drugset / Trial / NCT01261793

Study of Epratuzumab Versus Placebo in Subjects With Moderate to Severe General Systemic Lupus Erythematosus (SLE)

NCT01261793 ↗

Phase 3 Completed 791 enrolled UCB Pharma
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of the study is to confirm the clinical efficacy of epratuzumab in the treatment of subjects with Systemic Lupus Erythematosus (SLE).

Timeline

Start
2010-12
Primary completion
2015-05
Completion
2015-06

Outcome

Missed primary endpoint

paper There was no statistically significant difference in the primary end point between the groups PMID 27598855 ↗

registry Placebo Weekly (FAS) vs Epratuzumab 1200 mg Every Other Week (FAS); p =0.899 NCT01261793 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Epratuzumab Monoclonal antibody 600 mg Other
Subject Epratuzumab Monoclonal antibody 1200 mg Other