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Completed Phase 2 Interventional

Cannabidiol (CBD) for the Treatment of Social Anxiety Disorder

ClinicalTrials.gov ID: NCT05600114

Public ClinicalTrials.gov record NCT05600114. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 7, 2026, 12:02 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official 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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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).

Study identification

NCT ID
NCT05600114
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
EmpowerPharm Inc.
Industry
Enrollment
239 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 27, 2022 (Actual)
Primary completion
Dec 13, 2023 (Actual)
Completion
Dec 13, 2023 (Actual)
Last update posted
Nov 21, 2024

2022 – 2023

United States locations

U.S. sites
17
U.S. states
8
U.S. cities
17
Facility City State ZIP Site status
EPI-CBD-001 Site Encino California 91316 —
EPI-CBD-001 Site Lemon Grove California 91945 —
EPI-CBD-001 Site Los Alamitos California 90720 —
EPI-CBD-001-Site Oceanside California 92056 —
EPI-CBD-001 site San Jose California 95124 —
EPI-CBD-001 Site Jacksonville Florida 32256 —
EPI-CBD-001 Site Lauderhill Florida 33319 —
EPI-CBD-001 Site Maitland Florida 32751 —
EPI-CBD-001 Site Orlando Florida 32801 —
EPI-CBD-001 Site Chicago Illinois 60640 —
EPI-CBD-001 Site Cedarhurst New York 11516 —
EPI-CBD-001-Site New York New York 10036 —
EPI-CBD-001-Site Rochester New York 10036 —
EPI-CBD-001 Site Oklahoma City Oklahoma 73106 —
EPI-CBD-001 Site Portland Oregon 97210 —
EPI-CBD-001 site Wichita Falls Texas 76309 —
EPI-CBD-001 Site Bellevue Washington 98007 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05600114, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 21, 2024 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05600114 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →