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Completed Phase 2 Interventional

MEDI-522 in the Treatment of Patients With Metastatic Androgen-Independent Prostate Cancer

ClinicalTrials.gov ID: NCT00072930

Public ClinicalTrials.gov record NCT00072930. 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 22, 2026, 11:45 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

Phase II, Randomized, Open-Label, Two-Arm, Multicenter Study of MEDI-522, a HuMA Directed Against the Human Alpha V Beta 3 Integrin, in Combination With Docetaxel, Prednisone, and Zoledronic Acid in the Treatment of Patients With Metastatic Androgen-Independent Prostate Cancer

Brief summary

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

The primary objectives of this study are: 1. To explore the antitumor activity of MEDI-522 in combination with docetaxel, prednisone, and zoledronic acid in patients with metastatic Androgen-Independent Prostate Cancer (AIPC); and 2. To summarize the safety of MEDI-522 in combination with docetaxel, prednisone, and zoledronic acid in this patient population.

Study identification

NCT ID
NCT00072930
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
MedImmune LLC
Industry
Enrollment
150 participants

Conditions and interventions

Interventions

Biological

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
Dec 2003 (Type not available)
Primary completion
Apr 2007 (Estimated)
Completion
Jun 2007 (Actual)
Last update posted
Jan 15, 2008

2003 – 2007

United States locations

U.S. sites
36
U.S. states
21
U.S. cities
36
Facility City State ZIP Site status
Clinical Research Consultants, Inc. Hoover Alabama 35216 —
Highlands Oncology Group, P.A. Springdale Arizona 72764 —
Arizona Hematology-Oncology, P.C. Tucson Arizona 85704 —
South Valley Medical Plaza Gilroy California 95020-3535 —
San Bernardino Urological Associates San Bernardino California 92404 —
Saint Francis Memorial Hospital San Francisco California 94109 —
Stanford Advanced Medical Center Stanford California 94305-5826 —
Florida Cancer Specialist Fort Myers Florida 33901 —
The Florida Wellcare Alliance, L.C. Inverness Florida 34452 —
Hemotology/Oncology Associates Lake Worth Florida — —
Hawaii Medical Consultants Honolulu Hawaii 96817 —
University of Chicago Chicago Illinois 60637-1470 —
Ingalls Hospital Harvey Illinois 60426 —
The Community Hospital Munster Indiana 46321 —
Hematology Oncology Services, LLC New Orleans Louisiana 70115 —
Hubert H. Humphrey Cancer Center Robbinsdale Minnesota 55422 —
North Mississippi Hematology & Oncology Associates, Ltd. Tupelo Mississippi 38801 —
Washington University School of Medicine St Louis Missouri 63110-1010 —
Comprehensive Cancer Center of Nevada Las Vegas Nevada 89109 —
VA Sierra Nevada Health Care System Reno Nevada 89502 —
New Mexico Oncology Hematology, Consultants Ltd. Albuquerque New Mexico 87109 —
SUNY Down State Medical Center Brooklyn New York 11203 —
VA Western New York Healthcare System Buffalo New York 14215-1199 —
North Shore Hematology Oncology Assoc., PC East Setauket New York 11733 —
Columbia Presbyterian Medical Center New York New York 10032-3713 —
VA Medical Center Northport New York 11768 —
Raleigh Hematology Oncology Association Raleigh North Carolina 27609 —
Clinical Research Services Bismarck North Dakota — —
University of Cincinnati, Barrett Cancer Center Cincinnati Ohio 45267-0501 —
Santee Hematology/Oncology Sumter South Carolina 29150 —
Associates in Oncology and Hematology Chattanooga Tennessee 37404 —
Thompson Cancer Survival Center Knoxville Tennessee 37916 —
The Sarah Cannon Cancer Center Nashville Tennessee 37203 —
Danville Hematology and Oncology Danville Virginia 24541-4155 —
Virginia Cancer Institute Richmond Virginia 23230 —
Western Washington Oncology, Inc., P.S. Lacey Washington 98503 —

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 NCT00072930, 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 Jan 15, 2008 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00072930 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →