Efficacy and safety of four doses of glycopyrrolate/formoterol fumarate delivered via a metered dose inhaler compared with the monocomponents in patients with moderate-to-severe COPD.

Colin Reisner, James Pearle, Edward M Kerwin, Earl St Rose, Patrick Darken

Journal: International journal of chronic obstructive pulmonary disease 2019;13():1965-1977

PMID: 29950826

Abstract

PURPOSE

To determine the efficacy and safety of glycopyrrolate/formoterol fumarate metered dose inhaler (GFF MDI 36/9.6, 36/7.2, 18/9.6, 9/9.6 µg) using innovative co-suspension delivery technology, compared with glycopyrrolate (GP) MDI 36 µg and formoterol fumarate (FF) MDI 9.6 µg, in patients with moderate-to-severe COPD.

METHODS

In this Phase IIb, randomized, double-blind, balanced incomplete-block, two-period, cross-over study (NCT01349816), patients received treatment twice-daily for 7 days. The primary efficacy endpoint was forced expiratory volume in 1 second (FEV) area under the curve from 0 to 12 hours (AUC) on Day 7. Secondary efficacy endpoints were peak change from baseline in FEV through 2 hours; time to onset of action (≥10% improvement in mean FEV); proportion of patients achieving ≥12% improvement in FEV on Day 1; peak change from baseline in inspiratory capacity (IC) on Days 1 and 7; change from baseline in morning pre-dose FEV; peak change from baseline in FEV through 6 hours; and change from baseline in mean evening 12-hour post-dose trough FEV on Day 7. Safety was assessed.

RESULTS

All 185 randomized patients received treatment. All doses of GFF MDI significantly improved the primary endpoint compared with GP MDI 36 µg (all ≤0.0137). For peak change in FEV and IC and time to onset of action secondary endpoints, ≥2 doses of GFF MDI demonstrated superiority to GP MDI 36 µg. No significant differences were observed between GFF MDI and FF MDI 9.6 µg for primary and secondary endpoints. The incidence of adverse events was similar between treatments.

CONCLUSION

While all doses of GFF MDI were superior to GP MDI 36 µg for the primary end-point, in this study neither superiority of GFF MDI to FF MDI 9.6 µg nor a clear dose-response was observed. All treatments were well tolerated with no unexpected safety findings.

Address: Pearl - a member of the AstraZeneca Group, Morristown, NJ, USA.; AstraZeneca, Gaithersburg, MD, USA.; California Research Medical Group, Inc., Fullerton, CA, USA.; Clinical Research Institute of Southern Oregon, Medford, OR, USA.
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