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Clinical Trial Summary

The purpose of this study is to assess the safety, tolerability and preliminary efficacy of HRS-5041 in men with progressive metastatic castration resistant prostate cancer. The objective of this study was to determine the dose-limiting toxicity, maximum tolerance and recommended dose of HRS-5041 in phase II study.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05942001
Study type Interventional
Source Jiangsu HengRui Medicine Co., Ltd.
Contact Fei Luo
Phone +0518-81220121
Email fei.luo@hengrui.com
Status Recruiting
Phase Phase 1
Start date September 15, 2023
Completion date August 31, 2025

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