This study aims to investigate the efficacy and safety of SHR-1701 in combination with famitinib in the perioperative treatment of mucosal melanoma
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
70
Event-Free Survival, EFS
Time frame: From start of treatment to end of study, up to approximately 36 months
Overall Survival (OS)
Time frame: From start of treatment to end of study, up to approximately 36 months
Major Pathological Response (MPR)
Time frame: Perioperative
Recurrence-Free Survival (RFS)
Time frame: From surgery to end of study, up to ~36 months
Pathological Response Rate (pRR)
Time frame: Perioperative
Objective Response Rate (ORR)
Time frame: Perioperative
Adverse Events (AE)
Time frame: From informed consent to 30 days after last dose
Serious Adverse Events (SAE)
Time frame: From informed consent to 30 days after last dose
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