Phase II Study to Determine Predictive Markers of Response to BMS-734016 (MDX-010)
Completed · Phase 1/Phase 2
Conditions studied: Unresectable Stage III or IV Malignant Melanoma
In brief
The purpose of this study is to identify candidate markers predictive of response and/or serious toxicity to BMS-734016 (MDX-010).
Key facts
- Study ID
- NCT00261365
- Run by
- Bristol-Myers Squibb
- People needed
- 80
- Starts
- 2005-11-01
- Expected to finish
- 2007-10-01
- Last updated by the study team
- 2016-09-29
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Histologic or cytologic diagnosis of unresectable State III or IV malignant melanoma (excluding ocular melanoma); A pre- and post-treatment fresh core or excision tumor biopsy must be provided.
Where it is running
- Comprehensive Cancer Center — Palm Springs, California, United States
- The Angeles Clinic And Research Institution — Santa Monica, California, United States
- Beth Israel Deaconess Medical Center — Boston, Massachusetts, United States
- Local Institution — Aarhus C, Denmark
- Local Institution — Odense C, Denmark
- Local Institution — Jerusalem, Israel
- Local Institution — Bari, Italy
- Local Institution — Forlì, Italy
- Local Institution — Ravenna, Italy
- Local Institution — Rimini, Italy
- Local Institution — Oslo, Norway
- Local Institution — Lima, Lima Province, Peru
- Local Institution — Lima, Lima Province, Peru
- Local Institution — Gothenberg, Sweden
- Local Institution — Stockholm, Sweden
Full record on ClinicalTrials.gov
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