Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02581865 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by Neurocrine Biosciences.

Completed
Registry status
Phase 2
Development phase
124
Enrollment target

NCT02581865 is a Phase 2 study that has completed, run by Neurocrine Biosciences. The registered enrollment target is 124 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02581865, a Phase 2 study, has completed, sponsored by Neurocrine Biosciences.

COMPLETED
Registry status
Phase 2
Development phase
124 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 8 weeks of treatment. This study will enroll approximately 90 male and female subjects clinically diagnosed with Tourette Syndrome.

Interventions

  • DRUG Placebo
  • DRUG NBI-98854

Trial Details

FieldValue
Enrollment Target 124 participants
Start Date 2015-11
Est. Completion 2016-12
Phase Phase 2

Sponsor

Neurocrine Biosciences

65 total trials

What the Registry Record Tells You About NCT02581865

The ClinicalTrials.gov registry entry for NCT02581865 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 124 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.

NCT02581865 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02581865 about?

NCT02581865 is a clinical study titled "Safety and Efficacy Study of NBI-98854 in Adults 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 8 weeks of treatment. This study will enroll approximately 90 male and female subjects clinically diagnosed with Tourette Syndrome.

What is the current status of trial NCT02581865?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 124 participants. The study started on 2015-11. Estimated completion is 2016-12.

What interventions are being tested in trial NCT02581865?

The interventions under investigation include: Placebo (DRUG), NBI-98854 (DRUG).

Who is sponsoring clinical trial NCT02581865?

This trial is sponsored by Neurocrine Biosciences, which has 65 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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.