塞库金单抗
医学
银屑病
乌斯特基努马
阿达木单抗
伊克泽珠单抗
皮肤病科
白细胞介素23
临床试验
免疫系统
白细胞介素17
免疫学
疾病
银屑病性关节炎
内科学
作者
Egídio Freitas,Andrew Blauvelt,Tiago Torres
出处
期刊:Drugs
[Springer Nature]
日期:2021-10-01
卷期号:81 (15): 1751-1762
被引量:23
标识
DOI:10.1007/s40265-021-01612-z
摘要
Psoriasis is a chronic, systemic, immune-mediated disease, with prominent skin and joint manifestations, associated with several comorbidities. In the past few decades, advances in the knowledge of psoriasis pathogenesis have driven the development of highly effective targeted biologic therapies, transforming the treatment landscape of psoriasis. Bimekizumab is a humanized antibody that selectively binds and neutralizes the biologic functions of interleukin (IL)-17A and IL-17F. This article reviews the current knowledge about bimekizumab in psoriasis treatment. The results obtained in the phase 3 studies (BE VIVID, BE READY, BE RADIANT, BE SURE) corroborate the high levels of efficacy of bimekizumab seen in previous studies, and show superior efficacy over adalimumab, ustekinumab, and secukinumab in direct comparative studies. In all phase 3 trials, bimekizumab was also well tolerated, with a safety profile similar to the other biologic drugs tested, except for a higher frequency of oral candidiasis. Dual inhibition of IL-17A and IL-17F is a highly effective therapeutic option for the treatment of psoriasis, both for naïve patients and for those resistant to previous biologic treatments.
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