کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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4210565 | 1280597 | 2010 | 8 صفحه PDF | دانلود رایگان |

SummaryBackgroundAclidinium 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.MethodsThis double-blind, randomised, placebo-controlled, crossover study was conducted in patients with moderate to severe COPD (forced expiratory volume in 1 s [FEV1] <65% predicted). Patients were randomly assigned to one of four treatment sequences of aclidinium bromide 100, 300, 900 μg and placebo with a washout period between doses. The primary outcome was area under the FEV1 curve over the 0–24 h time interval.ResultsSeventeen patients with COPD were studied. Mean FEV1 over 24 h was 1.583 L for placebo, and 1.727 L, 1.793 L and 1.815 L for aclidinium bromide 100, 300 and 900 μg, respectively (p < 0.001 vs. placebo, all doses). Significant changes from baseline in FEV1 were detected 15 min post-dose for aclidinium bromide 300 and 900 μg, with a peak effect 2 h 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.ConclusionAclidinium bromide 100–900 μg produced sustained bronchodilation over 24 h in patients with COPD.
Journal: Respiratory Medicine - Volume 104, Issue 6, June 2010, Pages 865–872