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Clinical Trial Summary

This is an open-label, 104-week, multicenter, extension study designed to evaluate the long-term safety, tolerability and effectiveness of flexibly dosed lurasidone (20, 40, 60 or 80 mg/day) in pediatric subjects who have completed the 6-week treatment period in the preceding studies, D1050301, D1050325, and D1050326


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01914393
Study type Interventional
Source Sunovion
Contact
Status Completed
Phase Phase 3
Start date September 30, 2013
Completion date October 17, 2018

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