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Clinical Trial Summary

This randomized phase II trial compared pathologic response rates (pCR) of early breast cancer following neoadjuvant fluorouracil-epirubicin-cyclophosphamide(FEC) and capecitabine-epirubicin-cyclophosphamide (XEC).


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02115152
Study type Interventional
Source Guangxi Medical University
Contact Jianlun Liu
Email jianlunliu@hotmail.com
Status Not yet recruiting
Phase Phase 2
Start date June 2014

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