Overview

A Study to Evaluate Once-Daily Oral VT-464 in Patients With Castration-Resistant Prostate Cancer

Status:
Completed
Trial end date:
2018-06-01
Target enrollment:
Participant gender:
Summary
The goal of this clinical study is to determine the safety, tolerability, pharmacokinetics and activity of once-daily (QD) oral dosing of VT-464, a lyase-selective inhibitor of CYP17, in patients with castration-resistant prostate cancer (CRPC).
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
Innocrin Pharmaceutical