The primary objective for this study is to evaluate the efficacy of NBI-1117568 compared with placebo on improving manic symptoms in adults with bipolar I disorder who are currently experiencing an episode of mania with or without mixed features.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
150
Oral administration
Oral administration
Change From Baseline in Young Mania Rating Scale (YMRS) Total Score at Day 21
Time frame: Baseline, Day 21
Change From Baseline in Clinical Global Impression - Severity Scale (CGI-S) Score at Day 21
Time frame: Baseline, Day 21
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