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Clinical trial

A Phase 2, Open-Label, Dose Titration Study to Evaluate the Efficacy and Safety of NBI-98854 for the Treatment of Tardive Dyskinesia in Subjects With Schizophrenia or Schizoaffective Disorder

NCT01267188 is registered in ClinicalTrials.gov with Neurocrine Biosciences as lead sponsor.

NCT NCT01267188
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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase 2, Open-Label, Dose Titration Study to Evaluate the Efficacy and Safety of NBI-98854 for the Treatment of Tardive Dyskinesia in Subjects With Schizophrenia or Schizoaffective Disorder
Lead sponsor
Neurocrine Biosciences
Phase
Phase 2
Overall status
Completed
Start date
January 31, 2011
Completion date
March 31, 2011
Enrollment
10 (estimated)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

tardive dyskinesia