drugset / Trial / NCT00190684

Long-Term, Open Label Atomoxetine Study

NCT00190684

Phase 3 Completed 1553 enrolled Eli Lilly and Company
NaSingle-groupOpen-labelTreatment

Summary

To learn about the safety and any side effects of atomoxetine when given to children and adolescents for about 5 years (long-term) and to learn whether atomoxetine can help children and adolescents with attention-deficit/hyperactivity disorder (ADHD) who take the drug for about 5 years (long-term). Study participants can be atomoxetine naive, atomoxetine experienced whose therapy has been interrupted or, atomoxetine experienced on a known stable dose.

Timeline

Start
2000-08
Primary completion
2009-10
Completion
2009-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Atomoxetine Other / unclassified 0.5 mg/kg Oral
Subject Atomoxetine Other / unclassified 1.8 mg/kg Oral