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Clinical Trial Summary

This is a phase IIIb randomised, double-blind, double-dummy, multicentre, parallel group, 24 week study to assess the efficacy and safety of Glycopyrronium/Formoterol Fumarate (GFF) fixed-dose combination 7.2/4.8 μg 2 inhalations twice daily compared to Umeclidinium/Vilanterol (UV) 62.5/25 μg fixed-dose combination 1 inhalation once daily in Patients with moderate to very severe COPD.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03162055
Study type Interventional
Source AstraZeneca
Contact
Status Completed
Phase Phase 3
Start date May 25, 2017
Completion date May 4, 2018

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