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A Clinical Trial of MK-7262 and Enlicitide in Participants With High Lipoprotein(a) (MK-7262-004)

RecruitingPhase 2

A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of MK-7262 as Monotherapy and When Coadministered With Enlicitide Decanoate in Adults With Elevated Lipoprotein(a)

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

The main inclusion criteria include but are not limited to the following:

* Has Lp(a) ≥ 150 nmol/L
* Is receiving an optimized and stable dose of statin for ≥ 30 days with no planned additions, dose changes, or discontinuations through the duration of the study

Exclusion Criteria:

The main exclusion criteria include but are not limited to the following:

* Has a history of homozygous familial hypercholesterolemia (FH), compound heterozygous FH, or double heterozygous FH
* Has a history of class IV heart failure, severe ventricular systolic dysfunction, uncontrolled ventricular arrhythmia, markedly prolonged corrected QT interval, untreated hypertension, or a recent coronary, cerebrovascular, or peripheral ischemic event or arterial revascularization
* Has human immunodeficiency virus infection, unless the infection is controlled (i.e. undetectable viral load)
* Has an active hepatitis C virus infection or active or chronic hepatitis B virus infection
* Has a history of nephrotic syndrome
* Has severe renal insufficiency
* Has received certain therapies in the prohibited timeframe as specified in the protocol
* Has active or chronic hepatobiliary or hepatic disease
* Has poorly controlled Type 1 or Type 2 diabetes

About the study

Researchers designed a trial medicine called MK-7262 to lower levels of Lp(a) in the blood. Researchers want to learn about giving MK-7262 with another trial medicine called enlicitide (also known as MK-0616 or enlicitide decanoate). Enlicitide is in a group of medicines that lower the amount of low-density lipoprotein cholesterol (LDL-C).

The goals of this trial are to evaluate:

* if MK-7262 and enlicitide taken together work better than placebo at lowering Lp(a) and LDL-C levels in the blood * if MK-7262 alone works better than placebo at lowering Lp(a) levels in the blood * the safety and tolerability of taking MK-7262 and enlicitide alone and together

What is being tested

Sponsor: Merck Sharp & Dohme LLC · Participants: 750 · Started: Jun 30, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07614984

Locations in the U.S.

AlabamaAdvanced Cardiovascular - Alexander City ( Site 0158), Alexander City
AMR Clinical Mobile ( Site 0149), Mobile
CaliforniaNational Heart Institute ( Site 0113), Beverly Hills
Headlands Research CTR Lincoln ( Site 0127), Lincoln
ConnecticutChase Medical Research, LLC ( Site 0163), Waterbury
FloridaSoffer Health Institute ( Site 0123), Hollywood
Westside Center for Clinical Research ( Site 0161), Jacksonville
Inpatient Research Clinic ( Site 0110), Miami Lakes
Clinical Research Trials of Florida ( Site 0101), Tampa
Conquest Research LLC ( Site 0140), Winter Park
MarylandFlourish Research - Bowie ( Site 0106), Bowie
Velocity Clinical Research Rockville ( Site 0146), Rockville
MichiganArcturus Healthcare , PLC, Troy Internal Medicine Research Division ( Site 0132), Troy
MinnesotaMinneapolis Heart Institute - Minneapolis ( Site 0130), Minneapolis
MontanaMontana Medical Research, Inc. ( Site 0156), Missoula
New MexicoNew Mexico Clinical Research & Osteoporosis Center ( Site 0119), Albuquerque
New YorkLaurelton Heart Specialist PC ( Site 0155), Rosedale
North CarolinaVelocity Clinical Research, Durham ( Site 0145), Durham
OhioRemington-Davis, Inc. ( Site 0107), Columbus
TennesseeHolston Medical Group ( Site 0117), Kingsport
TexasCenter for Cardiometabolic Disease Prevention/Baylor College of Medicine ( Site 0154), Houston
DM Clinical Research ( Site 0115), Tomball
VirginiaCarient Heart & Vascular - Manassas ( Site 0165), Manassas
WashingtonRainier Clinical Research Center ( Site 0116), Renton

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.