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Completed Phase 2 Interventional

A Study Comparing AT-101 in Combination With Docetaxel and Prednisone Versus Docetaxel and Prednisone in Men With Chemotherapy-Naïve Metastatic Hormone Refractory Prostate Cancer (HRPC)

ClinicalTrials.gov ID: NCT00571675

Public ClinicalTrials.gov record NCT00571675. 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 Apr 29, 2026, 8:52 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, Multicenter, Phase 2 Study Comparing AT-101 in Combination With Docetaxel and Prednisone Versus Docetaxel and Prednisone in Men With Chemotherapy-Naïve Metastatic Hormone Refractory Prostate Cancer (HRPC)

Study identification

NCT ID
NCT00571675
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Ascenta Therapeutics
Industry
Enrollment
220 participants

Conditions and interventions

Interventions

  • AT-101, prednisone and docetaxel Drug
  • placebo, prednisone and docetaxel Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Sep 30, 2007
Primary completion
Aug 31, 2010
Completion
Aug 31, 2010
Last update posted
Nov 8, 2010

2007 – 2010

United States locations

U.S. sites
24
U.S. states
13
U.S. cities
24
Facility City State ZIP Site status
Not listed Colorado Springs Colorado
Not listed New Port Richey Florida
Not listed Ocoee Florida
Not listed Fishers Indiana
Not listed Burnsville Minnesota
Not listed Las Vegas Nevada
Not listed Albuquerque New Mexico
Not listed Las Cruces New Mexico
Not listed Raleigh North Carolina
Not listed Kettering Ohio
Not listed Eugene Oregon
Not listed Spartanburg South Carolina
Not listed Amarillo Texas
Not listed Arlington Texas
Not listed Austin Texas
Not listed Dallas Texas
Not listed Denton Texas
Not listed Midland Texas
Not listed Paris Texas
Not listed Webster Texas
Not listed Fairfax Virginia
Not listed Norfolk Virginia
Not listed Kennewick Washington
Not listed Vancouver Washington

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 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00571675, 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 Nov 8, 2010 · Synced Apr 29, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00571675 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →