Breast Cancer Clinical Trial

Study Of The Efficacy And Safety Of SU-014813 In Patients With Metastatic Breast Cancer

Summary

To determine the antitumor efficacy and the safety of SU-014813 at a dose of 100 mg orally once daily in patients with Metastatic Breast Cancer

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Histologically or cytologically proven diagnosis of metastatic breast adenocarcinoma that is not amenable to surgery, radiation, or combined modality therapy with curative intent.
Must have received prior treatment with an anthracycline and a taxane either concurrently or sequentially in the adjuvant and/or advanced disease treatment settings. Patients may have received as many as 2 other chemotherapy regimens in the advanced disease setting. Patients whose tumors are Her-2-positive must have received prior trastuzumab therapy. Prior hormonal therapy or immunotherapy in the adjuvant and/or advanced/metastatic disease settings is permitted. Prior treatment with surgery, radiotherapy, chemoembolization therapy, or cryotherapy is allowed if these therapies did not affect the areas of measurable disease.

Exclusion Criteria:

Prior treatment with >/= 3 regimens of chemotherapy in the metastatic disease setting beyond those containing anthracyclines and taxanes
Uncontrolled brain metastases, spinal cord compression, or carcinomatous meningitis, or new evidence of brain or leptomeningeal disease. Patients should have completed surgery or radiation therapy for existing brain metastases, should not have documented increase in size over the previous 3 months and should be asymptomatic

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

90

Study ID:

NCT00322517

Recruitment Status:

Completed

Sponsor:

Pfizer

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There are 21 Locations for this study

See Locations Near You

Pfizer Investigational Site
Los Angeles California, 90095, United States
Pfizer Investigational Site
Pasadena California, 91105, United States
Pfizer Investigational Site
Santa Monica California, 90404, United States
Pfizer Investigational Site
Valancia California, 91355, United States
Pfizer Investigational Site
Corinth Mississippi, 38834, United States
Pfizer Investigational Site
Southaven Mississippi, 38671, United States
Pfizer Investigational Site
Memphis Tennessee, 38104, United States
Pfizer Investigational Site
Memphis Tennessee, 38120, United States
Pfizer Investigational Site
Hamburg , 20246, Germany
Pfizer Investigational Site
Magdeburg , 39130, Germany
Pfizer Investigational Site
Marburg , 35043, Germany
Pfizer Investigational Site
Chieti Scalo , 66013, Italy
Pfizer Investigational Site
Milano , 20133, Italy
Pfizer Investigational Site
Mirano (VE) , 30035, Italy
Pfizer Investigational Site
Udine , 33100, Italy
Pfizer Investigational Site
Amsterdam , 1081 , Netherlands
Pfizer Investigational Site
Rotterdam , 3075 , Netherlands
Pfizer Investigational Site
Manchester M20 4bx, , United Kingdom
Pfizer Investigational Site
Sutton Surrey, SM2 5, United Kingdom
Pfizer Investigational Site
Edinburgh , EH4 2, United Kingdom
Pfizer Investigational Site
London , SE1 9, United Kingdom
Pfizer Investigational Site
London , SW3 6, United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

90

Study ID:

NCT00322517

Recruitment Status:

Completed

Sponsor:


Pfizer

How clear is this clinincal trial information?

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