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Completed Phase 2 Interventional

Oral Drug Study In Women With Refractory Metastatic Breast Cancer After First-line or Second-line Herceptin.

ClinicalTrials.gov ID: NCT00051103

Public ClinicalTrials.gov record NCT00051103. 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 4, 2026, 5:24 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

An Open-Label, Multicenter, Single Arm Phase II Study of Oral GW572016 as Single Agent Therapy in Subjects With Advanced or Metastatic Breast Cancer Who Have Progressed While Receiving Herceptin Containing Regimens

Brief summary

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

The purpose of this study is to determine the efficacy of an oral investigational drug for the treatment of metastatic breast cancer tumors that are known to overexpress HER2/neu.

Study identification

NCT ID
NCT00051103
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
Not listed

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
Oct 2002 (Type not available)
Primary completion
Jun 2005 (Actual)
Completion
Jun 2005 (Actual)
Last update posted
Apr 15, 2015

2002 – 2005

United States locations

U.S. sites
30
U.S. states
17
U.S. cities
27
Facility City State ZIP Site status
GSK Investigational Site Chula Vista California 91911 —
GSK Investigational Site Los Angeles California 90095 —
GSK Investigational Site Poway California 92064 —
GSK Investigational Site Fort Myers Florida 33901 —
GSK Investigational Site Plantation Florida 33324 —
GSK Investigational Site Savannah Georgia 31405 —
GSK Investigational Site Park Ridge Illinois 60068 —
GSK Investigational Site Skokie Illinois 60076 —
GSK Investigational Site Skokie Illinois 60077 —
GSK Investigational Site Bettendorf Iowa 52722 —
GSK Investigational Site Des Moines Iowa 50309 —
GSK Investigational Site Baltimore Maryland 21201 —
GSK Investigational Site Royal Oak Michigan 48073 —
GSK Investigational Site Billings Montana 59101 —
GSK Investigational Site Hooksett New Hampshire 03106 —
GSK Investigational Site Durham North Carolina 27710 —
GSK Investigational Site Greenville North Carolina 27834 —
GSK Investigational Site Hickory North Carolina 28602 —
GSK Investigational Site Fargo North Dakota 58103 —
GSK Investigational Site Oklahoma City Oklahoma 73112 —
GSK Investigational Site Tulsa Oklahoma 74136 —
GSK Investigational Site Pittsburgh Pennsylvania 15213 —
GSK Investigational Site Columbia South Carolina 29210 —
GSK Investigational Site Germantown Tennessee 38138 —
GSK Investigational Site Memphis Tennessee 38104 —
GSK Investigational Site Memphis Tennessee 38120 —
GSK Investigational Site Nashville Tennessee 37203 —
GSK Investigational Site Nashville Tennessee 37205 —
GSK Investigational Site Houston Texas 77025 —
GSK Investigational Site Salem Virginia 24153 —

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 NCT00051103, 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 Apr 15, 2015 · Synced Oct 4, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00051103 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →