drugset / Trial / NCT01138657

Efficacy and Safety of Adalimumab in Patients With Active Uveitis

NCT01138657 ↗

Phase 3 Completed 239 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A study comparing the safety and efficacy of adalimumab compared with placebo in patients with active uveitis.

Timeline

Start
2010-08
Primary completion
2014-07
Completion
2014-08

Outcome

Met primary endpoint

release “The VISUAL-I study found that compared to placebo, patients on HUMIRA were less likely to experience treatment failure (TF)” abbvie.com ↗

release “The VISUAL-I study found that compared to placebo, patients on HUMIRA were less likely to experience TF (hazard ratio=0.5; 95 percent CI, 0.36–0.70; P<0.001)” abbvie.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Adalimumab Monoclonal antibody 40 mg Subcutaneous
Background Prednisone Other / unclassified 60 mg Oral

Indications