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NCT07204249 · ClinicalTrials.gov registry record · Phase 2

Glutide for Ending Methamphetamine

A Phase 2 study, sponsored by San Francisco Department of Public Health.

Recruiting
Registry status
Phase 2
Development phase
162
Enrollment target

NCT07204249: Recruiting Phase 2 study, sponsored by San Francisco Department of Public Health.

NCT07204249 is a Phase 2 study that is actively recruiting participants, run by San Francisco Department of Public Health. The registered enrollment target is 162 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (22% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07204249, a Phase 2 study, is actively recruiting participants, sponsored by San Francisco Department of Public Health.

RECRUITING
Registry status
Phase 2
Development phase
162 participants
Enrollment target

Study Summary

GEM is a two-phase study to evaluate the use of semaglutide (Wegovy) for the treatment of methamphetamine use disorder (MeUD). The first phase is a pilot study, which will be an open-label, single-arm pilot study of 25 participants. Participants will receive Wegovy over a 12-week treatment period, with a subsequent follow-up visit at week 20. This phase will evaluate the feasibility, acceptability, and preliminary efficacy of Wegovy for MeUD. The second phase will be a phase IIb randomized-controlled trial to determine the efficacy of Wegovy in treating MeUD. This trial will be similar to the pilot with randomization to Wegovy or placebo and blinding of group assignment. The trial will enroll 162 participants across two sites.

Primary Outcome

Feasibility of Wegovy for MeUD treatment: Feasibility will be determined by measuring the ratio of eligible to enrolled participants

Interventions

  • DRUG Placebo
  • DRUG Semaglutide

Trial Details

FieldValue
Enrollment Target 162 participants
Start Date 2026-02-26
Est. Completion 2030-02-15
Phase Phase 2

What NCT07204249 shows while recruiting

NCT07204249 is an interventional study that assigns participants to a tested intervention. The registered 162 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (22% higher).

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

NCT07204249 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07204249 about?

NCT07204249 is a clinical study titled "Glutide for Ending Methamphetamine". GEM is a two-phase study to evaluate the use of semaglutide (Wegovy) for the treatment of methamphetamine use disorder (MeUD). The first phase is a pilot study, which will be an open-label, single-arm pilot study of 25 participants. Participants will receive Wegovy over a 12-week treatment period, ...

What is the current status of trial NCT07204249?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 162 participants. The study started on 2026-02-26. Estimated completion is 2030-02-15.

What interventions are being tested in trial NCT07204249?

The interventions under investigation include: Placebo (DRUG), Semaglutide (DRUG).

Who is sponsoring clinical trial NCT07204249?

This trial is sponsored by San Francisco Department of Public Health, which has 13 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07204249's enrollment target sits among peer trials

162 418th of 2000 higher than 1,579 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 NCT07204249, the US trial registry maintained by the National Library of Medicine. NCT07204249 (mid enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.