塞库金单抗
乌斯特基努马
医学
银屑病面积及严重程度指数
皮肤科生活质量指数
银屑病
安慰剂
随机对照试验
不利影响
皮肤病科
内科学
银屑病性关节炎
阿达木单抗
疾病
病理
替代医学
作者
Diamant Thaçi,Andrew Blauvelt,Kristian Reich,Tsen‐Fang Tsai,F. Vanaclocha,Külli Kingo,Michael Ziv,Andreas Pinter,Sophie Hugot,R. You,M. Milutinovic
标识
DOI:10.1016/j.jaad.2015.05.013
摘要
Secukinumab, a fully human anti-interleukin-17A monoclonal antibody, has shown superior efficacy to etanercept with similar safety in moderate to severe plaque psoriasis (FIXTURE study).We sought to directly compare efficacy and safety of secukinumab versus ustekinumab.In this 52-week, double-blind study (NCT02074982), 676 subjects were randomized 1:1 to subcutaneous injection of secukinumab 300 mg or ustekinumab per label. Primary end point was 90% or more improvement from baseline Psoriasis Area and Severity Index (PASI) score (PASI 90) at week 16.Secukinumab (79.0%) was superior to ustekinumab (57.6%) as assessed by PASI 90 response at week 16 (P < .0001). The 100% improvement from baseline PASI score at week 16 was also significantly greater with secukinumab (44.3%) than ustekinumab (28.4%) (P < .0001). The 75% or more improvement from baseline PASI score at week 4 was superior for secukinumab (50.0%) versus ustekinumab (20.6%) (P < .0001). Percentage of subjects with the Dermatology Life Quality Index score 0/1 (week 16) was significantly higher with secukinumab (71.9%) than ustekinumab (57.4%) (P < .0001). The safety profile of secukinumab was comparable with ustekinumab and consistent with pivotal phase III secukinumab studies.The study was not placebo-controlled and of short-term duration.Secukinumab is superior to ustekinumab in clearing skin of subjects with moderate to severe psoriasis and improving health-related quality of life with a comparable safety profile over 16 weeks.
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