drugset / Trial / NCT02268396

Glycopyrronium and Formoterol Fumarate (GFF) Metered Dose Inhaler (MDI) Dose Indicator Study in Adults With Moderate to Very Severe COPD

NCT02268396

Phase 3 Completed 138 enrolled Pearl Therapeutics, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label, multi-center study to evaluate the accuracy, reliability and functionality of the Glycopyrronium and Formoterol Fumarate (GFF) Metered Dose Inhaler (MDI) dose indicator in adult subjects with moderate to very severe COPD over a 4-week Treatment Period.

Timeline

Start
2014-11
Primary completion
2015-01
Completion
2015-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Formoterol Other / unclassified Inhaled
Subject Glycopyrronium Unknown Inhaled