The purposed of this research is to study the safety and clinical activity of the combination of nivolumab and cabiralizumab in people with resectable biliary tract cancers (BTC).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Nivolumab 3 mg/kg will be given intravenously (IV) through a vein in the arm over 30 minutes every 2 weeks. (Cycle length 2 weeks).
Cabiralizumab 4 mg/kg given IV for 30 minutes, 30 minutes after Nivolumab infusion is completed, every 2 weeks. (Cycle length 2 weeks).
Number of participants experiencing study drug-related toxicities
Number of participants experiencing drug-related adverse events as defined by CTCAE v5.0
Time frame: 4 years
Overall survival (OS)
Number of months from the date of first treatment until death or end of follow-up.
Time frame: 4 years
Disease free survival (DFS)
Number of months until disease recurrence.
Time frame: up to 4 years
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