Clinical Trial of Rybelsus (Semaglutide) Among Adults With Alcohol Use Disorder (AUD)

Last updated: February 6, 2025
Sponsor: University of Colorado, Denver
Overall Status: Active - Recruiting

Phase

2

Condition

Alcohol Use Disorder

Substance Abuse

Addictions

Treatment

Semaglutide 7 MG [Rybelsus]

Placebo

Semaglutide 3 MG [Rybelsus]

Clinical Study ID

NCT05892432
23-0261
R21AA031146
  • Ages > 21
  • All Genders

Study Summary

This study is a randomized controlled trial of oral semaglutide among treatment-seeking individuals with AUD. The investigators will randomly assign 50 participants to receive semaglutide (titrated to 7 milligrams (mg) per day) or matched placebo for 8 weeks. The primary aims are to assess the safety and tolerability of semaglutide in this population and to evaluate its effects, relative to placebo, on alcohol cue-elicited craving and alcohol consumption.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Age 21 or older.

  2. Meets Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5)criteria for current AUD of at least moderate severity, as assessed by the MiniInternational Neuropsychiatric Interview (MINI).

  3. Seeking pharmacological treatment for AUD and wants to stop or cut down on drinking.

  4. Has a body mass index (BMI) of at least 25 kg/m2.

  5. Able to read and understand questionnaires and informed consent.

  6. Lives within 50 miles of the study site.

Please contact clinical site for additional inclusion criteria.

Exclusion

Exclusion Criteria:

  1. Current DSM-5 diagnosis of any other substance use disorder of moderate or greaterseverity, except for Nicotine Use Disorder, as assessed by MINI.

  2. Urine drug screen at screening positive for any substance except cannabis.

  3. Current DSM-5 bipolar disorder, major depressive episode, or panic disorder, asassessed by MINI.

  4. Current or lifetime eating disorder (anorexia, bulimia, or binge eating disorder) orpsychotic disorder, as assessed by MINI.

  5. Current suicidal ideation or homicidal ideation.

  6. Current use of other psychotropic medications except antidepressants (for which dosemust be stable for at least the past 2 months).

  7. Current or past-month use of AUD pharmacotherapy, including (e.g., oral naltrexone,acamprosate, or disulfiram) or current or past 60-day use of injectable naltrexone.

  8. Current psychotherapy in which the primary focus is AUD. Attendance at AlcoholicsAnonymous (AA) meetings is not exclusionary.

  9. Current or past-month use of weight control medications.

  10. Current or past-month use of metformin for any indication.

  11. Any prior use of semaglutide or other GLP-1 agonists.

  12. History of severe alcohol withdrawal (e.g., seizure, delirium tremens), as evidencedby self- report and assessment with Clinical Institute Withdrawal Assessment forAlcohol-Revised (CIWA-Ar).

  13. Current or lifetime Type 1 or Type 2 diabetes diagnosis, or HbA1c >6.5%.

  14. Current or lifetime kidney disease or creatinine clearance <80 mL/min forparticipants <=55 years of age (<65 mL/min for those >55).

  15. Personal history of gastrointestinal disease (e.g., gastroparesis) or pancreatitis.

  16. Personal or family history of medullary thyroid carcinoma and/or multiple endocrineneoplasia syndrome type 2

  17. Current or past hepatocellular disease, as indicated by verbal report or elevationsof serum amylase, alanine aminotransferase (ALT) or aspartate aminotransferase (AST)greater than 3 times the upper limit of the normal range at screening.

  18. Uncontrolled hypertension (systolic BP >160 mmHg or diastolic >100 mmHg).

  19. Biological females of childbearing potential who are pregnant (by plasma HCG),nursing, or who are not using a reliable form of contraception.

  20. Lack of a stable living situation.

  21. (If participating in MRI sessions) Contraindications to MRI scanning, ferrous metalin the body including intracranial, intraorbital, or intraspinal metal, pacemakers,cochlear implants, other non-MRI-compatible devices, or other devices that couldcompromise the quality of the MRI images such as a permanent top retainer or braces.

  22. (If participating in MRI sessions) Severe claustrophobia or morbid obesity thatpreclude placement in the MRI scanner.

Study Design

Total Participants: 135
Treatment Group(s): 3
Primary Treatment: Semaglutide 7 MG [Rybelsus]
Phase: 2
Study Start date:
January 11, 2024
Estimated Completion Date:
June 30, 2025

Study Description

A screening visit will be conducted at which written informed consent will be obtained and inclusion/exclusion criteria will be assessed. Subsequently, eligible participants will be randomly assigned to take oral semaglutide or matched placebo for 8 weeks, with the semaglutide dose titrated from 3 milligrams (mg)/day for the first 4 weeks to 7 milligrams (mg)/day for the second 4 weeks. Participants will complete 7 additional clinic visits (weekly during the first 4 weeks of the treatment period and biweekly during the second 4 weeks). At each visit, participants will also engage in a computerized behavioral intervention. At screening and again at the Week 6 visit, participants will complete an alcohol cue reactivity task. At the Week 1 visit, before ingesting the first dose of study medication, and again at the Week 8 visit, participants will complete a functional MRI session.

Connect with a study center

  • University of Colorado Anschutz Medical Campus

    Aurora, Colorado 80045
    United States

    Active - Recruiting

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