drugset / Trial / NCT00615030

Study of Indacaterol Dosed in the Evening in Patients With Chronic Obstructive Pulmonary Disease (COPD)

NCT00615030 ↗

Phase 3 Completed 96 enrolled Novartis
RandomizedCrossoverDouble-blindTreatment

Summary

This study was conducted to provide detailed information on the efficacy of indacaterol (in terms of the spirometry assessment forced expiratory volume in 1 second \[FEV1\]) over the full 24-h time period

Timeline

Start
2008-01
Primary completion
2008-07
Completion
2008-08

Outcome

Met primary endpoint

paper difference vs. placebo in trough FEV(1) for PM indacaterol was 200 mL (p < 0.001 [primary analysis]) PMID 20850959 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Indacaterol Other / unclassified 300 ug Inhaled
Subject Salmeterol Other / unclassified 50 ug Inhaled