دورية أكاديمية
Phase 2B randomized study of nemolizumab in adults with moderate-to-severe atopic dermatitis and severe pruritus
العنوان: | Phase 2B randomized study of nemolizumab in adults with moderate-to-severe atopic dermatitis and severe pruritus |
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المؤلفون: | Silverberg, Jonathan I., Pinter, Andreas, Pulka, Grażyna, Poulin, Yves, Bouaziz, Jean-David, Wollenberg, Andreas, Murrell, Dedee F., Alexis, Andrew, Lindsey, Lisa, Ahmad, Faiz, Piketty, Christophe, Clucas, Alan |
سنة النشر: | 2020 |
المجموعة: | Jagiellonian University Repository |
مصطلحات موضوعية: | atopic dermatitis, humanized mAb, anti–IL-31 receptor |
الوصف: | Background: Nemolizumab targets the IL-31 receptor a subunit involved in atopic dermatitis (AD) pathogenesis. Objective: We sought to evaluate a new dosing strategy of nemolizumab in patients with AD. Methods: We performed a 24-week, randomized, double-blind, multicenter study of nemolizumab (10, 30, and 90 mg) subcutaneous injections every 4 weeks versus placebo, with topical corticosteroids in adults with moderate-to-severe AD, severe pruritus, and inadequate control with topical treatment (n 5 226). The Eczema Area and Severity Index (EASI), the peak pruritus (PP) numeric rating scale (NRS), and the Investigator’s Global Assessment (IGA) were assessed. Standard safety assessments were performed. Results: Nemolizumab improved EASI, IGA, and/or NRS-itch scores, with the 30-mg dose being most effective. Nemolizumab (30 mg) reduced EASI scores versus placebo at week 24 (268.8% vs 252.1%, P 5 .016); significant differences were observed by week 8 (P <_ .01). With significant improvement (P 5 .028) as early as week 4, IGA 0/1 rates were higher for 30 mg of nemolizumab versus placebo at week 16 (33.3% vs 12.3%, P 5 .008) but not week 24 because of an increased placebo/topical corticosteroid effect (36.8% vs 21.1%, P 5 .06). PP-NRS scores were improved for 30 mg of nemolizumab versus placebo at week 16 (268.6% vs 234.3%, P <.0001) and week 24 (267.3% vs 235.8%, P <.0001), with a difference by week 1 (P < .001). NRS response rates (>_4-point decrease) were greater for 30 mg of nemolizumab versus placebo at week 16 (P <_ .001) and week 24 (P <_ .01). Nemolizumab was safe and well tolerated. The most common adverse events were nasopharyngitis and upper respiratory tract infection. Conclusions: Nemolizumab resulted in rapid and sustained improvements in cutaneous signs of inflammation and pruritus in patients with AD, with maximal efficacy observed at 30 mg. Nemolizumab had an acceptable safety profile. (J Allergy Clin Immunol 2020;145:173-82.) |
نوع الوثيقة: | article in journal/newspaper |
اللغة: | English |
تدمد: | 0091-6749 1097-6825 |
العلاقة: | Journal of Allergy and Clinical Immunology, T. 145, nr 1, s. 173-182; https://ruj.uj.edu.pl/xmlui/handle/item/256918Test; https://www.jacionline.org/article/S0091-6749Test(19)31099-1/pdf |
DOI: | 10.1016/j.jaci.2019.08.013 |
الإتاحة: | https://doi.org/10.1016/j.jaci.2019.08.013Test https://ruj.uj.edu.pl/xmlui/handle/item/256918Test https://www.jacionline.org/article/S0091-6749Test(19)31099-1/pdf |
حقوق: | Udzielam licencji. Uznanie autorstwa - Użycie niekomercyjne - Bez utworów zależnych 4.0 Międzynarodowa ; http://creativecommons.org/licenses/by-nc-nd/4.0/pl/legalcodeTest |
رقم الانضمام: | edsbas.B4F6F5F4 |
قاعدة البيانات: | BASE |
تدمد: | 00916749 10976825 |
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DOI: | 10.1016/j.jaci.2019.08.013 |