US6197786B1
(en)
*
|
1998-09-17 |
2001-03-06 |
Pfizer Inc |
4-Carboxyamino-2-substituted-1,2,3,4-tetrahydroquinolines
|
GT199900147A
(es)
*
|
1998-09-17 |
1999-09-06 |
|
1, 2, 3, 4- tetrahidroquinolinas 2-sustituidas 4-amino sustituidas.
|
US6147089A
(en)
*
|
1998-09-17 |
2000-11-14 |
Pfizer Inc. |
Annulated 4-carboxyamino-2-methyl-1,2,3,4,-tetrahydroquinolines
|
US7115279B2
(en)
*
|
2000-08-03 |
2006-10-03 |
Curatolo William J |
Pharmaceutical compositions of cholesteryl ester transfer protein inhibitors
|
US20060287254A1
(en)
*
|
2001-01-26 |
2006-12-21 |
Schering Corporation |
Use of substituted azetidinone compounds for the treatment of sitosterolemia
|
SE0101161D0
(sv)
*
|
2001-03-30 |
2001-03-30 |
Astrazeneca Ab |
New compounds
|
EP1385501A2
(fr)
*
|
2001-04-11 |
2004-02-04 |
Atherogenics, Inc. |
Procedes d'accroissement des taux de cholesterol hdl du plasma et d'amelioration de la fonctionnalite hdl avec des monoesters de probucol
|
ES2259080T3
(es)
*
|
2001-04-30 |
2006-09-16 |
Pfizer Products Inc. |
Procedimientos e intermedios para preparar inhibidores cetp.
|
CZ20033341A3
(cs)
*
|
2001-06-21 |
2004-10-13 |
Pfizeráproductsáinc |
Samoemulgující se kompozice inhibitorů přenosového proteinu cholesterylesteru
|
EP1269994A3
(fr)
|
2001-06-22 |
2003-02-12 |
Pfizer Products Inc. |
Compositions Pharmaceutiques comprenant un médicament et un polymère permettant d'améliorer la concentration du médicament
|
TNSN03138A1
(fr)
*
|
2001-06-22 |
2005-12-23 |
Pfizer Prod Inc |
Compositions pharmaceutiques d'adsorbats d'un medicament amorphe
|
ATE444060T1
(de)
|
2001-06-22 |
2009-10-15 |
Pfizer Prod Inc |
Pharmazeutische zusammensetzungen enthaltend dispersionen aus arzneistoffen und neutralen polymeren
|
JP2005516941A
(ja)
*
|
2001-12-19 |
2005-06-09 |
アセロジエニクス・インコーポレイテツド |
カルコン誘導体及び疾患を治療するためのそれらの使用
|
WO2003053359A2
(fr)
|
2001-12-19 |
2003-07-03 |
Atherogenics, Inc. |
1,3-bis-(phenyl-substitue)-2-propyne-1-ones et leur utilisation pour le traitement d'affections
|
AU2002351748B2
(en)
*
|
2001-12-21 |
2009-07-09 |
Novo Nordisk A/S |
Amide derivatives as GK activators
|
EP1469833B1
(fr)
*
|
2002-02-01 |
2021-05-19 |
Bend Research, Inc. |
Procede de fabrication de dispersions medicamenteuses amorphes solides homogenes sechees par pulverisation au moyen d'un appareil de sechage par pulverisation modifie
|
DE60322665D1
(de)
*
|
2002-02-01 |
2008-09-18 |
Pfizer Prod Inc |
Pharmazeutische darreichungsform mit gesteuerter freigabe eines cholesterylester-transferproteininhibitors
|
CA2474838C
(fr)
|
2002-02-01 |
2009-01-06 |
Pfizer Products Inc. |
Compositions pharmaceutiques de dispersions amorphes de medicaments et materiaux formant des microphases lipophiles
|
AR038375A1
(es)
|
2002-02-01 |
2005-01-12 |
Pfizer Prod Inc |
Composiciones farmaceuticas de inhibidores de la proteina de transferencia de esteres de colesterilo
|
KR101116627B1
(ko)
*
|
2002-06-27 |
2012-10-09 |
노보 노르디스크 에이/에스 |
치료제로서 아릴 카르보닐 유도체
|
US7071210B2
(en)
*
|
2002-07-02 |
2006-07-04 |
Pfizer Inc. |
CETP inhibitors in combination with antihypertensive agents and uses thereof
|
US20040053842A1
(en)
*
|
2002-07-02 |
2004-03-18 |
Pfizer Inc. |
Methods of treatment with CETP inhibitors and antihypertensive agents
|
US7211672B2
(en)
*
|
2002-10-04 |
2007-05-01 |
Millennium Pharmaceuticals, Inc. |
PGD2 receptor antagonists for the treatment of inflammatory diseases
|
US7504508B2
(en)
|
2002-10-04 |
2009-03-17 |
Millennium Pharmaceuticals, Inc. |
PGD2 receptor antagonists for the treatment of inflammatory diseases
|
US20090181966A1
(en)
*
|
2002-10-04 |
2009-07-16 |
Millennium Pharmaceuticals, Inc. |
PGD2 receptor antagonists for the treatment of inflammatory diseases
|
DE60305724T2
(de)
*
|
2002-10-21 |
2006-11-09 |
Warner-Lambert Co. Llc |
Tetrahydrochinolin-derivate als crth2 antagonisten
|
AU2003289207A1
(en)
*
|
2002-12-06 |
2004-06-30 |
Kyowa Hakko Kogyo Co., Ltd. |
Anti-inflammatory agent
|
AU2003303239A1
(en)
*
|
2002-12-19 |
2004-07-14 |
Atherogenics, Inc. |
Process of making chalcone derivatives
|
US20040132771A1
(en)
*
|
2002-12-20 |
2004-07-08 |
Pfizer Inc |
Compositions of choleseteryl ester transfer protein inhibitors and HMG-CoA reductase inhibitors
|
BR0317521A
(pt)
|
2002-12-20 |
2005-11-16 |
Pfizer Prod Inc |
Formas de dosagem compreendendo um inibidor da cetp e um inibidor da redutase hmg-coa
|
EP1435356A1
(fr)
*
|
2003-01-06 |
2004-07-07 |
Warner-Lambert Company LLC |
Dérivés de la quinoléine en tant qu'antagonistes de CRTH2
|
WO2004072042A2
(fr)
*
|
2003-02-12 |
2004-08-26 |
Carex S.A. |
Modulation de l'activite de recepteurs nucleaires
|
MXPA05009848A
(es)
|
2003-03-17 |
2005-12-06 |
Japan Tobacco Inc |
Composiciones farmaceuticas de inhibidores de la proteina de transferencia del ester de colesterilo.
|
AU2004222436A1
(en)
*
|
2003-03-17 |
2004-09-30 |
Japan Tobacco Inc. |
Method for increasing the oral bioavailability of S-(2-(((1- (2-ethylbutyl) cyclohexyl)carbonyl) amino) phenyl)-2-methylpropanethioate
|
CN1795177A
(zh)
*
|
2003-03-28 |
2006-06-28 |
辉瑞产品公司 |
作为治疗动脉粥样硬化和肥胖症的cetp抑制剂的 1 , 2 , 4 , -取代的1,2,3,4,-四氢-和1,2二氢-喹啉以及1, 2 , 3 , 4-四氢-喹喔啉衍生物
|
US20040204450A1
(en)
*
|
2003-03-28 |
2004-10-14 |
Pfizer Inc |
Quinoline and quinoxaline compounds
|
TWI494102B
(zh)
*
|
2003-05-02 |
2015-08-01 |
Japan Tobacco Inc |
包含s-〔2(〔〔1-(2-乙基丁基)環己基〕羰基〕胺基)苯基〕2-甲基丙烷硫酯及hmg輔酶a還原酶抑制劑之組合
|
US7923467B2
(en)
|
2003-05-30 |
2011-04-12 |
Ranbaxy Laboratories, Inc. |
Substituted pyrrole derivatives and their use as HMG-CO inhibitors
|
CL2004001884A1
(es)
|
2003-08-04 |
2005-06-03 |
Pfizer Prod Inc |
Procedimiento de secado por pulverizacion para la formacion de dispersiones solidas amorfas de un farmaco y polimeros.
|
BRPI0413277A
(pt)
|
2003-08-04 |
2006-10-10 |
Pfizer Prod Inc |
composições farmacêuticas de adsorvatos de medicamentos amorfos e materiais que formam microfases lipofìlicas
|
BRPI0414822A
(pt)
|
2003-09-26 |
2006-11-14 |
Japan Tobacco Inc |
método de inibir a produção de lipoproteìna remanescente
|
WO2005033082A2
(fr)
*
|
2003-09-30 |
2005-04-14 |
Pfizer Products Inc. |
Inhibiteurs de la proteine de transfert d'ester de cholesteryle (cetp) et leurs metabolites
|
EP1670768B1
(fr)
|
2003-10-08 |
2009-09-09 |
Eli Lilly And Company |
Composes et techniques de traitement de la dyslipidemie
|
DE602004020649D1
(de)
*
|
2003-11-07 |
2009-05-28 |
Jj Pharma Inc |
Hdl-verstärkende kombinationstherapie-komplexe
|
JP4834840B2
(ja)
|
2004-01-06 |
2011-12-14 |
ノヴォ ノルディスク アー/エス |
ヘテロアリール尿素およびグルコキナーゼ活性化剤としてのその使用
|
US7932268B2
(en)
|
2004-03-05 |
2011-04-26 |
The Trustees Of The University Of Pennsylvania |
Methods for treating disorders or diseases associated with hyperlipidemia and hypercholesterolemia while minimizing side effects
|
US7262318B2
(en)
*
|
2004-03-10 |
2007-08-28 |
Pfizer, Inc. |
Substituted heteroaryl- and phenylsulfamoyl compounds
|
JP2007530550A
(ja)
|
2004-03-26 |
2007-11-01 |
イーライ リリー アンド カンパニー |
異脂肪血症を治療するための化合物および方法
|
MY139887A
(en)
*
|
2004-04-02 |
2009-11-30 |
Mitsubishi Tanabe Pharma Corp |
Tetrahydronaphthyridine derivatives and a process for preparing the same.
|
UA90269C2
(ru)
|
2004-04-02 |
2010-04-26 |
Мицубиси Танабе Фарма Корпорейшн |
Тетрагидрохинолиновые производные и способ их получения
|
US20050282812A1
(en)
*
|
2004-06-18 |
2005-12-22 |
JONES Zachary |
Inhibitors of cholesteryl ester transfer protein
|
WO2006012093A1
(fr)
*
|
2004-06-24 |
2006-02-02 |
Eli Lilly And Company |
Composés et procédés destinés à traiter la dyslipidémie
|
KR100859223B1
(ko)
*
|
2004-06-24 |
2008-09-18 |
일라이 릴리 앤드 캄파니 |
이상지혈증 치료를 위한 화합물 및 방법
|
WO2006004903A2
(fr)
*
|
2004-06-28 |
2006-01-12 |
Atherogenics, Inc. |
1,2-bis-(phenyl-substitue)-2-propen-1-ones et des compositions pharmaceutiques en contenant
|
US20050288340A1
(en)
*
|
2004-06-29 |
2005-12-29 |
Pfizer Inc |
Substituted heteroaryl- and phenylsulfamoyl compounds
|
DOP2005000123A
(es)
|
2004-07-02 |
2011-07-15 |
Merck Sharp & Dohme |
Inhibidores de cetp
|
WO2006026469A2
(fr)
|
2004-08-25 |
2006-03-09 |
Essentialis, Inc. |
Formulations pharmaceutiques d'activateurs de canaux potassiques atp, et utilisations correspondantes
|
US20060063803A1
(en)
*
|
2004-09-23 |
2006-03-23 |
Pfizer Inc |
4-Amino substituted-2-substituted-1,2,3,4-tetrahydroquinoline compounds
|
WO2006033004A1
(fr)
*
|
2004-09-23 |
2006-03-30 |
Pfizer Products Inc. |
Composes de quinoline en tant qu'inhibiteurs de cetp
|
ES2328384T3
(es)
*
|
2004-11-23 |
2009-11-12 |
Warner-Lambert Company Llc |
Derivados del acido 7-(2h-pirazol-3-il)-3,5-dihidroxi-heptanoico como inhibidores de hmg co-a reductasa para el tratamiento de la lipidemia.
|
WO2006069162A1
(fr)
*
|
2004-12-20 |
2006-06-29 |
Reddy Us Therapeutics, Inc. |
Nouveaux composes heterocycliques et leurs compositions pharmaceutiques
|
US8604055B2
(en)
|
2004-12-31 |
2013-12-10 |
Dr. Reddy's Laboratories Ltd. |
Substituted benzylamino quinolines as cholesterol ester-transfer protein inhibitors
|
DK1848430T3
(da)
|
2004-12-31 |
2017-11-06 |
Dr Reddys Laboratories Ltd |
Nye benzylamin-derivativer som cetp-inhibitors
|
EP1844078B1
(fr)
|
2005-02-03 |
2016-09-28 |
Bend Research, Inc |
Compositions pharmaceutiques a efficacite amelioree
|
AU2006216713A1
(en)
|
2005-02-24 |
2006-08-31 |
Millennium Pharmaceuticals, Inc. |
PGD2 receptor antagonists for the treatment of inflammatory diseases
|
WO2006098394A1
(fr)
*
|
2005-03-14 |
2006-09-21 |
Japan Tobacco Inc. |
Méthode pour inhiber l’absorption de lipides et l’inhibiteur de l'absorption de lipides
|
EP2985022B1
(fr)
*
|
2005-07-01 |
2018-09-12 |
Merck Sharp & Dohme Corp. |
Procédé de synthèse d'un inhibiteur de cetp
|
WO2007006761A1
(fr)
*
|
2005-07-08 |
2007-01-18 |
Novo Nordisk A/S |
Dicycloalkylcarbamoylurées en tant qu’activateurs de glucokinase
|
EP1904466A1
(fr)
*
|
2005-07-08 |
2008-04-02 |
Novo Nordisk A/S |
Activateurs de dicycloalkylurée glucokinase
|
CN101263131B
(zh)
*
|
2005-07-14 |
2013-04-24 |
特兰斯特克药品公司 |
脲葡糖激酶活化剂
|
GT200600381A
(es)
|
2005-08-25 |
2007-03-28 |
|
Compuestos organicos
|
JP4681526B2
(ja)
*
|
2005-09-29 |
2011-05-11 |
田辺三菱製薬株式会社 |
医薬組成物
|
JP4531027B2
(ja)
*
|
2005-09-29 |
2010-08-25 |
田辺三菱製薬株式会社 |
医薬組成物
|
WO2007048027A2
(fr)
|
2005-10-21 |
2007-04-26 |
Novartis Ag |
Combinaison de composes organiques
|
WO2007054896A1
(fr)
|
2005-11-08 |
2007-05-18 |
Ranbaxy Laboratories Limited |
Procede de preparation de sel hemicalcique d’acide (3r,5r)-7-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-[(4-hydroxymethylphenylamino)carbonyl]-pyrrol-1-yl]-3,5-dihydroxy-heptanoique
|
US7888376B2
(en)
|
2005-11-23 |
2011-02-15 |
Bristol-Myers Squibb Company |
Heterocyclic CETP inhibitors
|
EP3545958A1
(fr)
|
2006-01-05 |
2019-10-02 |
Essentialis, Inc. |
Sels d'ouverture de canal atp du potassium et leurs utilisations
|
UY30117A1
(es)
|
2006-01-31 |
2007-06-29 |
Tanabe Seiyaku Co |
Compuesto amina trisustituido
|
PE20071025A1
(es)
|
2006-01-31 |
2007-10-17 |
Mitsubishi Tanabe Pharma Corp |
Compuesto amina trisustituido
|
UY30244A1
(es)
|
2006-03-30 |
2007-11-30 |
Tanabe Seiyaku Co |
Un proceso para preparar derivados de tetrahidroquinolina
|
GB0615670D0
(en)
*
|
2006-08-07 |
2006-09-13 |
Syngenta Participations Ag |
Chemical compounds
|
US7750019B2
(en)
|
2006-08-11 |
2010-07-06 |
Kowa Company, Ltd. |
Pyrimidine compound having benzyl(pyridylmethyl)amine structure and medicament comprising the same
|
AR063275A1
(es)
*
|
2006-10-12 |
2009-01-14 |
Epix Delaware Inc |
Compuestos de carboxamida, una composicion farmaceutica que los comprende y su uso en la preparacion de un medicamento para el tratamiento de enfermedades mediadas por la activacion de ccr2.
|
ES2382009T3
(es)
|
2006-12-01 |
2012-06-04 |
Bristol-Myers Squibb Company |
Derivados de N-((3-bencil)-2,2-(bis-fenil-)-propan-1-amina como inhibidores de CETP para el tratamiento de aterosclerosis y enfermedades cardiovasculares
|
WO2008079398A1
(fr)
*
|
2006-12-21 |
2008-07-03 |
Aegerion Pharmaceuticals, Inc. |
Procédés de traitement de l'obésité à l'aide d'une combinaison comprenant un inhibiteur de mtp et un inhibiteur de l'absorption du cholestérol
|
JP2010515701A
(ja)
*
|
2007-01-09 |
2010-05-13 |
ノボ・ノルデイスク・エー/エス |
ウレアグルコキナーゼアクチベーター
|
EP2099777B1
(fr)
*
|
2007-01-11 |
2015-08-12 |
Novo Nordisk A/S |
Activateurs de l'urée glucokinase
|
CN101220021B
(zh)
*
|
2007-01-12 |
2010-12-08 |
上海医药工业研究院 |
4-取代苯氧基喹啉类化合物及其中间体、制备方法和应用
|
US7790737B2
(en)
|
2007-03-13 |
2010-09-07 |
Kowa Company, Ltd. |
Substituted pyrimidine compounds and their utility as CETP inhibitors
|
AU2008241904B2
(en)
|
2007-04-13 |
2012-06-07 |
Kowa Company, Ltd. |
Novel pyrimidine compound having dibenzylamine structure and medicament comprising the same
|
AU2008272923A1
(en)
*
|
2007-07-02 |
2009-01-08 |
Essentialis, Inc. |
Salts of potassium ATP channel openers and uses thereof
|
AU2008324243B2
(en)
|
2007-11-05 |
2012-03-08 |
Novartis Ag |
4-benzylamino-1-carboxyacyl-piperidine derivatives as CETP inhibitors useful for the treatment of diseases such as hyperlipidemia or arteriosclerosis
|
PL2404901T3
(pl)
|
2007-12-03 |
2013-10-31 |
Novartis Ag |
1,2-Dipodstawione pochodne 4-benzyloamino-pirolidyny jako inhibitory CETP użyteczne do leczenia chorób, takich jak hiperlipidemia lub stwardnienie tętnic
|
AU2008335135A1
(en)
|
2007-12-11 |
2009-06-18 |
Cytopathfinder, Inc. |
Carboxamide compounds and their use as chemokine receptor agonists
|
WO2010130773A2
(fr)
|
2009-05-15 |
2010-11-18 |
Novartis Ag |
Dérivés de benzoxazolone en tant qu'inhibiteurs d'aldostérone synthase
|
MX2011012198A
(es)
|
2009-05-15 |
2011-12-08 |
Novartis Ag |
Aril-piridinas como inhibidoras de sintasa de aldosterona.
|
ES2602902T3
(es)
|
2009-05-28 |
2017-02-22 |
Novartis Ag |
Derivados aminopropiónicos sustituidos como inhibidores de neprilisina
|
EP3048100A1
(fr)
|
2009-05-28 |
2016-07-27 |
Novartis AG |
Dérivés aminobutyriques substitués en tant qu'inhibiteurs de la néprilysine
|
AR077208A1
(es)
*
|
2009-06-30 |
2011-08-10 |
Lilly Co Eli |
Derivados del acido trans-4-[[(5s)-5-[[[3,5-bis(trifluorometil) fenil] metil] (2-metil-2h-tetrazol-5-il) amino) -2,3,4,5-tetrahidro-7,9-dimetil-1h-1-benzazepin-1-il) metil)-ciclohexancarboxilico y sus formas cristalinas, composiciones farmaceuticas que los comprenden, su uso para preparar un medicam
|
EP2501678B1
(fr)
|
2009-11-17 |
2015-09-23 |
Novartis AG |
Dérivés de l'arylpyridine comme inhibiteurs de l'aldosterone synthase.
|
JO2967B1
(en)
|
2009-11-20 |
2016-03-15 |
نوفارتس ايه جي |
Acetic acid derivatives of carbamoyl methyl amino are substituted as new NEP inhibitors
|
EP2507234B1
(fr)
|
2009-11-30 |
2014-03-12 |
Novartis AG |
Dérivés d'imidazole en tant qu'inhibiteurs de l'aldostérone synthase
|
EP2571860A1
(fr)
|
2010-05-21 |
2013-03-27 |
Pfizer Inc |
2-phénylbenzoylamides
|
US8877815B2
(en)
|
2010-11-16 |
2014-11-04 |
Novartis Ag |
Substituted carbamoylcycloalkyl acetic acid derivatives as NEP
|
US8673974B2
(en)
|
2010-11-16 |
2014-03-18 |
Novartis Ag |
Substituted amino bisphenyl pentanoic acid derivatives as NEP inhibitors
|
EP2668507B1
(fr)
|
2011-01-26 |
2017-08-23 |
INSERM - Institut National de la Santé et de la Recherche Médicale |
Méthode d'évaluation du risque d'un sujet de contracter une maladie cardiovasculaire
|
US20130345392A1
(en)
|
2011-03-04 |
2013-12-26 |
Pfizer Inc |
Edn3-like peptides and uses thereof
|
AU2012271661B8
(en)
|
2011-06-17 |
2016-11-10 |
Merck Sharp & Dohme Corp. |
Cycloalkyl-fused tetrahydroquinolines as CRTH2 receptor modulators
|
TWI537262B
(zh)
*
|
2011-08-17 |
2016-06-11 |
美國禮來大藥廠 |
供治療糖尿病使用之新穎1,2,3,4-四氫喹啉衍生物
|
JP5964965B2
(ja)
|
2011-08-18 |
2016-08-03 |
ドクター レディズ ラボラトリーズ リミテッド |
コレステリルエステル転送タンパク質(cetp)インヒビターとしての置換複素環式アミン化合物
|
JP6140168B2
(ja)
|
2011-09-27 |
2017-05-31 |
ドクター レディズ ラボラトリーズ リミテッド |
アテローム性動脈硬化症の処置のために有用なコレステリルエステル転送タンパク質(cetp)インヒビターとしての5−ベンジルアミノメチル−6−アミノピラゾロ[3,4−b]ピリジン誘導体
|
MX347400B
(es)
|
2012-06-29 |
2017-04-18 |
Univ Nac Autónoma De México |
Vacuna de aplicacion nasal contra el desarrollo de la enfermedad aterosclerotica y el higado graso.
|
UY35144A
(es)
|
2012-11-20 |
2014-06-30 |
Novartis Ag |
Miméticos lineales sintéticos de apelina para el tratamiento de insuficiencia cardiaca
|
CN105073762B
(zh)
|
2013-02-14 |
2017-03-08 |
诺华股份有限公司 |
作为nep(中性内肽酶)抑制剂的取代的联苯丁酰膦酸衍生物
|
BR112015026513A2
(pt)
|
2013-04-17 |
2017-07-25 |
Pfizer |
derivados de n-piperidin-3-ilbenzamida para tratar as doenças cardiovasculares
|
KR20160031551A
(ko)
|
2013-07-25 |
2016-03-22 |
노파르티스 아게 |
심부전의 치료를 위한 시클릭 폴리펩티드
|
AU2014293387B2
(en)
|
2013-07-25 |
2017-04-20 |
Novartis Ag |
Bioconjugates of synthetic apelin polypeptides
|
WO2016032324A1
(fr)
*
|
2014-08-28 |
2016-03-03 |
Dezima Pharma B.V. |
Composition pharmaceutique et combinaison thérapeutique comprenant un inhibiteur de protéine de transfert d'ester de cholestéryle et des inhibiteurs de hmg-coa réductase
|
MX2017002610A
(es)
|
2014-08-29 |
2017-10-11 |
Tes Pharma S R L |
INHIBIDORES DE ACIDO A-AMINO-ß-CARBOXIMUCONICO SEMIALDEHIDO DESCARBOXILASA.
|
WO2016055901A1
(fr)
|
2014-10-08 |
2016-04-14 |
Pfizer Inc. |
Composés d'amide substitué
|
US9931372B2
(en)
|
2015-01-23 |
2018-04-03 |
Novartis Ag |
Synthetic apelin fatty acid conjugates with improved half-life
|
JOP20190086A1
(ar)
|
2016-10-21 |
2019-04-18 |
Novartis Ag |
مشتقات نافثيريدينون جديدة واستخدامها في معالجة عدم انتظام ضربات القلب
|
UY38072A
(es)
|
2018-02-07 |
2019-10-01 |
Novartis Ag |
Compuestos derivados de éster butanoico sustituido con bisfenilo como inhibidores de nep, composiciones y combinaciones de los mismos
|
JP2021526130A
(ja)
|
2018-06-12 |
2021-09-30 |
ブイティーブイ・セラピューティクス・エルエルシー |
インスリンまたはインスリン類似体と組み合わせたグルコキナーゼ活性化薬の治療的使用
|
MA54261A
(fr)
|
2019-01-18 |
2022-04-27 |
Astrazeneca Ab |
Inhibiteurs de pcsk9 et leurs procédés d'utilisation
|
AR127698A1
(es)
|
2021-11-23 |
2024-02-21 |
Novartis Ag |
Derivados de naftiridinona para el tratamiento de una enfermedad o un trastorno
|