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Evaluate the Efficacy, Safety and Tolerability of TSUPPORT for Adults With Tourette Syndrome

Tourette Syndrome Clinical Trial

Official title:
Pilot Phase 2 Study to Evaluate the Efficacy, Safety and Tolerability of TSUPPORT (a Traditional Chinese Medicine) for Adults With Tourette Syndrome

Clinical Trial Summary

A 28-week single-arm trial to evaluate the efficacy, safety and tolerability of TSupport (a Traditional Chinese Medicine) for adults with Tourette Syndrome.

Clinical Trial Description

This study is to evaluate the efficacy, safety and tolerability of TSupport (a Traditional Chinese Medicine) for adults with Tourette Syndrome, which consists of a screening/wash-out period of up to 6 weeks, a 24-week supportive care period and a 4-week follow-up period. During the first 2-week follow-up period, subjects will continue to receive TSupport at half dose. After informed consent conducted and signed, subjects will receive TSupport orally twice daily. Morning dose and evening dose should be administrated at about the same time every day and irrelevant to meals. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05183594
Study type Interventional
Source Tasly Pharmaceuticals, Inc.
Contact Michael H Bloch, MD, PhD
Phone 203-974-7551
Email michael.bloch@yale.edu
Status Not yet recruiting
Phase N/A
Start date March 2022
Completion date September 2024
View Details
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