ClinicalTrials.gov record
Completed Phase 3 Interventional

Study to Assess the Efficacy, Safety, and Tolerability of Valbenazine for the Treatment of Dyskinesia Due to Cerebral Palsy

ClinicalTrials.gov ID: NCT05206513

Public ClinicalTrials.gov record NCT05206513. 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 18, 2026, 1:30 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 3, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy, Safety, and Tolerability of Valbenazine for the Treatment of Dyskinesia Due to Cerebral Palsy

Study identification

NCT ID
NCT05206513
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Neurocrine Biosciences
Industry
Enrollment
86 participants

Conditions and interventions

Conditions

Not listed

Interventions

Not listed

Eligibility (public fields only)

Age range
6 Years to 70 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
Apr 14, 2022
Primary completion
Oct 15, 2025
Completion
Mar 30, 2026
Last update posted
Apr 28, 2026

2022 – 2026

United States locations

U.S. sites
19
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
Neurocrine Clinical Site San Diego California 92123
Neurocrine Clinical Site Aurora Colorado 80045
Neurocrine Clinical Site Stamford Connecticut 06905
Neurocrine Clinical Site Gulf Breeze Florida 32561
Neurocrine Clinical Site Miami Florida 33155
Neurocrine Clinical Site Orlando Florida 32806
Neurocrine Clinical Site Chicago Illinois 60611
Neurocrine Clinical Site Baltimore Maryland 21205
Neurocrine Clinical Site Boston Massachusetts 02115
Neurocrine Clinical Site Farmington Hills Michigan 48334
Neurocrine Clinical Site Saint Paul Minnesota 55101
Neurocrine Clinical Site New York New York 10003
Neurocrine Clinical Site Cincinnati Ohio 45229
Neurocrine Clinical Site Columbus Ohio 43205
Neurocrine Clinical Site Oklahoma City Oklahoma 73120
Neurocrine Clinical Site Portland Oregon 97239
Neurocrine Clinical Site Dallas Texas 75390-8857
Neurocrine Clinical Site Fort Worth Texas 76104
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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05206513, 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 Apr 28, 2026 · Synced May 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05206513 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →