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Completed Phase 1Phase 2 Interventional Results available

Study Of SU011248 In Combination With Docetaxel (Taxotere) And Prednisone In Patients With Prostate Cancer

ClinicalTrials.gov ID: NCT00137436

Public ClinicalTrials.gov record NCT00137436. 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, 4:49 PM 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 Phase 1/2 Safety And Pharmacokinetic Study Of SU011248 In Combination With Docetaxel (Taxotere) And Prednisone In Patients With Metastatic Hormone Refractory Prostate Cancer (HRPC)

Brief summary

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

This is a multi-center, open-label, Phase 1/2 study of SU011248 (sunitinib malate, SUTENT) in combination with docetaxel and prednisone for the first-line treatment of metastatic hormone-refractory prostate cancer (mHRPC).

Study identification

NCT ID
NCT00137436
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
93 participants

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
Sep 30, 2005
Primary completion
Apr 30, 2008
Completion
Feb 28, 2010
Last update posted
Aug 28, 2011

2005 – 2010

United States locations

U.S. sites
24
U.S. states
8
U.S. cities
20
Facility City State ZIP Site status
Pfizer Investigational Site Harvey Illinois 60426
Pfizer Investigational Site Tinley Park Illinois 60477
Pfizer Investigational Site Hobart Indiana 46342
Pfizer Investigational Site Munster Indiana 46321
Pfizer Investigational Site Durham North Carolina 27710
Pfizer Investigational Site Portland Oregon 97239-3098
Pfizer Investigational Site Portland Oregon 97239
Pfizer Investigational Site Myrtle Beach South Carolina 29572
Pfizer Investigational Site Clarksville Tennessee 37043
Pfizer Investigational Site Franklin Tennessee 37067
Pfizer Investigational Site Gallarin Tennessee 37066
Pfizer Investigational Site Hermitage Tennessee 37076
Pfizer Investigational Site Lebanon Tennessee 37087
Pfizer Investigational Site Murfreesboro Tennessee 37130
Pfizer Investigational Site Nashville Tennessee 37203
Pfizer Investigational Site Nashville Tennessee 37205
Pfizer Investigational Site Nashville Tennessee 37207
Pfizer Investigational Site Nashville Tennessee 37211
Pfizer Investigational Site Smithville Tennessee 37166
Pfizer Investigational Site Smyrna Tennessee 37167
Pfizer Investigational Site Tullahoma Tennessee 37388
Pfizer Investigational Site Dallas Texas 75246
Pfizer Investigational Site Houston Texas 77030
Pfizer Investigational Site Madison Wisconsin 53792

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 NCT00137436, 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 Aug 28, 2011 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00137436 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →