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

Outcome

Met primary endpoint

registry analysis (superiority test); Anifrolumab 300 mg vs Placebo; p = 0.0013; Mean Difference (Final Values) 16.3 (95% CI 6.3 to 26.3) NCT02446899 ↗

paper The percentage of patients who had a BICLA response was 47.8% in the anifrolumab group and 31.5% in the placebo group (difference, 16.3 percentage points; 95% confidence interval, 6.3 to 26.3; P= 0.001). PMID 35157371 ↗

release “the Phase III TULIP 2 trial for anifrolumab, a potential new medicine for the treatment of systemic lupus erythematosus (SLE), met its primary endpoint” astrazeneca.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Anifrolumab Monoclonal antibody 300 mg Intravenous