Breast Cancer Clinical Trial
Trial of Paclitaxel, Bevacizumab, and Enzastaurin Versus Paclitaxel, Bevacizumab and Placebo for Breast Cancer
Summary
The purpose of this study is to determine efficacy and safety of paclitaxel, bevacizumab and enzastaurin versus paclitaxel, bevacizumab, and placebo in participants who are diagnosed with locally recurrent or metastatic breast cancer.
Eligibility Criteria
Inclusion Criteria:
Must have signed an inform consent document
Have histologic or cytologic diagnosis of breast cancer with evidence of unresectable locally recurrent or metastatic disease
Have not received any prior chemotherapy for locally recurrent or metastatic disease
Have not had adjuvant or neoadjuvant taxane therapy within 12 months prior to assignment to study treatment
Age 18 years or older at time of informed consent
Exclusion Criteria:
Have any clinical evidence of central nervous system (CNS) metastases
Have a history of seizure
Have had a major surgical procedure within 4 weeks prior to assignment to study treatment
Have had a minor surgical procedure, placement of an access device, or fine needle aspiration within 7 days prior to assignment to study treatment
Have symptomatic peripheral vascular disease
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There are 7 Locations for this study
Newark Delaware, 19713, United States
Galesburg Illinois, 61401, United States
Fort Wayne Indiana, 46815, United States
Goshen Indiana, 46526, United States
Indianapolis Indiana, 46202, United States
Lafayette Indiana, 47905, United States
Omaha Nebraska, 68114, United States
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