Overview

Indacaterol Delivered Via a Single Dose Dry Powder Inhaler (SDDPI) in Chronic Obstructive Pulmonary Disease (COPD)

Status:
Completed
Trial end date:
2007-01-01
Target enrollment:
Participant gender:
Summary
The study is designed to obtain safety and efficacy data on three dose levels of indacaterol when delivered via an SDDPI in patients with COPD. All patients will receive 1 day of treatment with each of the following: indacaterol 150 µg, once- indacaterol 300 µg, indacaterol 600 µg, placebo, and formoterol. Each treatment day will be followed by a washout-period of 1 week.
Phase:
Phase 2/Phase 3
Details
Lead Sponsor:
Novartis
Treatments:
Maleic acid