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Completed Phase 2 Interventional Results available

Pazopanib Plus Lapatinib Compared To Lapatinib Alone In Subjects With Advanced Or Metastatic Breast Cancer

ClinicalTrials.gov ID: NCT00347919

Public ClinicalTrials.gov record NCT00347919. 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 May 12, 2026, 7:21 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

A Phase II, Open-Label, Randomized, Multicenter Trial of GW786034 (Pazopanib) in Combination With Lapatinib (GW572016) Compared to Lapatinib Alone as First Line Therapy in Subjects With Advanced or Metastatic Breast Cancer With ErbB2 Fluorescence In Situ Hybridization (FISH) Positive Tumors

Study identification

NCT ID
NCT00347919
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
189 participants

Conditions and interventions

Interventions

  • lapatinib (GW572016) 1000 mg Drug
  • lapatinib (GW572016) 1500 mg Drug
  • pazopanib (GW786034) 400 mg Drug
  • pazopanib (GW786034) 800 mg Drug

Drug

Eligibility (public fields only)

Age range
21 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
Jun 30, 2006
Primary completion
Jul 31, 2008
Completion
Feb 28, 2015
Last update posted
Feb 24, 2016

2006 – 2015

United States locations

U.S. sites
19
U.S. states
8
U.S. cities
19
Facility City State ZIP Site status
GSK Investigational Site Jonesboro Arkansas 72401
GSK Investigational Site Alhambra California 91801
GSK Investigational Site Bakersfield California 93309
GSK Investigational Site Fullerton California 92835
GSK Investigational Site Long Beach California 90813
GSK Investigational Site Los Angeles California 90095-1752
GSK Investigational Site Northridge California 91328
GSK Investigational Site Oxnard California 93030
GSK Investigational Site Redondo Beach California 90277
GSK Investigational Site Santa Barbara California 93105
GSK Investigational Site Santa Maria California 93454
GSK Investigational Site Indianapolis Indiana 46202
GSK Investigational Site Metairie Louisiana 70006
GSK Investigational Site Henderson Nevada 89052
GSK Investigational Site The Bronx New York 10461
GSK Investigational Site Akron Ohio 44304
GSK Investigational Site Dallas Texas 75390-9113
GSK Investigational Site Lubbock Texas 79410
GSK Investigational Site San Antonio Texas 78207

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 65 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00347919, 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 Feb 24, 2016 · Synced May 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00347919 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →