| Literature DB >> 28000522 |
Warren Greth1, Gabriel J Robbie1, Philip Brohawn1, Micki Hultquist1, Bing Yao1.
Abstract
Dysregulation of the type I interferon (IFN) system is associated with various immunologic diseases, such as systemic lupus erythematosus (SLE). Targeting this dysregulation presents an attractive approach for SLE therapy. Sifalimumab, a fully human immunoglobulin G1 κ monoclonal antibody that binds to and neutralizes most IFN-α subtypes, has been recently evaluated in a Phase IIb study in patients with moderate to severe SLE. Insights gained from earlier studies were used to inform design of the Phase IIb study, to provide a more comprehensive evaluation of sifalimumab. Sifalimumab demonstrated broad efficacy across composite and organ-specific end points, suggesting that targeting of IFN-α is a promising treatment option for SLE, particularly for those patients whose disease is refractory to current standard of care.Entities:
Keywords: sifalimumab; systemic lupus erythematosus; type I interferon
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Year: 2017 PMID: 28000522 DOI: 10.2217/imt-2016-0090
Source DB: PubMed Journal: Immunotherapy ISSN: 1750-743X Impact factor: 4.196