This study will evaluate the efficacy of valbenazine on clinician- and patient-reported outcomes in participants with TD while receiving or after stopping a VMAT2 inhibitor.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
50
Valbenazine capsules for oral administration.
Neurocrine Clinical Site
Bryant, Arkansas, United States
RECRUITINGNeurocrine Clinical Site
Fountain Valley, California, United States
RECRUITINGNeurocrine Clinical Site
Orange, California, United States
RECRUITINGNeurocrine Clinical Site
Bonita Springs, Florida, United States
RECRUITINGNeurocrine Clinical Site
Hialeah, Florida, United States
RECRUITINGNeurocrine Clinical Site
Miami, Florida, United States
RECRUITINGNeurocrine Clinical Site
Tampa, Florida, United States
RECRUITINGNeurocrine Clinical Site
Marietta, Georgia, United States
RECRUITINGChange from Baseline in the Abnormal Involuntary Movement Scale (AIMS) Dyskinesia Total Score (AIMS 1-7) at Week 24
Time frame: Baseline, Week 24
Change from Baseline in the Clinical Global Impression of Severity - Tardive Dyskinesia (CGI-TD-S) Score at Week 24
Time frame: Baseline, Week 24
Change from Baseline in the Tardive Dyskinesia Impact Scale (TDIS) at Week 24
Time frame: Baseline, Week 24
Change from Baseline in the EuroQol-Visual Analogue Scale (EQ-VAS) at Week 24
Time frame: Baseline, Week 24
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