To further characterize the long-term safety and tolerability of brexpiprazole in adolescents with schizophrenia
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Number of Participants With Adverse Events (AEs)
Timeframe: From the first dose of study drug (including the conversion period and the open-label treatment period in the current study) up to 21 days after the last dose of study drug (up to approximately 25.6 months).
Number of Participants With Serious Treatment Emergent Adverse Events (TEAEs)
Timeframe: From the first dose of study drug (including the conversion period and the open-label treatment period in the current study) up to 21 days after the last dose of study drug (up to approximately 25.6 months).
Number of Participants Who Discontinued the Trial Due to AEs
Timeframe: From the first dose of study drug (including the conversion period and the open-label treatment period in the current study) up to 21 days after the last dose of study drug (up to approximately 25.6 months).