Efficacy and safety of AZD3199 vs formoterol in COPD: a randomized, double-blind study.

ABSTRACT:

Background

We investigated the efficacy and safety of AZD3199, a novel inhaled ultra-LABA, with the main aim of establishing a dose that would maintain 24-hour bronchodilation in patients with COPD.

Methods

Patients (n = 329) were randomized to AZD3199 (200, 400 or 800 μg o.d.), formoterol (9 μg b.i.d.) or placebo via Turbuhaler® in a parallel group study. The primary objective of the study was to compare the clinical efficacy of three doses of AZD3199 inhaled once daily with 9 μg formoterol twice daily and placebo, over a 4-week treatment period in adults with moderate-to-severe COPD. After 4 weeks, peak (0-4 h) and trough (24-26 h) forced expiratory volume in 1 second (FEV1) were assessed as the primary efficacy outcome variables.

Results

All AZD3199 doses significa

SUBMITTER: Kuna P 

PROVIDER: S-EPMC3691744 | biostudies-literature | 2013 Jun

REPOSITORIES: biostudies-literature