Overview A Long-term Administration Trial of SEP-363856 in Patients With Schizophrenia Status: NOT_YET_RECRUITING Trial end date: 2028-03-01 Target enrollment: Participant gender: Summary To evaluate the safety of SEP-363856 (75 mg/day or 100 mg/day) administered for 52 weeks in adult participants with schizophreniaPhase: PHASE3 Details Lead Sponsor: Otsuka Pharmaceutical Co., Ltd.Treatments: SEP-363856