drugset / Trial / NCT00254878

Placebo-Controlled Comparison of Two Different Brands of Modified-Release Oral Dosage Forms Regarding Safety and Efficacy in Children With Attention Deficit Hyperactivity Disorder (ADHD) Aged 6 - 14

NCT00254878

Phase 3 Completed 130 enrolled Novartis
RandomizedCrossoverDouble-blindTreatment

Summary

Currently two different brands of modified-release formulations are providing 50% immediate release beads/pellets and 50% extended release beads/pellets, resulting in a rapid onset and dual peak concentrations of plasma methylphenidate. One is manufactured by Novartis, the other one by Medice (Germany). The objective of the study is to test the hypothesis that the Novartis product is superior to placebo and is clinically not inferior to the formulation manufactured by Medice.

Timeline

Start
2005-10
Primary completion
Completion
2006-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Methylphenidate Small molecule 20 mg Oral