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Completed Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT02012920

Public ClinicalTrials.gov record NCT02012920. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 15, 2026, 10:34 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1/2 Open-Label Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Seviteronel in Subjects With Castration-Resistant Prostate Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The goal of this clinical study is to determine the safety, tolerability, pharmacokinetics and activity of Seviteronel, a lyase-selective inhibitor of CYP17, in patients with castration-resistant prostate cancer (CRPC).

Study identification

NCT ID
NCT02012920
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Innocrin Pharmaceutical
Industry
Enrollment
200 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2011
Primary completion
Nov 30, 2018
Completion
Dec 31, 2018
Last update posted
Jan 31, 2019

2011 – 2019

United States locations

U.S. sites
19
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
Urology Centers of Alabama Homewood Alabama 35209
H. Lee Moffitt Cancer and Research Institute Tampa Florida 33612
First Urology, PSC Jeffersonville Indiana 47130
Wichita Urology Wichita Kansas 67226
Urology Cancer Center Omaha Nebraska 68130
Comprehensive Cancer Centers of Nevada Las Vegas Nevada 86169
North Shore Hematology Oncology Associates East Setauket New York 11733
Associated Medical Professionals of NY Syracuse New York 13210
NY Cancer and Blood Specialists The Bronx New York 10469
Duke Cancer Institute at Cary: Medical Oncology Cary North Carolina 27518
Duke University Medical Center Durham North Carolina 27710
Gabrail Cancer Center Research Canton Ohio 44718
Urologic Consultants of Southeastern Pennsylvania Bala-Cynwyd Pennsylvania 19004
Charleston Hematology Oncology Associates Charleston South Carolina 29414
Carolina Urologic Research Center Myrtle Beach South Carolina 29572
Urology Clinics of North Texas Dallas Texas 75231
University of Texas MD Anderson Cancer Center Houston Texas 77030
Virginia Oncology Associates Norfolk Virginia 23502
University of Wisconsin Carbone Cancer Center Madison Wisconsin 53792

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02012920, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 31, 2019 · Synced Sep 15, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02012920 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →