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ACTIVE NOT RECRUITING Phase 3

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

NCT05206513 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this study is to evaluate the efficacy of valbenazine versus placebo on improving chorea in pediatric and adult participants who have dyskinesia due to cerebral palsy (DCP) with choreiform movements.

Interventions

  • DRUG Placebo
  • DRUG Valbenazine

Study Locations (20)

Florida

  • Neurocrine Clinical Site — Gulf Breeze
  • Neurocrine Clinical Site — Miami
  • Neurocrine Clinical Site — Orlando

Texas

  • Neurocrine Clinical Site — Dallas
  • Neurocrine Clinical Site — Fort Worth
  • Neurocrine Clinical Site — Houston

Ohio

  • Neurocrine Clinical Site — Cincinnati
  • Neurocrine Clinical Site — Columbus

California

  • Neurocrine Clinical Site — San Diego

Colorado

  • Neurocrine Clinical Site — Aurora

Connecticut

  • Neurocrine Clinical Site — Stamford

Illinois

  • Neurocrine Clinical Site — Chicago

Maryland

  • Neurocrine Clinical Site — Baltimore

Trial Details

FieldValue
Enrollment Target 86 participants
Start Date 2022-04-15
Est. Completion 2026-06
Phase Phase 3

Sponsor

Neurocrine Biosciences

47 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05206513

The ClinicalTrials.gov registry entry for NCT05206513 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 86 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Neurocrine Biosciences, which has 47 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Cerebral Palsy appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05206513 reports 20 study locations spanning 15 distinct geographic areas — top geographies include Florida, Texas, Ohio. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05206513 about?

NCT05206513 is a clinical study titled "Study to Assess the Efficacy, Safety, and Tolerability of Valbenazine for the Treatment of Dyskinesia Due to Cerebral Palsy". The primary objective of this study is to evaluate the efficacy of valbenazine versus placebo on improving chorea in pediatric and adult participants who have dyskinesia due to cerebral palsy (DCP) with choreiform movements.

What is the current status of trial NCT05206513?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 86 participants. The study started on 2022-04-15. Estimated completion is 2026-06.

What conditions does trial NCT05206513 study?

This clinical trial studies the following conditions: Cerebral Palsy, Dyskinesia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05206513?

The interventions under investigation include: Placebo (DRUG), Valbenazine (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05206513?

This trial is sponsored by Neurocrine Biosciences, which has 47 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05206513 being conducted?

This trial has 20 study locations across California, Colorado, Connecticut, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial