drugset / Trial / NCT02175342

Pharmacodynamic and Pharmacokinetic Dose Ranging Study of Tiotropium Bromide Administered Via Respimat Device in Patients With Chronic Obstructive Pulmonary Disease (COPD)

NCT02175342

Phase 2 Completed 202 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

This pharmacodynamic and pharmacokinetic dose-ranging study aims to determine the optimal dose of tiotropium inhaled as a solution from a Respimat device once a day for three weeks in patients with COPD.

Timeline

Start
1998-03-01
Primary completion
1999-04-01
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Tiotropium Other / unclassified 0.625 ug Inhaled
Subject Tiotropium Other / unclassified 1.25 ug Inhaled
Subject Tiotropium Other / unclassified 2.5 ug Inhaled
Subject Tiotropium Other / unclassified 5 ug Inhaled
Subject Tiotropium Other / unclassified 10 ug Inhaled
Subject Tiotropium Other / unclassified 18 ug Inhaled