International Journal of COPD (Sep 2020)

Clinically Important Deterioration Among Patients with Chronic Obstructive Pulmonary Disease (COPD) Treated with Nebulized Glycopyrrolate: A Post Hoc Analysis of Pooled Data from Two Randomized, Double-Blind, Placebo-Controlled Studies

  • Kerwin EM,
  • Murray L,
  • Niu X,
  • Dembek C

Journal volume & issue
Vol. Volume 15
pp. 2309 – 2318

Abstract

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Edward M Kerwin,1 Lindsey Murray,2 Xiaoli Niu,3 Carole Dembek3 1Clinical Research Institute of Southern Oregon, Medford, OR, USA; 2Evidera, Bethesda, MD, USA; 3Sunovion Pharmaceuticals Inc., Marlborough, MA, USACorrespondence: Xiaoli NiuSunovion Pharmaceuticals Inc., 84 Waterford Dr, Marlborough, MA 01752, USATel +1 508 357 7863Email [email protected]: Using a composite endpoint, pooled data from two 12-week Phase III placebo-controlled trials (GOLDEN 3, NCT02347761; GOLDEN 4, NCT02347774) were analyzed to determine whether glycopyrrolate inhalation solution (25 mcg and 50 mcg) administered twice daily (BID) via the eFlow® Closed System nebulizer (GLY) reduced the risk of clinically important deterioration (CID) in patients with moderate-to-very-severe COPD.Methods: CID was defined as ≥ 100-mL decrease from baseline in post-bronchodilator trough forced expiratory volume in one second (FEV1), or ≥ 4-unit increase in baseline St. George’s Respiratory Questionnaire (SGRQ) total score, or moderate/severe exacerbation. The relative treatment effect of GLY versus placebo on the odds of CID (any and by component endpoints) was expressed as the odds ratio (OR) and 95% confidence interval (CI). Subgroups categorized by age (< 65/≥ 65 years), sex, smoking status (current/former), long-acting beta agonist (LABA) use, FEV1 (< 50%/≥ 50%), and peak inspiratory flow rate (PIFR) (< 60 L/min/≥ 60 L/min) were analyzed.Results: Compared to placebo, GLY 25 mcg and 50 mcg BID over 12 weeks significantly reduced the risk of CID by 50% (OR: 0.50 [0.37– 0.68]) and 40% (OR: 0.60 [0.44– 0.80]), respectively. Subjects treated with GLY 25 mcg BID were 59% less likely to experience CID in FEV1 (OR: 0.41 [0.27– 0.62]) and 48% less likely to perceive CID in health status (OR: 0.52 [0.37– 0.73]). Statistically significant reductions were also observed at the higher dose. The incidence of moderate/severe exacerbations was low and comparable among the cohorts. GLY 25 mcg BID was significantly more effective than placebo (p< 0.05) in preventing CID irrespective of age, smoking status, LABA use, COPD severity, or PIFR. Subjects < 65 years (OR 0.45 [0.29– 0.68]) and those with PIFR < 60 L/min (OR 0.36 [0.20– 0.67]) exhibited the largest benefit.Conclusion: Nebulized GLY over 12 weeks significantly reduced the risk of CID and provided greater short-term stability in patients with moderate-to-very-severe COPD.Keywords: nebulized glycopyrrolate, clinically important deterioration, composite measure

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