drugset / Trial / NCT01986114

A Long-Term Study of SM-13496 in Patients With Bipolar I Disorder.

NCT01986114

Phase 3 Completed 495 enrolled Sumitomo Pharma Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

The study evaluates the long-term efficacy and safety of SM-13496 in patients with bipolar I disorder.

Timeline

Start
2014-01-29
Primary completion
2018-02-08
Completion
2018-02-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Lurasidone Small molecule 20 mg Oral
Subject Lurasidone Small molecule 120 mg Oral

Indications