drugset / Trial / NCT00393458

Efficacy, Safety, and Tolerability of Once Daily Indacaterol in Chronic Obstructive Pulmonary Disease (COPD) Using Formoterol Twice Daily as Active Control

NCT00393458

Phase 3 Completed 1732 enrolled Novartis
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study was designed to assess the efficacy and long-term safety of 300 and 600 µg doses of indacaterol when delivered via a single-dose dry-powder inhaler (SDDPI) in patients with chronic obstructive pulmonary disease (COPD). Patients were randomized to receive either indacaterol 300 µg once daily, indacaterol 600 µg once daily, formoterol 12 µg twice daily, or placebo.

Timeline

Start
2006-10
Primary completion
2008-07
Completion
2008-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator Formoterol Other / unclassified 12 ug Inhaled
Subject Indacaterol Other / unclassified 300 ug Inhaled
Subject Indacaterol Other / unclassified 600 ug Inhaled