drugset / Trial / NCT01670565
Belimumab for the Treatment of Diffuse Cutaneous Systemic Sclerosis
Phase 2
Completed
20 enrolled
Hospital for Special Surgery, New York
Human Genome Sciences Inc. · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Belimumab | Monoclonal antibody | 10 mg/kg | Intravenous |
| Background | Mycophenolate Mofetil | Small molecule | 1000 mg | — |