At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 98 enrolled
Drug / intervention
NBI-98854 +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Randomized, Double-Blind, Placebo-Controlled Study to Assess the Safety and Efficacy of NBI-98854 in Pediatric Subjects With Tourette Syndrome
In Brief
A Phase 2 clinical trial evaluating NBI-98854 and Placebo for Tourette Syndrome. Completed, enrolled 98 participants across 44 sites.
Detailed Summary
Phase 2, double-blind, placebo-controlled study to assess the safety and efficacy of NBI-98854 administered once daily (qd) for a total of 6 weeks of treatment. This study will enroll approximately 90 male and female pediatric subjects clinically diagnosed with Tourette Syndrome.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsTourette Syndrome
CountriesUnited States
Collaborators--
Timeline
Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedFeb 2016
Enrollment StartMar 2016
Primary CompletionApr 2017
TodayJul 2026
First PostedFeb 10, 2016
Enrollment StartMar 23, 2016
Primary CompletionApr 14, 2017
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 10.4 years ago
Interventions
NBI-98854drug
Placebodrug