drugset / Trial / NCT04800237

Evaluating the Effects of VQW-765 vs. Placebo in Performance Anxiety

NCT04800237 ↗

Phase 2 Completed 230 enrolled Vanda Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a multicenter, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of a single oral dose of VQW-765 compared to placebo in male and female participants with performance anxiety.

Timeline

Start
2021-02-23
Primary completion
2022-08-02
Completion
2022-08-02

Drugs

EvaluationDrugModalityDoseRoute
Subject VQW-765 Unknown — Oral

Indications

No indication recorded.