41
Participants
Start Date
August 16, 2007
Primary Completion Date
September 29, 2009
Study Completion Date
September 29, 2009
GSK461364
GSK461364 will be given intravenously as a 4 hour infusion in either a final volume of 500 or 1000 mLs. The starting dose for Stage A - Schedule 1 was 50 mg and doses were to be escalated as described in protocol until maximum tolerated dose established.
GSK Investigational Site, Sutton
GSK Investigational Site, Belfast, Northern Ireland
GSK Investigational Site, London
Lead Sponsor
GlaxoSmithKline
INDUSTRY