drugset / Trial / NCT02349061

A Phase 2a, Efficacy and Safety Study of Ustekinumab in Systemic Lupus Erythematosus

NCT02349061 ↗

Phase 2 Completed 102 enrolled Janssen Research & Development, LLC
RandomizedCrossoverDouble-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy of ustekinumab as measured by a reduction in disease activity for subjects with active Active Systemic Lupus Erythematosus (SLE - chronic disorder of connective tissue in which there can be skin rash, arthritis, kidney problems, and anemia, among other problems).

Timeline

Start
2015-10-15
Primary completion
2017-05-15
Completion
2019-03-13

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs Ustekinumab; p = 0.0057; Odds Ratio (OR) 3.28 (95% CI 1.41 to 7.63); Regression, Logistic NCT02349061 ↗

paper SRI-4 response rates were significantly greater in the ustekinumab group (62%) versus the placebo group (33%) in the week 24 primary end point analysis (P = 0.006) PMID 31769212 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ustekinumab Monoclonal antibody 90 mg Intravenous