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Completed Phase 3 Interventional Results available

Lapatinib Plus Capecitabine Versus Trastuzumab Plus Capecitabine in ErbB2 (HER2) Positive Metastatic Breast Cancer

ClinicalTrials.gov ID: NCT00820222

Public ClinicalTrials.gov record NCT00820222. 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 20, 2026, 11:42 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

A Randomized, Multicentre, Open-Label, Phase III Study of Lapatinib Plus Capecitabine Versus Trastuzumab Plus Capecitabine in Patients With Anthracycline- or Taxane-Exposed ErbB2-Positive Metastatic Breast Cancer

Brief summary

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

This open label study was designed to evaluate Lapatinib effect on incidence of brain metastases in ErbB2 (HER2) positive metastatic breast cancer patients exposed to prior taxanes or anthracyclines.

Study identification

NCT ID
NCT00820222
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
540 participants

Conditions and interventions

Interventions

Drug

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
Apr 14, 2009 (Actual)
Primary completion
Jun 11, 2012 (Actual)
Completion
Mar 22, 2018 (Actual)
Last update posted
Apr 2, 2019

2009 – 2018

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
17
Facility City State ZIP Site status
Novartis Investigative Site Goodyear Arizona 85338 —
Novartis Investigative Site Tucson Arizona 85715 —
Novartis Investigative Site Jonesboro Arkansas 72401 —
Novartis Investigative Site Anaheim California 92801 —
Novartis Investigative Site Greenbrae California 94904-2007 —
Novartis Investigative Site Sacramento California 95816 —
Novartis Investigative Site Santa Barbara California 93105 —
Novartis Investigative Site Washington D.C. District of Columbia 20007 —
Novartis Investigative Site Boca Raton Florida 33486 —
Novartis Investigative Site Coral Springs Florida 33065 —
Novartis Investigative Site Hollywood Florida 33021 —
Novartis Investigative Site Warrenville Illinois 60555 —
Novartis Investigative Site Metairie Louisiana 70006 —
Novartis Investigative Site St Louis Missouri 63110 —
Novartis Investigative Site Great Falls Montana 59405 —
Novartis Investigative Site Voorhees Township New Jersey 08043 —
Novartis Investigative Site Durham North Carolina 27710 —

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 147 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00820222, 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 2, 2019 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00820222 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →