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Clinical Trial Summary

This study will evaluate the efficacy and safety of SPN-812, an extended-release formulation of viloxazine, compared to placebo in children in an analog classroom setting.


Clinical Trial Description

This is a Phase 3, randomized, double-blind, placebo-controlled, parallel-group, 2-arm, analog classroom study to evaluate the efficacy and safety of 200 mg/day SPN-812 compared to placebo in the treatment of children aged 6 through 11 years with ADHD. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04016792
Study type Interventional
Source Supernus Pharmaceuticals, Inc.
Contact
Status Withdrawn
Phase Phase 3
Start date August 2019
Completion date November 2020

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