The purposed of this research is to study the safety and clinical activity of the combination of durvalumab and a CSF-1R inhibitor (SNDX-6352) in people with Intrahepatic Cholangiocarcinoma.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Objective Response Rate (ORR) Per mRECIST (Modified RECIST)
Timeframe: 8 months
Number of Participants Experiencing Study Drug-related Toxicities
Timeframe: up to 1 year