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Terminated Phase 2 Interventional

Efficacy and Safety Study of Etodolac and Propranolol in Patients With Clinically Progressive Prostate Cancer

ClinicalTrials.gov ID: NCT01857817

Public ClinicalTrials.gov record NCT01857817. 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 Jul 22, 2026, 10:54 AM 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 Randomized, Placebo Controlled, Multicenter Phase 2 Study of Etodolac and Propranolol in Patients With Clinically Progressive Prostate Cancer

Study identification

NCT ID
NCT01857817
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Vicus Therapeutics
Industry
Enrollment
35 participants

Conditions and interventions

Interventions

  • VT-122 Drug
  • Placebo Drug

Drug

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
May 31, 2013
Primary completion
Mar 31, 2016
Completion
Mar 31, 2016
Last update posted
Apr 25, 2018

2013 – 2016

United States locations

U.S. sites
16
U.S. states
10
U.S. cities
16
Facility City State ZIP Site status
Highlands Oncology Group Fayetteville Arkansas 72703
Redwood Regional Medical Group Santa Rosa California 95403
Advanced Urology Parker Colorado 80134
Manatee Medical Research Institute, LLC Bradenton Florida 34205
Baptist Cancer Institute Jacksonville Florida 32207
Midwestern Regional Medical Center Zion Illinois 60099
Karmanos Cancer Institute Detroit Michigan 48201
Detroit Clinical Research Center, PC Lansing Michigan 48912
Adult & Pediatric Urology Sartell Minnesota 56377
AccuMed Research Associates Garden City New York 11530
Premier Medical Group of the Hudson Valley PC Poughkeepsie New York 12601
Montefiore Medical Center The Bronx New York 10467
Hendrick Cancer Center Abilene Texas 79601
Oncology Consultants, P.A. Houston Texas 77030
Virginia Mason Medical Center Seattle Washington 98101
Medical Oncology Associates, PS Spokane Washington 99208

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01857817, 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 Apr 25, 2018 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01857817 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →