Lapatinib Combined With Paclitaxel For Patients With First-Line ErbB2-Amplified Metastatic Breast Cancer

PHASE2CompletedINTERVENTIONAL
Enrollment

57

Participants

Timeline

Start Date

May 31, 2006

Primary Completion Date

March 31, 2008

Study Completion Date

December 31, 2013

Conditions
Neoplasms, Breast
Interventions
DRUG

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.

DRUG

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.

Trial Locations (13)

117997

GSK Investigational Site, Moscow

197022

GSK Investigational Site, Saint Petersburg

197758

GSK Investigational Site, Saint Petersburg

LV3401

GSK Investigational Site, Liepāja

LV 1002

GSK Investigational Site, Riga

LV 1079

GSK Investigational Site, Riga

31-115

GSK Investigational Site, Krakow

10-228

GSK Investigational Site, Olsztyn

10-699

GSK Investigational Site, Olsztyn

02-781

GSK Investigational Site, Warsaw

022328

GSK Investigational Site, Bucharest

115 478

GSK Investigational Site, Moscow

129 128

GSK Investigational Site, Moscow

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY