NCT07772960RecruitingPhase 1
Semaglutide Dose Effects on Metabolic and Stress Hormone, Craving and Alcohol Use Outcomes
Source: ClinicalTrials.gov · Last updated 4 Nov 2026
Brief summary (registry, in English)
This study will examine two doses of 1.0 mg and 2.0 mg of Semaglutide versus placebo in patients with Alcohol Use Disorder (AUD) and Obesity (Ob) to assess if these doses improve alcohol craving, stress and alcohol use outcomes.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 1
- Study type
- Interventional
- Enrollment
- 90 (estimated)
- First submitted
- 13 Aug 2026
- Start date
- 1 Oct 2026
- Primary completion date
- 31 Oct 2031
- Lead sponsor
- Yale University
- Diseases
- Obesity
- NCT number
- NCT07772960
What you commit to
- Study type: Interventional · Phase 1
- Planned participants: 90
- From 1 Oct 2026 to the primary completion date, 31 Oct 2031
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Current use of any anti-obesity medications;
- Prior history of bariatric surgery or current intragastric balloon;
Other illness
- Meet current criteria for moderate to severe substance use disorders from abuse of any another psychoactive substance, excluding nicotine;
- Current use of psychiatric medications, including benzodiazepine-based sedatives/anxiolytics and anticonvulsants, non SSRI antidepressants, oral prescription analgesics (other than non-steroidal anti-inflammatory drugs), acamprosate, naltrexone, antabuse, baclofen, varenicline;
- Endocrine or immune disorders, including diagnosis of diabetes (T2D or T1D) by American Diabetes Association (ADA) criteria or a history of HgbA1c \>6.5% and on current medications for T2D treatment;
- Significant underlying medical conditions, including history of pancreatitis, acute kidney injury, medullary thyroid cancer, or MEN syndrome, as well as other cerebral, renal, thyroid or cardiac pathology that would preclude study participation;
Other
- Current use of opiates;
- Psychotic or otherwise severely psychiatrically disabled (i.e., suicidal, homicidal, current mania);
- Current participation in structured meal replacement or weight loss program;
- Weight loss of \>=10% over the preceding 6 months;
- Women who are pregnant, nursing or refuse use of reliable form of birth control.
Who the study is looking for
- Male and females ages 18-60 and BMI in 30-49.9 kg/m2;
- regular weekly alcohol use (at least 3X/week) prior to admission;
- must meet current DSM-V criteria for moderate to severe Alcohol Use Disorders (AUDs) using SCID-I for DSM-V;
- Good health as verified by screening and physical examination;
- Able to read English and complete study evaluation;
- Able to provide informed written and verbal consent.
Age in the registry: 18 years to 68 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Yale Stress Center Coordinator of this site? Confirm its status | New Haven | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.