The Safety of Ixekizumab in Chinese Adults with Moderate-to-Severe Plaque Psoriasis: Analyses from a Prospective, Single-Arm, Multicenter, 12-Week Observational Study

IF 4 2区 医学 Q1 PHARMACOLOGY & PHARMACY Drug Safety Pub Date : 2024-04-30 DOI:10.1007/s40264-024-01427-3
Ying Li, Lin Dang, Chengzhi Lv, Bingjiang Lin, Juan Tao, Nan Yu, Ya Deng, Huiping Wang, Xiaojing Kang, Hui Qin, Rong Chen, Jinnan Li, Yunsheng Liang, Yanhua Liang, Yuling Shi
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Abstract

Introduction

Ixekizumab, a monoclonal antibody against interleukin-17A, is efficacious and well tolerated for the treatment of moderate-to-severe plaque psoriasis. However, there are limited data on the real-world safety of ixekizumab in Chinese patient populations. We performed an observational study of ixekizumab for the treatment of moderate-to-severe plaque psoriasis in routine clinical practice in China. Here we present a further safety analysis of this study.

Methods

In this prospective, observational, single-arm, multicenter, post-marketing safety study, adults (≥18 years) with moderate-to-severe plaque psoriasis receiving ixekizumab were enroled at dermatology departments in hospitals across China and prospectively followed for 12 weeks or until their last dose of ixekizumab. In this analysis, we evaluated adverse events (AEs) of special interest (AESIs) identified using MedDRA® search strategies. We also analyzed AEs and AESIs occurring in greater than ten patients in subgroups by age (< 65/≥ 65 years), sex, body weight (< 60/60 kg to < 80/≥ 80 kg), renal impairment, hepatic impairment, history of tuberculosis, history of HBV infection, recent or active infection, history of allergic reaction/hypersensitivity, and number (0–1/2–4/5–7) of ixekizumab 80 mg injections after baseline until day 105.

Results

This analysis included 663/666 patients enrolled in the primary study. At least one AESI was reported in 224 (33.8%) patients and considered related to ixekizumab in 181 (27.3%); the most common were injection site reactions (n = 131, 19.8%), infections (n = 80, 12.1%), and allergic reactions/hypersensitivity events (n = 59, 8.9%). The proportion of patients with ≥ 1 AE was higher for females versus males (99/186, 53.2% versus 184/477, 38.6%, p = 0.0006). The proportion of patients with ≥ 1 AE increased with the number of ixekizumab injections after baseline [61/188 (32.4%) for zero to one injection, 151/338 (44.7%) for two to four injections, and 61/106 (57.5%) for five to seven injections; p = 0.0001].

Conclusions

In this real-world study, ixekizumab was well tolerated in Chinese patients with moderate-to-severe plaque psoriasis, with no difference in safety across most patient subgroups.

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伊昔单抗在中国成人中重度斑块状银屑病患者中的安全性:一项为期12周的前瞻性单臂多中心观察研究的分析结果
导言伊克珠单抗是一种抗白细胞介素-17A的单克隆抗体,治疗中重度斑块状银屑病疗效显著,耐受性良好。然而,有关ixekizumab在中国患者群体中的实际安全性的数据却很有限。我们在中国的常规临床实践中开展了一项ixekizumab治疗中重度斑块状银屑病的观察性研究。方法在这项前瞻性、观察性、单臂、多中心、上市后安全性研究中,中国各地医院的皮肤科登记了接受ixekizumab治疗的中重度斑块状银屑病成人患者(≥18岁),并对他们进行了为期12周或直至最后一次服用ixekizumab的前瞻性随访。在这项分析中,我们评估了使用 MedDRA® 搜索策略发现的特殊关注不良事件 (AEs)。我们还按年龄(65/≥65 岁)、性别、体重(60/60 千克至 80/≥80 千克)、肾功能损害、肝功能损害、结核病史、HBV 感染史、近期或活动性感染、过敏反应/过敏史以及基线后至第 105 天注射伊昔单抗 80 毫克的次数(0-1/2-4/5-7)对亚组中发生率超过 10 例的 AEs 和 AESI 进行了分析。结果这项分析包括663/666名参加主要研究的患者。224例(33.8%)患者报告了至少一种AESI,181例(27.3%)被认为与ixekizumab有关;最常见的是注射部位反应(131例,19.8%)、感染(80例,12.1%)和过敏反应/过敏事件(59例,8.9%)。女性与男性相比,发生≥1次AE的患者比例更高(99/186,53.2%;184/477,38.6%;P = 0.0006)。在这项真实世界研究中,中国中重度斑块状银屑病患者对ixekizumab的耐受性良好,大多数亚组患者的安全性没有差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug Safety
Drug Safety 医学-毒理学
CiteScore
7.60
自引率
7.10%
发文量
112
审稿时长
6-12 weeks
期刊介绍: Drug Safety is the official journal of the International Society of Pharmacovigilance. The journal includes: Overviews of contentious or emerging issues. Comprehensive narrative reviews that provide an authoritative source of information on epidemiology, clinical features, prevention and management of adverse effects of individual drugs and drug classes. In-depth benefit-risk assessment of adverse effect and efficacy data for a drug in a defined therapeutic area. Systematic reviews (with or without meta-analyses) that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. Original research articles reporting the results of well-designed studies in disciplines such as pharmacoepidemiology, pharmacovigilance, pharmacology and toxicology, and pharmacogenomics. Editorials and commentaries on topical issues. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Drug Safety Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
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