drugset / Trial / NCT00669617

Study to Determine the Onset of Action of Indacaterol in Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD)

NCT00669617

Phase 3 Completed 89 enrolled Novartis
RandomizedCrossoverTriple-blindTreatment

Summary

This study will evaluate the onset of action of indacaterol (150 and 300 µg) as compared to placebo, salbutamol 200 µg and salmeterol/fluticasone 50/500 µg

Timeline

Start
2008-04
Primary completion
2008-08
Completion
2008-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Indacaterol Other / unclassified 150 ug Inhaled
Subject Indacaterol Other / unclassified 300 ug Inhaled
Subject Salbutamol Unknown 200 ug Inhaled
Subject Salmeterol/fluticasone Unknown 50 ug Inhaled
Subject Salmeterol/fluticasone Unknown 500 ug Inhaled