A Clinical Study to Evaluate Enlicitide (MK-0616) Formulations in Healthy Adult Participants (MK-0616-035)
Part of paid clinical trials in Tempe, Arizona.
- Sponsor
- Merck Sharp & Dohme LLC
- Study ID
- NCT06880874
- Phase
- PHASE1
- Status
- Completed
Conditions
- Healthy
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 55 Years
- Healthy Volunteers
- Accepted
Interventions
- Enlicitide — DRUGOral Tablet
Study Details
The goal of the study is to learn what happens to different forms of enlicitide medications in a healthy person's body over time. Researchers will compare the amount of enlicitide in the healthy person's body over time when enlicitide is given in different formulations.
Key Dates
- Start date
- Apr 2, 2025
- Status verified
- Jun 2025
- Primary completion
- May 16, 2025
- Completion
- May 31, 2025
Study Design
- Enrollment
- 40 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- CROSSOVER
- Primary purpose
- BASIC_SCIENCE
Arms
- Experimental: Treatment A: enlicitide reference tabletParticipants receive a single oral dose of enlicitide reference tablet.
- Experimental: Treatment B: enlicitide test tabletParticipants receive a single oral dose of enlicitide test tablet.
Primary Outcome Measure
Area Under the Concentration-Time Curve from Time 0 to 24 hours (AUC0-24hrs) of enlicitide in plasma [ Time Frame: Pre-dose and at designated time points up to 24 hours post dose ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Celerion ( Site 0001) | Tempe | Arizona | 85283 | - |
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