Breast Cancer Clinical Trial

Study Evaluating Bosutinib-Exemestane Combination Vs Exemestane Alone in Post Menopausal Women With Breast Cancer

Summary

This is a phase 2, open-label, multicenter, 2-arm study of bosutinib administered in combination with exemestane versus exemestane alone. This is a 2-part study consisting of a safety lead-in phase and randomized phase 2 portion. Subjects in part 1 will receive bosutinib and exemestane daily, and will be closely monitored for 28 days. If no safety concerns arise, then future eligible subjects will be randomly assigned to the main phase of the study. They will either receive bosutinib daily combined with daily exemestane, or daily exemestane alone for a specified period of time. Subjects will be followed up for survival after treatment discontinuation.

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Full Description

This study was terminated on 19 Apr 2010 due to unfavorable risk benefit ratio which did not support continuation in part 2 of the study. Even if the safety profile of the combination of Bosutinib and Exemestane was acceptable 25% of subjects had treatment related liver events including 14% of severe liver events.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Woman aged 18 years or older.
Confirmed pathologic diagnosis of breast cancer.
Locally advanced, metastatic, or locoregional recurrent breast cancer not amenable to curative treatment with surgery or radiotherapy.
Surgically sterile or postmenopausal woman.
Documented ER+ and/or PgR+ and erbB2- tumor.
Progression of locally advanced or metastatic disease during treatment with a nonsteroidal AI or tamoxifen, or progression during treatment with (or within 6 months of discontinuation of) an adjuvant nonsteroidal AI.

Exclusion Criteria:

Prior exemestane, prior bosutinib, or any other prior anti-Src therapy.
More than 1 prior endocrine treatment for locally advanced or MBC.
More than 1 prior cytotoxic chemotherapy regimen in metastatic setting.
Bone or skin as the only site of disease.

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

42

Study ID:

NCT00793546

Recruitment Status:

Terminated

Sponsor:

Pfizer

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There are 25 Locations for this study

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Pfizer Investigational Site
Lake Worth Florida, 33461, United States
Pfizer Investigational Site
Joliet Illinois, 60435, United States
Pfizer Investigational Site
Boston Massachusetts, 02114, United States
Pfizer Investigational Site
Boston Massachusetts, 02115, United States
Pfizer Investigational Site
Detroit Michigan, 84202, United States
Pfizer Investigational Site
New Brunswick New Jersey, 08901, United States
Pfizer Investigational Site
New York New York, 10032, United States
Pfizer Investigational Site
Bethlehem Pennsylvania, 18015, United States
Pfizer Investigational Site
Philadelphia Pennsylvania, 19104, United States
Pfizer Investigational Site
Philadelphia Pennsylvania, 19104, United States
Pfizer Investigational Site
Seattle Washington, 98104, United States
Pfizer Investigational Site
South Brisbane Queensland, 4101, Australia
Pfizer Investigational Site
Brussels , 1000, Belgium
Pfizer Investigational Site
Leuven , 3000, Belgium
Pfizer Investigational Site
Liege , 4000, Belgium
Pfizer Investigational Site
Wilrijk , 2610, Belgium
Pfizer Investigational Site
Kelowna British Columbia, V1Y 5, Canada
Pfizer Investigational Site
Beijing , 10002, China
Pfizer Investigational Site
Hong Kong , , Hong Kong
Pfizer Investigational Site
Budapest , 1122, Hungary
Pfizer Investigational Site
Mumbai Maharashtra, 40001, India
Pfizer Investigational Site
Pune Maharashtra, 41100, India
Pfizer Investigational Site
Olsztyn , 10-51, Poland
Pfizer Investigational Site
Lynnwood Gauteng, 0081, South Africa
Pfizer Investigational Site
Barcelona , 08035, Spain
Pfizer Investigational Site
Madrid , 28040, Spain
Pfizer Investigational Site
Valencia , 46010, Spain
Pfizer Investigational Site
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How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

42

Study ID:

NCT00793546

Recruitment Status:

Terminated

Sponsor:


Pfizer

How clear is this clinincal trial information?

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