drugset / Trial / NCT01107496

Evaluation of Immediate-Release Viloxazine in Adults With ADHD

NCT01107496 ↗

Phase 1/2 Completed 52 enrolled Supernus Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindOther

Summary

This will be a randomized, double-blind, placebo-controlled, parallel group, safety and tolerability study in adults with ADHD. The target subjects are healthy male or female adults aged 18 to 64 years, inclusive, with a diagnosis of ADHD.

Timeline

Start
2010-06
Primary completion
2010-12
Completion
2010-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Viloxazine Small molecule 100 mg Oral