Background: Secukinumab (SEC), a fully human monoclonal antibody (mAb) that selectively neutralizes IL-17A, has significant efficacy in the treatment of moderate to severe plaque psoriasis (Pso) and psoriatic arthritis (PsA), demonstrating a rapid onset of action and sustained responses up to 5 years with a favorable safety profile and 0.4% immunogenicity in the Pso phase 3 program. SEC has previously demonstrated lower potential for immunogenicity compared with other mAbs used to treat Pso and PsA in in vitro assays.
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