drugset / Trial / NCT06666010

PEX010-Assisted Therapy for Stimulant Use Disorder: A Safety, Feasibility and Efficacy Study

NCT06666010 ↗

Phase 2 Not yet recruiting 86 enrolled Filament Health Corp. University of British Columbia · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The goal of this clinical trial is to learn if PEX010 is effective for the treatment of Stimulant Use Disorder in adults. The study will also assess the safety and feasibility of administering PEX010 to this population. The main questions it aims to answer are: Does PEX010 reduce stimulant use? What medical problems do participants experience when taking PEX010? Researchers will compare an active PEX010 dose containing 25 mg psilocybin to an active placebo arm, to see if PEX010 works to reduce stimulant use. Participants will: Take PEX010 or the active placebo once during the study, engage in cognitive behavioural therapy, and visit the clinic twice weekly for study intervention and follow-up assessments.

Timeline

Start
2025-01
Primary completion
2028-01
Completion
2028-07

Drugs

EvaluationDrugModalityDoseRoute
Subject PYEX Unknown 25 mg Oral