A phase III, randomised, double-blind, multicentre, parallel-group, placebo- and active-controlled, dose-optimisation safety and efficacy study of lisdexamfetamine dimesylate (LDX) in children and adolescents aged 6-17 with attention-deficit/ hyperactivity disorder (ADHD)
Laufzeit: 01.01.2008 - 31.12.2010