Efficacy and safety of a CXCR2 antagonist, AZD5069, in patients with uncontrolled persistent asthma: a randomised, double-blind, placebo-controlled trial

医学 安慰剂 哮喘 双盲 内科学 敌手 随机对照试验 麻醉 替代医学 病理 受体
作者
Paul M. O’Byrne,Hristo Metev,Margareta Puu,Kai Richter,Christina Keen,Mohib Uddin,Bengt Larsson,Marie Cullberg,Parameswaran Nair
出处
期刊:The Lancet Respiratory Medicine [Elsevier BV]
卷期号:4 (10): 797-806 被引量:232
标识
DOI:10.1016/s2213-2600(16)30227-2
摘要

Airway neutrophilic inflammation is a pathological feature in some patients with severe asthma. Stimulation of the chemokine receptor CXCR2 mediates neutrophil migration into the airways. We investigated the safety and efficacy of AZD5069, a CXCR2 antagonist, as an add-on therapy in patients with uncontrolled severe asthma.In this multicentre, randomised, double-blind, placebo-controlled, dose-finding trial, we enrolled patients aged 18 years or older with uncontrolled asthma despite combination therapy with long-acting β2 agonists and medium-dose or high-dose inhaled corticosteroids. Patients were randomised in a 1:1:1:1 ratio via an interactive voice-response or web-response system to receive 5, 15, or 45 mg oral AZD5069 twice daily or matched placebo. The primary endpoint was the number of severe asthma exacerbations in 6 months. Safety was assessed in the 6-month treatment period and an optional 6-month safety extension. This trial is registered with ClinicalTrials.gov, number NCT01704495.640 patients with a mean age of 52 (SD 11·8) years were randomised, 478 to receive AZD5069 (5 mg n=160, 15 mg n=156, and 45 mg n=162) and 162 placebo. No dose of AZD5069 reduced the rate of severe exacerbations compared with placebo (rate ratio for 5 mg 1·29, 90% CI 0·79-2·11; for 15 mg 1·53, 0·95-2·46; and for 45 mg 1·56, 0·98-2·49). Treatment with AZD5069 was generally well tolerated. The most commonly reported adverse event overall was nasopharyngitis, seen in 18 (11·5%) receiving 5 mg, 13 (8·5%) receiving 15 mg, and 18 (11·2%) receiving 45 mg AZD5069, and 31 (19·5%) of those receiving placebo.Treatment with this selective CXCR2 antagonist did not reduce the frequency of severe exacerbations in patients with uncontrolled severe asthma. These findings bring into question the role of CXCR2-mediated neutrophil recruitment in the pathobiology of exacerbations in severe refractory asthma.AstraZeneca.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
fenglin4620发布了新的文献求助10
刚刚
CipherSage应助科研通管家采纳,获得200
刚刚
Orange应助科研通管家采纳,获得20
刚刚
我是老大应助科研通管家采纳,获得10
刚刚
bkagyin应助科研通管家采纳,获得10
刚刚
FashionBoy应助科研通管家采纳,获得10
1秒前
1秒前
小库里2025完成签到 ,获得积分10
1秒前
1秒前
紧张的绿茶完成签到,获得积分10
2秒前
zhongjr_hz完成签到,获得积分10
3秒前
Remote完成签到,获得积分10
3秒前
爆米花应助alice采纳,获得10
3秒前
谨慎的哈密瓜完成签到 ,获得积分10
4秒前
wuxunxun2015完成签到,获得积分10
4秒前
Davey1220完成签到,获得积分10
5秒前
ranbo发布了新的文献求助10
5秒前
天行马完成签到,获得积分10
6秒前
BareBear应助碧蓝可乐采纳,获得10
7秒前
MrCoolWu完成签到,获得积分10
8秒前
活力数据线完成签到,获得积分10
8秒前
偶然847完成签到,获得积分10
10秒前
10秒前
安详秋完成签到 ,获得积分10
11秒前
12秒前
塞西尔完成签到,获得积分10
14秒前
haha完成签到,获得积分10
17秒前
17秒前
芝麻配海带完成签到,获得积分10
17秒前
18秒前
爆米花完成签到,获得积分10
18秒前
cistronic发布了新的文献求助10
18秒前
18秒前
一年发3篇JACS完成签到,获得积分10
19秒前
酷酷的安柏完成签到 ,获得积分10
21秒前
neo完成签到,获得积分10
21秒前
路明非完成签到,获得积分10
21秒前
丘比特应助豆豆采纳,获得10
22秒前
超级玛丽完成签到 ,获得积分10
22秒前
独立卫生间完成签到,获得积分10
22秒前
高分求助中
(禁止应助)【重要!!请各位详细阅读】【科研通的精品贴汇总】 10000
Semantics for Latin: An Introduction 1099
Biology of the Indian Stingless Bee: Tetragonula iridipennis Smith 1000
Robot-supported joining of reinforcement textiles with one-sided sewing heads 760
2024-2030年中国石英材料行业市场竞争现状及未来趋势研判报告 500
镇江南郊八公洞林区鸟类生态位研究 500
Thermal Quadrupoles: Solving the Heat Equation through Integral Transforms 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 4150175
求助须知:如何正确求助?哪些是违规求助? 3686226
关于积分的说明 11643900
捐赠科研通 3379146
什么是DOI,文献DOI怎么找? 1854557
邀请新用户注册赠送积分活动 916641
科研通“疑难数据库(出版商)”最低求助积分说明 830544