CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 22 enrolled
Drug / intervention
BHV-0223 +1 moredrug
Likely dose
BHV-0223 35mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03017508
NCT03017508Phase 3Completed

Double-Blind, Placebo-Controlled, Single-Dose Crossover Study Examining the Effects of Sublingual Riluzole (BHV-0223) on Public Speaking in Social Anxiety Disorder

Yale University·interventional·Posted Jan 11, 2017·Updated May 20, 2021

In Brief

A Phase 3 clinical trial evaluating BHV-0223 and Placebo for Social Anxiety Disorder and Performance Anxiety. Completed, enrolled 22 participants across 1 site.

Detailed Summary

The goal of the current proposal is to examine if sublingual riluzole can reduce anxiety in people with social anxiety disorder during a public speaking task.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 3CompletedFinished
2017201820192020202120222023202420252026
First PostedJan 11, 2017
Enrollment StartJan 1, 2017
Primary CompletionDec 1, 2019
Study CompletionJan 29, 2021
TodayJul 2, 2026
Enrollment to primary: 2.9 yearsPosted 9.5 years ago

Interventions

BHV-0223drug

35mg of sublingual riluzole before performing an anxiety provoking speech task. Participants will then be clinically assessed every hour for 3 hours.

Placebodrug

a sublingual tablet identical to the active drug will be given before performing an anxiety provoking speech task. Participants will then be clinically assessed every hour for three hours.