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
Chino, California, United States
RECRUITINGNeurocrine Clinical Site
Fountain Valley, California, United States
RECRUITINGNeurocrine Clinical Site
Long Beach, California, United States
RECRUITINGNeurocrine Clinical Site
Orange, California, United States
RECRUITINGNeurocrine Clinical Site
Redlands, California, United States
RECRUITINGNeurocrine Clinical Site
San Diego, California, United States
RECRUITINGNeurocrine Clinical Site
Bonita Springs, Florida, United States
RECRUITINGNeurocrine Clinical Site
Hialeah, Florida, United States
RECRUITINGNeurocrine Clinical Site
Hialeah, Florida, United States
RECRUITING...and 9 more locations
Change 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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