A randomized, double-blind, parallel-group, 52-week study to compare the effect of fluticasone propionate/salmeterol DISKUS 250/50mcg BID with salmeterol DISKUS 50mcg BID on the annual rate of moderate/severe exacerbations in subjects with chronic obstructive pulmonary disease (COPD)

Authors
Category Primary study
Registry of TrialsGSK Study Register
Year 2008
Study period: December 2004‐June 2007. Phase IV, randomized, double‐blind, parallel group study in 98 centres in the US and Canada.
Epistemonikos ID: 94f60012c837071252fd22d61543e1172102d319
First added on: Aug 21, 2024