Pulmonology Xagena

Xagena Mappa
Xagena Newsletter
Medical Meeting

Dual bronchodilator QVA149 compared with Glycopyrronium and Tiotropium in the chronic obstructive pulmonary disease exacerbations

Researchers have evaluated the effect of dual, long acting inhaled bronchodilator treatment on exacerbations in patients with severe and very severe chronic obstructive pulmonary disease ( COPD ).

In this parallel-group study, 2224 patients ( aged greater than or equal to 40 years, Global Initiative for Chronic Obstructive Lung Disease stages III-IV, and one or more moderate COPD exacerbation in the past year ) were randomly assigned ( 1:1:1; via interactive voice response or web system; stratified for smoking status ) to once-daily QVA149 ( fixed-dose combination of Indacaterol 110 mcg and Glycopyrronium 50 mcg; Ultibro Breezhaler ), Glycopyrronium 50 mcg, or Tiotropium 18 mcg for 64 weeks.
Assignment to QVA149 and Glycopyrronium was double-blind; Tiotropium was open-label.

Efficacy was assessed in all patients randomly assigned to treatment groups who received at least one dose of study drug; safety was assessed in all patients who received at least one dose whether or not they were assigned to a group.

The primary objective was to show superiority of QVA149 versus Glycopyrronium for rate of moderate to severe COPD exacerbations ( defined by worsening symptoms and categorised by treatment requirements ) during treatment.

During the period 2010-2012, 741 patients were randomly assigned to receive QVA149, 741 to receive Glycopyrronium, and 742 to receive Tiotropium ( 729, 739, and 737 patients, respectively, analysed for efficacy ).

QVA149 significantly reduced the rate of moderate to severe exacerbations versus Glycopyrronium by 12% ( annualised rate of exacerbations 0.84 vs 0.95; rate ratio 0.88; p=0.038 ).

Adverse events ( including exacerbations ) were reported for 678 ( 93% ) of 729 patients on QVA149, 694 ( 94% ) of 740 on Glycopyrronium, and 686 ( 93% ) of 737 on Tiotropium.
Incidence of serious adverse events was similar between groups ( 167 [ 23% ] patients on QVA149, 179 [ 24% ] on Glycopyrronium, and 165 [ 22% ] on Tiotropium ); COPD worsening was the most frequent serious adverse event ( 107 [ 15% ] patients on QVA149, 116 [ 16% ] on Glycopyrronium, 87 [ 12% ] on tiotropium ).

The dual bronchodilator QVA149 was superior in preventing moderate to severe COPD exacerbations compared with the single long acting antimuscarinic bronchodilator Glycopyrronium, with concomitant improvements in lung function and health status. These results indicate the potential of dual bronchodilation as a treatment option for patients with severe and very severe COPD. ( Xagena )

Wedzicha JA et al, The Lancet Respiratory Medicine 2013;1: 199-209