Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02679079 · ClinicalTrials.gov registry record · Phase 2
Safety and Efficacy Study of NBI-98854 in Children and Adolescents With Tourette Syndrome
A Phase 2 study, sponsored by Neurocrine Biosciences.
- Completed
- Registry status
- Phase 2
- Development phase
- 98
- Enrollment target
NCT02679079 is a Phase 2 study that has completed, run by Neurocrine Biosciences. The registered enrollment target is 98 participants.
The verdict
NCT02679079, a Phase 2 study, has completed, sponsored by Neurocrine Biosciences.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 98 participants
- Enrollment target
Study 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.
Interventions
- DRUG Placebo
- DRUG NBI-98854
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 98 participants |
| Start Date | 2016-03-23 |
| Est. Completion | 2017-04-14 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02679079
The ClinicalTrials.gov registry entry for NCT02679079 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 98 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Neurocrine Biosciences, which has 65 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT02679079 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02679079 about?
NCT02679079 is a clinical study titled "Safety and Efficacy Study of NBI-98854 in Children and Adolescents With Tourette Syndrome". 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.
What is the current status of trial NCT02679079?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 98 participants. The study started on 2016-03-23. Estimated completion is 2017-04-14.
What interventions are being tested in trial NCT02679079?
The interventions under investigation include: Placebo (DRUG), NBI-98854 (DRUG).
Who is sponsoring clinical trial NCT02679079?
This trial is sponsored by Neurocrine Biosciences, which has 65 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.