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A Clinical Trial of MK-1406 in Healthy Participants (MK-1406-008)

RecruitingPhase 1Healthy volunteers welcome

A Randomized, Open Label, Parallel Group Phase 1 Study to Compare Safety, Tolerability and Pharmacokinetics of Subcutaneously Administered MK-1406 as Three Injections Compared With Two Injections in Healthy Adult Participants

Who can join

Ages 18 to 64 · All sexes · Healthy volunteers welcome

Full eligibility criteria
Inclusion Criteria:

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

* Is in good health
* Has body mass index (BMI) 18.0 to 32.0 kg/m\^2

Exclusion Criteria:

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

* History of clinically significant endocrine, Gastrointestinal (GI), cardiovascular, hematological, hepatic, immunological, renal, respiratory, genitourinary, or major neurological (including stroke and chronic seizures) abnormalities or diseases
* History of cancer (malignancy)

About the study

The purpose of this trial is to compare what happens to MK-1406 in the body of healthy participants when it is given as 2-injections and 3-injections. Researchers also want to learn about the safety of MK-1406 and if people tolerate it.

What is being tested

Sponsor: Merck Sharp & Dohme LLC · Participants: 400 · Started: Sep 10, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07743151

Locations in the U.S.

FloridaResearch Centers of America ( Hollywood ) ( Site 0008), Hollywood
New JerseyHassman Research Institute Marlton Site ( Site 0001), Marlton
OhioVelocity Clinical Research, Cleveland ( Site 0005), Cleveland

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