AERIFY-1/-2:伊替匹单抗治疗中重度慢性阻塞性肺病前吸烟者的两项三期随机对照试验

IF 4.3 3区 医学 Q1 RESPIRATORY SYSTEM
Klaus F. Rabe, Fernando J. Martinez, Surya P. Bhatt, Tomotaka Kawayama, B. Cosío, Robert M. Mroz, Maarten M. Boomsma, Helene Goulaouic, M. Nivens, Michel Djandji, Xavier Soler, Ying Liu, M. Kosloski, Christine R. Xu, Nikhil Amin, H. Staudinger, David J. Lederer, R. Abdulai
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引用次数: 0

摘要

越来越多的数据表明,白细胞介素(IL)-33 是一种上皮细胞受损时局部释放的促炎细胞因子,与慢性阻塞性肺病(COPD)的发病机制有关。在一项二期研究中,针对IL-33的人类单克隆抗体伊替匹单抗(itepekimab)在慢性阻塞性肺病前吸烟者的亚组分析中减少了病情恶化,改善了肺功能,且安全性可接受。AERIFY-1/2(NCT04701983/NCT04751487)是两项3期随机、双盲、安慰剂对照试验,其主要目的是评估伊替匹单抗与安慰剂在中度至重度慢性阻塞性肺病前吸烟者中的疗效和安全性,时间长达52周。另外,AERIFY-2 还招募了另外一批当前吸烟者。这两项研究将招募患有慢性阻塞性肺病和慢性支气管炎的患者(年龄在 40-85 岁之间),这些患者尽管接受了标准的三联或双联背景治疗,但在过去一年中仍有≥2 次中度或≥1 次重度病情加重。所有参与者的吸烟史必须≥10包年,曾经吸烟者的戒烟时间必须≥6个月。主要终点是慢性阻塞性肺疾病中度或重度急性加重的年率。次要终点包括支气管扩张剂前后 FEV1 与基线相比的变化以及严重恶化的年化频率。症状终点包括慢性阻塞性肺病呼吸道症状评估、圣乔治呼吸道问卷、安全性和抗药物抗体反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
AERIFY-1/-2: 2 phase 3 randomised controlled trials of itepekimab in former smokers with moderate-to-severe COPD
Accumulating data implicate interleukin (IL)-33, a proinflammatory cytokine released locally upon epithelial cell damage, in the pathogenesis of chronic obstructive pulmonary disease (COPD). In a phase 2 study, itepekimab, a human monoclonal antibody against IL-33, reduced exacerbations and improved lung function in a subgroup analysis of former smokers with COPD with an acceptable safety profile.The study designs of AERIFY-1 and AERIFY-2 are described in this article.:The primary objective of AERIFY-1/2 (NCT04701983/NCT04751487), two phase 3 randomized, double-blind, placebo-controlled trials, is to assess the efficacy and safety of itepekimabversusplacebo in a population of former smokers with moderate-to-severe COPD over up to 52 weeks. An additional secondary population of current smokers are being enrolled in AERIFY-2. These two studies will enrol patients (aged 40–85 years) with COPD and chronic bronchitis who had ≥2 moderate or ≥1 severe exacerbations within the previous year despite standard-of-care triple or double background therapy. All participants are required to have ≥10-pack year smoking history, and ≥6 months since smoking cessation for former smokers. The primary endpoint is the annualized rate of moderate or severe acute exacerbation of COPD. Secondary endpoints include change from baseline in pre- and post-bronchodilator FEV1, and annualized frequency of severe exacerbations. Symptomatic endpoints include Evaluating Respiratory Symptoms in COPD, and St. George's Respiratory Questionnaire, safety and anti-drug antibody responses.
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来源期刊
ERJ Open Research
ERJ Open Research Medicine-Pulmonary and Respiratory Medicine
CiteScore
6.20
自引率
4.30%
发文量
273
审稿时长
8 weeks
期刊介绍: ERJ Open Research is a fully open access original research journal, published online by the European Respiratory Society. The journal aims to publish high-quality work in all fields of respiratory science and medicine, covering basic science, clinical translational science and clinical medicine. The journal was created to help fulfil the ERS objective to disseminate scientific and educational material to its members and to the medical community, but also to provide researchers with an affordable open access specialty journal in which to publish their work.
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