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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 Nov 7, 2026, 9:55 AM EST

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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)

Brief summary

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

This is a randomized, double-blind, placebo-controlled, multinational Phase 2 study to evaluate and compare oral AT-101 in combination with docetaxel and prednisone versus docetaxel and prednisone plus placebo in the treatment of chemotherapy-naïve metastatic hormone-refractory prostate cancer, who have received hormonal therapy but not chemotherapy.

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

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
Oct 2007 (Type not available)
Primary completion
Sep 2010 (Actual)
Completion
Sep 2010 (Actual)
Last update posted
Nov 9, 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 9, 2010 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00571675 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →