drugset / Trial / NCT00969618
A Long Term Follow-Up Study for Asian Adult Patients With Attention Deficit Hyperactivity Disorder
NaSingle-groupOpen-labelTreatment
Summary
The purpose of this study is to assess long-term safety and tolerability in adult patients who have completed a previous atomoxetine study.
Timeline
- Start
- 2009-11
- Primary completion
- 2012-01
- Completion
- 2012-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Atomoxetine | Other / unclassified | 40 mg | Oral |
| Subject | Atomoxetine | Other / unclassified | 120 mg | Oral |