Español24/7 enrollment line386-218-5911

At a glance

ConditionTardive Dyskinesia
Therapeutic areaNeurology
Principal investigatorDavid A. Riascos, MD, MSc
DurationVisit schedule confirmed during pre-screening
CompensationCompensation provided for time and travel
Trial registryNCT07105111

This study is registered on ClinicalTrials.gov, the U.S. National Library of Medicine's public trial registry. You can independently verify its details, sponsor, and status under identifier NCT07105111.

Who may qualify

The screening call takes about 5 minutes. Coordinators will walk you through the full eligibility criteria; the items below are the most common gates.

  • Adults with tardive dyskinesia who are still symptomatic
  • Currently on deutetrabenazine or recently discontinued a prior VMAT2 inhibitor, per protocol review
  • Able to complete study assessments and attend scheduled visits

What you receive

Tap any item for details.

Investigational treatment at no cost

The investigational treatment is provided at no cost throughout the study.

Study-related care at no cost
Travel reimbursement

You are reimbursed for travel and mileage to and from your study visits.

How to enroll

The fastest path is to submit the pre-qualification form on this page or call the enrollment line at 386-218-5911. A study coordinator will review your information and call you within one business day to schedule a free screening visit.

You are never obligated to continue. You can stop at any step — before signing consent, during screening, or at any point after enrollment.

About the site

This study is conducted at Optimal Research Sites, an independent clinical trial facility in Orange City, Florida. We've conducted Phase I–IV trials since 1994, with a dedicated 9-bed Phase I inpatient unit, certified sample processing laboratory, and a bilingual study team. Every trial runs under IRB oversight and ICH Good Clinical Practice standards.