Tardive Dyskinesia — Clinical Trial, Orange City FL
A clinical research study of an investigational treatment for adults with tardive dyskinesia — involuntary, repetitive movements often linked to long-term use of certain psychiatric medications.
At a glance
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 NCT07365462.
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 diagnosed or suspected tardive dyskinesia
- Ongoing abnormal involuntary movements
- Psychiatric or neurologic medication history reviewed at pre-screening
- Able to attend scheduled site visits in Orange City
What you receive
Tap any item for details.
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.
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