Clinical Trial

Psilocybin as a Novel Therapy for Residual Anhedonia

Not Yet Recruiting Phase 1
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Summary
The primary objective is to evaluate whether a single dose of psilocybin (25 mg), compared to placebo, can restore fronto-striatal reward circuit function and thereby improve anhedonia and emotional blunting in individuals with residual symptoms despite ongoing SSRI or SNRI treatment. This will be assessed using precision functional mapping (PFM), task-based fMRI, and clinical rating scales (DARS).
Trial Details
NCT Number NCT07607938
Lead Sponsor NYU Langone Health
Collaborators: National Institute of Mental Health (NIMH)
Conditions Anhedonia, Emotional Blunting
Enrollment 90 participants
Start Date 2026-07
Primary Completion 2030-08-01 (estimated)
Study Completion 2030-09-30 (estimated)
Updated on ClinicalTrials.gov 2026-05-27