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Clinical Trial Summary

This study will evaluate the efficacy and safety of high doses of SPN 812 in children with ADHD


Clinical Trial Description

This is a multicenter, randomized, double-blind, placebo-controlled, 3-arm, parallel-group study, to assess the efficacy and safety of SPN-812 as monotherapy for the treatment of children 6-11 years old with ADHD. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03247543
Study type Interventional
Source Supernus Pharmaceuticals, Inc.
Contact
Status Completed
Phase Phase 3
Start date October 31, 2017
Completion date October 17, 2018

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