Long-term Data Collection for Subjects in MDX-010 Studies

Completed

Conditions studied: Metastatic Melanoma

In brief

The objective of this study is to collect disease status and overall survival information for all Subjects in MDX-010 studies.

Key facts

Study ID

NCT00928031

Run by

Bristol-Myers Squibb

People needed

160

Starts

2007-06-01

Expected to finish

2009-04-01

Last updated by the study team

2010-04-26

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects who were previously enrolled in MDX-010 studies MDX010-02, MDX010-08, or MDX010-15.
• Subjects (or if applicable, next of kin), who are alive at the time of contact must have read, understood, and provided written informed consent and health Insurance Portability and Accountability Act (HIPAA) authorization after the nature of the study has been fully explained.
• For subjects who have died or have been lost to follow-up(the subject status at end of original ipilimumab study), approval from the appropriate site IRB, specifying or limiting appropriate means for obtaining information, must be granted prior to collection of any information.

Where it is running

• Arizona Cancer Center — Tuscon, Arizona, United States
• Pacific Shores Medical Group — Long Beach, California, United States
• The Angeles Clinic and Research Institute — Los Angeles, California, United States
• USC Norris Cancer Center — Los Angeles, California, United States
• University of Miami Sylvester Cancer Center — Miami, Florida, United States
• St. Francis Research Foundation — Beech Grove, Indiana, United States
• Dana-Farber Cancer Institute — Boston, Massachusetts, United States
• NYU Cancer Institute — New York, New York, United States
• Carolinas Cancer Care — Charlotte, North Carolina, United States
• Providence Portland Medical Center — Portland, Oregon, United States
• Huntsman Cancer Institute — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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