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Study identifier: NCT02291861 Synced from ClinicalTrials.gov · August 02, 2026
● Completed

Addressing Involuntary Movements in Tardive Dyskinesia

Condition: Tardive Dyskinesia  ·  Sponsor: Auspex Pharmaceuticals, Inc.

PhasePhase 3
Planned participants298
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

The purpose of this study is to determine whether fixed-doses of an investigational drug, SD-809 (deutetrabenazine), will reduce the severity of abnormal involuntary movements of tardive dyskinesia.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (106)

Teva Investigational Site 145Tuscaloosa, Alabama, United States
Teva Investigational Site 107Anaheim, California, United States
Teva Investigational Site 108Anaheim, California, United States
Teva Investigational Site 123Glendale, California, United States
Teva Investigational Site 177Imperial, California, United States
Teva Investigational Site 160Irvine, California, United States
Teva Investigational Site 106Irvine, California, United States
Teva Investigational Site 176Loma Linda, California, United States
Teva Investigational Site 121Los Angeles, California, United States
Teva Investigational Site 147Los Angeles, California, United States
Teva Investigational Site 174Norwalk, California, United States
Teva Investigational Site 170Oceanside, California, United States

+ 94 more locations — full list on the registry record.

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