16 |
2023-10-10 |
Eisai R&D Management Co., Ltd. |
Combinaison de proteine se liant au cre/inhibiteur de catenine et d'un inhibiteur de point de controle immunitaire servant au traitement du cancer
|
EP3344642A1
(fr)
*
|
2015-09-02 |
2018-07-11 |
AbbVie Inc. |
Dérivés anti-viraux de tétrahydrofurane
|
WO2017060661A1
(fr)
*
|
2015-10-05 |
2017-04-13 |
Nucana Biomed Limited |
Polythérapie
|
WO2017098252A1
(fr)
|
2015-12-11 |
2017-06-15 |
Nucana Biomed Limited |
Synthèse diastéréosélective de dérivés de phosphate et du promédicament de gemcitabine nuc-1031
|
IL261721B
(en)
|
2016-03-15 |
2022-07-01 |
Oryzon Genomics Sa |
Combinations of lsd1 inhibitors for use in the treatment of solid tumors
|
US11246905B2
(en)
|
2016-08-15 |
2022-02-15 |
President And Fellows Of Harvard College |
Treating infections using IdsD from Proteus mirabilis
|
WO2018094406A1
(fr)
|
2016-11-21 |
2018-05-24 |
Bexion Pharmaceuticals, Inc. |
Traitements combinés comprenant sapc-dops pour le traitement du cancer du pancréas
|
US11034667B2
(en)
|
2017-01-09 |
2021-06-15 |
Shuttle Pharmaceuticals, Inc. |
Selective histone deacetylase inhibitors for the treatment of human disease
|
US11584733B2
(en)
|
2017-01-09 |
2023-02-21 |
Shuttle Pharmaceuticals, Inc. |
Selective histone deacetylase inhibitors for the treatment of human disease
|
JP7247101B2
(ja)
|
2017-04-03 |
2023-03-28 |
エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト |
Steap-1に結合する抗体
|
CN110831605A
(zh)
|
2017-04-26 |
2020-02-21 |
托马斯·I.·卡尔曼 |
多靶标的核苷衍生物
|
CA3071599A1
(fr)
|
2017-08-07 |
2019-02-14 |
Amgen Inc. |
Traitement du cancer du sein triple negatif ou du cancer colorectal comportant des metastases hepatiques par un anticorps anti-pd-l1 et un virus oncolytique
|
EP4435009A2
(fr)
|
2017-09-18 |
2024-09-25 |
The Regents of the University of California |
Anticorps anti-claudine6 et méthodes de traitement du cancer
|
US10435429B2
(en)
|
2017-10-03 |
2019-10-08 |
Nucorion Pharmaceuticals, Inc. |
5-fluorouridine monophosphate cyclic triester compounds
|
CN112004537A
(zh)
|
2018-01-09 |
2020-11-27 |
穿梭药业公司 |
用于治疗人疾病的选择性组蛋白去乙酰化酶抑制剂
|
CA3088287A1
(fr)
|
2018-01-10 |
2019-07-18 |
Nucorion Pharmaceuticals, Inc. |
Composes de phosphore(n)amidatacetal et phosph(on)atalcetal
|
US11427550B2
(en)
|
2018-01-19 |
2022-08-30 |
Nucorion Pharmaceuticals, Inc. |
5-fluorouracil compounds
|
AU2019216531A1
(en)
|
2018-02-02 |
2020-09-24 |
Maverix Oncology, Inc. |
Small molecule drug conjugates of gemcitabine monophosphate
|
TW202002952A
(zh)
|
2018-03-15 |
2020-01-16 |
美商艾伯維有限公司 |
用於治療胰臟癌之abbv-621與抗癌劑之組合
|
WO2019222435A1
(fr)
|
2018-05-16 |
2019-11-21 |
Halozyme, Inc. |
Procédés de sélection de sujets pour une polythérapie anticancéreuse avec un ph20 soluble conjugué à un polymère
|
WO2020044252A1
(fr)
|
2018-08-31 |
2020-03-05 |
Novartis Ag |
Régimes posologiques pour anticorps anti-m-csf et utilisations associées
|
EP3669890A1
(fr)
|
2018-12-18 |
2020-06-24 |
Croda International PLC |
Nanoparticules filamenteuses ayant un effet d'adjuvant de vaccin
|
US20220087975A1
(en)
|
2019-01-11 |
2022-03-24 |
Lipomedix Pharmaceuticals Ltd. |
Liposome composition comprising liposomal prodrug of mitomycin c and method of manufacture
|
CA3134056A1
(fr)
|
2019-03-20 |
2020-09-24 |
The Regents Of The University Of California |
Anticorps de claudin-6 bispecifiques
|
WO2020191342A1
(fr)
|
2019-03-20 |
2020-09-24 |
The Regents Of The University Of California |
Anticorps anti-claudine-6 et conjugués de médicaments
|
BR112021021663A2
(pt)
|
2019-04-30 |
2022-05-17 |
Inst De Medicina Molecular Joao Lobo Antunes |
Inibidores da via rank em combinação com inibidores de cdk
|
US20220305081A1
(en)
|
2019-06-24 |
2022-09-29 |
Amgen Inc. |
Inhibitions of sirp-gamma for cancer treatment
|
US12110311B2
(en)
|
2019-07-17 |
2024-10-08 |
Nucorion Pharmaceuticals, Inc. |
Cyclic deoxyribonucleotide compounds
|
US20230218644A1
(en)
|
2020-04-16 |
2023-07-13 |
Som Innovation Biotech, S.A. |
Compounds for use in the treatment of viral infections by respiratory syndrome-related coronavirus
|
WO2021216427A1
(fr)
|
2020-04-21 |
2021-10-28 |
Ligand Pharmaceuticals, Inc. |
Composés de promédicaments nucléotidiques
|