Secukinumab is superior to ustekinumab in clearing skin of subjects with moderate to severe plaque psoriasis: CLEAR, a randomized controlled trial

被引:490
作者
Thaci, Diamant [1 ]
Blauvelt, Andrew [2 ]
Reich, Kristian [3 ,4 ]
Tsai, Tsen-Fang [5 ]
Vanaclocha, Francisco [6 ]
Kingo, Kuelli [7 ]
Ziv, Michael [8 ]
Pinter, Andreas [9 ]
Hugot, Sophie [10 ]
You, Ruquan [11 ]
Milutinovic, Marina [10 ]
机构
[1] Univ Hosp Schleswig Holstein, Comprehens Ctr Inflammat Med, D-23538 Lubeck, Germany
[2] Oregon Med Res Ctr, Portland, OR USA
[3] Dermatologikum Hamburg, Hamburg, Germany
[4] Univ Gottingen, Gottingen, Germany
[5] Natl Taiwan Univ, Coll Med, Natl Taiwan Univ Hosp, Taipei, Taiwan
[6] Hosp 12 Octubre, E-28041 Madrid, Spain
[7] Univ Tartu, Dermatol Clin, Tartu Univ Hosp, Dept Dermatol, Tartu, Estonia
[8] HaEmek Med Ctr, Dept Dermatol, Afula, Israel
[9] Goethe Univ Frankfurt, Frankfurt, Germany
[10] Novartis Pharma AG, Basel, Switzerland
[11] Beijing Novartis Pharma Co Ltd, Shanghai, Peoples R China
关键词
clear or almost clear skin; clinical trial; head to head; plaque psoriasis; secukinumab; superiority; ustekinumab; 90% or more improvement in baseline Psoriasis Area and Severity Index; INTERLEUKIN-12/23; MONOCLONAL-ANTIBODY; TO-SEVERE PSORIASIS; QUALITY INDEX DLQI; DOUBLE-BLIND; PHASE-III; EFFICACY; SAFETY; ETANERCEPT; THERAPY; PLACEBO;
D O I
10.1016/j.jaad.2015.05.013
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100227 [皮肤病学];
摘要
Background: 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). Objective: We sought to directly compare efficacy and safety of secukinumab versus ustekinumab. Methods: 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. Results: 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. Limitations: The study was not placebo-controlled and of short-term duration. Conclusions: 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.
引用
收藏
页码:400 / 409
页数:10
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