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CompletedPhase 2

Efficacy and Safety of COMP360 Psilocybin Therapy in Anorexia Nervosa: a Proof-of-concept Study

NCT05481736 · COMPASS Pathways

Closed to entry
Status
Not accepting participants
Phase 2
Phase
32
Target enrolment
5
Study sites
3 US states

What it is testing

Summary

Efficacy and Safety of COMP360 Psilocybin therapy in Anorexia Nervosa: a Proof-of-concept Study

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • Change from baseline in the Eating Disorder Examination (EDE) global score

    Measured over Week 4

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

18 Years
Ages
All
Sex
Not accepted
Healthy volunteers
Inclusion Criteria: 1. Any sex and aged 18 years or above at screening. 2. Meeting criteria for AN either restrictive or binge-purging type, according to the DSM-5, based on medical records, clinical assessment, BMI, and documented completion of MINI 7.0.2 and EDE at screening. 3. Have successfully discontinued all prohibited medications for a period of at least two weeks prior to baseline. For fluoxetine (Prozac), immediate cessation at screening period visit 1a followed by at least four weeks of washout will be required prior to baseline. 4. Has a history of disordered eating with duration of at least 3 years prior to screening, that is consistent with AN. 5. BMI ≥15 kg/m2 and ≤20 kg/m2. For participants with a BMI \<16 kg/m2 and \>18.5 kg/m2 at screening, approval from the Medical Monitor will be required. Any participant with a BMI \>18.5 kg/m2 must meet all of the criteria for AN except that, despite significant weight loss, the individual's weight is within or above the normal range. 6. Being otherwise medically stable at screening determined by clinical interview, clinical laboratory values, vital signs, ECG, and medical history. 7. Have at least one documented prior attempt at treatment in the past 3 years. Exclusion Criteria: 1. Prior or ongoing bipolar disorder, any psychotic disorder, including schizophrenia, schizophreniform disorder, schizoaffective disorder, brief psychotic disorder (unless substance induced or due to a medical condition), antisocial personality disorder, or any serious psychiatric comorbidity as assessed by medical history and a structured clinical interview (MINI 7.0.2). 2. Prior or ongoing paranoid, schizoid, schizotypal, histrionic, narcissistic personality disorder based on medical history and clinical judgment. 3. Borderline personality disorder as demonstrated by medical history, the MINI Plus - BPD and clinical judgment. 4. Significant suicide risk as defined by (1) suicidal ideation as endorsed on items 4 or 5 on the C-SSRS within the past year, at screening or at baseline, or; (2) suicidal behaviours within the past year or; (3) clinical assessment of significant suicidal risk during participant interview. 5. Current (within last year) alcohol or substance use disorder as informed by the DSM-5 assessed via the MINI 7.0.2, and urine toxicology at screening. 6. Other personal circumstances and behaviour judged to be incompatible with establishment of rapport or safe exposure to psilocybin. 7. Exposure to psilocybin, or any other psychedelics, such as ayahuasca, mescaline, LSD, or peyote within the past year.

Where

5 study sites

FacilityCityRegionCountry
Altman Clinical and Translational Research InstituteSan DiegoCaliforniaUnited States
Sheppard Pratt Health SystemBaltimoreMarylandUnited States
Dell Medical SchoolAustinTexasUnited States
Tallaght University HospitalDublinIreland
Kings College London, Institute of Psychiatry, Psychology and NeurologyLondonUnited Kingdom

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT05481736 on ClinicalTrials.gov →

Last updated in the registry 2024-12-04. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits