drugset / Trial / NCT04931563

Anifrolumab Asian PhIII Efficacy Study for Systemic Lupus Erythematosus (SLE)

NCT04931563

Phase 3 Completed 277 enrolled AstraZeneca
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of an intravenous treatment regimen of anifrolumab versus placebo in Asian participants with active systemic lupus erythematosus (SLE).

Timeline

Start
2021-09-13
Primary completion
2025-04-07
Completion
2025-06-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Anifrolumab Monoclonal antibody 300 mg Intravenous