drugset / Trial / NCT03247517

Evaluation of SPN-812 (Viloxazine Extended-release Capsule) Low Dose in Adolescents With ADHD

NCT03247517 ↗

Phase 3 Completed 310 enrolled Supernus Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will evaluate the efficacy and safety of low doses of SPN-812 in adolescents 12-17 years of age.

Timeline

Start
2017-11-02
Primary completion
2018-10-17
Completion
2018-10-17

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs 200mg SPN-812; p = 0.0232; Least Square Mean Difference -4.5 (95% CI -8.4 to -0.6) NCT03247517 ↗

registry analysis (superiority test); Placebo vs 400mg SPN-812; p = 0.0091; Least Square Mean Difference -5.1 (95% CI -8.9 to -1.3) NCT03247517 ↗

release “We are pleased with the positive topline results of the P302 study, in which SPN-812 showed statistical significance on the primary endpoint” supernus.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Viloxazine Small molecule 200 mg Oral
Subject Viloxazine Small molecule 400 mg Oral