Study of Psilocybin for Anorexia in Young Adults
NCT06399263 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 40
Last updated 2026-03-03
Summary
This is a single site trial of psilocybin therapy for the treatment of refractory Anorexia Nervosa in young adults. The psilocybin therapy will include three preparatory sessions, psilocybin dosing session one (20mg), two integration sessions, psilocybin dosing session two (up to 25mg), and three final integration sessions. Eating disorder symptoms will be measured pre and post treatment. One to two family member(s) of each young adult participant will be enrolled in the study. One of which will be required to attend a portion of two preparatory sessions and a portion of two integration sessions and receive psychoeducation about supporting the young adult participant through preparation and integration for psilocybin therapy. Investigators hypothesize that psilocybin will increase cognitive flexibility and that this increase will predict long-term changes in cognitive rigidity, habitual eating, and exercise behaviors in patients with Anorexia Nervosa.
Conditions
- Anorexia Nervosa
Interventions
- DRUG
-
The psilocybin will include two dose administration sessions, first a 20mg administration, and second an administration of up to 25mg.
- BEHAVIORAL
-
Preparation and Integration Sessions
The psilocybin therapy will include three preparatory sessions, two dose A integration sessions, and four final integration sessions.
Sponsors & Collaborators
-
Marissa Raymond-Flesch, MD, MPH
lead OTHER
Principal Investigators
-
Marissa Raymond-Flesch, MD · University of California, San Francisco
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 25 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-11-18
- Primary Completion
- 2029-11-30
- Completion
- 2029-11-30
- FDA Drug
- Yes
Countries
- United States
Study Locations
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