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Completed Phase 4 Interventional Results available

Study of the Effectiveness of Valbenazine on Patient- and Clinician-Reported Outcomes in Participants With Tardive Dyskinesia

ClinicalTrials.gov ID: NCT05859698

Public ClinicalTrials.gov record NCT05859698. 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 7, 2026, 8:39 PM EST

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Official title

A Phase 4, Single-Arm, Open-Label Study to Evaluate the Effectiveness of Valbenazine on Patient- and Clinician-Reported Outcomes in Subjects With Tardive Dyskinesia

Brief summary

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

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.

Study identification

NCT ID
NCT05859698
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Neurocrine Biosciences
Industry
Enrollment
59 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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
May 9, 2023 (Actual)
Primary completion
Dec 27, 2024 (Actual)
Completion
Dec 27, 2024 (Actual)
Last update posted
Jan 16, 2026

2023 – 2024

United States locations

U.S. sites
18
U.S. states
8
U.S. cities
18
Facility City State ZIP Site status
Neurocrine Clinical Site Bryant Arkansas 72022 —
Neurocrine Clinical Site Anaheim California 92805 —
Neurocrine Clinical Site Orange California 92868 —
Neurocrine Clinical Site Torrance California 90504 —
Neurocrine Clinical Site Bonita Springs Florida 34134 —
Neurocrine Clinical Site Miami Florida 33176 —
Neurocrine Clinical Site Miami Lakes Florida 33016 —
Neurocrine Clinical Site Okeechobee Florida 34972 —
Neurocrine Clinical Site Tampa Florida 33629 —
Neurocrine Clinical Site Atlanta Georgia 30328 —
Neurocrine Clinical Site Augusta Georgia 30912 —
Neurocrine Clinical Site Marietta Georgia 30060 —
Neurocrine Clinical Site Lincoln Nebraska 68526 —
Neurocrine Clinical Site Beechwood Ohio 44122 —
Neurocrine Clinical Site Oklahoma City Oklahoma 73112 —
Neurocrine Clinical Site DeSoto Texas 75115 —
Neurocrine Clinical Site El Paso Texas 79902 —
Neurocrine Clinical Site Houston Texas 77030 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05859698, 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 Jan 16, 2026 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05859698 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →