44
Participants
Start Date
September 1, 2012
Primary Completion Date
October 1, 2014
Study Completion Date
October 6, 2014
Dose 1 GSK2586881
Low dose GSK2586881 administered intravenously
Dose 2 GSK2586881
Medium dose GSK2586881 administered intravenously
Dose 3 GSK2586881
Medium-High dose GSK2586881 administered intravenously
Dose 4 GSK2586881
High dose GSK2586881 administered intravenously
Placebo (saline)
Administered intravenously to match intervention
GSK Investigational Site, New York
GSK Investigational Site, Philadelphia
GSK Investigational Site, Philadelphia
GSK Investigational Site, Greensboro
GSK Investigational Site, Winston-Salem
GSK Investigational Site, Durham
GSK Investigational Site, Charleston
GSK Investigational Site, Columbus
GSK Investigational Site, Ann Arbor
GSK Investigational Site, Chicago
GSK Investigational Site, Sacramento
GSK Investigational Site, Portland
GSK Investigational Site, Springfield
GSK Investigational Site, Vancouver
GSK Investigational Site, Vancouver
GSK Investigational Site, Halifax
GSK Investigational Site, Kingston
GSK Investigational Site, Greenfield Park
GSK Investigational Site, Sainte-Foy
Lead Sponsor
GlaxoSmithKline
INDUSTRY