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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05646303
Other study ID # CLA PSY 201
Secondary ID
Status Recruiting
Phase Phase 2
First received
Last updated
Start date May 2, 2022
Est. completion date October 2024

Study information

Verified date September 2023
Source Clairvoyant Therapeutics
Contact Teresa Yan
Email hello@clairvoyantrx.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical trial is to investigate treatment with psilocybin and psychotherapy for the treatment of people with Alcohol Use Disorder (AUD). The main question[s] it aims to answer are: - Does treatment with psilocybin and therapy help reduce alcohol consumption more than placebo and therapy? - Is treatment with psilocybin and therapy safe for participants? Participants will - Attend 13 study visits - Take part in therapy sessions including 2 treatment sessions with either psilocybin or placebo - Record their daily alcohol consumption on study specific device Researchers will compare psilocybin and placebo groups to see if alcohol consumption is decreased.


Recruitment information / eligibility

Status Recruiting
Enrollment 128
Est. completion date October 2024
Est. primary completion date May 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Moderate to severe diagnosis of AUD as measured by Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) criteria using Structured Clinical Interview for DSM-5 by the investigator. - Expressed a wish to reduce or stop alcohol consumption. - Generally healthy with no unstable medical conditions, as determined by medical history, physical examination, routine blood labs, electrocardiogram, urine analysis, and urine toxicology. Exclusion Criteria: - Diagnosed with or having a family history of any of the following concomitant psychiatric disorders: schizophrenia or prodromal symptoms, any bipolar disorder, obsessive compulsive disorder, or other psychotic episode. Recent (within last 12 months) diagnosis of a major depressive disorder (MDD) (HAM-D score >19), treatment resistant depression (TRD), post-traumatic stress disorder (PTSD), panic disorder, or eating disorders. - Subjects deemed unfit for psilocybin-assisted therapy based on the assessments made during psychotherapy sessions prior to the first psilocybin-assisted psychotherapy session. - History of hallucinogen use disorder, or any use in the past 1 year, or >25 lifetime uses.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Psilocybin
Psilocybin and psychotherapy
Placebo
Placebo and psychotherapy

Locations

Country Name City State
Canada Sabi Mind Calgary Alberta
Canada Centricity Research Halifax Nova Scotia
Canada MacAnxiety Research Centre Hamilton Ontario
Canada Okanagan Clinical Trials Kelowna British Columbia
Canada Department of Psychiatry, Queen's University Kingston Ontario
Canada Centre for Neurology Studies Surrey British Columbia
Canada Centre for Addiction and Mental Health Toronto Ontario
Canada University of British Columbia, Department of Psychiatry, BRAIN Lab Vancouver British Columbia
Finland Research Center Oxidi Oy / Addiktum Oy Helsinki
Finland A-Klinikka Kouvola
Finland Mentacare Oy Oulu
Finland Addiktum Oy Turku

Sponsors (2)

Lead Sponsor Collaborator
Clairvoyant Therapeutics Optimapharm

Countries where clinical trial is conducted

Canada,  Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Reduction in the number of Heavy Drinking Days Mean number of HDD from V5 (baseline) measured monthly (4 weeks) over the treatment period (Week 8), where heavy drinking is defined as the consumption of =60 g alcohol/day (if male) or =40 g alcohol/day (if female). 8 weeks
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