MA38949A1 - Forme saline d'hydrochlorure pour inhibition d'ezh2 - Google Patents
Forme saline d'hydrochlorure pour inhibition d'ezh2Info
- Publication number
- MA38949A1 MA38949A1 MA38949A MA38949A MA38949A1 MA 38949 A1 MA38949 A1 MA 38949A1 MA 38949 A MA38949 A MA 38949A MA 38949 A MA38949 A MA 38949A MA 38949 A1 MA38949 A1 MA 38949A1
- Authority
- MA
- Morocco
- Prior art keywords
- dgat1
- ezh2
- hydrochloride
- inhibition
- saline form
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
L'invention concerne de nouveaux composés qui sont des inhibiteurs d'acyl-coenzyme a: diacylglycérol transférase 1 (dgat1), des compositions pharmaceutiques les contenant, des procédés pour leur préparation, ainsi que leur utilisation en thérapie, seuls ou en combinaison avec des thérapies de gestion du poids ou autre thérapie de diminution des triglycérides pour la prévention ou le traitement de maladies liées à un dysfonctionnement de dgat1 ou dans lesquelles une modulation de l'activité de dgat1 peut avoir un bénéfice thérapeutique.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361891786P | 2013-10-16 | 2013-10-16 | |
PCT/US2014/060724 WO2015057859A1 (fr) | 2013-10-16 | 2014-10-15 | Forme saline d'hydrochlorure pour inhibition d'ezh2 |
Publications (1)
Publication Number | Publication Date |
---|---|
MA38949A1 true MA38949A1 (fr) | 2017-07-31 |
Family
ID=52828660
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA38949A MA38949A1 (fr) | 2013-10-16 | 2014-10-15 | Forme saline d'hydrochlorure pour inhibition d'ezh2 |
Country Status (24)
Country | Link |
---|---|
US (3) | US10040782B2 (fr) |
EP (2) | EP4324525A3 (fr) |
JP (2) | JP6608812B2 (fr) |
KR (1) | KR102142177B1 (fr) |
CN (1) | CN105829302B (fr) |
AU (2) | AU2014337300B2 (fr) |
CA (1) | CA2925889C (fr) |
CL (1) | CL2016000866A1 (fr) |
DK (1) | DK3057962T3 (fr) |
EA (1) | EA038869B1 (fr) |
ES (1) | ES2960953T3 (fr) |
FI (1) | FI3057962T3 (fr) |
HU (1) | HUE063984T2 (fr) |
IL (1) | IL244787B (fr) |
LT (1) | LT3057962T (fr) |
MA (1) | MA38949A1 (fr) |
MX (1) | MX2016004703A (fr) |
MY (1) | MY179802A (fr) |
PE (1) | PE20161273A1 (fr) |
PL (1) | PL3057962T3 (fr) |
PT (1) | PT3057962T (fr) |
SG (2) | SG11201602269QA (fr) |
SI (1) | SI3057962T1 (fr) |
WO (1) | WO2015057859A1 (fr) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2745016T3 (es) | 2012-04-13 | 2020-02-27 | Epizyme Inc | Bromhidrato de N-((4,6-dimetil-2-oxo-L,2-dihidropiridin-3-il)metil)-5-(etil(tetrahidro-2H-piran-4-il)amino)-4-metil-4'-(morfolinometil)-[L,1'-bifenil]-3-carboxamida para su uso en el tratamiento de un trastorno proliferativo celular del sistema hematológico |
HUE063984T2 (hu) | 2013-10-16 | 2024-02-28 | Epizyme Inc | Hidroklorid só forma az EZH2 gátlásához |
BR112016012713A2 (pt) | 2013-12-06 | 2017-08-08 | Epizyme Inc | Método para tratamento de câncer em um paciente necessitado, e, método de selecionar um paciente para um método de tratamento |
SG10201811128RA (en) | 2014-06-17 | 2019-01-30 | Epizyme Inc | Ezh2 inhibitors for treating lymphoma |
IL289947B2 (en) | 2014-10-16 | 2024-06-01 | Epizyme Inc | A method for treating cancer |
PL3220916T3 (pl) | 2014-11-17 | 2023-08-14 | Epizyme, Inc. | Sposób leczenia raka n-((4,6-dimetylo-2-okso-1,2-dihydropirydyn-3-ylo)metylo)-5-(etylo(tetrahydro-2h-piran-4-ylo)amino)-4-metylo-4'-(morfolinometylo)-[1,1'-bifenylo]-3-karboksyamidem |
SG11201708286PA (en) | 2015-04-20 | 2017-11-29 | Epizyme Inc | Combination therapy for treating cancer |
WO2016201328A1 (fr) | 2015-06-10 | 2016-12-15 | Epizyme, Inc. | Inhibiteurs d'ezh2 pour traiter le lymphome |
WO2017035234A1 (fr) | 2015-08-24 | 2017-03-02 | Epizyme, Inc. | Méthode de traitement du cancer |
AU2017211331A1 (en) | 2016-01-29 | 2018-06-07 | Epizyme, Inc. | Combination therapy for treating cancer |
CA3025933A1 (fr) | 2016-06-01 | 2017-12-07 | Epizyme, Inc. | Utilisation d'inhibiteurs de ezh2 pour le traitement du cancer |
EP3471830A4 (fr) | 2016-06-17 | 2020-02-26 | Epizyme Inc | Inhibiteurs d'ezh2 pour traiter le cancer |
JP7125353B2 (ja) | 2017-01-19 | 2022-08-24 | 第一三共株式会社 | Htlv-1関連脊髄症を治療することに用いるための医薬組成物 |
WO2018183885A1 (fr) | 2017-03-31 | 2018-10-04 | Epizyme, Inc. | Multithérapie pour le traitement du cancer |
JP2020522687A (ja) | 2017-06-02 | 2020-07-30 | エピザイム,インコーポレイティド | 癌を処置するためのezh2阻害剤の使用 |
CA3074720A1 (fr) | 2017-09-05 | 2019-03-14 | Epizyme, Inc. | Polytherapie pour le traitement du cancer |
WO2020011607A1 (fr) | 2018-07-09 | 2020-01-16 | Fondation Asile Des Aveugles | Inhibition de sous-unités de prc2 permettant de traiter des troubles oculaires |
JP2022545467A (ja) | 2019-08-22 | 2022-10-27 | ジュノー セラピューティクス インコーポレイテッド | T細胞療法とzesteホモログ2エンハンサー(EZH2)阻害剤との併用療法および関連方法 |
AU2023262308A1 (en) | 2022-04-27 | 2024-10-03 | Astrazeneca Uk Limited | Combination of antibody-drug conjugate with ezh1 and/or ezh2 inhibitor |
Family Cites Families (63)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0733729A (ja) | 1993-07-26 | 1995-02-03 | Kirin Brewery Co Ltd | N−シアノ−n′−置換−アリールカルボキシイミダミド化合物の製造法 |
HUT74450A (en) | 1993-12-27 | 1996-12-30 | Eisai Co Ltd | Anthranilic acid derivative and pharmaceutical compns. contg. such compds. |
DE19516776A1 (de) | 1995-05-10 | 1996-11-14 | Boehringer Ingelheim Int | Chromatin-Regulatorgene |
US5741819A (en) | 1995-06-07 | 1998-04-21 | 3-Dimensional Pharmaceuticals, Inc. | Arylsulfonylaminobenzene derivatives and the use thereof as factor Xa inhibitors |
JP3906935B2 (ja) | 1995-12-18 | 2007-04-18 | 杏林製薬株式会社 | N−置換ジオキソチアゾリジルベンズアミド誘導体及びその製造法 |
AU6060099A (en) | 1998-09-30 | 2000-04-17 | Procter & Gamble Company, The | 2-substituted ketoamides |
UA71587C2 (uk) | 1998-11-10 | 2004-12-15 | Шерінг Акцієнгезелльшафт | Аміди антранілової кислоти та їхнє застосування як лікарських засобів |
US6710058B2 (en) | 2000-11-06 | 2004-03-23 | Bristol-Myers Squibb Pharma Company | Monocyclic or bicyclic carbocycles and heterocycles as factor Xa inhibitors |
ATE438624T1 (de) | 2000-12-28 | 2009-08-15 | Shionogi & Co | 2-pyridonderivate mit affinität für den cannabinoid-typ-2-rezeptor |
US7700293B2 (en) | 2001-08-02 | 2010-04-20 | The Regents Of The University Of Michigan | Expression profile of prostate cancer |
EP2130820A1 (fr) | 2002-02-19 | 2009-12-09 | Shionogi & Co., Ltd. | Antiprurigineux |
TW200306155A (en) | 2002-03-19 | 2003-11-16 | Du Pont | Benzamides and advantageous compositions thereof for use as fungicides |
US7442685B2 (en) | 2003-06-13 | 2008-10-28 | The University Of North Carolina At Chapel Hill | DOT1 histone methyltransferases as a target for identifying therapeutic agents for leukemia |
EP1765994B1 (fr) | 2004-06-01 | 2009-11-18 | The University of North Carolina at Chapel Hill | Complexe d'histone methyltransferase reconstitue et methodes associees d'identification de modulateurs |
JO2787B1 (en) | 2005-04-27 | 2014-03-15 | امجين إنك, | Alternative amide derivatives and methods of use |
DE602006019423D1 (de) | 2005-06-02 | 2011-02-17 | Univ North Carolina | Reinigung, charakterisierung und wiederherstellung einer ubiquitin-e3-ligase |
FR2889526B1 (fr) | 2005-08-04 | 2012-02-17 | Aventis Pharma Sa | 7-aza-indazoles substitues, compositions les contenant, procede de fabrication et utilisation |
KR101347102B1 (ko) | 2005-10-19 | 2014-01-03 | 그뤼넨탈 게엠베하 | 신규한 바닐로이드 수용체 리간드 및 약제를 제조하기 위한이의 용도 |
AU2006306541B2 (en) | 2005-10-21 | 2011-07-14 | Merck Sharp & Dohme Corp. | Potassium channel inhibitors |
ATE547514T1 (de) | 2005-10-28 | 2012-03-15 | Univ North Carolina | Protein-demethylasen mit einer jmjc-domäne |
WO2007070818A1 (fr) | 2005-12-14 | 2007-06-21 | Bristol-Myers Squibb Company | Heterocycles a six elements utiles en tant qu’inhibiteurs de serine protease |
EP1974055A4 (fr) | 2006-01-20 | 2010-01-27 | Univ North Carolina | Cibles diagnostiques et therapeutiques pour la leucemie |
AU2007333021A1 (en) | 2006-05-15 | 2008-06-19 | Irm Llc | Terephthalamate compounds and compositions, and their use as HIV integrase inhibitors |
WO2007136592A2 (fr) | 2006-05-18 | 2007-11-29 | Amphora Discovery Corporation | Compositions à base de quinolones substituées et leurs utilisations |
EP2086318A4 (fr) | 2006-10-10 | 2009-12-23 | Burnham Inst Medical Research | Compositions neuroprotectrices et procédés correspondants |
US8314087B2 (en) | 2007-02-16 | 2012-11-20 | Amgen Inc. | Nitrogen-containing heterocyclyl ketones and methods of use |
US8338437B2 (en) | 2007-02-28 | 2012-12-25 | Methylgene Inc. | Amines as small molecule inhibitors |
WO2008113006A1 (fr) | 2007-03-14 | 2008-09-18 | Xenon Pharmaceuticals Inc. | Procédés d'utilisation de composés à base de quinolinone dans le traitement des maladies ou des affections associées aux canaux sodiques |
DE102007017884A1 (de) | 2007-04-13 | 2008-10-16 | Grünethal GmbH | Neue Vanilloid-Rezeptor Liganden und ihre Verwendung zur Herstellung von Arzneimitteln |
US20090012031A1 (en) | 2007-07-03 | 2009-01-08 | The Regents Of The University Of Michigan | EZH2 Cancer Markers |
JP2011502148A (ja) | 2007-10-31 | 2011-01-20 | メルク・シャープ・エンド・ドーム・コーポレイション | 疼痛の治療用としてのp2x3受容体アンタゴニスト |
AU2008337286B2 (en) | 2007-12-19 | 2014-08-07 | Cancer Research Technology Limited | Pyrido[2,3-b]pyrazine-8-substituted compounds and their use |
WO2009124137A2 (fr) | 2008-04-01 | 2009-10-08 | Mount Sinai School Of Medicine Of New York University | Procédé de suppression d’une transcription de gène par méthylation d’histone lysine |
US20100113415A1 (en) | 2008-05-29 | 2010-05-06 | Rajapakse Hemaka A | Epha4 rtk inhibitors for treatment of neurological and neurodegenerative disorders and cancer |
CA2730064A1 (fr) | 2008-08-08 | 2010-02-11 | Asim Kumar Debnath | Inhibiteurs a petite molecule d'assemblage et de maturation retroviraux |
FR2934995B1 (fr) | 2008-08-14 | 2010-08-27 | Sanofi Aventis | Composes d'azetidines polysubstitues, leur preparation et leur application en therapeutique |
WO2010111653A2 (fr) | 2009-03-27 | 2010-09-30 | The Uab Research Foundation | Modulation de la traduction à médiation par les séquences ires |
WO2011011366A2 (fr) | 2009-07-20 | 2011-01-27 | Constellation Pharmaceuticals | Agents pour stimuler l'activité d'enzymes de modification par méthyle et procédés d'utilisation de ceux-ci |
US8329149B2 (en) | 2009-12-30 | 2012-12-11 | Avon Products, Inc. | Topical lightening composition and uses thereof |
PT2566327T (pt) | 2010-05-07 | 2017-05-26 | Glaxosmithkline Llc | Indoles |
ES2534804T3 (es) | 2010-05-07 | 2015-04-28 | Glaxosmithkline Llc | Indazoles |
WO2012005805A1 (fr) | 2010-05-07 | 2012-01-12 | Glaxosmithkline Llc | Aza-indazoles |
US9175331B2 (en) | 2010-09-10 | 2015-11-03 | Epizyme, Inc. | Inhibitors of human EZH2, and methods of use thereof |
RU2765155C2 (ru) | 2010-09-10 | 2022-01-26 | Эпизайм, Инк. | Ингибиторы ezh2 человека и способы их применения |
WO2012068589A2 (fr) | 2010-11-19 | 2012-05-24 | Constellation Pharmaceuticals | Modulateurs d'enzymes de modification par méthylation, compositions et utilisations associées |
JP5908493B2 (ja) | 2010-12-01 | 2016-04-26 | グラクソスミスクライン・リミテッド・ライアビリティ・カンパニーGlaxoSmithKline LLC | インドール |
AU2011336272A1 (en) | 2010-12-03 | 2013-06-20 | Epizyme, Inc. | 7-deazapurine modulators of histone methyltransferase, and methods of use thereof |
WO2012118812A2 (fr) | 2011-02-28 | 2012-09-07 | Epizyme, Inc. | Composés hétéroaryles bicycliques substitués condensés en 6,5 |
JO3438B1 (ar) | 2011-04-13 | 2019-10-20 | Epizyme Inc | مركبات بنزين مستبدلة بأريل أو أريل غير متجانس |
TW201733984A (zh) | 2011-04-13 | 2017-10-01 | 雅酶股份有限公司 | 經取代之苯化合物 |
ES2718900T3 (es) | 2012-03-12 | 2019-07-05 | Epizyme Inc | Inhibidores de EZH2 humana y métodos de uso de los mismos |
ES2745016T3 (es) | 2012-04-13 | 2020-02-27 | Epizyme Inc | Bromhidrato de N-((4,6-dimetil-2-oxo-L,2-dihidropiridin-3-il)metil)-5-(etil(tetrahidro-2H-piran-4-il)amino)-4-metil-4'-(morfolinometil)-[L,1'-bifenil]-3-carboxamida para su uso en el tratamiento de un trastorno proliferativo celular del sistema hematológico |
JP6340361B2 (ja) | 2012-04-13 | 2018-06-06 | エピザイム,インコーポレイティド | がんを処置するための組合せ治療 |
WO2013173441A2 (fr) | 2012-05-16 | 2013-11-21 | Glaxosmithkline Llc | Inhibiteurs d'homologue d'activateur de zeste 2 |
PT2908823T (pt) | 2012-10-15 | 2019-11-04 | Epizyme Inc | Métodos para tratamento do cancro |
BR112015008487B1 (pt) | 2012-10-15 | 2022-05-31 | Epizyme, Inc | Compostos de benzeno substituído, composição farmacêutica compreendendo os ditos compostos e uso terapêutico dos mesmos para tratar um distúrbio mediado por ezh2 |
EP2935214B1 (fr) | 2012-12-21 | 2019-02-20 | Epizyme, Inc. | Composés 1,4-pyridones |
WO2014100665A1 (fr) | 2012-12-21 | 2014-06-26 | Epizyme, Inc. | Composés hétéroaryles bicycliques 1,4-pyridone |
CA2903572A1 (fr) | 2013-03-15 | 2014-10-23 | Epizyme, Inc. | Composes de benzene substitues |
US9776996B2 (en) | 2013-03-15 | 2017-10-03 | Epizyme, Inc. | Substituted 6,5-fused bicyclic heteroaryl compounds |
US9624205B2 (en) | 2013-07-19 | 2017-04-18 | Epizyme, Inc. | Substituted 6,5-fused bicyclic heteroaryl compounds |
EP3022184B1 (fr) | 2013-07-19 | 2017-09-27 | Epizyme, Inc. | Composés de benzène substitués |
HUE063984T2 (hu) | 2013-10-16 | 2024-02-28 | Epizyme Inc | Hidroklorid só forma az EZH2 gátlásához |
-
2014
- 2014-10-15 HU HUE14854272A patent/HUE063984T2/hu unknown
- 2014-10-15 EP EP23203529.5A patent/EP4324525A3/fr active Pending
- 2014-10-15 LT LTEPPCT/US2014/060724T patent/LT3057962T/lt unknown
- 2014-10-15 CA CA2925889A patent/CA2925889C/fr active Active
- 2014-10-15 MA MA38949A patent/MA38949A1/fr unknown
- 2014-10-15 MY MYPI2016000542A patent/MY179802A/en unknown
- 2014-10-15 FI FIEP14854272.3T patent/FI3057962T3/fi active
- 2014-10-15 JP JP2016519378A patent/JP6608812B2/ja active Active
- 2014-10-15 US US15/029,848 patent/US10040782B2/en active Active
- 2014-10-15 SI SI201432051T patent/SI3057962T1/sl unknown
- 2014-10-15 CN CN201480056428.6A patent/CN105829302B/zh active Active
- 2014-10-15 MX MX2016004703A patent/MX2016004703A/es active IP Right Grant
- 2014-10-15 PL PL14854272.3T patent/PL3057962T3/pl unknown
- 2014-10-15 KR KR1020167011534A patent/KR102142177B1/ko active IP Right Grant
- 2014-10-15 DK DK14854272.3T patent/DK3057962T3/da active
- 2014-10-15 SG SG11201602269QA patent/SG11201602269QA/en unknown
- 2014-10-15 SG SG10201901977XA patent/SG10201901977XA/en unknown
- 2014-10-15 EA EA201690650A patent/EA038869B1/ru unknown
- 2014-10-15 EP EP14854272.3A patent/EP3057962B1/fr active Active
- 2014-10-15 WO PCT/US2014/060724 patent/WO2015057859A1/fr active Application Filing
- 2014-10-15 PT PT148542723T patent/PT3057962T/pt unknown
- 2014-10-15 PE PE2016000506A patent/PE20161273A1/es unknown
- 2014-10-15 ES ES14854272T patent/ES2960953T3/es active Active
- 2014-10-15 AU AU2014337300A patent/AU2014337300B2/en active Active
-
2016
- 2016-03-28 IL IL244787A patent/IL244787B/en unknown
- 2016-04-13 CL CL2016000866A patent/CL2016000866A1/es unknown
-
2018
- 2018-06-05 US US16/000,539 patent/US10710987B2/en active Active
- 2018-12-11 JP JP2018231817A patent/JP2019052181A/ja active Pending
-
2019
- 2019-04-02 AU AU2019202246A patent/AU2019202246A1/en not_active Abandoned
-
2020
- 2020-06-03 US US16/891,427 patent/US20210017163A1/en active Pending
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MA38949A1 (fr) | Forme saline d'hydrochlorure pour inhibition d'ezh2 | |
MA45985B1 (fr) | Inhibiteurs de diacylglycérol acyltransférase 2 | |
MA38380A1 (fr) | Inhibiteurs quinazoline de l'activation des formes mutantes du récepteur de croissance épidermique (egfr) | |
MA40290A1 (fr) | Agents immunorégulateurs | |
MA39753B1 (fr) | Inhibiteurs de diacylglycérol acyltransférase pour le traitement de troubles métaboliques ou analogues | |
MX2014002459A (es) | Inhibidores de quinurenina-3-monooxigenasa, composiciones farmaceuticas y metodos de uso de los mismos. | |
MA42410A (fr) | Oxystérols et leurs méthodes d'utilisation | |
EA200901166A1 (ru) | Соединения и композиции в качестве модуляторов активности gpr 119 | |
GEP20237541B (en) | Methods for treating and/or preventing graft-versus-host disease and/or diffuse alveolar hemorrhage and/or veno-occlusive disease associated with hematopoietic stem cell transplant | |
TW201613919A (en) | Inhibitors of Bruton's tyrosine kinase | |
MA32393B1 (fr) | Composés et compositions servant d'inhibiteurs de kinases | |
MX2014002460A (es) | Inhibidores de la quinurenina-3-monooxigenasa, sus composiciones farmaceuticas y metodos para uso. | |
EA201490163A1 (ru) | Ингибиторы кинуренин-3-монооксигеназы, фармацевтические композиции и способы их применения | |
MA38810B1 (fr) | Inhibiteurs de rorc2 méthodes d'utilisation associées | |
MA35945B1 (fr) | Inhibiteurs de la bêta-sécrétase | |
MA37763A1 (fr) | Difluoro-hexahydro-cyclopentaoxazinyles et difluoro-hexahydro-benzooxazinyles en tant qu'inhibiteurs de bace1 | |
MA38253A1 (fr) | Compositions comprenant de la vortioxétine et du donépézil | |
MA39447A1 (fr) | (s)-pirlindole ou ses sels pharmaceutiquement acceptables pour une utilisation en médecine | |
MA49839B1 (fr) | Inhibiteurs bicycliques de la histone déacétylase | |
MA39448A1 (fr) | (r)-pirlindole et ses sels pharmaceutiquement acceptables destinés à un usage médical | |
MX2016010892A (es) | Agente para suprimir el progreso de o para mejorar la enfermedad renal cronica. | |
UA109359C2 (xx) | Лікування захворювань і станів шкіри 7-(1h-імідазол-4-ілметил)-5,6,7,8-тетрагідрохіноліном | |
MA38102A1 (fr) | Nouveaux composés utilisés comme inhibiteurs de diacylglycérol acyltransférase | |
PH12015501109A1 (en) | Novel compounds as diacylglycerol acyltransferase inhibitors | |
MA45990B1 (fr) | Combinaison d'agonistes inverses du récepteur de l'histamine-3 avec des inhibiteurs de l'acétylcholinestérase |