Frontlight ResearchEarly access
CompletedPhase 2
Efficacy and Safety of COMP360 Psilocybin Therapy in Anorexia Nervosa: a Proof-of-concept Study
Key facts
- Who runs it
- COMPASS Pathways
- Where
- Austin, Baltimore, and San Diego, United StatesSee the 3 sitesAlso in 2 other countries, 2 sites
- Trial code
- Status
- Completed
- Phase
- Phase 2
- People taking part
- 32 people enrolled
- Started
- 12 Oct 2022
- Ended
- 18 Nov 2024
- Type of study
- Interventional, 2 groupsOne group gets an existing treatment, for comparison.
- Treatments tested
- Psilocybin
- Record updated
- 4 December 2024
Who can take part
- Age
- 18 years and older
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
Show all 14 criteriaShow less
Who can take part
- Any sex and aged 18 years or above at screening
- 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
- 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
- Has a history of disordered eating with duration of at least 3 years prior to screening, that is consistent with AN
- 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
- Being otherwise medically stable at screening determined by clinical interview, clinical laboratory values, vital signs, ECG, and medical history
- Have at least one documented prior attempt at treatment in the past 3 years
Who cannot take part
- 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)
- Prior or ongoing paranoid, schizoid, schizotypal, histrionic, narcissistic personality disorder based on medical history and clinical judgment
- Borderline personality disorder as demonstrated by medical history, the MINI Plus - BPD and clinical judgment
- 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
- 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
- Other personal circumstances and behaviour judged to be incompatible with establishment of rapport or safe exposure to psilocybin
- Exposure to psilocybin, or any other psychedelics, such as ayahuasca, mescaline, LSD, or peyote within the past year
Where in United States
Also in 2 other countries, 2 sites
- Dell Medical SchoolAustin, United States
- Sheppard Pratt Health SystemBaltimore, United States
- Altman Clinical and Translational Research InstituteSan Diego, United States
About the trial
What the trial wants to find out
Efficacy and Safety of COMP360 Psilocybin therapy in Anorexia Nervosa: a Proof-of-concept Study
The 2 groups in the trial
- 25 mg COMP360 PsilocybinTreatment being tested
Treatment: Psilocybin
- 1 mg COMP360 PsilocybinExisting treatment, for comparison
Treatment: Psilocybin
Data and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Record updated
- 4 December 2024