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Drug Safety Evaluation

The safety of belimumab for the treatment of systemic lupus erythematosus

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Pages 1133-1144 | Received 14 Aug 2019, Accepted 24 Oct 2019, Published online: 31 Oct 2019
 

ABSTRACT

Introduction: Systemic lupus erythematosus (SLE) is a systemic autoimmune inflammatory disease with extensive clinical variability. In 2011, the anti-BAFF monoclonal antibody, belimumab, became the first FDA-approved drug for SLE in 50+ years. As with all immunomodulating medications, the benefits must be weighed against the adverse side effects. This is especially pertinent for SLE patients, given the chronic nature of their disease and their need for long-term treatment. The focus of the present review is the safety of belimumab, including data gleaned from clinical trials, their open-label extensions, and ‘real-world’ clinical settings.

Areas covered: Safety data from phase I, phase II, phase III, extension open-label trials, and ‘real-world’ observational studies of belimumab are reviewed and discussed.

Expert opinion: As the only FDA-approved treatment for SLE in the past 60+ years, belimumab has demonstrated significant, albeit modest, efficacy and a reassuring safety profile. Long-term data to date show that it is well-tolerated with a low risk of side effects, even when administered for up to 13 years. Given that belimumab allows providers to decrease daily corticosteroid doses over time (and, thereby, decrease the serious risks associated with chronic corticosteroid use), it should be seen as a valuable tool in the rheumatologist’s arsenal.

Box 1. Drug Summary Box

Declaration of interest

W Stohl has received clinical trial support from GlaxoSmithKline and Pfizer. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.

Reviewer disclosures

Peer reviewers on this manuscript have no relevant financial or other relationships to disclose.

Additional information

Funding

This work was supported in part by the Thomas D. Beardmore, MD Memorial Endowment Fund and by the Selena Gomez Fund for Lupus Research.

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