Department of Respiratory Medicine, Ghent University Hospital, De Pintelaan 185, B9000 Ghent, Belgium.
Respir Med. 2010 Jun;104(6):865-72. doi: 10.1016/j.rmed.2009.12.003. Epub 2009 Dec 30.
Aclidinium bromide is a novel, long-acting, inhaled muscarinic antagonist bronchodilator currently in Phase III clinical development for the treatment of chronic obstructive pulmonary disease (COPD). This study evaluated the pharmacodynamics, pharmacokinetics, safety and tolerability of ascending doses of aclidinium bromide in patients with COPD.
This double-blind, randomised, placebo-controlled, crossover study was conducted in patients with moderate to severe COPD (forced expiratory volume in 1s [FEV(1)] <65% predicted). Patients were randomly assigned to one of four treatment sequences of aclidinium bromide 100, 300, 900microg and placebo with a washout period between doses. The primary outcome was area under the FEV(1) curve over the 0-24h time interval.
Seventeen patients with COPD were studied. Mean FEV(1) over 24h was 1.583L for placebo, and 1.727L, 1.793L and 1.815L for aclidinium bromide 100, 300 and 900microg, respectively (p<0.001 vs. placebo, all doses). Significant changes from baseline in FEV(1) were detected 15min post-dose for aclidinium bromide 300 and 900microg, with a peak effect 2h post-dose (all doses). Aclidinium bromide was undetected in plasma. The majority of adverse events was unrelated to study medication and did not result in discontinuation.
Aclidinium bromide 100-900microg produced sustained bronchodilation over 24h in patients with COPD.
阿地溴铵是一种新型长效吸入性毒蕈碱拮抗剂支气管扩张剂,目前正处于治疗慢性阻塞性肺疾病(COPD)的 III 期临床开发阶段。本研究评估了阿地溴铵递增剂量在 COPD 患者中的药效学、药代动力学、安全性和耐受性。
这是一项双盲、随机、安慰剂对照、交叉研究,在中重度 COPD 患者(FEV1<65%预计值)中进行。患者随机分配到阿地溴铵 100、300、900μg 和安慰剂的四个治疗序列之一,每个剂量之间有洗脱期。主要终点是 0-24h 时间间隔内 FEV1 曲线下面积。
17 例 COPD 患者入组。安慰剂组的平均 24h FEV1 为 1.583L,阿地溴铵 100、300 和 900μg 组分别为 1.727L、1.793L 和 1.815L(均与安慰剂相比,p<0.001)。阿地溴铵 300 和 900μg 组在给药后 15min 即出现 FEV1 与基线相比的显著变化,2h 时达到峰值效应(所有剂量)。血浆中未检测到阿地溴铵。大多数不良事件与研究药物无关,且未导致停药。
阿地溴铵 100-900μg 在 COPD 患者中产生了持续 24h 的支气管扩张作用。