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Completed Phase 2 Interventional

Evaluating The Antitumor Activity Of MEDI-522 With Or Without Dacarbazine In Patients With Metastatic Melanoma

ClinicalTrials.gov ID: NCT00066196

Public ClinicalTrials.gov record NCT00066196. 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 24, 2026, 1:41 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

A Phase II, Randomized, Open-Label Study Evaluating The Antitumor Activity Of MEDI-522, A Humanized Monoclonal Antibody Directed Against The Human Alpha V Beta 3 Integrin, ± Dacarbazine In Patients With Metastatic Melanoma

Study identification

NCT ID
NCT00066196
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
MedImmune LLC
Industry
Enrollment
110 participants

Conditions and interventions

Interventions

  • MEDI--522 Biological
  • Integrin + Dacarbazine Biological

Biological

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Jul 31, 2003
Primary completion
Mar 31, 2007
Completion
May 31, 2007
Last update posted
Jan 14, 2008

2003 – 2007

United States locations

U.S. sites
25
U.S. states
16
U.S. cities
23
Facility City State ZIP Site status
Mayo Clinic Arizona Scottsdale Arizona 85259
Pacific Shores Medical Group Long Beach California 90813
Saint Francis Memorial Hospital San Francisco California 94109
Cancer Institute Medical Group Santa Monica California 90404
Medical Group of North County Vista California 92083
Yale University School of Medicine New Haven Connecticut 06520
University of Miami Miami Florida 33136
Winship Cancer Institute of Emory University Atlanta Georgia 30322
Oncology Specialists, S.C. Park Ridge Illinois 60069
Indiana Oncology Hematology Consultants Indianapolis Indiana 46202
Indiana University Medical Center Indianapolis Indiana 46202
Johns Hopkins University - SKCC at Johns Hopkins Lutherville Maryland 21093
Boston Medical Center Boston Massachusetts 02118
Kansas City Oncology & Hematology Group Kansas City Missouri 64131
The Melanoma Center of St. Louis St Louis Missouri 63131
HemOnc Care, P.C. Brooklyn New York 11235
Memorial Sloan-Kettering Cancer Center New York New York 10021
UNC-Chapel Hill Chapel Hill North Carolina 27599
Blumenthal Cancer Center Charlotte North Carolina 28203
Providence Portland Medical Center Portland Oregon 97213
Thomas Jefferson University Philadelphia Pennsylvania 19107
University of Pittsburgh Cancer Institute Pittsburgh Pennsylvania 15232
Vanderbilt University Medical Center Nashville Tennessee 37232
Discovery Alliance Houston Texas 77030
The University of Texas, MD Anderson Cancer Center Houston Texas 77030

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 NCT00066196, 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 14, 2008 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00066196 live on ClinicalTrials.gov.

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