Study of the Effectiveness of Valbenazine on Patient- and Clinician-Reported Outcomes in Participants With Tardive Dyskinesia
Completed · Phase 4
Conditions studied: Schizophrenia, Schizoaffective Disorder, Bipolar Disorder, Major Depressive Disorder, Tardive Dyskinesia
In brief
This study will evaluate the effectiveness of valbenazine on patient- and clinician-reported outcomes assessing health-related quality of life, functioning, and treatment effect in participants with tardive dyskinesia (TD) who are receiving valbenazine for up to 24 weeks.
Key facts
- Study ID
- NCT05859698
- Run by
- Neurocrine Biosciences
- People needed
- 59
- Starts
- 2023-05-09
- Expected to finish
- 2024-12-27
- Last updated by the study team
- 2026-01-16
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Neurocrine Clinical Site — Bryant, Arkansas, United States
- Neurocrine Clinical Site — Anaheim, California, United States
- Neurocrine Clinical Site — Orange, California, United States
- Neurocrine Clinical Site — Torrance, California, United States
- Neurocrine Clinical Site — Bonita Springs, Florida, United States
- Neurocrine Clinical Site — Miami, Florida, United States
- Neurocrine Clinical Site — Miami Lakes, Florida, United States
- Neurocrine Clinical Site — Okeechobee, Florida, United States
- Neurocrine Clinical Site — Tampa, Florida, United States
- Neurocrine Clinical Site — Atlanta, Georgia, United States
- Neurocrine Clinical Site — Augusta, Georgia, United States
- Neurocrine Clinical Site — Marietta, Georgia, United States
- Neurocrine Clinical Site — Lincoln, Nebraska, United States
- Neurocrine Clinical Site — Beechwood, Ohio, United States
- Neurocrine Clinical Site — Oklahoma City, Oklahoma, United States
- Neurocrine Clinical Site — DeSoto, Texas, United States
- Neurocrine Clinical Site — El Paso, Texas, United States
- Neurocrine Clinical Site — Houston, Texas, United States
Full record on ClinicalTrials.gov
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