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

Primary Purpose

Anorexia Nervosa

Status
Recruiting
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
Psilocybin
Sponsored by
COMPASS Pathways
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anorexia Nervosa

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept 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.

Sites / Locations

  • Altman Clinical and Translational Research InstituteRecruiting
  • Sheppard Pratt Health SystemRecruiting
  • New York State Psychiatric Institute
  • Tallaght University HospitalRecruiting
  • Kings College London, Institute of Psychiatry, Psychology and NeurologyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

25 mg COMP360 Psilocybin

1 mg COMP360 Psilocybin

Arm Description

25 mg COMP360 Psilocybin

1 mg COMP360 Psilocybin

Outcomes

Primary Outcome Measures

Change from baseline in the Eating Disorder Examination (EDE) global score
The EDE is a structured clinical interview (investigator rated) used to measure severity of the characteristic psychopathology of eating disorders

Secondary Outcome Measures

Safety
Proportion of patients with adverse events (AEs)
Change from baseline in Yale-Brown Obsessive Compulsive Scale (Y-BOCS)
The Y-BOCS self-rated version consists of a 10 item measure with a total score ranging from 0 to 40, with higher scores indicating increased severity of symptoms
Change from baseline in weight

Full Information

First Posted
July 28, 2022
Last Updated
July 11, 2023
Sponsor
COMPASS Pathways
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1. Study Identification

Unique Protocol Identification Number
NCT05481736
Brief Title
Efficacy and Safety of COMP360 Psilocybin Therapy in Anorexia Nervosa: a Proof-of-concept Study
Official Title
Efficacy and Safety of COMP360 Psilocybin Therapy in Anorexia Nervosa: a Proof-of-concept Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 12, 2022 (Actual)
Primary Completion Date
November 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
COMPASS Pathways

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Efficacy and Safety of COMP360 Psilocybin therapy in Anorexia Nervosa: a Proof-of-concept Study
Detailed Description
This study aims to explore the efficacy and safety of COMP360 25 mg as compared to COMP360 1 mg (control condition) administered with psychological support in participants with Anorexia Nervosa

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anorexia Nervosa

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
25 mg COMP360 Psilocybin
Arm Type
Experimental
Arm Description
25 mg COMP360 Psilocybin
Arm Title
1 mg COMP360 Psilocybin
Arm Type
Active Comparator
Arm Description
1 mg COMP360 Psilocybin
Intervention Type
Drug
Intervention Name(s)
Psilocybin
Other Intervention Name(s)
COMP360
Intervention Description
COMP360 Psilocybin administered under supportive conditions
Primary Outcome Measure Information:
Title
Change from baseline in the Eating Disorder Examination (EDE) global score
Description
The EDE is a structured clinical interview (investigator rated) used to measure severity of the characteristic psychopathology of eating disorders
Time Frame
Week 4
Secondary Outcome Measure Information:
Title
Safety
Description
Proportion of patients with adverse events (AEs)
Time Frame
Up to 12 weeks
Title
Change from baseline in Yale-Brown Obsessive Compulsive Scale (Y-BOCS)
Description
The Y-BOCS self-rated version consists of a 10 item measure with a total score ranging from 0 to 40, with higher scores indicating increased severity of symptoms
Time Frame
Week 4
Title
Change from baseline in weight
Time Frame
Up to 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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. Exclusion Criteria: 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. 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. 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. 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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Medical Director, MD
Email
COMP401trial@compasspathways.com
Facility Information:
Facility Name
Altman Clinical and Translational Research Institute
City
San Diego
State/Province
California
ZIP/Postal Code
92037
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jessie Kim
Email
jbk005@health.ucsd.edu
First Name & Middle Initial & Last Name & Degree
Alexandra Babakanian
Email
alexandrambabakanian@gmail.com
First Name & Middle Initial & Last Name & Degree
Walter Kaye, MD
Facility Name
Sheppard Pratt Health System
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21044
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kimberly Swartz
Email
kimberly.swartz@sheppardpratt.org
First Name & Middle Initial & Last Name & Degree
Audrey Shoultz
Email
audrey.shoultz@sheppardpratt.org
First Name & Middle Initial & Last Name & Degree
Scott Aaronson, MD
Facility Name
New York State Psychiatric Institute
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Caroline Touzeau
Email
caroline.touzeau@nyspi.columbia.edu
First Name & Middle Initial & Last Name & Degree
Evelyn Attia
Facility Name
Tallaght University Hospital
City
Dublin
Country
Ireland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Annie Baker
Email
psilocybin@crp.healthcare
First Name & Middle Initial & Last Name & Degree
John Kelly, MD
Facility Name
Kings College London, Institute of Psychiatry, Psychology and Neurology
City
London
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Katie Rowlands
Email
katie.rowlands@kcl.ac.uk
First Name & Middle Initial & Last Name & Degree
Hubertus Himmerich

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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

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