drugset / Trial / NCT01670565

Belimumab for the Treatment of Diffuse Cutaneous Systemic Sclerosis

NCT01670565

RandomizedParallel-groupDouble-blindTreatment

Summary

This is a 48 week, phase IIa, single center, randomized, double-blind, placebo-controlled, proof-of-concept pilot study. All participants will first be treated with mycophenolate mofetil (MMF, Cellcept) and titrated up to a dose of 2 grams/day. Following this period, half will be given either a belimumab (Benlysta®) or placebo intravenous infusion to treat early diffuse cutaneous systemic sclerosis. Belimumab/MMF is expected to improve disease activity measured by an improvement in skin thickening and stability of pulmonary function test measurements when compared to patients treated with placebo/MMF.

Timeline

Start
2012-08
Primary completion
2015-11
Completion
2016-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Belimumab Monoclonal antibody 10 mg/kg Intravenous
Background Mycophenolate Mofetil Small molecule 1000 mg

Indications