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Psilocybin therapy for adult females with anorexia nervosa: pilot study.

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, Tim Read, Allan Blemings, Adele Lafrance, Dasha Nicholls, David Erritzøe, Rebecca J. Park, David J. Nutt, Robin L. Carhart-Harris

Br J Psychiatry July 8, 2026 DOI: 10.1192/bjp.2026.10687 via PubMed

Summary

AI-generated from the abstract

In a small pilot study, 21 women with anorexia nervosa received three doses of psilocybin (COMP360) over six weeks, combined with talk therapy and usual care. The treatment was well tolerated; common side effects were headache, nausea, and dizziness. Two serious adverse events (suicide attempts) occurred in one participant during the 6–12 month period. Eating disorder symptoms significantly improved at six months, and motivation to change improved at twelve months, though individual responses varied widely. The findings provide preliminary support for the feasibility and safety of psilocybin therapy in this population, but larger, more rigorous studies are needed.

Study at a glance

Characteristics Single-blind, within-individual pilot study Peer reviewed
Sample size 21
Population Adult females with anorexia nervosa
Intervention Psilocybin (COMP360)
Dose 1 mg, 25 mg, 25 mg
Duration 6-week intervention, 3-month follow-up, 6-month follow-up, 12-month remote follow-up
Key finding Psilocybin therapy was associated with significant improvements in eating disorder symptoms and motivation to change in adult females with anorexia nervosa, with large individual variation in outcomes.

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.

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