Breast Cancer Clinical Trial

CPG 7909 Plus Herceptin® In Patients With Metastatic Breast Cancer

Summary

To determine the safety and efficacy of CPG 7909 Injection given with Herceptin to patients with metastatic breast cancer.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Histologically confirmed breast cancer with metastases
Tumor that has overexpression of HER2 as documented by being either FISH-positive or HER2/neu 3+ confirmed by immunohistochemistry
Patients may have had up to three prior chemotherapy regimens for metastatic disease, which may have been given in combination with Herceptin® and which may have been discontinued due to toxicities. In addition, patients may have had adjuvant chemotherapy.
Phase II only: Must have measurable disease by RECIST criteria (defined in section 8) with at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded) as > 20 mm with conventional techniques, or as > 10 mm with spiral CT scan

Exclusion Criteria:

Any prior therapy with anthracycline + Herceptin® concurrently
Significant cardiovascular disease (e.g., NYHA class 3 congestive heart failure, myocardial infarction within the past 6 months, unstable angina; coronary angioplasty within the past 6 months, uncontrolled atrial or ventricular cardiac arrhythmias) or left ventricular ejection fraction < 50%
Pre-existing autoimmune or antibody-mediated diseases including but not limited to: systemic lupus erythematosus, rheumatoid arthritis, multiple sclerosis, Sjogren's syndrome, autoimmune thrombocytopenia

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

16

Study ID:

NCT00043394

Recruitment Status:

Completed

Sponsor:

Pfizer

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There are 12 Locations for this study

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Pfizer Investigational Site
Berkely California, 94704, United States
Pfizer Investigational Site
Orange California, 92868, United States
Pfizer Investigational Site
Palm Springs California, 92262, United States
Pfizer Investigational Site
New Haven Connecticut, 06510, United States
Pfizer Investigational Site
Washington District of Columbia, 20007, United States
Pfizer Investigational Site
Plantation Florida, 33324, United States
Pfizer Investigational Site
Ann Arbor Michigan, 48109, United States
Pfizer Investigational Site
Dearborn Michigan, 48126, United States
Pfizer Investigational Site
Detroit Michigan, 48202, United States
Pfizer Investigational Site
West Bloomfield Michigan, 48322, United States
Pfizer Investigational Site
Cleveland Ohio, 44195, United States
Pfizer Investigational Site
Burlington Vermont, 05401, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

16

Study ID:

NCT00043394

Recruitment Status:

Completed

Sponsor:


Pfizer

How clear is this clinincal trial information?

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