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Набира участници Фаза 3 NCT07216482

A Clinical Study of Enlicitide in Participants With High Cholesterol (MK-0616-037)

Фаза 3 – широко изпитване преди одобрение
Заболявания: Hyperlipidemia

Спонсор: Merck Sharp & Dohme LLC

Налично на: БГ
Обобщение
Researchers designed a study medicine called enlicitide to lower low-density lipoprotein cholesterol (LDL-C). In this study, researchers want to learn about giving enlicitide with another medicine called rosuvastatin. Rosuvastatin is a standard (usual) treatment to lower LDL-C. The goal of this study is to learn if enlicitide given with rosuvastatin works better than placebo on lowering LDL-C in a person's blood. A placebo looks like the study medicine but has no study medicine in it. Using a placebo helps researchers better understand the effects of a study medicine.
Кой може да участва
Inclusion Criteria: -Has either not received lipid-lowering therapy (LLT) or has not received certain LLTs within a specified time period prior to the study. Exclusion Criteria: * Has a history of homozygous familial hypercholesterolemia (FH), compound heterozygous FH, or double heterozygous FH. * Had a heart failure hospitalization within 3 months before Screening. * Is unwilling to take a statin, and/or has a history of statin-associated muscle symptoms or other statin-related AEs to any statin and dose, and/or is known to be intolerant to 1 or more statins. * Has a history of any of the following conditions: (1) Myopathy, myositis, rhabdomyolysis, or unexplained muscle pain; (2) Muscular or neuromuscular disease; (3) Neuropathy, fibromyalgia, or chronic pain; or (4) Has a personal or family history of hereditary muscular disorders. * Has active or chronic hepatobiliary or hepatic disease. * Has known human immunodeficiency virus (HIV) infection. * Is undergoing or previously underwent an LDL-C apheresis program within 3 months before Screening or plans to initiate an LDL-C apheresis program. * Has received any medication that may interact with rosuvastatin within 5 half-lives prior to Screening or is planning to initiate such treatment.
Интервенции
Enlicitide
DRUG
Rosuvastatin
DRUG
Placebo for Enlicitide
DRUG
Placebo for Rosuvastatin
DRUG
Места на провеждане 88
Argentina (7)
CIPREC-CIPREC Sede Arenales ( Site 0200)
Buenos Aires , Buenos Aires F.D.
Study Coordinator
CEMEDIC ( Site 0201)
CABA , Buenos Aires
Study Coordinator
Centro Medico Dra. Laura Maffei- Investigacion Clinica Aplicada ( Site 0206)
CABA
Study Coordinator
Instituto de Cardiología "Juana F. Cabral"-Cardiología ( Site 0205)
Corrientes
Study Coordinator
Instituto de Investigaciones Clínicas Mar del Plata ( Site 0202)
Mar del Plata , Buenos Aires
Study Coordinator
Fundacion Estudios Clinicos ( Site 0203)
Rosario , Santa Fe Province
Study Coordinator
Instituto de Investigaciones Clinicas Rosario ( Site 0204)
Rosario , Santa Fe Province
Study Coordinator
Австралия (6)
Emeritus Research ( Site 0904)
Camberwell , Victoria
Study Coordinator
Baker - HeartWest ( Site 0902)
Hoppers Crossing , Victoria
Study Coordinator
Australian Clinical Research Network ( Site 0900)
Maroubra , New South Wales
Study Coordinator
Fusion Clinical Research ( Site 0901)
Norwood , South Australia
Study Coordinator
Momentum Darlinghurst ( Site 0906)
Sydney , New South Wales
Study Coordinator
Momentum Clinical Research Taringa ( Site 0907)
Taringa , Queensland
Study Coordinator
Бразилия (5)
Centro de Pesquisa Clinica do Coracao ( Site 0303)
Aracaju , Sergipe
Study Coordinator
Hospital Universitário São Francisco de Assis - Bragança Paulista ( Site 0305)
Bragança Paulista , São Paulo
Study Coordinator
Centro de Pesquisas em Diabetes e Doenças Endócrino-Metabólicas ( Site 0306)
Fortaleza , Ceará
Study Coordinator
IBPClin - Instituto Brasil de Pesquisa Clínica ( Site 0302)
Rio de Janeiro
Study Coordinator
Fundação Faculdade Regional de Medicina de São José do Rio Preto ( Site 0309)
São José do Rio Preto , São Paulo
Study Coordinator
Канада (6)
Milestone Research Inc. ( Site 0111)
London , Ontario
Study Coordinator
Centricity Research Mirabel Multispecialty ( Site 0107)
Mirabel , Quebec
Study Coordinator
G A Research Associates ( Site 0102)
Moncton , New Brunswick
Study Coordinator
North York Diagnostic and Cardiac Centre ( Site 0110)
North York , Ontario
Study Coordinator
Recherche Clinique Sigma Inc ( Site 0108)
Québec , Quebec
Study Coordinator
Care Access - Thunder Bay ( Site 0130)
Thunder Bay , Ontario
Study Coordinator
Унгария (4)
Lausmed Egészségügyi Szolgáltató ( Site 1105)
Baja , Bács-Kiskun county
Study Coordinator
DRC Gyógyszervizsgáló Központ ( Site 1109)
Balatonfüred , Veszprém megye
Study Coordinator
Debreceni Egyetem Klinikai Kozpont-Belgyógyászati Klinika (Anyagcsere Tanszék) ( Site 1102)
Debrecen
Study Coordinator
Borbánya Praxis ( Site 1103)
Nyíregyháza , Szabolcs-Szatmár-Bereg
ACTIVE_NOT_RECRUITING
Израел (5)
Barzilai Medical Center ( Site 0504)
Ashkelon
Study Coordinator
Linn Medical Center ( Site 0503)
Haifa
Study Coordinator
Rambam Health Care Campus ( Site 0500)
Haifa
Study Coordinator
Meir Medical Center. ( Site 0501)
Kfar Saba
Study Coordinator
Clalit Health Services - Sakhnin Community Clinic ( Site 0502)
Sakhnin
Study Coordinator
New Zealand (5)
Pacific Clinical Research Network - Forte ( Site 1004)
Christchurch , Canterbury
Study Coordinator
Lakeland Clinical Trials Waikato ( Site 1000)
Nawton , Waikato Region
Study Coordinator
Pacific Clinical Research Network - Tasman ( Site 1003)
Nelson , Tasman District
Study Coordinator
Pacific Clinical Research Network - Rotorua ( Site 1001)
Rotorua , Bay of Plenty
Study Coordinator
Lakeland Clinical Trials Wellington ( Site 1002)
Upper Hutt , Wellington Region
Study Coordinator
Испания (3)
EAP Sardenya ( Site 0601)
Barcelona
Study Coordinator
EBA Centelles ( Site 0600)
Barcelona
Study Coordinator
Centro de Salud Concepcion Arenal ( Site 0603)
Santiago de Compostela , Galicia
Study Coordinator
Турция (7)
Ufuk University Dr.Ridvan Ege Hospital ( Site 0709)
Ankara
Study Coordinator
Eskisehir Osmangazi University ( Site 0705)
Eskişehir
Study Coordinator
Istanbul Universitesi - Cerrahpasa Kardiyoloji Enstitusu ( Site 0703)
Istanbul
Study Coordinator
Ege Universitesi Hastanesi ( Site 0708)
Izmir
Study Coordinator
Erciyes Universitesi Tıp Fakultesi Hastaneleri ( Site 0701)
Kayseri
Study Coordinator
İnönü Üniversitesi Turgut Özal Tıp Merkezi ( Site 0702)
Malatya
Study Coordinator
Hacettepe Universite Hastaneleri ( Site 0700)
Sıhhiye , Ankara
Study Coordinator
Великобритания (5)
Velocity Clinical Research, Bristol ( Site 0803)
Bristol , Bristol, City of
Study Coordinator
Lakeside Surgery ( Site 0802)
Corby , Northamptonshire
Study Coordinator
Velocity Clinical Research Havering ( Site 0804)
London , Havering
Study Coordinator
William Harvey Heart Centre ( Site 0800)
London , London, City of
Study Coordinator
West Walk Surgery ( Site 0801)
Yate , Gloucestershire
Study Coordinator
САЩ (35)
New Mexico Clinical Research & Osteoporosis Center, Inc. ( Site 0027)
Albuquerque , New Mexico
Study Coordinator
Conquest Research ( Site 0045)
Arlington , Virginia
Study Coordinator
Central Research Associates ( Site 0009)
Birmingham , Alabama
Study Coordinator
Trialmed ( Site 0026)
Chicago , Illinois
Study Coordinator
Great Lakes Clinical Trials - Ravenswood ( Site 0018)
Chicago , Illinois
Study Coordinator
Legacy Clinical Trials ( Site 0044)
Colorado Springs , Colorado
Study Coordinator
Cardiovascular Associates of the Delaware Valley ( Site 0035)
Elmer , New Jersey
Study Coordinator
G&L Research ( Site 0024)
Foley , Alabama
Study Coordinator
Alliance for Multispecialty Research, LLC ( Site 0040)
Fort Myers , Florida
Study Coordinator
Soffer Health Institute ( Site 0046)
Hollywood , Florida
Study Coordinator
Provecta Research Network LLC ( Site 0022)
Houston , Texas
Study Coordinator
Midwest Institute For Clinical Research ( Site 0033)
Indianapolis , Indiana
Study Coordinator
East Coast Institute for Research ( Site 0041)
Lake City , Florida
Study Coordinator
Chemidox Clinical Trials ( Site 0008)
Lancaster , California
Study Coordinator
Jubilee Clinical Research ( Site 0031)
Las Vegas , Nevada
Study Coordinator
Monroe Biomedical Research ( Site 0004)
Louisville , Kentucky
Study Coordinator
Manassas Clinical Research Center ( Site 0002)
Manassas , Virginia
Study Coordinator
Inpatient Research Clinic ( Site 0017)
Miami Lakes , Florida
ACTIVE_NOT_RECRUITING
Health Research of Hampton Roads, Inc. ( Site 0013)
Newport News , Virginia
Study Coordinator
Alliance for Multispecialty Research, LLC ( Site 0048)
Newton , Kansas
Study Coordinator
Alliance for Multispecialty Research, LLC - Norman ( Site 0043)
Norman , Oklahoma
Study Coordinator
Permian Research Foundation ( Site 0005)
Odessa , Texas
Study Coordinator
LinQ Research ( Site 0025)
Pearland , Texas
Study Coordinator
Synexus Clinical Research US, Inc. - Phoenix Central ( Site 0030)
Phoenix , Arizona
Study Coordinator
Rainier Clinical Research ( Site 0023)
Renton , Washington
Study Coordinator
National Clinical Research, Inc ( Site 0028)
Richmond , Virginia
Study Coordinator
Clinical Trials Research ( Site 0036)
Sacramento , California
Study Coordinator
Clinical Trials of Texas, Inc. ( Site 0010)
San Antonio , Texas
Study Coordinator
Stone Oak, LLC dba Discovery Clinical Trials (DCT) ( Site 0021)
San Antonio , Texas
Study Coordinator
Clinical Research Trials of Florida ( Site 0001)
Tampa , Florida
Study Coordinator
Alliance for Multispecialty Research LLC ( Site 0049)
Tempe , Arizona
Study Coordinator
LinQ Research - Tomball ( Site 0047)
Tomball , Texas
Study Coordinator
Cotton O'Neil Clinical Research Center ( Site 0006)
Topeka , Kansas
Study Coordinator
Clinical Site Partners LLC, dba CSP Orlando ( Site 0014)
Winter Park , Florida
Study Coordinator
Cardiology Consultants of Philadelphia Yardley ( Site 0016)
Yardley , Pennsylvania
Study Coordinator
Технически детайли
Статус
Набира участници
Фаза
Фаза 3
Вид изследване
INTERVENTIONAL
Пол
Мъже и жени
Минимална възраст
18 Years
Максимална възраст
64 Years
Здрави доброволци
Не
Начална дата
11.11.2025
Крайна дата
01.03.2027
Регистрационен номер
NCT07216482
Източник
clinicaltrials.gov
Запитване за медицински туризъм

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