Cancer Clinical Trial
Official title:
INST: Phase I-II Study of Carboplatin, Vinorelbine and Capecitabine in Patients With Metastatic Breast Cancer
1. Determine the response rate with this regimen in an anthracycline and taxane resistant cohort of patients.
1. Determine the response rate with this regimen in an anthracycline and taxane resistant
cohort of patients.
2. Determine a maximum tolerated dose of capecitabine in combination with vinorelbine and
carboplatin for this patient population.
3. Determine the time to relapse after the administration of this regimen.
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Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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