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Completed Phase 2 Interventional Results available

Vidaza to Restore Hormone Thx Prostate

ClinicalTrials.gov ID: NCT00384839

Public ClinicalTrials.gov record NCT00384839. 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 11, 2026, 4:53 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

Phase II Study for the Use of Vidaza™ to Restore Responsiveness of Patients' Prostate Cancers to Hormonal Therapy

Brief summary

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

The purpose of this research study is to find out what effects (good and bad) Vidaza has on patients with prostate cancer. This investigational drug is not approved by the Food and Drug Administration (FDA) for the treatment of prostate cancer; however, it is approved in myelodysplastic syndrome - a bone marrow disease. The pharmaceutical company involved in this study, Pharmion Corporation, is the manufacturer of Vidaza.

Study identification

NCT ID
NCT00384839
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
US Oncology Research
Industry
Enrollment
36 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
Mar 31, 2006
Primary completion
Oct 31, 2009
Completion
Oct 31, 2009
Last update posted
Oct 24, 2018

2006 – 2009

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
Rocky Mountain Cancer Center-Midtown Denver Colorado 80218
Cancer Centers of Florida, P.A. Ocoee Florida 34761
Minnesota Oncology Hematology, P.A. Minneapolis Minnesota 55404
Comprehensive Cancer Centers of Nevada Las Vegas Nevada 89109
New York Oncology Hematology, P.C. Albany New York 12208
Raleigh Hematology Oncology Associates Cary North Carolina 27511
Northwestern Carolina Oncology Hematology Hickory North Carolina 28602
Texas Oncology, P.A. Dallas Texas 75246
Texas Oncology, P.A. Fort Worth Texas 76104
Tyler Cancer Center Tyler Texas 75702
Deke Slayton Cancer Center Webster Texas 77598
Virginia Oncology Associates Norfolk Virginia 23502
Cancer Care Nrothwest-South Spokane Washington 99202

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

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About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00384839, 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 24, 2018 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00384839 live on ClinicalTrials.gov.

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