15
Participants
Start Date
October 3, 2011
Primary Completion Date
March 5, 2012
Study Completion Date
March 5, 2012
Drug: GSK2251052
Reconstituted, added to 250mL 0.9% NaCl solution and administered via IV infusion
Meropenem
Reconstituted, added to 100mL 0.9% NaCl solution and administered via IV infusion
Placebo
saline placebo
GSK Investigational Site, Prague
GSK Investigational Site, Buffalo
GSK Investigational Site, Richmond
GSK Investigational Site, Madrid
GSK Investigational Site, Nîmes
GSK Investigational Site, Jacksonville
GSK Investigational Site, Mobile
GSK Investigational Site, Verona
GSK Investigational Site, Columbus
GSK Investigational Site, Lima
GSK Investigational Site, Council Bluffs
GSK Investigational Site, Topeka
GSK Investigational Site, Strasbourg
GSK Investigational Site, New Orleans
GSK Investigational Site, Limoges
GSK Investigational Site, Las Vegas
GSK Investigational Site, Torrance
GSK Investigational Site, Long Beach
GSK Investigational Site, Saint Petersburgh
GSK Investigational Site, Smolensk
GSK Investigational Site, Perm
GSK Investigational Site, Perm
GSK Investigational Site, Irkutsk
GSK Investigational Site, Chicoutimi
GSK Investigational Site, Sherbrooke
GSK Investigational Site, Trois-Rivières
GSK Investigational Site, Saskatoon
GSK Investigational Site, Prague
GSK Investigational Site, Alicante
GSK Investigational Site, Elche (Alicante)
GSK Investigational Site, Pama de Mallorca
Lead Sponsor
GlaxoSmithKline
INDUSTRY