drugset / Trial / NCT04016792

Classroom Study of SPN-812 in Children With ADHD

NCT04016792 ↗

Phase 3 Withdrawn Supernus Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

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.

Timeline

Start
2019-08
Primary completion
2020-09
Completion
2020-11

Outcome

Outcome not reported

Stopped (Enrollment): “Study stopped before enrollment due to non-safety related corporate decision.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Viloxazine Small molecule 200 mg —