drugset / Trial / NCT02327013

Investigating the Effect of Vortioxetine in Adult ADHD Patients

NCT02327013 ↗

Phase 2 Completed 227 enrolled H. Lundbeck A/S
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose is to determine the effect of vortioxetine treatment on ADHD symptoms in adult patients with ADHD in a 12 weeks study.

Timeline

Start
2014-12
Primary completion
2016-09
Completion
2016-09

Outcome

Missed primary endpoint

registry analysis (superiority test); Placebo, Combined vs Vortioxetine 10mg, Combined; p = 0.9723; Mean Difference (Final Values) -0.1 (95% CI -3.6 to 3.5); weighed z-score NCT02327013 ↗

registry analysis (superiority test); Placebo, Combined vs Vortioxetine 20mg, Combined; p = 0.6010; Mean Difference (Final Values) 1.0 (95% CI -2.8 to 4.8); weighed z-score NCT02327013 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Vortioxetine Unknown 10 mg Oral
Subject Vortioxetine Unknown 20 mg Oral