20
Participants
Start Date
February 28, 2011
Primary Completion Date
July 31, 2012
Study Completion Date
July 31, 2012
pazopanib
oral agent, administered at 800 mg daily (400 mg tablets x 2). Dose can be reduced, interrupted or discontinued due to adverse events or intolerance
pemetrexed
pemetrexed IV 500 mg/m2 once every 3 weeks
GSK Investigational Site, Latham
GSK Investigational Site, Raleigh
GSK Investigational Site, Charleston
GSK Investigational Site, Chattanooga
GSK Investigational Site, Pikeville
GSK Investigational Site, Indianapolis
GSK Investigational Site, Ames
GSK Investigational Site, Fargo
GSK Investigational Site, Skokie
GSK Investigational Site, Skokie
GSK Investigational Site, Columbia
GSK Investigational Site, Overland Park
GSK Investigational Site, Garland
GSK Investigational Site, Mesquite
GSK Investigational Site, Dallas
GSK Investigational Site, Dallas
GSK Investigational Site, Dallas
GSK Investigational Site, Tyler
GSK Investigational Site, Bedford
GSK Investigational Site, Houston
GSK Investigational Site, San Marcos
GSK Investigational Site, Tucson
GSK Investigational Site, Las Vegas
GSK Investigational Site, Everett
GSK Investigational Site, Vancouver
Lead Sponsor
GlaxoSmithKline
INDUSTRY