68
Participants
Start Date
March 31, 2008
Primary Completion Date
April 30, 2011
Study Completion Date
January 31, 2015
Lapatinib and Capecitabine
oral lapatinib (1250mg) administered as a monotherapy run-in followed by its combination with capecitabine
GSK Investigational Site, Taipei
GSK Investigational Site, Taipei
GSK Investigational Site, Taipei
GSK Investigational Site, Changhua
GSK Investigational Site, Washington D.C.
GSK Investigational Site, Ann Arbor
GSK Investigational Site, Southgate
GSK Investigational Site, Jefferson City
GSK Investigational Site, Shreveport
GSK Investigational Site, Dallas
GSK Investigational Site, Los Angeles
GSK Investigational Site, Loma Linda
GSK Investigational Site, Saint Petersburg
GSK Investigational Site, Astrakhan
GSK Investigational Site, Ufa
GSK Investigational Site, Chelyabinsk
GSK Investigational Site, Montreal
GSK Investigational Site, Mexico City
GSK Investigational Site, Hwasun
GSK Investigational Site, Seoul
GSK Investigational Site, Seoul
GSK Investigational Site, Suwon, Gyeonggi-do
Lead Sponsor
GlaxoSmithKline
INDUSTRY