|
DE2236930A1
(de)
|
1971-08-03 |
1973-02-15 |
Cameroun Etat |
Verfahren zur herstellung von desmosterol
|
|
GB1447456A
(en)
|
1973-06-20 |
1976-08-25 |
Teijin Ltd |
Process for preparing desmosterols
|
|
GB8607294D0
(en)
|
1985-04-17 |
1986-04-30 |
Ici America Inc |
Heterocyclic amide derivatives
|
|
DE3823318A1
(de)
|
1988-07-09 |
1990-02-22 |
Bayer Ag |
(hetero)aryloxynaphthaline mit ueber schwefel gebundenen substituenten
|
|
US5229115A
(en)
|
1990-07-26 |
1993-07-20 |
Immunex Corporation |
Adoptive immunotherapy with interleukin-7
|
|
MX9200161A
(es)
|
1991-01-16 |
1992-07-01 |
Schering Corp |
Uso de interleucina-10 en inmunoterapia adoptiva de cancer
|
|
TW263508B
(enExample)
|
1991-02-12 |
1995-11-21 |
Pfizer |
|
|
US5229109A
(en)
|
1992-04-14 |
1993-07-20 |
Board Of Regents, The University Of Texas System |
Low toxicity interleukin-2 analogues for use in immunotherapy
|
|
JP3414433B2
(ja)
|
1993-03-01 |
2003-06-09 |
日本化薬株式会社 |
電子写真用トナー
|
|
DE19523446A1
(de)
|
1995-06-28 |
1997-01-02 |
Bayer Ag |
Benzotriazole
|
|
AU6490396A
(en)
|
1995-07-14 |
1997-02-18 |
Smithkline Beecham Corporation |
Substituted-pent-4-ynoic acids
|
|
RU2170735C2
(ru)
|
1995-08-10 |
2001-07-20 |
Байер Аг |
Производные галогензамещенного бензимидазола и их кислотно-аддитивные соли, промежуточные соединения и фунгицидное средство
|
|
IL124969A
(en)
|
1995-12-28 |
2002-09-12 |
Fujisawa Pharmaceutical Co |
History of benzimidazole, processes for their preparation and pharmaceutical preparations containing them
|
|
EP2223920A3
(en)
|
1996-06-19 |
2011-09-28 |
Aventis Pharma Limited |
Substituted azabicyclic compounds
|
|
EP0915825B1
(en)
|
1996-06-21 |
2004-05-06 |
Allergan, Inc. |
Substituted tetrahydronaphthalene and dihydronaphthalene derivatives having retinoid and/or retinoid antagonist-like biological activity
|
|
ATE264318T1
(de)
|
1996-11-19 |
2004-04-15 |
Amgen Inc |
Aryl und heteroaryl substituierte kondensierte pyrrole als entzündunghemmende mittel
|
|
US6392010B1
(en)
|
1996-12-19 |
2002-05-21 |
Aventis Pharmaceuticals Inc. |
Process for the solid phase synthesis of aldehyde, ketone, oxime, amine, hydroxamic acid and αβ-unsaturated carboxylic acid and aldehyde compounds
|
|
US6828344B1
(en)
|
1998-02-25 |
2004-12-07 |
Genetics Institute, Llc |
Inhibitors of phospholipase enzymes
|
|
JP4327915B2
(ja)
|
1998-03-30 |
2009-09-09 |
株式会社デ・ウエスタン・セラピテクス研究所 |
スルフォンアミド誘導体
|
|
DE69928414T2
(de)
|
1998-09-18 |
2006-08-03 |
Abbott Gmbh & Co. Kg |
4-aminopyrrolopyrimidine als kinaseinhibitoren
|
|
US6348032B1
(en)
|
1998-11-23 |
2002-02-19 |
Cell Pathways, Inc. |
Method of inhibiting neoplastic cells with benzimidazole derivatives
|
|
AU6762400A
(en)
|
1999-08-12 |
2001-03-13 |
Cor Therapeutics, Inc. |
Inhibitors of factor xa
|
|
HUP0202469A3
(en)
|
1999-08-13 |
2004-06-28 |
Biogen Idec Ma Inc Cambridge |
Cell adhesion inhibitor compound and pharmaceutical composition containing thereof
|
|
AU7315700A
(en)
|
1999-09-20 |
2001-04-24 |
Takeda Chemical Industries Ltd. |
Melanin concentrating hormone antagonist
|
|
WO2002014361A2
(en)
|
2000-08-17 |
2002-02-21 |
Agensys, Inc. |
NUCLEIC ACIDS AND CORRESPONDING PROTEINS ENTITLED 83P2H3 AND CaTrF2E11 USEFUL IN TREATMENT AND DETECTION OF CANCER
|
|
DE60136490D1
(de)
|
2000-11-09 |
2008-12-18 |
Neopharm Inc |
Sn-38-lipidkomplexe und verfahren zu ihrer verwendung
|
|
TWI239942B
(en)
|
2001-06-11 |
2005-09-21 |
Dainippon Pharmaceutical Co |
N-arylphenylacetamide derivative and pharmaceutical composition containing the same
|
|
ATE515495T1
(de)
|
2001-08-03 |
2011-07-15 |
Schering Corp |
Gamma sekretase inhibitoren
|
|
CA2457575C
(en)
|
2001-08-17 |
2010-12-21 |
Sankyo Agro Company, Limited |
3-phenoxy-4-pyridazinol derivatives and herbicidal composition containing the same
|
|
US7563882B2
(en)
|
2002-06-10 |
2009-07-21 |
University Of Rochester |
Polynucleotides encoding antibodies that bind to the C35 polypeptide
|
|
DE10229777A1
(de)
|
2002-07-03 |
2004-01-29 |
Bayer Ag |
Indolin-Phenylsulfonamid-Derivate
|
|
FR2845382A1
(fr)
|
2002-10-02 |
2004-04-09 |
Sanofi Synthelabo |
Derives d'indazolecarboxamides, leur preparation et leur utilisation en therapeutique
|
|
US6894061B2
(en)
*
|
2002-12-04 |
2005-05-17 |
Wyeth |
Substituted dihydrophenanthridinesulfonamides
|
|
UA80171C2
(en)
|
2002-12-19 |
2007-08-27 |
Pfizer Prod Inc |
Pyrrolopyrimidine derivatives
|
|
BR0317572A
(pt)
|
2002-12-20 |
2005-11-22 |
Warner Lambert Co |
Benzoxazinas e seus derivados como inibidores de pi3ks
|
|
JP4601038B2
(ja)
|
2003-03-26 |
2010-12-22 |
第一三共株式会社 |
インドリルマレイミド類
|
|
US20080199486A1
(en)
|
2003-05-12 |
2008-08-21 |
Yair Argon |
Grp94-based compositions and methods of use thereof
|
|
WO2005028434A2
(en)
|
2003-09-18 |
2005-03-31 |
Conforma Therapeutics Corporation |
Novel heterocyclic compounds as hsp90-inhibitors
|
|
AU2004275444A1
(en)
|
2003-09-26 |
2005-04-07 |
Forbes Medi-Tech Inc. |
Method of inhibiting the expression of a multi-drug resistance genes and inhibiting the production of proteins resulting from the expression of such genes thereby enhancing the effectiveness of chemotherapeutic agents to treat cancers
|
|
WO2005033048A2
(en)
|
2003-09-29 |
2005-04-14 |
The Johns Hopkins University |
Wnt pathway antagonists
|
|
US8067608B2
(en)
|
2003-09-29 |
2011-11-29 |
The Johns Hopkins University |
Hedgehog pathway antagonists
|
|
SE0302760D0
(sv)
|
2003-10-20 |
2003-10-20 |
Biovitrum Ab |
New compounds
|
|
US7420059B2
(en)
|
2003-11-20 |
2008-09-02 |
Bristol-Myers Squibb Company |
HMG-CoA reductase inhibitors and method
|
|
DE602004008668T2
(de)
|
2003-12-09 |
2008-06-12 |
F. Hoffmann-La Roche Ag |
Benzoxazinderivate und deren verwendungen
|
|
CA2548326A1
(en)
|
2003-12-23 |
2005-07-14 |
Novartis Ag |
Bicyclic heterocyclic p-38 kinase inhibitors
|
|
WO2005084208A2
(en)
|
2004-02-27 |
2005-09-15 |
New York University |
A novel class of sterol ligands and their uses in regulation of cholesterol and gene expression
|
|
WO2005120558A2
(en)
|
2004-05-25 |
2005-12-22 |
University Of Connecticut Health Center |
Methods for making compositions comprising heat shock proteins or alpha-2-macroglobulin for the treatment of cancer and infectious disease
|
|
US20110104186A1
(en)
|
2004-06-24 |
2011-05-05 |
Nicholas Valiante |
Small molecule immunopotentiators and assays for their detection
|
|
CA2572334A1
(en)
|
2004-07-01 |
2006-01-19 |
New York University |
Compositions and methods for modulation of ror.gamma.t
|
|
FR2874011B1
(fr)
|
2004-08-03 |
2007-06-15 |
Sanofi Synthelabo |
Derives de sulfonamides, leur preparation et leur application en therapeutique
|
|
US20070010537A1
(en)
|
2004-08-20 |
2007-01-11 |
Kazumasa Hamamura |
Fused pyramidine derivative and use thereof
|
|
US7304073B2
(en)
|
2004-08-20 |
2007-12-04 |
Wyeth |
Method of treating myocardial ischemia-reperfusion injury using NF-kB inhibitors
|
|
US7652043B2
(en)
|
2004-09-29 |
2010-01-26 |
The Johns Hopkins University |
WNT pathway antagonists
|
|
PT1809321E
(pt)
|
2004-10-08 |
2012-05-17 |
Us Gov Health & Human Serv |
Imunoterapia adotiva com sobrevivência aumentada de linfócitos
|
|
US20060269973A1
(en)
|
2004-11-24 |
2006-11-30 |
Cassian Yee |
Methods of using IL-21 for adoptive immunotherapy and identification of tumor antigens
|
|
AR051780A1
(es)
|
2004-11-29 |
2007-02-07 |
Japan Tobacco Inc |
Compuestos en anillo fusionados que contienen nitrogeno y utilizacion de los mismos
|
|
GB0514911D0
(en)
|
2005-07-20 |
2005-08-24 |
Univ Birmingham |
T cell memory assay
|
|
US8003624B2
(en)
|
2005-08-25 |
2011-08-23 |
Schering Corporation |
Functionally selective ALPHA2C adrenoreceptor agonists
|
|
CA2620171A1
(en)
|
2005-08-25 |
2007-03-01 |
Schering Corporation |
Imidazole derivatives as functionally selective alpha2c adrenoreceptor agonists
|
|
ATE543813T1
(de)
|
2005-09-01 |
2012-02-15 |
Janssen Pharmaceutica Nv |
Neue benzopyranderivate als kaliumkanalöffner
|
|
BRPI0616246A2
(pt)
|
2005-09-15 |
2011-06-14 |
Hoffmann La Roche |
compostos, processo para a sua manufatura, composiÇÕes farmacÊuticas que os compreendem, mÉtodo para o tratamento terapÊutico e/ou profilÁtico de enfermidades que sço moduladas por inibidores de l-cpt1 e uso dos compostos
|
|
FR2896798A1
(fr)
|
2006-01-27 |
2007-08-03 |
Sanofi Aventis Sa |
Derives de sulfonamides, leur preparation et leur application en therapeutique
|
|
CN101379044B
(zh)
|
2006-02-13 |
2012-04-11 |
霍夫曼-拉罗奇有限公司 |
用于治疗糖尿病的杂双环磺酰胺衍生物
|
|
DK1984357T3
(da)
|
2006-02-17 |
2014-01-13 |
Rigel Pharmaceuticals Inc |
2,4-pyrimidindiaminforbindelser til behandling eller forebyggelse af autoimmunsygdomme
|
|
CA2643337C
(en)
|
2006-03-01 |
2016-01-12 |
Janssen Pharmaceutica N.V. |
Cancer treatment combining lymphodepleting agent with ctls and cytokines
|
|
WO2007113337A1
(en)
|
2006-04-06 |
2007-10-11 |
Tibotec Pharmaceuticals Ltd. |
A homogeneous time resolved fluorescence based test system
|
|
CA2651072A1
(en)
|
2006-05-01 |
2007-11-08 |
Pfizer Products Inc. |
Substituted 2-amino-fused heterocyclic compounds
|
|
US20080305169A1
(en)
|
2006-05-26 |
2008-12-11 |
Japan Tobacco Inc. |
Pharmaceutical Compositions Comprising Nitrogen-Containing Fused Ring Coumpounds
|
|
MX2008015329A
(es)
|
2006-06-01 |
2008-12-12 |
Wyeth Corp |
Derivados 1-sulfonilindazolilamina y -amida como ligandos de 5-hidroxitriptamina-6.
|
|
BRPI0712898A2
(pt)
|
2006-07-03 |
2013-01-08 |
Biovitrum Ab |
indàis como moduladores de 5-ht6
|
|
EP2038301A4
(en)
|
2006-07-12 |
2010-01-20 |
Oncotx Inc |
COMPOSITIONS AND METHODS OF TARGETING CANCER-SPECIFIC TRANSCRIPTION COMPLEXES
|
|
TWI315304B
(en)
|
2006-08-31 |
2009-10-01 |
Univ Taipei Medical |
Indoline-sulfonamides compounds
|
|
US8389739B1
(en)
|
2006-10-05 |
2013-03-05 |
Orphagen Pharmaceuticals |
Modulators of retinoid-related orphan receptor gamma
|
|
US20090275586A1
(en)
|
2006-10-06 |
2009-11-05 |
Kalypsys, Inc. |
Heterocyclic inhibitors of pde4
|
|
WO2008062740A1
(fr)
|
2006-11-20 |
2008-05-29 |
Japan Tobacco Inc. |
Composé azoté à anneaux fusionnés et son utilisation
|
|
US7799933B2
(en)
|
2006-12-21 |
2010-09-21 |
Hoffman-La Roche Inc. |
Sulfonamide derivatives
|
|
US20080186971A1
(en)
|
2007-02-02 |
2008-08-07 |
Tarari, Inc. |
Systems and methods for processing access control lists (acls) in network switches using regular expression matching logic
|
|
WO2008150827A1
(en)
|
2007-05-29 |
2008-12-11 |
Smithkline Beecham Corporation |
Naphthyridine, derivatives as p13 kinase inhibitors
|
|
JP2010529843A
(ja)
|
2007-06-03 |
2010-09-02 |
オンコティーエックス インコーポレイテッド |
バイオマーカーおよび薬物標的としての、転写因子複合体の構成要素のがん関連アイソフォーム
|
|
US7776877B2
(en)
|
2007-06-22 |
2010-08-17 |
Chemocentryx, Inc. |
N-(2-(hetaryl)aryl) arylsulfonamides and N-(2-(hetaryl) hetaryl arylsulfonamides
|
|
WO2009032667A1
(en)
|
2007-08-29 |
2009-03-12 |
Smithkline Beecham Corporation |
Thiazole and oxazole kinase inhibitors
|
|
US7960376B2
(en)
|
2007-09-14 |
2011-06-14 |
Cara Therapeutics, Inc. |
Benzo-fused heterocycles
|
|
US8541185B2
(en)
|
2007-09-24 |
2013-09-24 |
Technion Research & Development Foundation Limited |
Method of predicting responsiveness to autologous adoptive cell transfer therapy
|
|
US20090131523A1
(en)
|
2007-10-15 |
2009-05-21 |
Enzymotec Ltd. |
Lipid compositions for the treatment and prevention of proliferative diseases and for the reduction of incidences of mutagenesis and carinogenesis
|
|
RU2364597C1
(ru)
|
2007-12-14 |
2009-08-20 |
Андрей Александрович Иващенко |
ГЕТЕРОЦИКЛИЧЕСКИЕ ИНГИБИТОРЫ Hh-СИГНАЛЬНОГО КАСКАДА, ЛЕКАРСТВЕННЫЕ КОМПОЗИЦИИ НА ИХ ОСНОВЕ И СПОСОБ ЛЕЧЕНИЯ ЗАБОЛЕВАНИЙ, СВЯЗАННЫХ С АББЕРАНТНОЙ АКТИВНОСТЬЮ Hh СИГНАЛЬНОЙ СИСТЕМЫ
|
|
WO2009120660A2
(en)
|
2008-03-28 |
2009-10-01 |
Cara Therapeutics, Inc. |
Substituted pyridoxazines
|
|
US8163743B2
(en)
|
2008-06-05 |
2012-04-24 |
GlaxoGroupLimited |
4-carboxamide indazole derivatives useful as inhibitors of PI3-kinases
|
|
WO2009147190A1
(en)
|
2008-06-05 |
2009-12-10 |
Glaxo Group Limited |
Novel compounds
|
|
JP5508400B2
(ja)
|
2008-06-05 |
2014-05-28 |
グラクソ グループ リミテッド |
Ｐｉ３キナーゼの阻害剤としてのベンズピラゾール誘導体
|
|
EP2288605B1
(en)
|
2008-06-09 |
2014-06-25 |
Sanofi |
Annelated pyrrolidin sulfonamides with oxadiazolone headgroup, processes for their preparation and their use as pharmaceuticals
|
|
JP2011523664A
(ja)
|
2008-06-09 |
2011-08-18 |
サノフィ−アベンティス |
オキサジアゾロン頭部基を有する、環付加された（ａｎｎｅｌａｔｅｄ）Ｎ−複素環式スルホンアミド、それらの製造方法および医薬としてのそれらの使用
|
|
US20110130384A1
(en)
|
2008-06-25 |
2011-06-02 |
Takeda Pharmaceutical Company Limited |
Amide compound
|
|
CN104844531A
(zh)
|
2008-07-09 |
2015-08-19 |
日产化学工业株式会社 |
异*唑啉取代的苯甲酰胺化合物的制造方法
|
|
WO2010017827A1
(en)
|
2008-08-14 |
2010-02-18 |
European Molecular Biology Laboratory |
6-substituted 1-sulfonyl-2, 3-dihydro-indole derivatives for the treatment of proliferative diseases
|
|
US20110236363A1
(en)
|
2008-09-11 |
2011-09-29 |
Lung-Ji Chang |
System and method for producing t cells
|
|
AU2009300607C1
(en)
|
2008-10-02 |
2014-08-07 |
Taisho Pharmaceutical Co., Ltd. |
7-piperidinoalkyl-3,4-dihydroquinolone derivative
|
|
EP2181710A1
(en)
|
2008-10-28 |
2010-05-05 |
Phenex Pharmaceuticals AG |
Ligands for modulation of orphan receptor-gamma (NR1F3) activity
|
|
WO2010057101A2
(en)
|
2008-11-17 |
2010-05-20 |
Schering Corporation |
Compounds useful as hiv blockers
|
|
WO2010059602A2
(en)
|
2008-11-19 |
2010-05-27 |
Schering Corporation |
Inhibitors of diacylglycerol acyltransferase
|
|
JP6069755B2
(ja)
|
2008-11-24 |
2017-02-01 |
ヘルムホルツ・ツェントルム・ミュンヘン・ドイチェス・フォーシュンクスツェントルム・フュア・ゲズントハイト・ウント・ウンベルト・ゲーエムベーハー |
高親和性ｔ細胞受容体およびその用途
|
|
UA104447C2
(uk)
|
2008-12-19 |
2014-02-10 |
Сіртріз Фармасьютікалз, Інк. |
Тіазолопіридинові сполуки, що модулюють сиртуїн
|
|
TW201030007A
(en)
|
2009-02-06 |
2010-08-16 |
Gruenenthal Gmbh |
Substituted spiro-amides as b1r modulators
|
|
ES2542551T3
(es)
|
2009-03-09 |
2015-08-06 |
Glaxo Group Limited |
4-Oxadiazol-2-il-indazoles como inhibidores de PI3 cinasas
|
|
TW201102391A
(en)
|
2009-03-31 |
2011-01-16 |
Biogen Idec Inc |
Certain substituted pyrimidines, pharmaceutical compositions thereof, and methods for their use
|
|
WO2010123139A1
(ja)
|
2009-04-24 |
2010-10-28 |
持田製薬株式会社 |
スルファモイル基を有するアリールカルボキサミド誘導体
|
|
UY32585A
(es)
|
2009-04-30 |
2010-11-30 |
Glaxo Group Ltd |
Nuevos derivados del indazol utiles como inhibidores de la familia fosfoinositida 3´oh quinasa
|
|
SG10201502330TA
(en)
|
2009-08-03 |
2015-05-28 |
Univ Miami |
Method for in vivo expansion of t regulatory cells
|
|
WO2011019634A2
(en)
|
2009-08-10 |
2011-02-17 |
Taipei Medical University |
Aryl substituted sulfonamide compounds and their use as anticancer agents
|
|
US8383099B2
(en)
|
2009-08-28 |
2013-02-26 |
The United States Of America, As Represented By The Secretary, Department Of Health And Human Services |
Adoptive cell therapy with young T cells
|
|
EP2493888B1
(en)
|
2009-10-29 |
2016-04-06 |
GlaxoSmithKline LLC |
Bicyclic pyridines and analogs as sirtuin modulators
|
|
WO2011067364A1
(en)
|
2009-12-03 |
2011-06-09 |
Glaxo Group Limited |
Novel compounds
|
|
JP2013512879A
(ja)
|
2009-12-03 |
2013-04-18 |
グラクソ グループ リミテッド |
Ｐｉ３キナーゼの阻害剤としてのベンズピラゾール誘導体
|
|
JP2013512880A
(ja)
|
2009-12-03 |
2013-04-18 |
グラクソ グループ リミテッド |
Ｐｉ３−キナーゼ阻害剤としてのインダゾール誘導体
|
|
US8956860B2
(en)
|
2009-12-08 |
2015-02-17 |
Juan F. Vera |
Methods of cell culture for adoptive cell therapy
|
|
US20110142814A1
(en)
|
2009-12-16 |
2011-06-16 |
New York University |
Methods for Using Protein Kinase C-Theta Inhibitors in Adoptive Immunotherapy
|
|
RU2581367C2
(ru)
|
2010-03-01 |
2016-04-20 |
Джи Ти Икс, ИНК. |
Соединения для лечения рака
|
|
DK2542590T4
(da)
|
2010-03-05 |
2020-07-13 |
Univ Johns Hopkins |
Sammensætninger og fremgangsmåde til målrettede immunomodulatoriske antistof-fer og fusionproteiner
|
|
WO2011115892A1
(en)
|
2010-03-15 |
2011-09-22 |
Griffin Patrick R |
Modulators of the retinoic acid receptor-related orphan receptors
|
|
GB201004551D0
(en)
|
2010-03-19 |
2010-05-05 |
Immatics Biotechnologies Gmbh |
NOvel immunotherapy against several tumors including gastrointestinal and gastric cancer
|
|
GB201013443D0
(en)
|
2010-08-11 |
2010-09-22 |
Cytovac As |
Compositions and methods for producing dendritic cells
|
|
PL2614058T3
(pl)
|
2010-09-08 |
2015-12-31 |
Glaxosmithkline Ip Dev Ltd |
Polimorfy i sole n-[5-[4-(5-{[(2r,6s)-2,6-dimetylo-4-morfolinylo]-metylo}-1,3-oksazol-2-ilo)-1h-indazol-6-ilo]-2-(metyloksy)-3-pirydynylo]metanosulfonamidu
|
|
JP5876051B2
(ja)
|
2010-09-08 |
2016-03-02 |
グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドＧｌａｘｏｓｍｉｔｈｋｌｉｎｅ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ Ｄｅｖｅｌｏｐｍｅｎｔ Ｌｉｍｉｔｅｄ |
インフルエンザウィルス感染の治療に使用するためのインダゾール誘導体
|
|
WO2012037108A1
(en)
|
2010-09-13 |
2012-03-22 |
Glaxosmithkline Llc |
Aminoquinoline derivatives as antiviral agents
|
|
JP6063870B2
(ja)
|
2010-11-08 |
2017-01-18 |
ライセラ・コーポレイション |
ＲＯＲγ活性の阻害用のＮ−スルホニル化テトラヒドロキノリンおよび関連二環化合物および病気の治療
|
|
PH12013501201A1
(en)
|
2010-12-09 |
2013-07-29 |
Univ Pennsylvania |
Use of chimeric antigen receptor-modified t cells to treat cancer
|
|
EP2487159A1
(en)
|
2011-02-11 |
2012-08-15 |
MSD Oss B.V. |
RorgammaT inhibitors
|
|
WO2012129394A2
(en)
|
2011-03-22 |
2012-09-27 |
Brigham And Women's Hospital, Inc. |
Methods and compositions for the treatment of cancer
|
|
SG193591A1
(en)
|
2011-03-23 |
2013-10-30 |
Hutchinson Fred Cancer Res |
Method and compositions for cellular immunotherapy
|
|
WO2012127464A2
(en)
|
2011-03-23 |
2012-09-27 |
Gavish-Galilee Bio Applications Ltd |
Constitutively activated t cells for use in adoptive cell therapy
|
|
EP2511263A1
(en)
|
2011-04-14 |
2012-10-17 |
Phenex Pharmaceuticals AG |
Pyrrolo sulfonamide compounds for modulation of orphan nuclear receptor RAR-related orphan receptor-gamma (RORgamma, NR1F3) activity and for the treatment of chronic inflammatory and autoimmune diseases
|
|
US9586928B2
(en)
|
2011-05-16 |
2017-03-07 |
The Scripps Research Institute |
Modulators of the nuclear hormone receptor ROR
|
|
MX367850B
(es)
|
2011-06-24 |
2019-09-09 |
Gri Bio Inc |
Prevención y tratamiento de condiciones inflamatorias.
|
|
BR112014003704A2
(pt)
|
2011-09-19 |
2017-03-07 |
Eth Zuerich |
moduladores ror gama
|
|
GB201116641D0
(en)
|
2011-09-27 |
2011-11-09 |
Glaxo Group Ltd |
Novel compounds
|
|
WO2013074916A1
(en)
|
2011-11-18 |
2013-05-23 |
Board Of Regents, The University Of Texas System |
Car+ t cells genetically modified to eliminate expression of t- cell receptor and/or hla
|
|
RU2627185C1
(ru)
|
2012-03-16 |
2017-08-03 |
Коваген Аг |
Новые связывающие молекулы с противоопухолевой активностью
|
|
JP6236067B2
(ja)
*
|
2012-05-08 |
2017-11-22 |
メルク・シャープ・アンド・ドーム・コーポレーションＭｅｒｃｋ Ｓｈａｒｐ ＆ Ｄｏｈｍｅ Ｃｏｒｐ． |
ＲＯＲγ活性を阻害し疾患を治療するための二環式スルホン化合物
|
|
US9394315B2
(en)
|
2012-05-08 |
2016-07-19 |
Lycera Corporation |
Tetrahydro[1,8]naphthyridine sulfonamide and related compounds for use as agonists of RORγ and the treatment of disease
|
|
AU2013259737A1
(en)
|
2012-05-08 |
2014-10-02 |
Lycera Corporation |
Tetrahydronaphthyridine and related bicyclic compounds for inhibition of RORgamma activity and the treatment of disease
|
|
WO2013167136A1
(en)
|
2012-05-08 |
2013-11-14 |
Herlev Hospital |
Improving adoptive cell therapy with interferon gamma
|
|
WO2013176740A1
(en)
|
2012-05-25 |
2013-11-28 |
Health Diagnostic Laboratory, Inc. |
Rapid and high-throughput analysis of sterols/stanols or derivatives thereof
|
|
WO2014026329A1
(en)
|
2012-08-15 |
2014-02-20 |
Merck Sharp & Dohme Corp. |
N-alkylated indole and indazole compounds as rorgammat inhibitors and uses thereof
|
|
WO2014026327A1
(en)
|
2012-08-15 |
2014-02-20 |
Merck Sharp & Dohme Corp. |
4-heteroaryl substituted benzoic acid compounds as rorgammat inhibitors and uses thereof
|
|
WO2014028669A1
(en)
|
2012-08-15 |
2014-02-20 |
Biogen Idec Ma Inc. |
Novel compounds for modulation of ror-gamma activity
|
|
WO2014026328A1
(en)
|
2012-08-15 |
2014-02-20 |
Merck Sharp & Dohme Corp. |
3-cyclohexenyl substituted indole and indazole compounds as rorgammat inhibitors and uses thereof
|
|
WO2014026330A1
(en)
|
2012-08-15 |
2014-02-20 |
Merck Sharp & Dohme Corp. |
3-AMINOCYCLOALKYL COMPOUNDS AS RORgammaT INHIBITORS AND USES THEREOF
|
|
PL2888283T3
(pl)
|
2012-08-24 |
2019-03-29 |
The Regents Of The University Of California |
Przeciwciała i szczepionki do stosowania w leczeniu nowotworów z ekspresją ROR1 i w hamowaniu przerzutu
|
|
US20150329483A1
(en)
|
2012-12-17 |
2015-11-19 |
INSERM (Institut National de la Santé et de la Recherche Médicale) |
Methods and Pharmaceutical Compositions for the Treatment of X-Linked Charcot-Marie-Tooth
|
|
WO2014201378A1
(en)
|
2013-06-13 |
2014-12-18 |
Massachusetts Institute Of Technology |
Synergistic tumor treatment with extended-pk il -2 and adoptive cell therapy
|
|
WO2015095792A1
(en)
|
2013-12-20 |
2015-06-25 |
Merck Sharp & Dohme Corp. |
Carbamate benzoxaxine propionic acids and acid derivatives for modulation of rorgamma activity and the treatment of disease
|
|
WO2015095788A1
(en)
|
2013-12-20 |
2015-06-25 |
Merck Sharp & Dohme Corp. |
2-ACYLAMIDOMETHYL AND SULFONYLAMIDOMETHYL BENZOXAZINE CARBAMATES FOR INHIBITION OF RORgamma ACTIVITY AND THE TREATMENT OF DISEASE
|
|
WO2015095795A1
(en)
|
2013-12-20 |
2015-06-25 |
Merck Sharp & Dohme Corp. |
TETRAHYDRONAPHTHYRIDINE, BENZOXAZINE, AZA-BENZOXAZINE, AND RELATED BICYCLIC COMPOUNDS FOR INHIBITION OF RORgamma ACTIVITY AND THE TREATMENT OF DISEASE
|
|
US10532088B2
(en)
|
2014-02-27 |
2020-01-14 |
Lycera Corporation |
Adoptive cellular therapy using an agonist of retinoic acid receptor-related orphan receptor gamma and related therapeutic methods
|
|
US10189777B2
(en)
|
2014-05-05 |
2019-01-29 |
Lycera Corporation |
Benzenesulfonamido and related compounds for use as agonists of RORγ and the treatment of disease
|
|
CA2947290A1
(en)
|
2014-05-05 |
2015-11-12 |
Lycera Corporation |
Tetrahydroquinoline sulfonamide and related compounds for use as agonists of rory and the treatment of disease
|
|
EP3292119A4
(en)
|
2015-05-05 |
2018-10-03 |
Lycera Corporation |
DIHYDRO-2H-BENZO[b][1,4]OXAZINE SULFONAMIDE AND RELATED COMPOUNDS FOR USE AS AGONISTS OF RORy AND THE TREATMENT OF DISEASE
|