The U.S. Food and Drug Administration today approved Benlysta (belimumab) intravenous (IV)  of children with systemic lupus erythematosus (SLE) often referred to as simply “lupus” a serious chronic disease that causes inflammation and damage to various body tissues and organs. This is the first time that the FDA has approved a treatment for pediatric patients with SLE. Benlysta has been approved for use in adult patients since 2011.

Infusion for treatment

“The agency expedited the review and approval of this application because Benlysta IV fulfils an unmet need for therapies, specifically in pediatric patients with SLE. While there is no cure for lupus; treatment can help our youngest patients control their disease with the hope of improving their quality of life and lowering their risk of long-term organ damage and disability;” said Janet Woodcock, M.D., director of the FDA’s Center for Drug Evaluation and Research.

While childhood-onset SLE is rare; when diagnosed, it is generally more active in children and adolescents than adult patients, particularly in how it impacts organs such as the kidneys and central nervous system. As a result of the disease starting early in life; pediatric patients with SLE are at a higher risk for developing increase organ damage and complications from the disease as well as adverse events from the life-long treatments usually required.

Central nervous system

The efficacy of Benlysta IV for the treatment of SLE in pediatric patients was studied over 52 weeks in 93 pediatric patients with SLE. The proportion of pediatric patients achieving the composite primary endpoint, the SLE response index (SRI-4), was higher in pediatric patients receiving Benlysta IV plus standard therapy compare to placebo plus standard therapy.

Pediatric patients who received Benlysta IV plus standard therapy also had a lower risk of experiencing a severe flare; as well as longer duration of time until a severe flare (160 days versus 82 days). The drug’s safety and pharmacokinetic profiles in pediatric patients were consistent with those in adults with SLE.

Experiencing a severe flare

Benlysta’s doctor and patient information includes a warning for mortality, serious infections; hypersensitivity and depression; base on data from the clinical studies in adults with SLE. The drug should not be administer with live vaccines. The manufacturer is require to provide a Medication Guide to inform patients of the risks associate with Benlysta.
The most common side effects in patients included nausea, diarrhea and fever. Patients also commonly experience infusion reactions, so healthcare professionals are advised to pre-treat patients with an antihistamine. The FDA granted this application a Priority Review designation. The FDA granted the approval of Benlysta to GlaxoSmithKline.