This is a multicenter, randomized, double-blind, placebo-controlled, parallel-group, fixed-dose study in adult patients with a primary diagnosis of schizophrenia according to criteria of the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, (DSM-5).
The study will be conducted in the following 5 phases: * A no-drug Screening Phase up to 7 days in duration during which patient eligibility will be assessed; * A 6-week, open-label Run-in Phase (RIP) during which all patients will receive oral lumateperone 42 mg/day; * A 12-week, open-label Stabilization Phase (SP) during which all patients will receive oral lumateperone 42 mg/day; * A Double-blind Treatment Phase (DBTP) 26 weeks in duration during which patients receive either lumateperone 42 mg or placebo (1:1 ratio); * A 2-week Safety Follow-up (SFU) Phase.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
228
Lumateperone 42 mg capsules administered orally, once daily.
Matching capsules administered orally, once daily.
Time to first symptom relapse during the Double-blind Treatment Phase
Time frame: Number of days from the randomization date to the first relapse date up to 26 weeks.
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Clinical Site
Little Rock, Arkansas, United States
Clinical Site
Bellflower, California, United States
Clinical Site
Cerritos, California, United States
Clinical Site
Culver City, California, United States
Clinical Site
Garden Grove, California, United States
Clinical Site
Lemon Grove, California, United States
Clinical Site
Montclair, California, United States
Clinical Site
Orange, California, United States
Clinical Site
Hollywood, Florida, United States
Clinical Site
Miami Lakes, Florida, United States
...and 33 more locations