drugset / Trial / NCT02361086

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

NCT02361086

Phase 1/2 Completed 21 enrolled Innocrin Pharmaceutical
Non-randomizedParallel-groupOpen-labelTreatment

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).

Timeline

Start
2014-06
Primary completion
2017-12
Completion
2018-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Seviteronel Small molecule Oral