drugset / Trial / NCT01119937

Long Term Safety and Tolerability of NVA237 Versus Tiotropium in Japanese Patients

NCT01119937

Phase 3 Completed 211 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a 52-week, multi-center, randomized, open label, parallel group study to assess the long term safety and tolerability of once-daily NVA237, using tiotropium as an active control, in Japanese patients with moderate to severe chronic obstructive pulmonary disease (COPD) .

Timeline

Start
2010-05
Primary completion
2011-11
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Glycopyrrolate Small molecule 50 ug Inhaled
Subject Tiotropium Other / unclassified 18 ug Inhaled