A study testing whether a GLP-1 and GIP medicine, tirzepatide, can help people with alcohol use disorder drink less.

Recruiting now. Registry record last updated July 28, 2026.

Who can join
Adults 21 to 65, have alcohol use disorder, BMI 23+.
What you take
Tirzepatide, given as part of the study. Check ClinicalTrials.gov for this trial's study groups, including any placebo or comparison medicine.
How long it lasts
The full study runs about 6 years.
What you get
Costs vary by study. Ask the study team what this one covers, including the study medicine, visits and travel, before you sign the consent form.
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Phase Phase 1Sponsor National Institute on Alcohol Abuse and Alcoholism (NIAAA)Drug tirzepatideClass GLP-1/GIPSites 1 USEnrollment target 176

What this study is for

Primary condition: Alcohol Use Disorder (AUD).

Full scientific study title: Tirzepatide s Dopaminergic Effects in Alcohol Use Disorders (AUD).

Who can join

Age21 to 65SexAnyBMI23 to 35

Adults 21 to 65, have alcohol use disorder, BMI 23+. A site coordinator confirms whether you qualify during a free screening visit. The exact medical requirements are below.

Full medical eligibility (for you and your doctor)verbatim from the registry

This is the exact wording from ClinicalTrials.gov, including clinical measures (lab values, imaging scores). Bring it to your doctor if any of it is unclear.

Key inclusion criteria

  • Enrollment in 14AA0181.
  • Stated willingness to comply with all study procedures and availability for the duration of the study.
  • Male or female, ages 21-65 years old.
  • Ability to understand and willingness to sign a written informed consent document.
  • Have or had any prior experience with stimulant drugs including cocaine, methylphenidate, amphetamine or methamphetamine, or prescription stimulants (prescription or recreational use), whether or not they have had a past substance use disorder.

Key exclusion criteria

  • Presence of ferromagnetic objects in the body that are contraindicated for MRI of the head, fear of enclosed spaces, or other standard contraindication to MRI
  • Cannot lie comfortably flat on his/her back for up to 2 hours in the PET/MRI scanner.
  • BMI \<23 or \>35 (but no more than 500 lbs). The PET/MRI scanner bed is tested to a weight limit of 500 lbs.
  • Have had previous radiation exposure (from X-rays, PET scans, or other exposure) that, with the exposure from this study, would exceed NIH annual research limits as determined by medical history and physical exam.
  • Pregnant or breast-feeding: Females of childbearing potential, or with tubal ligation, or are post-menopausal and are age 55 or less will undergo a urine pregnancy test and it must be negative to continue participation. Urine pregnancy tests will be repeated on subsequent days of study (i.e., within 24 hours before study procedures). Females must not be currently breastfeeding.

Where this trial is enrolling

This trial has 1 sites across 1 state. Contact a site coordinator directly to start screening.

Maryland1 site
  • National Institutes of Health Clinical Center
    Bethesda, Maryland
    NIH Clinical Center Office of Patient Recruitment (OPR)800-411-1222ccopr@nih.gov

Timeline

Started enrolling: May 20, 2026. Expected completion: December 31, 2031. Last updated on ClinicalTrials.gov: July 28, 2026.

Official source

Every Monday we check this trial against ClinicalTrials.gov, the federal registry for clinical research. Last checked September 4, 2026. Confirm the current status there before you contact a site:

View on ClinicalTrials.gov →

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