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Clinical Trial Summary

The trial was designed to study the efficacy and safety of neoadjuvant docetaxel, epirubicin in combination with cyclophosphamide(DEC) plus human recombinant endostatin (endostar) for breast cancer patients. The hypothesis of this protocol is that the combined an active angiogenesis agent to chemotherapy could enhance the pathological responce rate and further benefit breast cancer patients.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01907529
Study type Interventional
Source Hebei Medical University Fourth Hospital
Contact
Status Enrolling by invitation
Phase Phase 2/Phase 3
Start date August 2019
Completion date December 2021

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