This study is an open, multicenter Phase II clinical trial to evaluate the efficacy and safety of the SHR-A1811 combination in HER2 positive patients with locally advanced or metastatic biliary tract cancer.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
54
Affiliated Cancer Hospital of Harbin Medical University
Harbin, Heilongjiang, China
RECRUITINGZhongshan Hospital, Fudan University
Shanghai, Shanghai Municipality, China
RECRUITINGObjective response rate (ORR) of the SHR-A1811 combination evaluated by investigators
Time frame: Screening up to study completion, an average of 3 year.
Duration of response (DoR) of the SHR-A1811 combination evaluated by investigators
Time frame: Screening up to study completion, an average of 3 year.
Disease control rate (DCR) of the SHR-A1811 combination evaluated by investigators
Time frame: Screening up to study completion, an average of 3 year.
Progression free survival (PFS) of the SHR-A1811 combination evaluated by investigators
Time frame: Screening up to study completion, an average of 3 year.
Overall survival (OS) of the SHR-A1811 combination evaluated by investigators
Time frame: Screening up to study completion, an average of 3 year.
Adverse events (AEs)
Time frame: Screening up to study completion, an average of 3 year.
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