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Terminated Phase 2 Interventional Results available

Brain Metastases In ErbB2-Positive Breast Cancer

ClinicalTrials.gov ID: NCT00437073

Public ClinicalTrials.gov record NCT00437073. 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 27, 2026, 3:18 PM EDT

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

Official title

Study EGF107671 - a Phase II Study of Lapatinib Plus Topotecan or Lapatinib Plus Capecitabine in the Treatment of Recurrent Brain Metastases From ErbB2-Positive Breast Cancer Following Cranial Radiotherapy

Brief summary

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

This study is for patients with ErbB2 overexpressing breast cancer that has spread to the brain and is still progressing there even after radiation treatment using WBRT (whole brain radiotherapy) or SRS (stereotactic radiosurgery) to the brain. The study will determine how safe and effective lapatinib is when given in combination with capecitabine to treat patients with ErbB2 overexpressing breast cancer that has spread to the brain. Lapatinib is an oral drug that will be taken every day. Tests for safety and efficacy will be performed regularly during the course of the study.

Study identification

NCT ID
NCT00437073
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
22 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
May 2007 (Type not available)
Primary completion
Jan 2009 (Actual)
Completion
Feb 2010 (Actual)
Last update posted
Oct 15, 2015

2007 – 2010

United States locations

U.S. sites
13
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
GSK Investigational Site Washington D.C. District of Columbia 20007 —
GSK Investigational Site Indianapolis Indiana 46202 —
GSK Investigational Site Sioux City Iowa 51101-1733 —
GSK Investigational Site Boston Massachusetts 02115 —
GSK Investigational Site Minneapolis Minnesota 55455 —
GSK Investigational Site Rochester Minnesota 55905 —
GSK Investigational Site Albuquerque New Mexico 87131-0001 —
GSK Investigational Site Cary North Carolina 27518 —
GSK Investigational Site Portland Oregon 97239 —
GSK Investigational Site Philadelphia Pennsylvania 19104 —
GSK Investigational Site Pittsburgh Pennsylvania 15213 —
GSK Investigational Site Spartanburg South Carolina 29303 —
GSK Investigational Site Dallas Texas 75230 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 31 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00437073, 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 Oct 15, 2015 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00437073 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →