A Study of Enlicitide Decanoate (MK-0616) and Semaglutide in Healthy Adult Participants (MK-0616-023)
Part of paid clinical trials in Lincoln, Nebraska.
- Sponsor
- Merck Sharp & Dohme LLC
- Study ID
- NCT06699329
- Phase
- PHASE1
- Status
- Completed
Conditions
- Healthy
Eligibility Criteria
- Sex
- ALL
- Age
- 19 Years - 55 Years
- Healthy Volunteers
- Accepted
Interventions
- Enlicitide Decanoate — DRUGmultiple doses, oral tablet
- Semaglutide — DRUGmultiple doses, oral tablet
Study Details
The goal of this study is to learn what happens in a person's body over time when they take enlicitide decanoate and semaglutide alone or at the same time. Enlicitide decanoate is a new medicine that lowers the amount of cholesterol in a person's blood. Semaglutide is a drug used to treat type 2 diabetes. Researchers want to learn what happens to the amount of semaglutide and enlicitide decanoate in a person's blood when each drug is taken alone and when they are taken together.
Key Dates
- Start date
- Jan 22, 2024
- Status verified
- Nov 2024
- Primary completion
- May 24, 2024
- Completion
- May 24, 2024
Study Design
- Enrollment
- 38 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- BASIC_SCIENCE
Arms
- Experimental: Enlicitide Decanoate and SemaglutidePeriod 1: Participants receive an oral dose of enlicitide decanoate every day for 1 week. Period 2: Participants receive an oral dose of semaglutide every day for 6 weeks. Period 3: Participants receive an oral dose of both enlicitide decanoate and semaglutide every day for 1 week.
Primary Outcome Measure
Area Under the Concentration-Time Curve from Time 0 to 24 hours (AUC0-24hrs) of Enlicitide Decanoate [ Time Frame: At designated timepoints (up to 24 hours postdose) ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Celerion (Site 0001) | Lincoln | Nebraska | 68502 | - |
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