drugset / Trial / NCT02951312

Assessment of the Safety and Ability of a Once-a-day Dose of an Orally Inhaled Medicine [ie, Glycopyrrolate Inhalation Solution = GIS] to Improve Airflow in the Lungs When Delivered With an Electronic eFlow Nebulizer System in Patients With Chronic Obstructive Pulmonary Disease (COPD)

NCT02951312

Phase 2 Completed 12 enrolled Sunovion Respiratory Development Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

The study assessed the safety and ability of several doses of an orally inhaled medicine \[ie, Glycopyrrolate Inhalation Solution = GIS\] to improve airflow in the lungs when delivered with an electronic eFlow nebulizer system in patients with Chronic Obstructive Pulmonary Disease (COPD). The study was conducted in 12 patients in 2 parts. Part 1 was designed to find the once-a- day GIS dose that produced the highest improvement in lung airflow. Part 2 tested the GIS dose with the highest improvement in lung airflow and a placebo (ie, no drug) delivered by a general purpose nebulizer. The airflow improvements of the same GIS dose were compared between the two nebulizer systems to determine what effect the device had on GIS delivery.

Timeline

Start
2009-05
Primary completion
2009-07
Completion
2009-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Glycopyrrolate Small molecule 25 ug Inhaled
Subject Glycopyrrolate Small molecule 75 ug Inhaled
Subject Glycopyrrolate Small molecule 200 ug Inhaled
Subject Glycopyrrolate Small molecule 500 ug Inhaled
Subject Glycopyrrolate Small molecule 1000 ug Inhaled