The safety, tolerability, pharmacokinetics and pharmacodynamics/efficacy profiles of two different doses of GSK233705 will be compared with 2 active comparators and placebo, all medication delivered via dry powder inhaler.
A multi-centre, randomised, partially blinded, placebo-controlled, three-way crossover, incomplete block design study to investigate the, safety, tolerability, pharmacodynamics/efficacy and pharmacokinetics of dual bronchodilator therapy with salmeterol 50 mcg twice daily plus two different doses of GSK233705 (20 and 50 mcg twice daily), compared with placebo, salmeterol 50 mcg twice daily alone, and tiotropium 18 mcg once daily alone, in subjects with chronic obstructive pulmonary disease
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
60
GSK Investigational Site
Helsinki, Finland
GSK Investigational Site
Wiesbaden, Hesse, Germany
GSK Investigational Site
Großhansdorf, Schleswig-Holstein, Germany
Bronchodilator effect of GSK233705 plus salmeterol at day 7, compared with placebo in COPD subjects.
Bronchodilator effect of salmeterol alone and tiotropium alone compared with placebo and GSK233705 at day 7. Safety and tolerability of GSK233705 plus salmeterol and the 2 active comparators at day 7.
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GSK Investigational Site
Almelo, Netherlands
GSK Investigational Site
Eindhoven, Netherlands
GSK Investigational Site
Heerlen, Netherlands
GSK Investigational Site
Veldhoven, Netherlands
GSK Investigational Site
Moscow, Russia
GSK Investigational Site
Saint Petersburg, Russia
GSK Investigational Site
Upton Road, Slough, Berkshire, United Kingdom
...and 1 more locations