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NCT Number: NCT07225712

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

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

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Jimbo Kokorono Clinic

Fukuoka, Japan

Location status: Recruiting

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Japanese male or female participants 18 years of age or older at the time of informed consent
  • Diagnosed with schizophrenia according to the DSM-5®
  • Judged by the investigator to be clinically stable for at least 8 weeks prior to screening
  • PANSS total score of 80 or less and CGI-S score 4 or less at both screening and baseline
  • No changes in antipsychotic medication for at least 6 weeks before screening (excluding minor dose adjustments for tolerability)

Exclusion criteria

  • History of psychiatric hospitalization within 8 weeks prior to screening
  • Treatment-resistant to antipsychotic therapy (ie, within 1 year to screening, despite administration of two or more marketed antipsychotics at appropriate doses for at least 4 weeks [28 consecutive days] in accordance with the package insert, psychiatric symptoms did not improve)
  • History of treatment with clozapine
  • Unwillingness, before or during the trial period, to comply with the requirements for prior and concomitant medications/therapies as specified in the protocol or use of prohibited medications at screening or baseline as specified in the protocol.

Treatment and study plan

SEP-363856

Drug

Tablet, once daily, for 52 weeks

Primary outcomes

  1. ・Incidence of treatment-emergent adverse events (TEAEs)

    Time frame: 52 weeks

Study contacts

Contact information is provided by the study sponsor or research team.

Drug Information Center

CONTACT

+81-3-6361-7314

Sponsors and collaborators

Lead sponsor

Otsuka Pharmaceutical Co., Ltd.

Industry

Registry information

Official study title

A Multicenter, Uncontrolled, Open-label Trial to Evaluate the Tolerability, Safety, and Efficacy of Long-term Administration of SEP-363856 in Patients With Schizophrenia

Important dates

Study start
2025
Primary completion
2028
Study completion
2028
First posted
Nov 10, 2025
Registry last updated
Jan 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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