ClinicalTrials.gov record
Recruiting Phase 4 Interventional

A Study to Evaluate the Effectiveness of Valbenazine in Adult Participants With Tardive Dyskinesia (TD) Who Remain Symptomatic While Receiving or After Stopping a Vesicular Monoamine Transporter 2 (VMAT2) Inhibitor

ClinicalTrials.gov ID: NCT07105111

Public ClinicalTrials.gov record NCT07105111. 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 May 20, 2026, 1:24 PM EDT

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

Official title

A Phase 4, Open-Label Study to Evaluate the Efficacy of Valbenazine on Clinician- and Patient-Reported Outcomes in Patients With Tardive Dyskinesia (TD) Who Remain Symptomatic While on Deutetrabenazine or After Discontinuing Prior TD Treatment With a Vesicular Monoamine Transporter 2 (VMAT2) Inhibitor

Study identification

NCT ID
NCT07105111
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 4
Lead sponsor
Neurocrine Biosciences
Industry
Enrollment
50 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
Aug 28, 2025
Primary completion
Dec 31, 2026
Completion
Dec 31, 2026
Last update posted
May 7, 2026

2025 – 2027

United States locations

U.S. sites
21
U.S. states
8
U.S. cities
20
Facility City State ZIP Site status
Neurocrine Clinical Site Bryant Arkansas 72022 Recruiting
Neurocrine Clinical Site Chino California 91710 Recruiting
Neurocrine Clinical Site Fountain Valley California 92708 Recruiting
Neurocrine Clinical Site Fresno California 93720 Recruiting
Neurocrine Clinical Site Long Beach California 90807 Recruiting
Neurocrine Clinical Site Orange California 92866 Recruiting
Neurocrine Clinical Site Redlands California 92373 Recruiting
Neurocrine Clinical Site San Diego California 92123 Recruiting
Neurocrine Clinical Site Bonita Springs Florida 34134 Recruiting
Neurocrine Clinical Site Hialeah Florida 33012 Recruiting
Neurocrine Clinical Site Miami Florida 33144 Recruiting
Neurocrine Clinical Site Miami Florida 33176 Recruiting
Neurocrine Clinical Site Orange City Florida 32763 Recruiting
Neurocrine Clinical Site Port Charlotte Florida 33980 Recruiting
Neurocrine Clinical Site Tampa Florida 33629 Recruiting
Neurocrine Clinical Site Augusta Georgia 30912 Recruiting
Neurocrine Clinical Site Marietta Georgia 30060 Recruiting
Neurocrine Clinical Site Naperville Illinois 60563 Recruiting
Neurocrine Clinical Site Omaha Nebraska 68124 Recruiting
Neurocrine Clinical Site Independence Ohio 44131 Recruiting
Neurocrine Clinical Site Richmond Virginia 23226 Recruiting

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 NCT07105111, 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 May 7, 2026 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07105111 live on ClinicalTrials.gov.

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