Table 4. Pre-dose FEV1 improvements in studies of ICS/LABA combinations in COPD.
Clinical studies | Pre-dose FEV 1 at baselinea (ml) | Pre-dose FEV 1 versus baselineb (ml) | Pre-dose FEV 1 versus LABAb (ml) | Timepoint considered for FEV 1 comparison |
---|---|---|---|---|
Calverley2 ,c | 1,266 | 120 | 73 | 52 weeks |
Ferguson4 ,c | 950 | 102 | 74 | 52 weeks |
Szafranski5 ,d | 960 | 80 | 80 | 12 months |
Calverley3 ,d | 980 | N/A | 50 | 12 months |
Wedzicha28 ,e | 1,052 | 70 | 65 | 48 weeks |
Calverley20 ,e | 1,140 | 77 | 50 | 48 weeks |
Rennard7 ,d | 1,020 | 120 | 90 | 12 months |
Sharafkhaneh44 ,d | 1,000 | 70 | 30 | 12 months |
Dransfield6 ,f | N/A | N/A | 40 | 52 weeks |
Studies >6 months duration were included. Studies with pre-dose FEV1 presented were included.
Abbreviations: LABA, long-acting β2-agonist; N/A, not available.
FEV1 before first dose (baseline).
Change in FEV1 caused by ICS/LABA.
Studies conducted with: fluticasone propionate/salmeterol.
Budesonide/formoterol fumarate.
Beclometasone dipropionate/formoterol fumarate.
Fluticasone furoate/vilanterol.