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A Study of Enlicitide Decanoate (MK-0616, an Oral PCSK9 Inhibitor) in Children and Adolescents With Heterozygous Familial Hypercholesterolemia (MK-0616-029)

RecruitingPhase 2/3

An Operationally Seamless Phase 2/3 Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Enlicitide Decanoate in Pediatric Participants With Heterozygous Familial Hypercholesterolemia

Who can join

Ages 6 to 17 · All sexes

Full eligibility criteria
Inclusion Criteria:

Inclusion criteria include, but are not limited to:

* Has possible or definite diagnosis of HeFH based on a locally accepted diagnostic algorithm or diagnosis by genetic testing results
* Has a fasted LDL-C value (evaluated by the central laboratory) that is ≥130 mg/dL
* Is receiving either:

  * An optimized daily dose of statin (± nonstatin LLT)
  * A nonstatin LLT with documented intolerance to at least 2 different statins, or documented intolerance to 1 statin plus refusal of statin therapy by the participant or legally acceptable representative
* Is on a stable dose of all background LLTs for at least 30 days prior to screening, with no medication or dose changes planned during participation in Part A or Part B

Exclusion Criteria:

Exclusion criteria include, but are not limited to:

* Has a history of homozygous FH based on genetic or clinical criteria, or history of known compound heterozygous FH, or double heterozygous FH
* Has a history of nephrotic syndrome
* Has any clinically significant malabsorption condition based on investigator assessment
* Was previously treated/is being treated with certain other cholesterol lowering medications, including proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors without adequate washout

About the study

This study is designed to learn if enlicitide decanoate is safe and effective to treat children and adolescents with heterozygous familial hypercholesterolemia (HeFH) and high amounts of low-density lipoprotein cholesterol (LDL-C) in the blood.

The goals of this study are to learn about the safety of enlicitide and if children tolerate it, what happens to enlicitide in a child's body over time, and if enlicitide works to lower cholesterol levels in children more than a placebo.

What is being tested

Sponsor: Merck Sharp & Dohme LLC · Participants: 153 · Started: Aug 21, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07058077

Locations in the U.S.

DelawareNemours/Alfred I. duPont Hospital for Children ( Site 0001), Wilmington
District of ColumbiaChildren's National Medical Center ( Site 0015), Washington D.C.
FloridaExcel Medical Clinical Trials ( Site 0008), Boca Raton
GeorgiaChildren's Healthcare of Atlanta Cardiology ( Site 0026), Atlanta
MassachusettsBoston Children's Hospital ( Site 0018), Boston
MissouriSt. Louis Children's Hospital ( Site 0014), St Louis
OhioCincinnati Children's Hospital Medical Center ( Site 0016), Cincinnati
West VirginiaWest Virginia University ( Site 0013), Morgantown

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