Nemolizumab plus topical agents in patients with atopic dermatitis (AD) and moderate-to-severe pruritus provide improvement in pruritus and signs of AD for up to 68 weeks: results from two phase III, long-term studies

被引:86
作者
Kabashima, K. [1 ]
Matsumura, T. [2 ]
Komazaki, H. [2 ]
Kawashima, M. [3 ]
机构
[1] Kyoto Univ, Grad Sch Med, Dept Dermatol, Kyoto, Japan
[2] Maruho Co Ltd, Clin Dev Dept, Kyoto, Japan
[3] Tokyo Womens Med Univ, Tokyo, Japan
关键词
ORIENTED ECZEMA MEASURE; CLINICAL-TRIALS; INDEX; IL-31; RESPONSIVENESS; VALIDATION; ANTIBODY; RECEPTOR; CHILDREN; AREA;
D O I
10.1111/bjd.20873
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Interleukin (IL)-31 affects the inflammatory response, is involved in epidermal barrier disruption in atopic dermatitis (AD) and plays a key role in pruritus. Nemolizumab, a humanized monoclonal antibody against IL-31 receptor A, reduced pruritus in patients with AD after a 16-week administration period. Objectives To examine the long-term effectiveness and safety of nemolizumab in patients aged >= 13 years with AD and inadequately controlled moderate-to-severe pruritus. Methods In two long-term phase III studies, nemolizumab 60 mg every 4 weeks (Q4W) was administered subcutaneously, concomitantly with topical treatments. Study-JP01 patients received double-blind nemolizumab or placebo for 16 weeks, and then entered a 52-week extension period in which all patients received nemolizumab (nemolizumab/nemolizumab and placebo/nemolizumab groups). Study-JP02 patients received nemolizumab for 52 weeks. Both studies included an 8-week follow-up period. Results Study-JP01 nemolizumab/nemolizumab and placebo/nemolizumab, and Study-JP02 nemolizumab groups comprised 143, 72 and 88 patients, respectively. In the nemolizumab/nemolizumab group, there were clinically meaningful improvements from the start of treatment to week 68 in the pruritus visual analogue scale (66% decrease) and Eczema Area and Severity Index (78% decrease). Quality of life (QoL) indicators improved after the first nemolizumab dose; improvements were maintained during the follow-up period. The long-term safety profile was consistent with previous studies, with no unexpected late-onset adverse events. Conclusions Nemolizumab 60 mg Q4W with concomitant topical treatments in patients with AD and inadequately controlled moderate-to-severe pruritus produced a continuous improvement in pruritus, signs of AD, and QoL for up to 68 weeks, with a favourable safety profile.
引用
收藏
页码:642 / 651
页数:10
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