The Safety and Effectiveness of Latuda® Post-marketing Surveillance in the Treatment of Chinese Schizophrenia Patients

NCT04432688 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3192

Last updated 2024-04-18

No results posted yet for this study

Summary

It's a prospective, non-interventional, observational Post-marketing Surveillance..

Conditions

Interventions

DRUG

Lurasidone HCl

This is a non-interventional, observational study

Sponsors & Collaborators

  • Sumitomo Pharma (Suzhou) Co., Ltd.

    lead INDUSTRY

Principal Investigators

  • Yifeng Xu · Shanghai Mental Health Center

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-12-01
Primary Completion
2023-03-18
Completion
2023-06-18
FDA Drug
Yes

Countries

  • China

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04432688 on ClinicalTrials.gov