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From trial to clinic: psilocybin’s efficacy in routine treatment-resistant depression

Vassilis Martiadis

The Lancet Regional Health - Europe July 15, 2026 DOI: 10.1016/j.lanepe.2026.101780 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Observational cohort Randomized Peer reviewed
Sample size 19
Population Adults with treatment-resistant depression
Intervention Psilocybin
Topics Depression Psilocybin
Keywords Depression economics Clinical trial Medline Disease Population
Key findings Among 19 adults with treatment-resistant depression treated with psilocybin in routine clinical practice, clinician-rated depressive symptoms decreased substantially, with a Montgomery–Åsberg reduction of approximately 11 points and Hedges' g ≈ 1.4.

Abstract

The question of whether the striking antidepressant effects of psilocybin reported in randomised trials can be reproduced in everyday care remains largely unanswered. This is because those trials enrol highly selected patients, withdraw concomitant medication and deliver treatment under tightly standardised protocols. In this issue, Jungwirth et al. provide one of the first responses from routine clinical practice.1 Among 19 adults with treatment-resistant depression (TRD) who were treated with psilocybin under Switzerland’s limited medical use framework, clinician-rated symptoms decreased substantially (a Montgomery–Åsberg reduction of approximately 11 points; Hedges’ g ≈ 1.4).