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NCT03169244 · ClinicalTrials.gov registry record · Phase 2

Buproprion for Binge Drinking

A Phase 2 study, sponsored by University of North Carolina, Chapel Hill.

Completed
Registry status
Phase 2
Development phase
42
Enrollment target

NCT03169244: Completed Phase 2 study, sponsored by University of North Carolina, Chapel Hill.

NCT03169244 is a Phase 2 study that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 42 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (68% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03169244, a Phase 2 study, has completed, sponsored by University of North Carolina, Chapel Hill.

COMPLETED
Registry status
Phase 2
Development phase
42 participants
Enrollment target

Study Summary

The present proposal is an innovative and translational clinical trial derived from exciting preclinical findings to test the hypothesis that treatment with the melanocortin activator bupropion can reduce binge drinking in humans. Furthermore, pilot data on moderating effects of coexisting nicotine use on the efficacy of bupropion for binge drinking population will be obtained. Evidence for an efficacy signal with good tolerability with this FDA approved medication would form the foundation to conduct a well-powered Phase II b trial. The development of an effective pharmacotherapy for binge drinking would be a significant clinical advance. .

Primary Outcome

Frequency is assessed as number of binge episodes/time in trial controlling for missing data.

Interventions

  • DRUG Placebo Oral Tablet
  • DRUG Bupropion

Trial Details

FieldValue
Enrollment Target 42 participants
Start Date 2017-09-04
Est. Completion 2019-09-17
Phase Phase 2

What the finished NCT03169244 record still lists

NCT03169244 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 42 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (68% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo Oral Tablet is the first listed.

NCT03169244 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03169244 about?

NCT03169244 is a clinical study titled "Buproprion for Binge Drinking". The present proposal is an innovative and translational clinical trial derived from exciting preclinical findings to test the hypothesis that treatment with the melanocortin activator bupropion can reduce binge drinking in humans. Furthermore, pilot data on moderating effects of coexisting nicotine ...

What is the current status of trial NCT03169244?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 42 participants. The study started on 2017-09-04. Estimated completion is 2019-09-17.

What interventions are being tested in trial NCT03169244?

The interventions under investigation include: Placebo Oral Tablet (DRUG), Bupropion (DRUG).

Who is sponsoring clinical trial NCT03169244?

This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03169244's enrollment target sits among peer trials

42 1339th of 2000 higher than 649 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03169244, the US trial registry maintained by the National Library of Medicine. NCT03169244 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.