drugset / Trial / NCT03465787

A 6-week Study to Evaluate the Efficacy and Safety of Lurasidone HCL in Acutely Psychotic Patients With Schizophrenia

NCT03465787

Phase 3 Completed 210 enrolled Bukwang Pharmaceutical
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a study designed to evaluate the efficacy and safety of lurasidone in acutely psychotic patients with chronic schizophrenia and to confirm the non-inferiority of lurasidone relative to quetiapine XR.

Timeline

Start
2018-04-09
Primary completion
2022-10-26
Completion
2022-10-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Lurasidone Small molecule 160 mg
Comparator Quetiapine Small molecule 600 mg

Indications