Overview

Dose-Optimization Study Evaluating the Efficacy, Safety and Tolerability of Vyvanse (Lisdexamfetamine Dimesylate) in Children Aged 6-12 Diagnosed With ADHD

Status:
Completed
Trial end date:
2008-01-02
Target enrollment:
Participant gender:
Summary
Assess the efficacy & tolerability of Vyvanse when children aged 6-12 years diagnosed with ADHD are dosed to optimal effect.
Phase:
Phase 4
Details
Lead Sponsor:
Shire
Treatments:
Lisdexamfetamine Dimesylate