Abstract
Objective: To assess the efficacy of inhaled, repeat doses (28 days) of the glucocorticoid agonist GW870086, which has been designed to inhibit gene transrepression of the glucocorticoid receptor while preserving its transactivation. Methods: This was a randomised, placebo-controlled, two-way crossover study, approved by the independent ethics committees of the study centres. Subjects with FEV1 40–85% of the predicted normal value (n = 36) received GW870086 (1 mg, once-daily) and placebo. Results: No significant change from baseline in forced expiratory volume in one second (FEV1) was seen following administration of GW8780086 1 mg relative to placebo; mean FEV1 (day 28), relative to placebo, was (95% confidence intervals [CI]) −0.077 L (−0.192, 0.038). A moderate positive placebo response was observed on Days 14 and 28: Mean FEV1 (95% CI) was 0.115 L (0.040, 0.189) and 0.115 L (0.019, 0.212), respectively. The placebo response was more notable in treatment period 1 and was larger than the response to GW870086 1 mg on day 28, irrespective of period. Peak expiratory flow rate results were consistent with FEV1 and no difference was seen between the GW870086 and placebo for rescue medication usage. Conclusion: This total lack of effect suggests that repeat-dose GW8700861 mg has suboptimal efficacy in mild to moderate asthma.
Acknowledgements
The authors thank the subjects and staff who participated in the studies and acknowledge Dawn Webber (GlaxoSmithKline Discovery Biometrics) for providing statistical support during the study design and conduct stages.
Notice of Correction:
The version of this article published online ahead of print on 01 Oct 2013 contained an error on page 1. Alison C. Donald's degrees should have read "BSc Hon, MSc" and not “BSc, MSc”. The error has been corrected for this version.