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RECRUITING
NCT06554288
PHASE1

Pharmacogenomic Contributions to Trihexyphenidyl Biotransformation and Response in Children With Dystonic Cerebral Palsy

Sponsor: Children's Mercy Hospital Kansas City

View on ClinicalTrials.gov

Summary

This study looks at how a medicine called trihexyphenidyl works in children with dystonic cerebral palsy. The study aims to understand how trihexyphenidyl is broken down and used in the body of pediatric patients and whether this is impacted by a person's genetics. Information from this study will also be used to design future clinical trials.

Official title: Pharmacogenomic Contribution to the Biotransformation of Trihexyphenidyl and Development of a Precision Dosing Model for Children With Dystonia and Cerebral Palsy

Key Details

Gender

All

Age Range

5 Years - 17 Years

Study Type

INTERVENTIONAL

Enrollment

40

Start Date

2024-10-15

Completion Date

2029-12-31

Last Updated

2025-07-18

Healthy Volunteers

No

Interventions

DRUG

Trihexyphenidyl

6-week dose escalation up to 0.25mg/kg TID, followed by a 9-week maintenance period at this dose

Locations (1)

Children's Mercy Hospital Kansas City

Kansas City, Missouri, United States