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OpenTrials
Completed

NCT Number: NCT05600114

Cannabidiol (CBD) for the Treatment of Social Anxiety Disorder

A phase 2, multicenter, double-blind, parallel group, placebo-controlled, randomized clinical study, designed to compare the efficacy, safety, and tolerability of 2 dose levels of CBD and a matching placebo for the treatment of subjects with Social Anxiety Disorder (SAD).

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

EPI-CBD-001 Site, Encino, California, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinically predominant diagnosis of Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) SAD
  • LSAS score of 70 or higher
  • Females of childbearing potential must test negative for pregnancy and agree to use a reliable birth control method. Male subjects must also agree to use highly effective methods of contraception.
  • Read, understand, and sign the informed consent form.
  • No significant physical health abnormalities based on physical exam, ECG and laboratory tests.

Exclusion criteria

  • Other current psychiatric disorder as the clinically predominant diagnosis.
  • Lifetime diagnosis of schizophrenia or any other psychosis, MDD with psychotic features, intellectual disability, autism spectrum disorders, bipolar disorder type 1, and cannabis use disorder
  • Previous 6 months diagnosis of Post-traumatic stress disorder, obsessive compulsive disorder, moderate to severe alcohol use disorder, and substance abuse disorder (except tobacco use disorder or mild alcohol use disorder)
  • Severe MDD
  • Use of oral psychoactive medications or beta adrenergic antagonists in the past 4 weeks, or depot neuroleptics within 12 weeks
  • Electroconvulsive therapy within 6 months, psychotherapy or transcranial magnetic stimulation within 3 months
  • Clinically significant abnormality or clinically significant unstable medical condition
  • Impaired liver function
  • Significant risk of suicide or homicide
  • Pregnancy/lactation
  • Sensitivity to CBD or excipients
  • Current cannabis use; past frequent cannabis use
  • Illegal drug use

Treatment and study plan

Cannabidiol Oral Solution

Drug

CBD 150 mg BID

Placebo

Drug

Placebo BID

Primary outcomes

  1. Mean change from baseline to endpoint in the Liebowitz Social Anxiety Scale (LSAS)

    Time frame: 10 weeks

Sponsors and collaborators

Lead sponsor

EmpowerPharm Inc.

Industry

Registry information

Official study title

A Randomized, Double-Blind, Parallel Group, Placebo-Controlled Study, Evaluating the Efficacy, Safety, and Tolerability of Cannabidiol Oral Solution in Subjects With Social Anxiety Disorder

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Oct 31, 2022
Registry last updated
Nov 21, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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