57
Participants
Start Date
May 31, 2006
Primary Completion Date
March 31, 2008
Study Completion Date
December 31, 2013
Lapatinib oral tablets
Lapatinib will be given as tablets contain 410 mg of lapatinib ditosylate monohydrate, equivalent to 250 mg lapatinib free base per tablet. Subjects will be given a 4 week supply of lapatinib tables and instructed to take 6 tablets daily (1500 mg daily dose) orally at the same time each day. Subjects will receive a daily dose of lapatinib until disease progression or withdrawal from study treatment due to unacceptable toxicity or withdrawal of consent.
Paclitaxel infusion
Subjects will receive weekly paclitaxel (80 mg/m2 IV for 3 weeks in a 4 week cycle). Subjects will be treated with paclitaxel for at least 6 months, and may continue on paclitaxel at the discretion of the Investigator, or discontinued sooner if the subject has disease progression, an unacceptable toxicity or withdraws consent.
GSK Investigational Site, Moscow
GSK Investigational Site, Saint Petersburg
GSK Investigational Site, Saint Petersburg
GSK Investigational Site, Liepāja
GSK Investigational Site, Riga
GSK Investigational Site, Riga
GSK Investigational Site, Krakow
GSK Investigational Site, Olsztyn
GSK Investigational Site, Olsztyn
GSK Investigational Site, Warsaw
GSK Investigational Site, Bucharest
GSK Investigational Site, Moscow
GSK Investigational Site, Moscow
Lead Sponsor
GlaxoSmithKline
INDUSTRY