The purpose of this study is to see if BMS-986205 combined with nivolumab, compared to nivolumab by itself, is more effective in treating Melanoma that has spread or is unable to be removed by surgery, and has not previously been treated
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
20
specified dose on specified day
Specified dose on specified day
Specified dose on specified day
Number of Participants Experiencing Adverse Events
Number of participants experiencing different types of Adverse Events, including Death, Any cause Adverse Events (AEs), Drug-related AEs, Any cause Serious Adverse Events (SAEs), Drug-related SAEs, SAEs leading to discontinuation, and Drug-related Non-serious AEs leading to discontinuation
Time frame: From first dose to 30 days following last dose (up to approximately 25 months)
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Angeles Clinic and Research Institute
Los Angeles, California, United States
University Of Colorado
Aurora, Colorado, United States
Mount Sinai Comprehensive Cancer Center
Miami Beach, Florida, United States
University Of Chicago
Chicago, Illinois, United States
Oregon Health & Science University
Portland, Oregon, United States
Local Institution
Seattle, Washington, United States
Local Institution
Blacktown, New South Wales, Australia
Melanoma Institute Australia
North Sydney, New South Wales, Australia
Local Institution
Greenslopes, Queensland, Australia
Local Institution
Woolloongabba, Queensland, Australia
...and 53 more locations