NBI-98854
Sponsors
Neurocrine Biosciences
Conditions
Tardive DyskinesiaTourette Syndrome
Phase 1
Phase 2
Efficacy and Safety of NBI-98854 in Subjects With Tardive Dyskinesia
CompletedNCT01267188
Start: 2011-01-31End: 2011-03-31Target: 10Updated: 2011-04-20
NBI-98854 for the Treatment of Tardive Dyskinesia in Subjects With Schizophrenia or Schizoaffective Disorder
CompletedNCT01393600
Start: 2011-08-31End: 2012-02-29Updated: 2017-08-10
NBI-98854 for the Treatment of Tardive Dyskinesia in Subjects With Schizophrenia or Schizoaffective Disorder (KINECT Study)
CompletedNCT01688037
Start: 2012-09-30End: 2013-10-31Updated: 2017-11-08
NBI-98854 Dose Titration Study for the Treatment of Tardive Dyskinesia
CompletedNCT01733121
Start: 2012-12-31End: 2013-12-31Updated: 2017-08-10
Safety and Efficacy Study of NBI-98854 in Adults With Tourette Syndrome
CompletedNCT02581865
Start: 2015-11-30End: 2016-12-31Updated: 2020-05-07
Safety and Efficacy Study of NBI-98854 in Children and Adolescents With Tourette Syndrome
CompletedNCT02679079
Start: 2016-03-23End: 2017-04-14Updated: 2021-01-15
Rollover Study for Continuing NBI-98854 Administration in Pediatric Subjects With Tourette Syndrome
TerminatedNCT03732534
Start: 2018-10-17End: 2019-02-18Updated: 2022-04-19
Phase 3
Related Papers
13 more papers not shown