drugset / Trial / NCT01458340

A Study of TD-9855 in Adults With Attention-Deficit/Hyperactivity Disorder (ADHD)

NCT01458340

Phase 2 Completed 295 enrolled Theravance Biopharma
RandomizedParallel-groupTriple-blindTreatment

Summary

The safety and efficacy of multiple dosages of TD-9855, administered once daily, will be evaluated in adult males with ADHD.

Timeline

Start
2011-12
Primary completion
2013-10
Completion
2013-11

Drugs

EvaluationDrugModalityDoseRoute
Subject ampreloxetine Small molecule Oral