drugset / Trial / NCT03774056

A Study Evaluating Tolerability, Pharmacokinetics, and Preliminary Efficacy of HC-1119 in Patients.

NCT03774056

NaSequentialOpen-labelTreatment

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.

Timeline

Start
2017-02-10
Primary completion
2018-09-26
Completion
2019-08-28

Drugs

EvaluationDrugModalityDoseRoute
Subject HC-1119 Unknown 40 mg Oral
Subject HC-1119 Unknown 80 mg Oral
Subject HC-1119 Unknown 160 mg Oral
Subject HC-1119 Unknown 200 mg Oral