Abstract

Background: Glycopyrrolate administered by a novel, investigational eFlow® Closed System (CS) nebulizer (eFlow CS) is being evaluated for the maintenance treatment of chronic obstructive pulmonary disease (COPD). The eFlow CS is a hand-held, vibrating membrane nebulizer optimized to deliver 1 mL of glycopyrrolate solution into the lung in <3 minutes. Clinical studies have shown improvements in lung function of subjects treated with nebulized glycopyrrolate.Methods: The aerosol performance of the eFlow CS nebulizer was characterized by delivered dose, aerodynamic droplet size distribution and nebulization time. Simulated use nebulizer performance over 60 days was assessed by volume median diameter (VMD), nebulized amount, and nebulization time. Nebulization outputs were assayed to ensure adequate delivery of glycopyrrolate with an acceptable impurity profile. Aerosol condensates were analyzed for glycopyrrolate concentration and impurities by ultra-high-performance liquid chromatography and compared with non-nebulized samples.Results: The mean mass median aerodynamic diameter, geometric standard deviation, and fine particle fraction were 3.7 μm, 1.7, and 72%, respectively, and independent of formulation strength (25 and 50 μg/mL). Delivered dose was 88% of the nominal dose for both formulation strengths. The mean delivered dose, assessed by breathing simulation, was 56.8% for 25 μg/mL and 62.6% for 50 μg/mL. Nebulization times were 1–2.5 minutes with no apparent increasing trend with use over a 60-day period. The nebulized amount showed no significant changes, whereas the VMD showed a slight, but not pharmaceutically relevant, increase (0.1–0.2 μm) after 60-day simulated use. Glycopyrrolate concentration and impurity levels of nebulized samples were statistically similar to those of non-nebulized samples.Conclusion: The eFlow CS generates glycopyrrolate aerosols with high delivered dose, short treatment time, and small droplet size with narrow size distribution suitable for central and peripheral airway deposition. The unit dose vial mitigates medication misuse and ensures dose uniformity. Results support the use of glycopyrrolate/eFlow CS for the treatment of COPD.

Highlights

  • There are no approved nebulized longacting muscarinic antagonists (LAMAs) for the treatment of chronic obstructive pulmonary disease (COPD)

  • Thirty investigational eFlow Closed System (CS) nebulizers selected from seven production lots were used in the study, and 15 devices were tested with both glycopyrrolate dosing regimens (1 mL of the 25 or 50 lg/mL solution)

  • The Next Generation Impactor (NGI) deposition profiles of aerosols generated from the 25 and 50 lg/mL glycopyrrolate strengths are similar, indicating that the aerodynamic size distribution of glycopyrrolate aerosol is independent of formulation strength

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Summary

Introduction

There are no approved nebulized longacting muscarinic antagonists (LAMAs) for the treatment of chronic obstructive pulmonary disease (COPD). SUN-101 (glycopyrrolate inhalation solution for nebulization) was developed for use in combination with the eFlow CS nebulizer by patients with moderate-to-verysevere COPD who cannot use MDI and DPI inhalers effectively (e.g., due to the inability to inhale quickly with force, coordinate single-breath actuation, or hold breath for the required time after dose delivery), as it allows the patient to take the dose using tidal breathing. Glycopyrrolate administered by a novel, investigational eFlowÒ Closed System (CS) nebulizer (eFlow CS) is being evaluated for the maintenance treatment of chronic obstructive pulmonary disease (COPD). Methods: The aerosol performance of the eFlow CS nebulizer was characterized by delivered dose, aerodynamic droplet size distribution and nebulization time. Conclusion: The eFlow CS generates glycopyrrolate aerosols with high delivered dose, short treatment time, and small droplet size with narrow size distribution suitable for central and peripheral airway deposition. Results support the use of glycopyrrolate/eFlow CS for the treatment of COPD

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