Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06303648Phase 1Completed
Phase 1, open-label trial of methylone in post-traumatic stress disorder (PTSD) (5 cohorts), sponsored by Transcend Therapeutics. Primary endpoints: Maximum Observed Plasma Concentration for methylone at 48 hours and Area under the plasma concentration-time curve for methylone at 48 hours. Started Mar 2024; status: completed.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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