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Clinical Trial Summary

Compare the efficacy of bicalutamide with conventional chemotherapy (Treatment of Physician's Choice,TPC) in first-line treatment of AR positive metastatic triple negative breast


Clinical Trial Description

This is a phase III,Multi-center,prospective,randomized clinical trials. The objective compare the efficacy of bicalutamide with conventional chemotherapy (Treatment of Physician's Choice,TPC) in first-line treatment of AR positive metastatic triple negative breast cancer.Primary endpoint is 16-week clinical benefit rate (CBR).By centre randomized grouping bicalutamide (experimental Group) or TPC (Control Group). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03055312
Study type Interventional
Source Sun Yat-sen University
Contact
Status Terminated
Phase Phase 3
Start date December 20, 2016
Completion date November 15, 2020

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