This study is an open-label, multicenter, single-arm Phase II clinical study to evaluate the effectiveness of cadonilimab (AK104) in combination with anlotinib in the treatment of locally advanced or metastatic melanoma.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Injectable solution
capsule
Response Rate
ORR is the proportion of patients with best response of complete response (CR) and PR
Time frame: from the frst drug administration up to two years
Progression-free Survival (PFS)
Time from the date of frst study treatment administration to the date of first
Time frame: from the frst drug administration up to two years
Disease Control Rate (DCR)
Proportion of patients whose best overall response is either CR, PR, or SD
Time frame: from the frst drug administration up to two years
Safety and tolerability
Incidence, nature, and severity of adverse events graded according to the NCI CTCAE
Time frame: from the frst drug administration up to two years
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