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Terminated Phase 2 Interventional Results available

Lapatinib In Combination With Chemotherapy In Subjects With Relapsed Breast Cancer

ClinicalTrials.gov ID: NCT00479856

Public ClinicalTrials.gov record NCT00479856. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 8:23 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-label, Multi-centre Study of Lapatinib in Combinationwith Chemotherapy in Patients With ErbB2 Overexpressing Breastcancer After Trastuzumab Failure in the Neoadjuvant or Adjuvantsetting.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will evaluate the safety and efficacy of lapatinib in combination with chemotherapy (capecitabine, docetaxel, nab-paclitaxel) in subjects with ErbB2-overexpressing breast cancer whose disease has progressed during or within 12 months after completion of trastuzumab-containing therapy in the neoadjuvant or adjuvant setting.

Study identification

NCT ID
NCT00479856
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
9 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2007 (Type not available)
Primary completion
Sep 2009 (Actual)
Completion
Mar 2010 (Actual)
Last update posted
Jun 5, 2012

2007 – 2010

United States locations

U.S. sites
28
U.S. states
18
U.S. cities
28
Facility City State ZIP Site status
GSK Investigational Site Hot Springs Arkansas 71913 —
GSK Investigational Site Anaheim California 92801 —
GSK Investigational Site Burbank California 91505 —
GSK Investigational Site Highland California 92346 —
GSK Investigational Site Long Beach California 90806 —
GSK Investigational Site Sacramento California 95819 —
GSK Investigational Site Washington D.C. District of Columbia 20007 —
GSK Investigational Site Fort Lauderdale Florida 33328 —
GSK Investigational Site Hollywood Florida 33021 —
GSK Investigational Site Orlando Florida 32806 —
GSK Investigational Site Atlanta Georgia 30341 —
GSK Investigational Site Lawrenceville Georgia 30045 —
GSK Investigational Site Zion Illinois 60099 —
GSK Investigational Site Indianapolis Indiana 46227 —
GSK Investigational Site Metairie Louisiana 70006 —
GSK Investigational Site New Orleans Louisiana 70112 —
GSK Investigational Site Baltimore Maryland 21237 —
GSK Investigational Site Minneapolis Minnesota 55426 —
GSK Investigational Site Tupelo Mississippi 38801 —
GSK Investigational Site Voorhees Township New Jersey 08043 —
GSK Investigational Site Albuquerque New Mexico 87131-0001 —
GSK Investigational Site New York New York 10016 —
GSK Investigational Site Sumter South Carolina 29150 —
GSK Investigational Site Austin Texas 78705 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Ogden Utah 84403 —
GSK Investigational Site Abingdon Virginia 24211 —
GSK Investigational Site Fairfax Virginia 22031 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00479856, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 5, 2012 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00479856 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →