{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","value":"2"}]}],"title":"3 months"},{"categories":[{"measurements":[{"groupId":"OG000","value":"2"}]}],"title":"6 months"},{"categories":[{"measurements":[{"groupId":"OG000","value":"2"}]}],"title":"9 months"},{"categories":[{"measurements":[{"groupId":"OG000","value":"2"}]}],"title":"12 months"}],"denoms":[{"counts":[{"groupId":"OG000","value":"3"}],"units":"Participants"}],"description":"Progression-Free Survival will be measured as number of patients alive at 3, 6, 9 and 12 months.","groups":[{"description":"Nivolumab is a human monoclonal antibody (HuMAb; immunoglobulin G4 \\[IgG4\\]-S228P) that targets the programmed death-1 (PD-1) cluster of differentiation 279 (CD279) cell surface membrane receptor. PD-1 is a negative regulatory molecule expressed by activated T and B lymphocytes.1 Binding of PD-1 to its ligands, programmed death-ligands 1 (PD-L1) and 2 (PD-L2), results in the down-regulation of lymphocyte activation. Inhibition of the interaction between PD-1 and its ligands promotes immune responses and antigen-specific T-cell responses to both foreign antigens as well as self-antigens. Nivolumab will be delivered intravenously at a fixed dose of 240 mg on day 1 of 14 day cycles.\n\nCabiralizumab is a recombinant, humanized Immunoglobulin G4 (IgG4) monoclonal antibody that binds to human colony stimulating factor 1 receptor (CSF1R; c-fms). Cabiralizumab will be delivered intravenously at a dosage of 4 mg/kg on day 1 of 14 day cycles.","id":"OG000","title":"Nivolumab + Cabiralizumab"}],"paramType":"COUNT_OF_PARTICIPANTS","reportingStatus":"POSTED","timeFrame":"3, 6, 9 and 12 months post starting study treatment","title":"Progression-Free Survival (PFS)","type":"SECONDARY","unitOfMeasure":"Participants"}