84
Participants
Start Date
September 11, 2006
Primary Completion Date
November 25, 2008
Study Completion Date
November 25, 2008
mepolizumab
Participants received mepolizumab 0.55 milligrams (mg)/kilogram (kg), 2.5 mg/kg , or 10 mg/kg by intravenous (IV) infusion for 30 minutes on Day 1, Week 4 and Week 8.
GSK Investigational Site, Brisbane
GSK Investigational Site, New York
GSK Investigational Site, Norfolk
GSK Investigational Site, Atlanta
GSK Investigational Site, Tampa
GSK Investigational Site, Birmingham
GSK Investigational Site, Cincinnati
GSK Investigational Site, Indianapolis
GSK Investigational Site, Evansville
GSK Investigational Site, Southfield
GSK Investigational Site, Troy
GSK Investigational Site, Milwaukee
GSK Investigational Site, Minneapolis
GSK Investigational Site, Sioux Falls
GSK Investigational Site, Springfield
GSK Investigational Site, St Louis
GSK Investigational Site, Kansas City
GSK Investigational Site, Dallas
GSK Investigational Site, Dallas
GSK Investigational Site, San Diego
GSK Investigational Site, Worcester
GSK Investigational Site, Hamilton
GSK Investigational Site, Kingston
GSK Investigational Site, London
GSK Investigational Site, Montreal
GSK Investigational Site, Liverpool
GSK Investigational Site, London
GSK Investigational Site, Sheffield
GSK Investigational Site, Watford
Lead Sponsor
GlaxoSmithKline
INDUSTRY