drugset / Trial / NCT02198794

Reducing Involuntary Movements in Participants With Tardive Dyskinesia

NCT02198794 ↗

Phase 3 Completed 343 enrolled Auspex Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the long-term safety, tolerability, and efficacy of SD-809 in reducing the severity of abnormal involuntary movements of moderate to severe tardive dyskinesia. The purpose of part B is to establish the durability of effect of SD-809 following 1-week period of randomized withdrawal (SD-809 and placebo), followed by 12 weeks of maintenance with SD-809.

Timeline

Start
2014-10-20
Primary completion
2019-12-06
Completion
2020-12-14

Outcome

Missed primary endpoint

registry p = 0.121; Least Square (LS) Mean Difference -0.6 (95% CI -1.42 to 0.17) NCT02198794 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Deutetrabenazine Unknown — Oral

Indications