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A Phase 2 Study of BNC210 for the Acute Treatment of Social Anxiety Disorder — PREVAIL  

Social Anxiety Disorder Clinical Trial

Official title:
A Phase 2, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of BNC210 Compared to Placebo for the Acute Treatment of Social Anxiety Disorder

Clinical Trial Summary

The purpose of this study is to assess the effects of an acute dose of BNC210 compared to placebo on reducing anxiety provoked by a speaking challenge and measured using the Subjective Units of Distress Scale (SUDS) in patients with Social Anxiety Disorder (SAD).

Clinical Trial Description

This is a randomized, double-blind, placebo-controlled, 3-arm, parallel-group, multi-center study. Participants will attend a Screening Visit to confirm eligibility and then return to the clinic within 14 days to be randomized into the study. Randomized participants will receive a single dose of their allocated study intervention (225 mg BNC210, 675 mg BNC210 or placebo) and approximately 1 hour later participate in a speaking challenge. After 1 week, a safety follow-up assessment will be conducted by phone/video conference. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05193409
Study type Interventional
Source Bionomics Limited
Contact
Status Completed
Phase Phase 2
Start date February 2, 2022
Completion date October 17, 2022
View Details
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