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Completed Phase 3 Interventional Results available

Cabazitaxel Versus Docetaxel Both With Prednisone in Patients With Metastatic Castration Resistant Prostate Cancer

ClinicalTrials.gov ID: NCT01308567

Public ClinicalTrials.gov record NCT01308567. 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 Jul 22, 2026, 4:22 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

Randomized, Open Label, Multi-Center Study Comparing Cabazitaxel at 25 mg/m^2 and at 20 mg/m^2 in Combination With Prednisone Every 3 Weeks to Docetaxel in Combination With Prednisone in Patients With Metastatic Castration Resistant Prostate Cancer Not Pretreated With Chemotherapy

Study identification

NCT ID
NCT01308567
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sanofi
Industry
Enrollment
1,168 participants

Conditions and interventions

Interventions

  • Cabazitaxel (XRP6258) Drug
  • Docetaxel (XRP6976) Drug
  • Prednisone Drug

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
May 4, 2011
Primary completion
Aug 31, 2015
Completion
Apr 30, 2018
Last update posted
Jun 4, 2019

2011 – 2018

United States locations

U.S. sites
32
U.S. states
22
U.S. cities
31
Facility City State ZIP Site status
Investigational Site Number 840004 Muscle Shoals Alabama 35661
Investigational Site Number 840009 Anaheim California 92801
Investigational Site Number 840014 Bakersfield California 93309
Investigational Site Number 840030 Sacramento California 95816
Investigational Site Number 840003 San Bernardino California 92404
Investigational Site Number 840012 San Francisco California 94143
Investigational Site Number 840019 Denver Colorado 80262
Investigational Site Number 840013 Boca Raton Florida 33486
Investigational Site Number 840035 Jacksonville Florida 32256
Investigational Site Number 840001 Port Saint Lucie Florida 34952
Investigational Site Number 840015 Decatur Illinois 62526
Investigational Site Number 840018 Wichita Kansas 67214
Investigational Site Number 840010 Paducah Kentucky 42002
Investigational Site Number 840008 New Orleans Louisiana 70112
Investigational Site Number 840006 Rockville Maryland 20850
Investigational Site Number 840238 Boston Massachusetts 02114
Investigational Site Number 840138 Boston Massachusetts 02115
Investigational Site Number 840038 Brookline Massachusetts 02115
Investigational Site Number 840005 Detroit Michigan 48202
Investigational Site Number 840021 Saint Louis Park Minnesota 55416
Investigational Site Number 840016 Kansas City Missouri 64128
Investigational Site Number 840020 Lincoln Nebraska 68506
Investigational Site Number 840017 East Orange New Jersey 07018
Investigational Site Number 840033 Albuquerque New Mexico 87109
Investigational Site Number 840036 Raleigh North Carolina 27607
Investigational Site Number 840011 Washington North Carolina 27889
Investigational Site Number 840026 Akron Ohio 44302
Investigational Site Number 840023 Cleveland Ohio 44106
Investigational Site Number 840032 Dunmore Pennsylvania 18512
Investigational Site Number 840007 Pawtucket Rhode Island 02860
Investigational Site Number 840037 Myrtle Beach South Carolina 29572
Investigational Site Number 840028 Chattanooga Tennessee 37421

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 135 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01308567, 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 Jun 4, 2019 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01308567 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →