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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 Oct 26, 2026, 7:17 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
Oct 2005 (Type not available)
Primary completion
May 2008 (Actual)
Completion
Mar 2010 (Actual)
Last update posted
Aug 29, 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 29, 2011 · Synced Oct 26, 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 public registry record, listed eligibility criteria, and available contact information for NCT00137436 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →