A Clinical Study to Evaluate Enlicitide (MK-0616) Formulations in Healthy Adult Participants (MK-0616-035)
NCT ID: NCT06880874
Last Updated: 2025-06-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
40 participants
INTERVENTIONAL
2025-04-02
2025-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
NONE
Study Groups
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Treatment A: enlicitide reference tablet
Participants receive a single oral dose of enlicitide reference tablet.
Enlicitide
Oral Tablet
Treatment B: enlicitide test tablet
Participants receive a single oral dose of enlicitide test tablet.
Enlicitide
Oral Tablet
Interventions
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Enlicitide
Oral Tablet
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Has body mass index (BMI) ≥18 kg/m\^2 and ≤32 kg/m\^2
Exclusion Criteria
* Has history of cancer (malignancy)
* Has positive results for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), or hepatitis C virus (HCV)
18 Years
55 Years
ALL
Yes
Sponsors
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Merck Sharp & Dohme LLC
INDUSTRY
Responsible Party
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Principal Investigators
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Medical Director
Role: STUDY_DIRECTOR
Merck Sharp & Dohme LLC
Locations
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Celerion ( Site 0001)
Tempe, Arizona, United States
Countries
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Related Links
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Merck Clinical Trials Information
Other Identifiers
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MK-0616-035
Identifier Type: OTHER
Identifier Source: secondary_id
0616-035
Identifier Type: -
Identifier Source: org_study_id
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