Psilocybin therapy for adult females with anorexia nervosa: pilot study

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Authors: Hannah M. Douglass, Meg J. Spriggs, Kate Godfrey, Jennifer L. Danby, Frederico J. C. de Magalhaes, Lauren Macdonald, Kirsty L. Alderton, Stephanie Archer, Kirran Ahmad, Jonny Martell, Jennifer T. Frias, Gabriela Sawicka
+8 more Tim Read, Allan Blemings, Adèle Lafrance, Dasha Nicholls, David Erritzøe, Rebecca J. Park, David Nutt, Robin L. Carhart-Harris
Cited by: 1
References: 31

Abstract

Background Anorexia nervosa is a debilitating eating disorder with high mortality and chronicity rates owing to the paucity of effective existing treatments. Several clinical trials using psilocybin therapy have demonstrated therapeutic efficacy and safety in psychiatric conditions, including anorexia nervosa. Aims This study aimed to further assess the safety, feasibility and potential efficacy of psilocybin therapy in anorexia nervosa. Method This single-blind, within-individual pilot study recruited 21 females with anorexia nervosa, who underwent three dosing sessions with oral psilocybin (COMP360) over 6 weeks in a fixed order (1 mg, 25 mg, 25 mg), alongside talk therapy and adjunctive to treatment as usual. Adverse events were monitored throughout the study. Primary clinical outcome measures were global Eating Disorder Examination Interview (EDE) and Readiness and Motivation Questionnaire (RMQ) precontemplation scores. Primary time points for the EDE were the 6-week final visit, 3-month follow-up and 6-month follow-up; and for the RMQ, they were the 6-week final visit and comparison between dosing days. Global EDE Questionnaire scores were a key secondary outcome. Key time points were the 6-week final visit and comparison between dosing days. There was a 12-month remote follow-up. Results Psilocybin was well tolerated by all participants. The most common adverse events were headache, nausea and dizziness. Two serious adverse events (suicide attempts) were reported for one participant within the 6–12-month period. Relative to baseline, participants displayed significant improvements in their eating disorder symptoms (EDE scores: p < 0.0001, d = 0.98, 6 months) and motivation to change (RMQ scores: p = 0.0017, d = 0.65, 12 months). However, there was a large variation in improvement and maintenance during the follow-up. Conclusions This study further provides preliminary support for the feasibility, safety and potential efficacy of this intervention to treat adult females with anorexia nervosa, and warrants further investigation in larger and more rigorously designed studies.

Fields of Study & Subjects

Psychedelics and Drug Studies Pain Management and Placebo Effect Body Image and Dysmorphia Studies

Publication details

Journal / source
The British Journal of Psychiatry
Publisher
Royal College of Psychiatrists
Pages
1–9
Publication date
8 July 2026
Language
EN