drugset / Trial / NCT00962104

Atomoxetine to Treat Asian Adult Patients With Attention-Deficit/Hyperactivity Disorder

NCT00962104 ↗

Phase 3 Completed 391 enrolled Eli Lilly and Company
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess the efficacy, the quality of life, and the safety of multiple dosing atomoxetine in Asian adult subjects with attention deficit/hyperactivity disorder (ADHD).

Timeline

Start
2009-08
Primary completion
2011-02
Completion
2011-02

Outcome

Met primary endpoint

registry analysis (superiority or other test); Atomoxetine vs Placebo; p <0.001; Least Squares Mean Difference -5.78 (95% CI -7.66 to -3.91); ANCOVA; NCT00962104 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Atomoxetine Other / unclassified 80 mg Oral
Subject Atomoxetine Other / unclassified 120 mg Oral