Parameter Point Estimate 90% CI
FF dose proportionality
AUC(0–t’) (pg•h/mL) Log (dose) 0.910 (0.843, 0.978)
Cmax (pg/mL) Log (dose) 0.484 (0.400, 0.569)
VI equivalence
AUC(0–t’) (pg•h/mL) Log (dose) 0.029 (–0.018, 0.077)
Cmax (pg/mL) Log (dose) 0.055 (–0.010, 0.121)
AUC(0-t’) = area under the curve from zero (pre-dose) to the time of last common measurable time point within subject; CI = confidence interval; Cmax = maximum plasma concentration; FF = fluticasone furoate; VI = vilanterol.
Table 2: Results of power model assessment of FF dose proportionality and VI equivalence following a single inhaled administration of FF/VI (200/100 μg, 400/100 μg and 800/100 μg; dose proportionality Study 1).
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