NCT00214981

Evaluate the Safety and Efficacy of Modafinil in Children and Adolescents With ADHD

A 1-Year, Open-Label, Flexible-Dosage Study to Evaluate the Safety and Continued Efficacy of Modafinil (Film-coated Tablet Formulation) in Children and Adolescents With Attention-Deficit/Hyperactivity Disorder (Followed by an Open-Ended Extension Period)

• Status: Completed
• Phase: Phase 3
• Study type: Interventional
• Enrollment: —
• Sponsor: Cephalon · Industry
• Sex: All
• Age: 6 Years – 17 Years
• Healthy volunteers: Not accepted

Summary

Primary objective of this study is to evaluate the safety of treatment with modafinil film-coated tablet.

Conditions

• Attention Deficit/Hyperactivity Disorder
• ADHD

Interventions

Type	Name	Description
DRUG	Modafinil

Timeline

• Start date: 2003-09-01
• Primary completion: 2006-09-01
• Completion: 2006-09-01
• First posted: 2005-09-22
• Last updated: 2012-07-26

Locations

57 sites across 1 country: United States