drugset / Trial / NCT03247530

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

NCT03247530 ↗

Phase 3 Completed 477 enrolled Supernus Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will evaluate the efficacy and safety of low doses of SPN-812 in children 6-11 years of age diagnosed with ADHD.

Timeline

Start
2017-10-20
Primary completion
2018-09-12
Completion
2018-09-12

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs 100mg SPN-812; p = 0.0004; Least Square Mean Difference -5.8 (95% CI -8.9 to -2.6); Mixed Models for Repeated Measures NCT03247530 ↗

registry analysis (superiority test); Placebo vs 200mg SPN-812; p <0.0001; Least Square Mean Difference -6.9 (95% CI -10.0 to -3.8); Mixed Models for Repeated Measures NCT03247530 ↗

release “Each study, P301 and P303, met primary endpoint with robust statistical significance” supernus.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Viloxazine Small molecule 100 mg Oral
Subject Viloxazine Small molecule 200 mg Oral