drugset / Trial / NCT07225712

A Long-term Administration Trial of SEP-363856 in Patients With Schizophrenia

NCT07225712

Phase 3 Recruiting 100 enrolled Otsuka Pharmaceutical Co., Ltd.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To evaluate the safety of SEP-363856 (75 mg/day or 100 mg/day) administered for 52 weeks in adult participants with schizophrenia

Timeline

Start
2025-12-22
Primary completion
2028-03
Completion
2028-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Ulotaront Small molecule 75 mg
Subject Ulotaront Small molecule 100 mg

Indications