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Clinical Trial Summary

This is a phase I study evaluating tolerability, pharmacokinetics, and preliminary efficacy of HC-1119 in patients with metastatic castration-resistant prostate cancer. The study objective is to study the tolerability, safety, and dose-limiting toxicities (DLT) of HC-1119 in patients with mCRPC.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03774056
Study type Interventional
Source Hinova Pharmaceuticals Inc.
Contact
Status Completed
Phase Phase 1
Start date February 10, 2017
Completion date August 28, 2019

See also
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