Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Addressing Involuntary Movements in Tardive Dyskinesia

ClinicalTrials.gov ID: NCT02291861

Public ClinicalTrials.gov record NCT02291861. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 1, 2026, 2:31 AM EST

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled, Fixed-Dose Study of SD-809 (Deutetrabenazine) for the Treatment of Moderate to Severe Tardive Dyskinesia

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT02291861
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Auspex Pharmaceuticals, Inc.
Industry
Enrollment
298 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2014 (Actual)
Primary completion
Aug 19, 2016 (Actual)
Completion
Aug 19, 2016 (Actual)
Last update posted
Jun 23, 2026

2014 – 2016

United States locations

U.S. sites
53
U.S. states
24
U.S. cities
46
Facility City State ZIP Site status
Teva Investigational Site 145 Tuscaloosa Alabama 35404 —
Teva Investigational Site 107 Anaheim California 92804 —
Teva Investigational Site 108 Anaheim California 92805 —
Teva Investigational Site 123 Glendale California 91206 —
Teva Investigational Site 177 Imperial California 92251 —
Teva Investigational Site 160 Irvine California 92614 —
Teva Investigational Site 106 Irvine California 92697 —
Teva Investigational Site 176 Loma Linda California 92354 —
Teva Investigational Site 121 Los Angeles California 90033 —
Teva Investigational Site 147 Los Angeles California 90095-1769 —
Teva Investigational Site 174 Norwalk California 90650 —
Teva Investigational Site 170 Oceanside California 92056 —
Teva Investigational Site 102 Orange California 92868 —
Teva Investigational Site 104 San Bernardino California 92408 —
Teva Investigational Site 110 San Diego California 92108 —
Teva Investigational Site 169 San Rafael California 94901 —
Teva Investigational Site 129 Englewood Colorado 80113 —
Teva Investigational Site 139 New Haven Connecticut 06519 —
Teva Investigational Site 156 Washington D.C. District of Columbia 20007 —
Teva Investigational Site 157 Boca Raton Florida 33486 —
Teva Investigational Site 117 Gainesville Florida 32607 —
Teva Investigational Site 150 Lake City Florida 32025 —
Teva Investigational Site 153 Miami Florida 33135 —
Teva Investigational Site 162 Miami Florida 33165 —
Teva Investigational Site 112 Orlando Florida 32803 —
Teva Investigational Site 144 Port Charlotte Florida 33980 —
Teva Investigational Site 155 Augusta Georgia 30912 —
Teva Investigational Site 165 Decatur Georgia 30033 —
Teva Investigational Site 131 Chicago Illinois 60611 —
Teva Investigational Site 113 Chicago Illinois 60612 —
Teva Investigational Site 164 Kansas City Kansas 66160 —
Teva Investigational Site 154 Baltimore Maryland 21287 —
Teva Investigational Site 101 Glen Burnie Maryland 21061 —
Teva Investigational Site 135 Boston Massachusetts 02215 —
Teva Investigational Site 118 Creve Coeur Missouri 63141 —
Teva Investigational Site 142 Kansas City Missouri 64108 —
Teva Investigational Site 175 St Louis Missouri 63104 —
Teva Investigational Site 161 St Louis Missouri 63109 —
Teva Investigational Site 178 Lincoln Nebraska 68526-9467 —
Teva Investigational Site 128 Albuquerque New Mexico 87106 —
Teva Investigational Site 172 Commack New York 11725 —
Teva Investigational Site 148 New York New York 10032 —
Teva Investigational Site 138 Asheville North Carolina 28805 —
Teva Investigational Site 146 Raleigh North Carolina 27610 —
Teva Investigational Site 133 Charleston South Carolina 29425 —
Teva Investigational Site 149 Memphis Tennessee 38163 —
Teva Investigational Site 151 Fort Worth Texas 76104 —
Teva Investigational Site 115 Salt Lake City Utah 84105 —
Teva Investigational Site 141 Salt Lake City Utah 84108 —
Teva Investigational Site 168 Burlington Vermont 05401 —
Teva Investigational Site 171 Charlottesville Virginia 22903 —
Teva Investigational Site 167 Richland Washington 99352 —
Teva Investigational Site 166 Waukesha Wisconsin 53188 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 53 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02291861, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 23, 2026 · Synced Nov 1, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02291861 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →