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Clinical Trial Summary

The primary purpose of this study is to determine what proportion of participants will achieve complete pathological response with epirubicin+ cyclophosphamide followed by docetaxel +carboplatin. This will also examine the potential of using signals in the blood (biomarkers) to identify resistance to chemotherapy in Nigerian women with triple negative breast cancer (TNBC). All enrollment to this trial will occur at sites in Nigeria. University of Chicago is serving as coordinating center and will be involved in data analysis.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06291064
Study type Interventional
Source University of Chicago
Contact Ilona Siljander
Phone 773-834-6542
Email isiljander1@bsd.uchicago.edu
Status Not yet recruiting
Phase Phase 2
Start date June 2024
Completion date June 2032

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