GLP-1 Receptor Agonists to Decrease Ethanol and CVD Risk in HIV
Purpose
The goal of this clinical trial is to learn if the drug semaglutide works to reduce alcohol intake among adults living with HIV. The main questions it aims to answer are: 1. Does semaglutide lower the average number of alcoholic beverages participants drink per week? 2. Does semaglutide lower the average number of cigarettes participants smoke per day? 3. Does semaglutide decrease the risk for cardiovascular disease among people living with HIV who drink alcohol and/or smoke tobacco? Researchers will compare the effects of semaglutide to a placebo (a look-alike substance that contains no drug) to see if semaglutide works to lower the alcohol intake among participants each week. Participants will: 1. Take semaglutide for 3 months 2. Visit the research clinic 3 times for checkups and tests 3. Provide blood samples, stool samples, and saliva samples for tests.
Conditions
- HIV
- Alcohol
- Smoking Cigarette
- Cardiovascular Disease Prevention
Eligibility
- Eligible Ages
- Between 18 Years and 89 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Ages 18-89 - Prior diagnosis of HIV-1 - Affiliated with Vanderbilt Comprehensive Care Clinic - On current ART regimen for at least 90 days prior to study entry with no missed doses for at least 7 consecutive days. - Most recent absolute CD4 count ≥ 300 cells/mm3 and drawn within 12 months of study enrollment - BMI ≥ 23 (calculated at screening) - Self-report of consuming alcohol in past 90 days - AUDIT-C ≥ 3 (male)/ ≥ 2 (female) - Has an established stable address at which they can receive mail and can be reached for the next 6 months - Willing and able to complete study procedures and follow-ups
Exclusion Criteria
- Known allergy to semaglutide - Currently taking GLP-1 RA (in the past 3 months) - History of diabetes defined by diagnosis in Problems List in medical record - History of pancreatitis - History of gastroparesis - Gallbladder disease (in the past 3 months) - History of medullary thyroid carcinoma - Family history of medullary thyroid carcinoma - History of multiple endocrine neoplasia syndrome type 2 - Family history of multiple endocrine neoplasia syndrome type 2 - Cognitive inability to consent - Barrier to speaking, hearing, reading, or writing English - Pregnant or breastfeeding, or planning to become pregnant in the next 6 months - Too ill to complete study procedures
Study Design
- Phase
- Phase 2
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Treatment
- Masking
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Semaglutide |
drug intervention |
|
|
Placebo Comparator Placebo |
|
Recruiting Locations
Nashville, Tennessee 37232
More Details
- Status
- Recruiting
- Sponsor
- Vanderbilt University Medical Center