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Completed Phase 2 Interventional Results available

Open Label Study Of SU011248 In Combination With Trastuzumab For Patients With Metastatic Breast Cancer

ClinicalTrials.gov ID: NCT00243503

Public ClinicalTrials.gov record NCT00243503. 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 Sep 27, 2026, 4:06 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 2 Efficacy And Safety Study Of SU011248 In Combination With Trastuzumab As Treatment For Metastatic Disease In Patients With Breast Cancer

Brief summary

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

The current study is to evaluate: Overall response rate for the combination of trastuzumab and SU011248 in metastatic or locally recurrent breast cancer; evaluate safety and tolerability of the combination; measure duration of tumor control and survival; assess patient reported outcomes; assess PK in combination with trastuzumab and compare efficacy and safety.

Study identification

NCT ID
NCT00243503
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
60 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
Jan 31, 2006
Primary completion
Mar 31, 2009
Completion
Jun 30, 2010
Last update posted
Jul 21, 2011

2006 – 2010

United States locations

U.S. sites
16
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
Pfizer Investigational Site Montgomery Alabama 36106 —
Pfizer Investigational Site Newark Delaware 19713 —
Pfizer Investigational Site Newark Delaware 19718-6001 —
Pfizer Investigational Site Wilmington Delaware 19899 —
Pfizer Investigational Site Fort Lauderdale Florida 33308 —
Pfizer Investigational Site Harvey Illinois 60426 —
Pfizer Investigational Site Tinley Park Illinois 60477 —
Pfizer Investigational Site Munster Indiana 46321 —
Pfizer Investigational Site Lafayette Louisiana 70503 —
Pfizer Investigational Site New Iberia Louisiana 70563 —
Pfizer Investigational Site Corinth Mississippi 38834 —
Pfizer Investigational Site Southaven Mississippi 38671 —
Pfizer Investigational Site Las Vegas Nevada 89135 —
Pfizer Investigational Site New York New York 10021 —
Pfizer Investigational Site Memphis Tennessee 38104 —
Pfizer Investigational Site Memphis Tennessee 38120 —

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 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00243503, 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 Jul 21, 2011 · Synced Sep 27, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00243503 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →