Lapatinib in Combination With Vinorelbine

PHASE2CompletedINTERVENTIONAL
Enrollment

29

Participants

Timeline

Start Date

April 30, 2009

Primary Completion Date

March 31, 2012

Study Completion Date

March 31, 2012

Conditions
Cancer
Interventions
DRUG

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.

Trial Locations (8)

21280

GSK Investigational Site, Diyarbakır

34390

GSK Investigational Site, Istanbul

34668

GSK Investigational Site, Istanbul

38039

GSK Investigational Site, Kayseri

337088

GSK Investigational Site, Diskapi / Ankara

06100

GSK Investigational Site, Ankara

06500

GSK Investigational Site, Ankara

06590

GSK Investigational Site, Ankara

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY