Impact of GLP-1 Receptor Agonist Therapy on Alcohol Pharmacokinetics
Part of paid clinical trials in Madison, Wisconsin.
- Sponsor
- University of Wisconsin, Madison
- Study ID
- NCT07758231
- Phase
- PHASE1
- Status
- Not Yet Recruiting
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Conditions
- Alcohol
- GLP-1
Eligibility Criteria
- Sex
- ALL
- Age
- 21 Years - 55 Years
- Healthy Volunteers
- Accepted
Interventions
- Acute Ethanol Dose — DRUGTime 0, participants will self-administer an oral ethanol beverage (vodka and sugar-free cherry Kool aid) calculated to reach a peak Breath Alcohol Concentration (BrAC) of 0.08 g/dL using the Widmark formula. A total time of 30 minutes will be given for completion of beverage consumption. This will be followed by a breakfast.
Study Details
This study is to learn how the weight loss drug tirzepatide (Zepbound) changes the way a body handles alcohol. 5 participants aged 21-55 who take Zepbound will be enrolled and can expect to be on study for up to 4 weeks.
Key Dates
- First listed
- Aug 11, 2026
- Start date
- Oct 31, 2026
- Status verified
- Aug 2026
- Primary completion
- Mar 31, 2027
- Completion
- Mar 31, 2027
Study Design
- Enrollment
- 5 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- BASIC_SCIENCE
Arms
- Experimental: Healthy adults on TirzepatideParticipants will complete a screening and enrollment visit, one study visit, and a follow-up correspondence over the course of approximately 4 weeks.
Primary Outcome Measure
Maximum Ethanol Concentration (Cmax) [ Time Frame: prior to dosing (-25 minutes), start of dosing (0 minutes), 15 minutes, 30 minutes, 60 minutes, 90 minutes, 120 minutes, 150 minutes, 180 minutes, 240 minutes, 300 minutes, 350 minutes ]
Central Contacts
- Heather Barkholtz, PhD608-890-1967
- Michael Chen, MD
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Wisconsin | Madison | Wisconsin | 53792 | - |
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