Efficacy and Safety of Aclidinium Bromide Compared with Placebo and Tiotropium in Patients with Moderate-to-Severe Chronic Obstructive Pulmonary Disease: Results from a 6-week, Randomized, Controlled Phase IIIb Study

被引:92
作者
Beier, Jutta [1 ]
Kirsten, Anne-Marie [2 ]
Mroz, Robert [3 ,4 ]
Segarra, Rosa [5 ]
Chuecos, Ferran [5 ]
Caracta, Cynthia [6 ]
Garcia Gil, Esther [5 ]
机构
[1] Insaf Resp Res Inst, D-65187 Wiesbaden, Germany
[2] Hosp Grosshansdorf, Pulm Res Inst, Grosshansdorf, Germany
[3] Med Univ Bialystok, ISPL Ctr Med, Bialystok, Poland
[4] Med Univ Bialystok, Dept Lung Dis & TB, Bialystok, Poland
[5] Almirall, Barcelona, Spain
[6] Forest Res Inst, Jersey City, NJ USA
关键词
24-hour; bronchodilation; long-acting muscarinic antagonist; nighttime; symptoms; COPD PATIENTS; CIRCADIAN VARIATION; OXYGEN-SATURATION; LUNG-FUNCTION; METAANALYSIS; SLEEP;
D O I
10.3109/15412555.2013.814626
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
100201 [内科学];
摘要
Background: This randomized, double-blind, Phase IIIb study evaluated the 24-hour bronchodilatory efficacy of aclidinium bromide versus placebo and tiotropium in patients with moderate-to-severe chronic obstructive pulmonary disease (COPD). Methods: Patients received aclidinium 400 mu g twice daily (morning and evening), tiotropium 18 mu g once daily (morning), or placebo for 6 weeks. The primary endpoint was change from baseline in forced expiratory volume in 1 second area under the curve for the 24-hour period post-morning dose (FEV1 AUC(0-24)) at week 6. Secondary and additional endpoints included FEV1 AUC(12-24), COPD symptoms (EXAcerbations of chronic pulmonary disease Tool-Respiratory Symptoms [E-RS] total score and additional symptoms questionnaire), and safety. Results: Overall, 414 patients were randomized and treated (FEV1 1.63 L [55.8% predicted]). Compared with placebo, FEV1 AUC0-24 and FEV1 AUC12-24 were significantly increased from baseline with aclidinium (Delta = 150 mL and 160 mL, respectively; p < 0.0001) and tiotropium (Delta = 140 mL and 123 mL, respectively; p < 0.0001) at week 6. Significant improvements in E-RS total scores over 6 weeks were numerically greater with aclidinium (p < 0.0001) than tiotropium (p < 0.05) versus placebo. Only aclidinium significantly reduced the severity of early-morning cough, wheeze, shortness of breath, and phlegm, and of nighttime symptoms versus placebo (p < 0.05). Adverse-event (AE) incidence (28%) was similar between treatments. Few anticholinergic AEs (<1.5%) or serious AEs (<3%) occurred in any group. Conclusions: Aclidinium provided significant 24-hour bronchodilation versus placebo from day 1 with comparable efficacy to tiotropium after 6 Improvements in COPD symptoms were consistently numerically greater aclidinium versus tiotropium. Aclidinium was generally well tolerated.
引用
收藏
页码:511 / 522
页数:12
相关论文
共 34 条
[1]
Night-time symptoms: a forgotten dimension of COPD [J].
Agusti, A. ;
Hedner, J. ;
Marin, J. M. ;
Barbe, F. ;
Cazzola, M. ;
Rennard, S. .
EUROPEAN RESPIRATORY REVIEW, 2011, 20 (121) :183-194
[2]
Avoiding confusion in COPD: from risk factors to phenotypes to measures of disease characterisation [J].
Agusti, A. ;
Celli, B. .
EUROPEAN RESPIRATORY JOURNAL, 2011, 38 (04) :749-751
[3]
Effect of tiotropium bromide on circadian variation in airflow limitation in chronic obstructive pulmonary disease [J].
Calverley, PMA ;
Lee, A ;
Towse, L ;
van Noord, J ;
Witek, TJ ;
Kelsen, S .
THORAX, 2003, 58 (10) :855-860
[4]
Outcomes for COPD pharmacological trials:: from lung function to biomarkers [J].
Cazzola, M. ;
MacNee, W. ;
Martinez, F. J. ;
Rabe, K. F. ;
Franciosi, L. G. ;
Barnes, P. J. ;
Brusasco, V. ;
Burge, P. S. ;
Calverley, P. M. A. ;
Celli, B. R. ;
Jones, P. W. ;
Mahler, D. A. ;
Make, B. ;
Miravitlles, M. ;
Page, C. P. ;
Palange, P. ;
Parr, D. ;
Pistolesi, M. ;
Rennard, S. I. ;
Moelken, M. P. Rutten-Van ;
Stockley, R. ;
Sullivan, S. D. ;
Wedzicha, J. A. ;
Wouters, E. F. .
EUROPEAN RESPIRATORY JOURNAL, 2008, 31 (02) :416-468
[5]
CHRYSTYN H, 2012, BRIT THOR SOC WINT M
[6]
Comparative safety of inhaled medications in patients with chronic obstructive pulmonary disease: systematic review and mixed treatment comparison meta-analysis of randomised controlled trials [J].
Dong, Yaa-Hui ;
Lin, Hsien-Ho ;
Shau, Wen-Yi ;
Wu, Yun-Chun ;
Chang, Chia-Hsuin ;
Lai, Mei-Shu .
THORAX, 2013, 68 (01) :48-56
[7]
Donohue James F, 2005, COPD, V2, P111
[8]
A 6-month, placebo-controlled study comparing lung function and health status changes in COPD patients treated with tiotropium or salmeterol [J].
Donohue, JF ;
van Noord, JA ;
Bateman, ED ;
Langley, SJ ;
Lee, A ;
Witek, TJ ;
Kesten, S ;
Towse, L .
CHEST, 2002, 122 (01) :47-55
[9]
Efficacy of Aclidinium Bromide 400 μg Twice Daily Compared With Placebo and Tiotropium in Patients With Moderate to Severe COPD [J].
Fuhr, Rainard ;
Magnussen, Helgo ;
Sarem, Kristina ;
Ribera Llovera, Anna ;
Kirsten, Anne-Marie ;
Falques, Meritxell ;
Caracta, Cynthia F. ;
Garcia Gil, Esther .
CHEST, 2012, 141 (03) :745-752
[10]
GAVALDA A, 2008, EUR RESP SOC ANN C B