Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
A Study of Brenipatide in Participants With Alcohol Use Disorder
NCT07219953 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to see if brenipatide when compared to a placebo works and is safe for participants with Alcohol Use Disorder (AUD) and hazardous alcohol use. Participation in this study will last approximately 56 weeks.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG LY3537031
Study Locations (20)
Florida
- Accel Research Sites - Lakeland Clinical Research Unit — Lakeland
- Innovative Clinical Research — Lauderhill
- K2 Medical Research - Maitland — Maitland
- K2 Medical Research ORLANDO — Maitland
- Life Arc Research Centers - Miami — Miami
- Wellness Research Center — Miami
- Life Medical Research Group Corp — Miami Gardens
- Charter Research - Orlando — Orlando
- K2 Medical Research - Tampa — Tampa
California
- UCLA Clinical & Translational Research Center (CTRC) — Los Angeles
- Artemis Institute for Clinical Research — Riverside
- Artemis Institute for Clinical Research — San Diego
- UCSF Weill Institute for Neurosciences - Substance Use Disorders Clinic - Mission Bay — San Francisco
Maryland
- Maryland Treatment Centers - Mountain Manor Treatment Center — Baltimore
- Maryland Treatment Centers - Avery Road Treatment Center — Rockville
Alabama
- Parkway Medical Center — Birmingham
Arizona
- Headlands Research - Scottsdale — Scottsdale
Arkansas
- Woodland International Research Group — Little Rock
Illinois
- Re:Cognition Health - Chicago — Chicago
Massachusetts
- Adams Clinical Boston — Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,100 participants |
| Start Date | 2025-10-16 |
| Est. Completion | 2028-04 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07219953
The ClinicalTrials.gov registry entry for NCT07219953 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eli Lilly and Company, which has 704 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Alcohol Use Disorder appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT07219953 reports 20 study locations spanning 8 distinct geographic areas — top geographies include Florida, California, Maryland. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT07219953 about?
NCT07219953 is a clinical study titled "A Study of Brenipatide in Participants With Alcohol Use Disorder". The purpose of this study is to see if brenipatide when compared to a placebo works and is safe for participants with Alcohol Use Disorder (AUD) and hazardous alcohol use. Participation in this study will last approximately 56 weeks.
What is the current status of trial NCT07219953?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 1,100 participants. The study started on 2025-10-16. Estimated completion is 2028-04.
What conditions does trial NCT07219953 study?
This clinical trial studies the following conditions: Alcohol Use Disorder. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07219953?
The interventions under investigation include: Placebo (DRUG), LY3537031 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07219953?
This trial is sponsored by Eli Lilly and Company, which has 704 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07219953 being conducted?
This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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