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首页> 外文期刊>Journal of the American Academy of Dermatology >Efficacy and safety of itolizumab, a novel anti-CD6 monoclonal antibody, in patients with moderate to severe chronic plaque psoriasis: Results of a double-blind, randomized, placebo-controlled, phase-III study
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Efficacy and safety of itolizumab, a novel anti-CD6 monoclonal antibody, in patients with moderate to severe chronic plaque psoriasis: Results of a double-blind, randomized, placebo-controlled, phase-III study

机译:新型抗CD6单克隆抗体itolizumab在中度至重度慢性斑块状牛皮癣患者中的功效和安全性:一项双盲,随机,安慰剂对照,III期研究的结果

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Background Itolizumab, a humanized monoclonal antibody to CD6, is a novel therapeutic agent evaluated in chronic plaque psoriasis. Objective We sought to assess the safety and efficacy of itolizumab in moderate to severe chronic plaque psoriasis. Methods A total of 225 patients were randomized (2:2:1) to 2 different itolizumab arms (A or B; A = 4-week loading dose of 0.4 mg/kg/wk followed by 1.6 mg/kg every 2 weeks; B = 1.6/mg every 2 weeks) or placebo. At week 12, the placebo arm was switched to 1.6 mg/kg itolizumab every 2 weeks. The primary end point was the proportion of patients with at least 75% improvement in Psoriasis Area and Severity Index score at week 12. Results At week 12, 27.0% in arm A (P =.0172 vs placebo), 36.4% in B (P =.0043 vs placebo), and 2.3% in the placebo arm had at least 75% improvement in Psoriasis Area and Severity Index score. At week 28, the proportion with at least 75% improvement in Psoriasis Area and Severity Index score was comparable: 46.1%, 45.5%, and 41.9% for A, B, and placebo, respectively. In weeks 1 to 12, the incidence of all adverse events was comparable across arms (A, 43%; B, 38%; placebo, 47%) and the incidence of infections was not greater than placebo (11.1%, 8.9%, and 18.6% for A, B, and placebo). Limitations No active comparator is a limitation. Conclusions Itolizumab is an effective and well-tolerated novel biological therapy in moderate to severe psoriasis.
机译:背景技术Itolizumab是一种针对CD6的人源化单克隆抗体,是一种在慢性斑块状牛皮癣中评估的新型治疗药物。目的我们试图评估阿托珠单抗在中度至重度慢性斑块状牛皮癣中的安全性和有效性。方法将总共225例患者(2:2:1)随机分配到2个不同的依托珠单抗组(A或B; A = 4周负荷剂量0.4 mg / kg / wk,然后每2周1.6 mg / kg); B =每2周1.6 mg / mg)或安慰剂。在第12周时,每2周将安慰剂组换为1.6 mg / kg托珠单抗。主要终点是在第12周时牛皮癣面积和严重性指数得分至少改善75%的患者比例。结果在第12周,A组27.0%(P = .0172 vs安慰剂),B组36.4%( P = .0043 vs安慰剂),安慰剂组2.3%的牛皮癣面积和严重性指数得分至少提高了75%。在第28周时,牛皮癣面积和严重性指数得分至少改善75%的比例相当:A,B和安慰剂分别为46.1%,45.5%和41.9%。在第1周到第12周,各组所有不良事件的发生率相当(A,43%; B,38%;安慰剂,47%),感染发生率不大于安慰剂(11.1%,8.9%,和A,B和安慰剂的18.6%)。限制没有活动的比较器是一个限制。结论Itolizumab是一种对中至重度牛皮癣有效且耐受良好的新型生物疗法。

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