drugset / Trial / NCT01484496

A Study of Belimumab Administered Subcutaneously in Subjects With Systemic Lupus Erythematosus (SLE)

NCT01484496 ↗

Phase 3 Completed 839 enrolled GlaxoSmithKline GlaxoSmithKline · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy, safety and tolerability of belimumab administered subcutaneously (SC) to adult subjects with Systemic Lupus Erythematosus (SLE).

Timeline

Start
2011-11-16
Primary completion
2015-02-13
Completion
2015-10-01

Outcome

Met primary endpoint

registry Placebo SC vs Belimumab 200 mg SC; p = 0.0006; Odds Ratio (OR) 1.68 (95% CI 1.25 to 2.25) NCT01484496 ↗

paper More patients who received belimumab were SRI4 responders than those who received placebo (61.4% versus 48.4% PMID 28118533 ↗

release “For the primary efficacy endpoint (Systemic Lupus Erythematosus Responder Index (SRI) at Week 52), significantly more patients treated with belimumab administered subcutaneously plus SoC (60.8%)” gsk.com ↗

release “BLISS-SC is the third successful Phase III study for belimumab in SLE.” gsk.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Belimumab Monoclonal antibody 200 mg Subcutaneous