29
Participants
Start Date
April 30, 2009
Primary Completion Date
March 31, 2012
Study Completion Date
March 31, 2012
lapatinib and Vinorelbine
Patients will receive 1250mg lapatinib once a day and vinorelbine 25mg/sqm IV Day 1and Day 8, every 3 week for 24 weeks.
GSK Investigational Site, Diyarbakır
GSK Investigational Site, Istanbul
GSK Investigational Site, Istanbul
GSK Investigational Site, Kayseri
GSK Investigational Site, Diskapi / Ankara
GSK Investigational Site, Ankara
GSK Investigational Site, Ankara
GSK Investigational Site, Ankara
Lead Sponsor
GlaxoSmithKline
INDUSTRY