drugset / Trial / NCT00150592

Safety, Tolerability and Efficacy of SPD503 in Treating ADHD in Children Aged 6-17

NCT00150592

Phase 2 Completed 182 enrolled Shire
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to determine the effects of SPD503 compared to placebo on tasks of sustained attention in children and adolescents aged 6-17 diagnosed with ADHD.

Timeline

Start
2005-05-12
Primary completion
2005-10-05
Completion
2005-10-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Guanfacine Small molecule 1 mg
Subject Guanfacine Small molecule 2 mg
Subject Guanfacine Small molecule 3 mg