429
Participants
Start Date
October 31, 2006
Primary Completion Date
December 31, 2007
Study Completion Date
December 31, 2007
Abciximab
Intravenous bolus of 0.25 mg/kg followed by continuous intravenous infusion of 0.125 mcg/kg/min (max. 10 mcg/min) for 12 h after PCI.
Eptifibatide
Intravenous bolus of 180 mcg/kg followed immediately by a continuous infusion of 2.0 mdg/kg/ min for 20-24 h after end of PCI, and a second bolus of 180 mcg/kg administered 10 min after the first bolus.
GSK Investigational Site, Caen
GSK Investigational Site, Bordeaux
GSK Investigational Site, Pessac
GSK Investigational Site, Mönchengladbach
GSK Investigational Site, Neuss
GSK Investigational Site, Dortmund
GSK Investigational Site, Aachen
GSK Investigational Site, Nancy
GSK Investigational Site, Vandœuvre-lès-Nancy
GSK Investigational Site, Lille
GSK Investigational Site, Alençon
GSK Investigational Site, Offenbach
GSK Investigational Site, Pau
GSK Investigational Site, Perpignan
GSK Investigational Site, Homburg
GSK Investigational Site, Ludwigshafen am Rhein
GSK Investigational Site, Heidelberg
GSK Investigational Site, Melun
GSK Investigational Site, Melun
GSK Investigational Site, Freiburg im Breisgau
GSK Investigational Site, Toulon
GSK Investigational Site, Ollioules
GSK Investigational Site, Créteil
GSK Investigational Site, Würzburg
Lead Sponsor
GlaxoSmithKline
INDUSTRY