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Completed Phase 2 Interventional

Efficacy and Safety of Patupilone in Men (≥18 Years) With Metastatic Hormone Refractory Prostate Cancer

ClinicalTrials.gov ID: NCT00411528

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT00411528. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 14, 2026, 10:22 PM EST

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Official title

A Randomized Multicenter Phase II Trial of Patupilone (EPO906) Plus Prednisone Versus Docetaxel Plus Prednisone in Patients With Metastatic Hormone Refractory Prostate Cancer

Brief summary

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

The objective of this study is to assess the response of patupilone plus prednisone compared to docetaxel plus prednisone on prostate specific antigen (PSA) in patients with metastatic hormone refractory prostate cancer. Additionally, this study will assess the response on measureable disease and the effects on patient-reported outcomes.

Study identification

NCT ID
NCT00411528
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
185 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
Sep 2006 (Type not available)
Primary completion
Sep 2012 (Actual)
Completion
Sep 2012 (Actual)
Last update posted
Dec 17, 2020

2006 – 2012

United States locations

U.S. sites
11
U.S. states
9
U.S. cities
11
Facility City State ZIP Site status
University of California San Diego Dept of Moores Cancer Center La Jolla California 92093-0658 —
University of Colorado Dept. of Univ. of Colorado Aurora Colorado 80045 —
Norwalk Hospital Norwalk Connecticut 06856 —
Georgetown University/Lombardi Cancer Center Dept.of Lombardi Cancer Center Washington D.C. District of Columbia 20007-2197 —
MD Anderson Cancer Center - Orlando CEPO906A2229 Orlando Florida 32806 —
H. Lee Moffitt Cancer Center/University of South Florida Department of Genitourology Tampa Florida 33612 —
Palm Beach Cancer Institute West Palm Beach Florida 33401 —
NorthWest Georgia Oncology Centers Marietta Center Marietta Georgia 30060 —
University Chicago Hospital StudyCoordinator:CEPO906A2229 Chicago Illinois 60637 —
Queens Cancer Center of Queens Hospital Jamaica New York 11432 —
Oregon Health & Science University StudyCoordinator:CEPO906A2229 Portland Oregon 97239 —

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 21 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00411528, 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 Dec 17, 2020 · Synced Nov 14, 2026

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