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Completed Phase 2 Interventional Results available

Safety and Efficacy Study of NBI-98854 in Children and Adolescents With Tourette Syndrome

ClinicalTrials.gov ID: NCT02679079

Public ClinicalTrials.gov record NCT02679079. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 26, 2026, 3:06 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled Study to Assess the Safety and Efficacy of NBI-98854 in Pediatric Subjects With Tourette Syndrome

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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 identification

NCT ID
NCT02679079
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Neurocrine Biosciences
Industry
Enrollment
98 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
6 Years to 17 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 23, 2016 (Actual)
Primary completion
Apr 14, 2017 (Actual)
Completion
Apr 14, 2017 (Actual)
Last update posted
Jan 15, 2021

2016 – 2017

United States locations

U.S. sites
44
U.S. states
19
U.S. cities
44
Facility City State ZIP Site status
Not listed Sun City Arizona — —
Not listed Springdale Arkansas — —
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Not listed Loxahatchee Groves Florida — —
Not listed Melbourne Florida — —
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Not listed Chicago Illinois — —
Not listed Naperville Illinois — —
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Not listed Ann Arbor Michigan — —
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Not listed Nashua New Hampshire — —
Not listed Marlton New Jersey — —
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Not listed Dallas Texas — —
Not listed DeSoto Texas — —
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Not listed Houston Texas — —
Not listed Irving Texas — —
Not listed Orem Utah — —
Not listed Salt Lake City Utah — —
Not listed Kirkland Washington — —
Not listed Seattle Washington — —
Not listed Spokane Washington — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02679079, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 15, 2021 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02679079 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →