drugset / Trial / NCT01472991

Safety & Efficacy of TC-5619 in Adults With Inattentive-predominant Attention Deficit/Hyperactivity Disorder (ADHD)

NCT01472991 ↗

Phase 2 Completed 250 enrolled Targacept Inc.
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

EvaluationDrugModalityDoseRoute
Subject TC-5619-238 Unknown 5 mg —
Subject TC-5619-238 Unknown 25 mg —