drugset / Trial / NCT03866174

A Study of Psilocybin for Major Depressive Disorder (MDD)

NCT03866174 ↗

Phase 2 Completed 347 enrolled Usona Institute The Emmes Company, LLC · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

One hundred participants, ages 21 to 65, who meet Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria for major depressive disorder (MDD) will be stratified by study site and randomized with a 1-to-1 allocation under double-blind conditions to receive a single 25 mg oral dose of psilocybin or a single 100 mg oral dose of niacin. Niacin will serve as an active placebo. The purpose of this study is to evaluate the potential efficacy of a single 25 mg oral dose of psilocybin for MDD compared to the active placebo in otherwise medically-healthy participants, assessed as the difference between groups in changes in depressive symptoms from Baseline to Day 43 post-dose.

Timeline

Start
2020-01-23
Primary completion
2022-06-28
Completion
2022-06-28

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Psilocybin Other / unclassified 25 mg Oral