This is a multicenter, randomized, open-label clinical study to evaluate the efficacy and safety of Adebrelimab plus Apatinib (cohort 1), or Adebrelimab plus Bevacizumab (cohort 2), or Camrelizumab plus Apatinib (cohort 3) as first-line treatment of unresectable HCC.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
111
Adebrelimab 1200mg intravenously every 3 weeks plus Apatinib 250mg orally once daily
Adebrelimab 1200mg intravenously plus Bevacizumab 15 mg/kg intravenously every 3 weeks
camrelizumab 200mg intravenously every 2 weeks plus Apatinib 250mg orally once daily
Beijing Cancer Hospital
Beijing, Beijing Municipality, China
RECRUITING12-month overall survival rate
Time frame: Up to approximately 3 years
ORR
Assessed by the investigator per RECIST v1.1 criteria
Time frame: Up to approximately 3 years
DCR
Assessed by the investigator per RECIST v1.1 criteria
Time frame: Up to approximately 3 years
DoR
Assessed by the investigator per RECIST v1.1 criteria
Time frame: Up to approximately 3 years
TTR
Assessed by the investigator per RECIST v1.1 criteria
Time frame: Up to approximately 3 years
TTP
Assessed by the investigator per RECIST v1.1 criteria
Time frame: Up to approximately 3 years
PFS
Assessed by the investigator per RECIST v1.1 criteria
Time frame: Up to approximately 3 years
OS
Time frame: Up to approximately 3 years
safety according to NCI Common Terminology Criteria for Adverse Events, version 5.0.
Time frame: Up to approximately 3 years
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