کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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4208090 | 1280427 | 2015 | 7 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Tiotropium Respimat® in cystic fibrosis: Phase 3 and Pooled phase 2/3 randomized trials Tiotropium Respimat® in cystic fibrosis: Phase 3 and Pooled phase 2/3 randomized trials](/preview/png/4208090.png)
BackgroundTiotropium Respimat® improved lung function in a phase 2 trial in patients with cystic fibrosis (CF). We investigated its efficacy and safety in a phase 3 trial, including a pre-specified pooled analysis of the phase 2 and 3 trials.Methods12-week, randomized, double-blind, placebo-controlled trial of tiotropium Respimat® 5 μg once daily in patients with CF (N = 463).ResultsCo-primary efficacy endpoints showed no statistical difference between tiotropium and placebo: percent-predicted forced expiratory volume in 1 s (FEV1) area under the curve from 0–4 h (AUC0–4 h) (95% CI): 1.64% (0.27,3.55; p = 0.092); percent-predicted trough FEV1 (95% CI) 1.40% (0.50,3.30; p = 0.15). Adverse events were similar between groups. Pooled phase 2/3 trial results showed a treatment difference in favor of tiotropium: percent-predicted FEV1 AUC0–4 h (95% CI): 2.62% (1.34,3.90).ConclusionTiotropium was well tolerated in patients with CF; lung function improvements compared with placebo were not statistically significant in the phase 3 trial.Clinical trialsThese studies are registered with clinical trial identifier numbers NCT00737100 and NCT01179347. These studies are also registered with the EudraCT number: 2008-001156-43 and 2010-019802-17.
Journal: Journal of Cystic Fibrosis - Volume 14, Issue 5, September 2015, Pages 608–614