Abstract
BACKGROUND: Umeclidinium (UMEC; long-acting muscarinic antagonist) plus vilanterol (VI; long-acting beta2 agonist [LABA]) and the LABA/inhaled corticosteroid fluticasone propionate/salmeterol (FP/SAL) are approved maintenance treatments for chronic obstructive pulmonary disease (COPD). This 12-week, multicentre, double-blind, parallel-group, double-dummy study compared the efficacy and safety of these treatments in symptomatic patients with moderate-to-severe COPD with no exacerbations in the year prior to enrolment. METHODS: Patients (n = 717) were randomised 1:1 to once-daily UMEC/VI 62.5/25 mcg or twice-daily FP/SAL 500/50 mcg. Endpoints included 0-24 h weighted mean (wm) forced expiratory volume in 1 s (FEV1) (Day 84; primary), trough FEV1 (Day 85; secondary), other lung function endpoints, symptoms, quality of life (QoL) and safety. RESULTS: Improvements with UMEC/VI versus FP/SAL were 0.080 L (95 % confidence interval: 0.046-0.113; wmFEV1) and 0.090 L (0.055-0.125; trough FEV1) (both p
Original language | English |
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Journal | BMC Pulmonary Medicine |
Volume | 15 |
DOIs | |
Publication status | Published - 2015 |
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Umeclidinium/vilanterol versus fluticasone propionate/salmeterol in COPD: a randomised trial
Singh, S. (Contributor), Worsley, S. (Contributor), Zhu, C. (Contributor), Hardaker, L. (Contributor) & Church, A. (Contributor), figshare , 19 Aug 2015
DOI: 10.6084/m9.figshare.c.3642377.v1, https://figshare.com/collections/Umeclidinium_vilanterol_versus_fluticasone_propionate_salmeterol_in_COPD_a_randomised_trial/3642377/1
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