drugset / Trial / NCT01472991
Safety & Efficacy of TC-5619 in Adults With Inattentive-predominant Attention Deficit/Hyperactivity Disorder (ADHD)
RandomizedParallel-groupQuadruple-blindTreatment
Summary
Study is to assess if TC-5619 improves symptoms for adults diagnosed with the inattentive-predominant subtype of ADHD over a 4-week treatment period.
Timeline
- Start
- 2011-11
- Primary completion
- 2012-07
- Completion
- 2012-07
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | TC-5619-238 | Unknown | 5 mg | — |
| Subject | TC-5619-238 | Unknown | 25 mg | — |