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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

NCT00087958 Phase 2 COMPLETED

The purpose of this clinical trial is to determine if the investigational drug is able to reduce/shrink advanced breast cancer tumors in patients who no longer benefit from anthracyclines, taxanes and capecitabine.

Details

Lead sponsorSanofi
PhasePhase 2
StatusCOMPLETED
Enrolment168
Start date2004-08
Completion2009-04

Conditions

Interventions

Primary outcomes

Countries

United States, Argentina, Belgium, Canada, Colombia, Denmark, France, Germany, Italy, Netherlands, South Africa, South Korea, Spain, Switzerland, Turkey (Türkiye)