drugset / Trial / NCT02242279

Study to Evaluate Efficacy and Safety of Inhaled BEA 2180 BR in COPD Patients

NCT02242279

Phase 2 Completed 37 enrolled Boehringer Ingelheim
RandomizedCrossoverDouble-blindTreatment

Summary

Study to investigate the dose-dependent bronchodilator effect and the safety of single inhalation doses of BEA 2180 inhaled via Respimat® compared to placebo in patients with stable Chronic Obstructive Pulmonary Disease (COPD)

Timeline

Start
2004-06
Primary completion
2004-12
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject BEA 2180 BR Unknown 80 ug Inhaled
Subject BEA 2180 BR Unknown 200 ug Inhaled
Subject BEA 2180 BR Unknown 800 ug Inhaled
Comparator Tiotropium Other / unclassified 72 ug