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Completed Phase 2 Interventional

A Phase II Study of MDX-060 in Subjects With Relapsed or Refractory Hodgkin's Disease

ClinicalTrials.gov ID: NCT00284804

Public ClinicalTrials.gov record NCT00284804. 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 3, 2026, 8:53 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

An Open-label, Randomized, Multicenter, Phase II Study of MDX-060 in Combination With Gemcitabine, MDX060 in Combination With Dexamethasone, and Gemcitabine Monotherapy in Patients With Relapsed or Refractory Hodgkin's Disease

Brief summary

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

This study is designed to determine the objective response rate in patients with relapsed or refractory Hodgkin's disease treated with MDX-060 in combination with gemcitabine or gemcitabine alone.

Study identification

NCT ID
NCT00284804
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
74 participants

Conditions and interventions

Interventions

Drug

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
Oct 31, 2005
Primary completion
Apr 30, 2008
Completion
Sep 30, 2009
Last update posted
Oct 11, 2015

2005 – 2009

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
City of Hope, National Medical Center Duarte California 91010
California Oncology of the Central Valley Fresno California 93710
University of California, San Diego/Moores UCSD Cancer Center La Jolla California 92093-0698
H. Lee Moffitt Cancer & Research Institute Tampa Florida 33612
Rush Cancer Institute Chicago Illinois 60612
St. Francis Hospital Center Beech Grove Indiana 46107
American Health Network of Indiana Indianapolis Indiana 46237
Division of Hematology/Oncology, Tufts-New England Medical Center Boston Massachusetts 02111
Henry Ford Health System Detroit Michigan 48202
Mayo Clinic Rochester Minnesota 55905
Nevada Cancer Institute Las Vegas Nevada 89135
The Cancer Institute of New Jersey New Brunswick New Jersey 08901
Roswell Park Cancer Center Buffalo New York 14263
Mount Sinai School of Medicine New York New York 10029
Carolina BioOncology Institute, PLLC Huntersville North Carolina 28078
M.D. Anderson Cancer Center, The University of Texas Houston Texas 77030
Mary Babb Randolph Cancer Center Morgantown West Virginia 26506-9162

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 NCT00284804, 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 Oct 11, 2015 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00284804 live on ClinicalTrials.gov.

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