To evaluate the efficacy and safety of Cadonilimab in combination with Regorafenib and Gem-Cis chemotherapy in advanced biliary tract Cancer
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Cadonilimab:10mg/kg, iv,q3w,D1 Regorafenib: 80mg, po, orally once daily Gemcitabine:1000 mg/m2, iv, Q3W,D1,D8 Cisplatin:25 mg/m2, iv, Q3W, D1,D8
Tianjin Cancer Hospital Airport Hospital
Tianjin, Tianjin Municipality, China
RECRUITINGOverall response rate ( ORR) per RECIST 1.1
Defined as proportion of patients who have a best response of CR or PR
Time frame: Up to 1 year
Overall survival (OS)
Defined as the time from enrollment to death from any cause
Time frame: Up to two years
Progress Free Survival (PFS)
Defined as the time from enrollment to disease progression or death (whichever occurs first)
Time frame: Up to two years
Adverse Events (AEs)
Defined as the proportion of patients with AE, treatment-related AE (TRAE), immune-related AE (irAE), serious adverse event (SAE), assessed by NCI CTCAE v5.0
Time frame: Up to two years
Disease control rate (DCR) per RECIST 1.1
Defined as proportion of patients who have CR or PR or SD
Time frame: Up to 1 year
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