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A Study of BMS-986249 Alone and in Combination With Nivolumab in Advanced Solid Tumors
Trial Status: complete
The purpose of this study is to determine whether BMS-986249 both by itself and in
combination with Nivolumab is safe and tolerable in the treatment of advanced solid
tumors
Inclusion Criteria
Histologic or cytologic confirmation of a solid tumor that is advanced (metastatic, recurrent, and/or unresectable) with measurable disease or metastatic disease documented by either bone lesions on radionuclide bone scan and/or soft tissue lesions on CT/MRI for prostate cancer and have at least 1 lesion accessible for biopsy. For Part 2B participants with HCC, intermediate disease is allowed.
Eastern Cooperative Oncology Group Performance Status of 0 or 1
Must have received, and then progressed, relapsed, or been intolerant to, at least 1 standard treatment regimen in the advanced or metastatic setting according to tumor type, if such a therapy exists
Prior anti-cancer treatments such as chemotherapy, radiotherapy, or hormonal are permitted for some participants
Willing and able to comply with all study procedures
Exclusion Criteria
Primary central nervous system (CNS) malignancies, tumors with CNS metastases as the only site of disease or active brain metastases will be excluded
Other active malignancy requiring concurrent intervention
Prior organ allograft
Active, known, or suspected autoimmune disease Other protocol-defined inclusion/exclusion criteria apply
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT03369223.
Locations matching your search criteria
United States
Maryland
Baltimore
Johns Hopkins University/Sidney Kimmel Cancer Center