Purpose

Efficacy, Safety, and Tolerability of a single administration of COMP360 in participants with treatment-resistant depression (TRD)

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  1. Aged ≥18 years at Screening 2. Major depression without psychotic features (single or recurrent episode as informed by the Diagnostic and Statistical Manual of Mental Disorders, 5th edition [DSM-5]) 3. If the current major depressive episode is the participant's first lifetime episode of depression, the length of the current episode must be ≥3 months and ≤2 years at Screening 4. MADRS total score ≥20 at Screening and Baseline to ensure at least moderate severity of depression 5. TRD, defined as failure to respond to an adequate dose and duration of two, three, or four different pharmacological treatments for the current episode as determined through the Massachusetts General Hospital Antidepressant Treatment Response Questionnaire (MGH-ATRQ) and using the supplementary advice on additional antidepressants not included in MGH-ATRQ. 6. At Screening, agreement to discontinue all prohibited medications.

Exclusion Criteria

Psychiatric 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 as assessed by a structured clinical interview (MINI 7.0.2) 2. Lifetime paranoid, schizoid, schizotypal, histrionic, narcissistic personality disorder, or any ongoing serious psychiatric comorbidity based on medical history and clinical judgement 3. Borderline personality disorder as demonstrated by medical history or the Mini International Neuropsychiatric Interview Plus (MINI plus) - borderline personality disorder module 4. Ongoing post-traumatic stress disorder, obsessive-compulsive disorder, or anorexia nervosa as assessed by medical history and a structured clinical interview (MINI 7.0.2) 5. Psychiatric inpatient within the past 12 months prior to Screening 6. Use of electroconvulsive therapy, deep brain stimulation, or vagus nerve stimulation during the current depressive episode 7. Transcranial magnetic stimulation within the past six months prior to Screening 8. Current enrolment in a psychological therapy programme that will not remain stable for the duration of the study. Psychological therapies cannot have been initiated within 30 days prior to Screening 9. Exposure to COMP360 psilocybin therapy prior to Screening

Study Design

Phase
Phase 3
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
25 mg COMP360 Psilocybin
25 mg COMP360 Psilocybin
  • Drug: Psilocybin
    COMP360 Psilocybin administered under supportive conditions
    Other names:
    • COMP360
Placebo Comparator
Placebo
Matched placebo
  • Drug: Psilocybin
    COMP360 Psilocybin administered under supportive conditions
    Other names:
    • COMP360

Recruiting Locations

University of Arizona College of Medicine - Tuscon
Tucson, Arizona 85724
Contact:
Clinical and Translational Sciences Research Center (CATS)
520-626-8000
cats-med@arizona.edu

ProScience Research Group
Culver City, California 90230
Contact:
Victoria Garin
424-227-8127
Victoria.garin@proscience.com

Collaborative Neuroscience Network, LLC
Garden Grove, California 92845
Contact:
David Walling, MD
866-787-4257

Kadima Neuropsychiatry Institute
La Jolla, California 92037
Contact:
Kadima Neuropsychiatry Institute
858-412-4130
Research@Kadimanp.com

University California San Diego
La Jolla, California 92037
Contact:
Jennifer Crowhurst
858-249-0161
jcrowhurst@health.ucsd.edu

California Center for Psychedelic Therapy
Los Angeles, California 90004
Contact:
New School Research
comp005info@newschoolresearch.com

CalNeuro Research Group, Inc
Los Angeles, California 90025
Contact:
Navy Kaiser
310-208-7144
nkaiser@calneuroresearch.com

Clarity Clinical Research, LLC
Los Angeles, California 90064
Contact:
Raul Gonzalez
949-506-8486

ATP Clinical Research, Inc.
Orange, California 92868
Contact:
ATP Clinical Research
949-354-5353

Artemis Institute for Clinical Research
San Diego, California 92103
Contact:
Artemis Recruitment
recruitment@artemis-research.com

Lumos Clinical Research Center
San Jose, California 95124
Contact:
408-402-5424
asklumos@lumosclinical.com

Stanford University
Stanford, California 94305
Contact:
Maureen Chang
650-725-4620
mhchang@stanford.edu

ASCLEPES Research Centers
Thousand Oaks, California 93012
Contact:
Mandeep Sublok
747-998-0394
msablok@asclepes.com

Comprehensive Psychiatric Care
Norwich, Connecticut 06360
Contact:
Lauren Vilchinsky
203-741-8876
lvilchinsky@cpccare.com

Clinical Neurosciecne Solutions, Inc. dba CNS Healthcare
Orlando, Florida 32801
Contact:
Felipe Suplicy, MD
407-425-5100
awesterfeld@cnshealthcare.com

APG Research, LLC
Orlando, Florida 32803
Contact:
Morteza Nadjafi, MD
407-423-7149
sarahvapg@gmail.com

DMI Health Care Group, Inc
Tampa, Florida 33782
Contact:
Schiara Kitwood
727-506-3421
skitwood@dmiresearch.com

Meridien Research/Accel Research
Tampa, Florida 33803
Contact:
Colleen Figueroa
863-940-2087

Psych Atlanta
Atlanta, Georgia 30060
Contact:
Jennifer Kane
770-422-2846
jenniferk@psychatlanta.com

Emory University
Atlanta, Georgia 30329-2209
Contact:
Tanja Mletzko
404-778-6663
tmletzk@emory.edu

Uptown Research Institute, LLC
Chicago, Illinois 60640
Contact:
Stephen Schneider
773-989-8313
sschneider@uptownresearch.com

Sheppard Pratt Health System
Baltimore, Maryland 21044
Contact:
Scott Aaronson, MD
iadtclinicaltrials@sheppardpratt.org

CBH Health, LLC
Gaithersburg, Maryland 20877
Contact:
Logan Gaither
301-251-4702
l.gaither@cenexel.com

Pharmasite Research, Inc
Pikesville, Maryland 21208
Contact:
Phyllis Erickson
667-770-6495
perickson@pharmasiteresearch.com

University of Massachusetts Medical School
North Worcester, Massachusetts 01655
Contact:
508-856-1882
CPRTResearchOffice@umassmed.edu

University of Minnesota
Minneapolis, Minnesota 55416
Contact:
Maryam Sham Dim
952-525-4505
ipl@umn.edu

University of Missouri
Columbia, Missouri 65212
Contact:
Mihiri De Silva
573-424-4632
desilvam@health.missouri.edu

Midwest Research Group
Saint Charles, Missouri 63304

Washington University School of Medicine
Saint Louis, Missouri 63110
Contact:
Demetrius Perry
314-747-5514
perry.demetrius@wustl.edu

Alivation Research, LLC.
Lincoln, Nebraska 68526
Contact:
Grant Wessel
402-817-2240
gwessel@alivation.com

Bio Behavioral Health
Toms River, New Jersey 08755
Contact:
Jessica Sutton
732-244-2299
jessica@bbhnj.com

New York State Psychiatric Institute
New York, New York 10032
Contact:
Genevieve Falabella
DESdesk@nyspi.columbia.edu

The Medical Research Network, LLC
New York, New York 10128
Contact:
Matt T
212-595-5012
MTurzilli@medicalresearchnetwork.com

Neuro-Behaviroral Clinical Research, Inc.
North Canton, Ohio 44720
Contact:
Crystal Blackford
Cblackford@nb-cr.com

Rivus Wellness & Research Institute
Oklahoma City, Oklahoma 73112
Contact:
Melissa Kelton
405-517-4201
melissa@rivusinstitute.com

Global Medical Institutes, LLC, Scranton Medical Institute
Moosic, Pennsylvania 18507
Contact:
Zoha Babar
zbabar@gminstitutes.com

UT Health Science Center at Houston (UTHSC-H)
Houston, Texas 77030
Contact:
Jair C. Soares, MD
713-486-2697
UTMoodDisorders@uth.tmc.edu

Cedar Clinical Research
Draper, Utah 84020
Contact:
Lovelle Goldenpenny
lovelle.goldenpenny@numinus.com

Core Clinical Research
Everett, Washington 98201
Contact:
Maria Golescu
425-443-9551
maria.golescu@ccrtrial.com

More Details

NCT ID
NCT05624268
Status
Recruiting
Sponsor
COMPASS Pathways

Study Contact

Medical Director, MD
COMP005@compasspathways.com

Detailed Description

This is a phase III, international, multi-centre, randomised, parallel group, fixed single-dose, double-blind, placebo-controlled study. The study population will include participants aged ≥18 years with TRD. Overall, 255 participants will be randomised in a 2:1 ratio to receive COMP360 25 mg or placebo. The study comprises three parts (A, B, and C) and will last approximately 62 weeks including a three- to ten-week Screening Period. Part A will include a six-week follow-up from initial investigational product (IP) administration. In this study, the primary aim is to assess the efficacy and safety of a single dose of COMP360 25 mg versus placebo for reducing symptom severity in TRD, when administered with psychological support. This will be assessed in a 6-week, single-dose, double-blind, placebo-controlled part of the study (Part A). Durability of efficacy and long-term safety, and the efficacy and safety of re-treatment will be assessed in a 20-week single-dose, double-blind re-treatment part (Part B), and a 26-week open-label treatment part (Part C).

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.