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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
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 sponsor | Sanofi |
|---|---|
| Phase | Phase 2 |
| Status | COMPLETED |
| Enrolment | 168 |
| Start date | 2004-08 |
| Completion | 2009-04 |
Conditions
- Breast Cancer
Interventions
- XRP9881
Primary outcomes
- Objective response rate as assessed by Response Evaluation Criteria in Solid Tumors
Countries
United States, Argentina, Belgium, Canada, Colombia, Denmark, France, Germany, Italy, Netherlands, South Africa, South Korea, Spain, Switzerland, Turkey (Türkiye)