drugset / Trial / NCT02446899

Efficacy and Safety of Anifrolumab Compared to Placebo in Adult Subjects With Active Systemic Lupus Erythematosus

NCT02446899

Phase 3 Completed 373 enrolled AstraZeneca PRA Health Sciences · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of an intravenous treatment regimen of anifrolumab versus placebo in adult participants with moderately to severely active, autoantibody-positive systemic lupus erythematosus (SLE).

Timeline

Start
2015-07-09
Primary completion
2018-09-27
Completion
2018-09-27

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Anifrolumab Monoclonal antibody 300 mg Intravenous