drugset / Trial / NCT00150618

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

NCT00150618

Phase 3 Completed 324 enrolled Shire
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to determine the efficacy of SPD503 compared to placebo in the treatment of children and adolescents aged 6-17 with ADHD.

Timeline

Start
2004-03-30
Primary completion
2004-10-07
Completion
2004-10-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Guanfacine Small molecule 1 mg Oral
Subject Guanfacine Small molecule 2 mg Oral
Subject Guanfacine Small molecule 3 mg Oral
Subject Guanfacine Small molecule 4 mg Oral