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Completed Phase 2 Interventional Results available

Androgen Deprivation Therapy and Vorinostat Followed by Radical Prostatectomy in Treating Patients With Localized Prostate Cancer

ClinicalTrials.gov ID: NCT00589472

Public ClinicalTrials.gov record NCT00589472. 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 5, 2026, 5:41 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

Neoadjuvant Androgen Depletion in Combination With Vorinostat Followed by Radical Prostatectomy for Localized Prostate Cancer: Total Androgen-Receptor Gene Expression Targeted Therapy (TARGET)

Brief summary

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

This phase II trial studies how well androgen deprivation therapy and vorinostat followed by radical prostatectomy works in treating patients with prostate cancer that has not spread to other parts of the body. Androgens can cause the growth of prostate cancer cells. Antihormone therapy, such as bicalutamide, goserelin acetate, and leuprolide acetate, may lessen the amount of androgens made by the body. Vorinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving androgen deprivation therapy and vorinostat before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed.

Study identification

NCT ID
NCT00589472
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
19 participants

Conditions and interventions

Eligibility (public fields only)

Age range
19 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
Oct 31, 2007
Primary completion
May 31, 2010
Completion
May 31, 2010
Last update posted
Oct 5, 2017

2007 – 2010

United States locations

U.S. sites
15
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
UCLA / Jonsson Comprehensive Cancer Center Los Angeles California 90095
UCSF Medical Center-Parnassus San Francisco California 94143
University of Chicago Comprehensive Cancer Center Chicago Illinois 60637
Johns Hopkins University/Sidney Kimmel Cancer Center Baltimore Maryland 21287
Dana-Farber Cancer Institute Boston Massachusetts 02115
University of Michigan Comprehensive Cancer Center Ann Arbor Michigan 48109
Wayne State University/Karmanos Cancer Institute Detroit Michigan 48201
Mayo Clinic Rochester Minnesota 55905
UMDNJ - New Jersey Medical School Newark New Jersey 07103
Memorial Sloan-Kettering Cancer Center New York New York 10065
Duke University Medical Center Durham North Carolina 27710
Oregon Health and Science University Portland Oregon 97239
M D Anderson Cancer Center Houston Texas 77030
University of Washington Medical Center Seattle Washington 98195
University of Wisconsin Hospital and Clinics 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00589472, 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 Oct 5, 2017 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00589472 live on ClinicalTrials.gov.

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