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(Türkiye)",{"type":25,"coordinates":150},[151,152],28.94966,41.01384,{"lat":152,"lon":151},{"type":7,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":155,"oldOrganization":156},"ICD Study Director","sanofi-aventis","100064363","phase-2-intravenous-rpr109881-in-male-or-female-patients-with-advanced-breast-cancer-who-no-longer-respond-to-anthracycline-taxane-and-capecitabine-treatment-100064363",false,"NCT00087958","Intravenous RPR109881 in Male or Female Patients With Advanced Breast Cancer Who no Longer Respond to Anthracycline, Taxane and Capecitabine Treatment","Phase II Multi-Center, Open-Label, Non-Randomized Study of Intravenous RPR109881 Given Every 3 Weeks in Patients With Metastatic Breast Cancer Progressing After Therapy With Anthracyclines, Taxanes and Capecitabine","Inclusion Criteria:\n\nIn order to be eligible for this trial you must:\n\n* Have a diagnosis of breast cancer that is now metastatic (meaning the cancer has spread beyond its original location) or a recurrence of the cancer in its original location that cannot be removed by surgery.\n* Have received previous treatment with anthracyclines (e.g. doxorubicin \\[Adriamycin or Doxil\\] or epirubicin \\[Ellence\\]), taxanes (paclitaxel \\[Taxol or Abraxane\\] or docetaxel \\[Taxotere\\]) and capecitabine (e.g. Xeloda) for your breast cancer and your doctor has determined that these treatments are no longer of benefit to you.\n* Be at least 18 years of age\n* Not be taking other treatments for your cancer at the time you enter the trial.\n* Not be pregnant\n* Additionally, there are other criteria for study entry that a doctor participating in this study will need to review in detail with you and clinical assessments may need to be performed (lab tests, CT scans).\n\nExclusion Criteria:\n\n* None listed here. 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