drugset / Trial / NCT02680197

Study to Evaluate Efficacy/Safety of 4 Doses of CHF5259 Via Dry Powder Inhaler (DPI) in Patients With COPD

NCT02680197

Phase 2 Completed 262 enrolled Chiesi Farmaceutici S.p.A.
RandomizedCrossoverQuadruple-blindTreatment

Summary

The study was designed to investigate the efficacy and safety of different doses CHF5259 a long acting muscarinic antagonist in patients with moderate to severe COPD.

Timeline

Start
2016-02-29
Primary completion
2017-02-06
Completion
2017-02-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Glycopyrronium Unknown 6.25 ug Inhaled
Subject Glycopyrronium Unknown 12.5 ug Inhaled
Subject Glycopyrronium Unknown 25 ug Inhaled
Subject Glycopyrronium Unknown 50 ug Inhaled