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Safety and Tolerability Study of NBI-98854 for the Treatment of Subjects With Tourette Syndrome

Tourette Syndrome Clinical Trial

Clinical Trial Summary

Phase 2, open-label, fixed-dose titration study to evaluate the safety and tolerability of NBI-98854 administered once daily for a total of 24 weeks in children, adolescents, and adults with Tourette Syndrome (TS).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02879578
Study type Interventional
Source Neurocrine Biosciences
Contact
Status Completed
Phase Phase 2
Start date July 25, 2016
Completion date November 1, 2017
View Details
See also
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