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Clinical Trial Summary

This study includes Single agent/combination dose exploration study and the phase II study. The primary purpose of this study is to determine the maximum tolerated dose(MTD)/recommended phase II dose(RP2D) of XZP-3287 and its efficacy and safety in hormone receptor(HR) positive, human epidermal growth factor receptor 2(HER2) negative advanced breast cancer.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04539496
Study type Interventional
Source Sihuan Pharmaceutical Holdings Group Ltd.
Contact Binghe Xu, Doctor
Phone (+86)(10)(87788826)
Email xubinghe@csco.org.cn
Status Recruiting
Phase Phase 1/Phase 2
Start date May 22, 2018
Completion date December 30, 2022

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