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Withdrawn Phase 3 Interventional

Study of a Drug [DCVax (tm)-Prostate] to Treat Prostate Cancer When Hormone Therapy is no Longer Effective.

ClinicalTrials.gov ID: NCT00043212

Public ClinicalTrials.gov record NCT00043212. 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, 5:41 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, Double-blind, Placebo-controlled Phase III Clinical Trial Evaluating DCVax(tm)-Prostate, Autologous Dendritic Cells Loaded With Recombinant PSMA for the Treatment of Metastatic Hormone Refractory Prostate Cancer

Brief summary

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

The purpose of this clinical research study is to assess the safety and efficacy of an investigational therapy called DCVax(TM)-Prostate.

Study identification

NCT ID
NCT00043212
Recruitment status
Withdrawn
Study type
Interventional
Phase
Phase 3
Lead sponsor
Northwest Biotherapeutics
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

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
Not listed
Primary completion
Not listed
Completion
Not listed
Last update posted
Apr 30, 2013

United States locations

U.S. sites
16
U.S. states
14
U.S. cities
16
Facility City State ZIP Site status
Highlands Oncology Group Springdale Arkansas
University of California, Los Angeles Los Angeles California
University of California, San Diego Medical Center San Diego California
Walter Reed Army Medical Center Washington D.C. District of Columbia
Cancer Centers of Florida, P.A. Orlando Florida
St. Francis Medical Center Peoria Illinois
Louisiana State University New Orleans Louisiana
Clinical Research Solutions Las Vegas Nevada
Albany Regional Cancer Center Albany New York
Carolinas HealthCare System Charlotte North Carolina
Cleveland Clinic Foundation Cleveland Ohio
Mary Crowley Medical Research Center Dallas Texas
Tyler Cancer Center Tyler Texas
University of Utah Salt Lake City Utah
Cancer Care Northwest Spokane Washington
St. Luke's Medical Center Milwaukee Wisconsin

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 NCT00043212, 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 30, 2013 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00043212 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →