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Clinical Trial Summary

The study primary objective is to evaluate the effect of HC-1119 soft capsules versus placebo on overall survival (OS) in mCRPC patients who have failed or become intolerant to the treatments with both abiraterone acetate and docetaxel, or who are not suitable for docetaxel treatment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03851640
Study type Interventional
Source Hinova Pharmaceuticals Inc.
Contact Zhonghua Zhou, Master
Phone +862885058465
Email zhzhou1@hinovapharma.com
Status Recruiting
Phase Phase 3
Start date April 12, 2019
Completion date December 2024

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