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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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Yale Stress Center
Coordinator of this site? Confirm its status
New HavenUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.