A Phase III Study of SM-13496 in Patients With Bipolar I Depression.

Status Completed

Clinical Trial Summary

The study evaluates the efficacy and safety of SM-13496 compared with placebo in patients with Bipolar I Depression.

Clinical Trial Description

The primary objective is to compare the efficacy of SM-13496 (20-60 or 80-120 mg/day) monotherapy with that of placebo in patients with depressive symptoms associated with bipolar I disorder by assessing the change from baseline in the MADRS total score at Week 6. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01986101
Study type	Interventional
Source	Sumitomo Pharma Co., Ltd.
Contact
Status	Completed
Phase	Phase 3
Start date	February 19, 2014
Completion date	February 16, 2017

View Details

See also
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