This is an open-label, phase II,multi-center study to evaluate the efficacy, safety and tolerability of KN026 in combination with KN046 in subjects with HER2-positive solid tumors.
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Objective response rate (ORR )
Timeframe: Throughout the duration of the study; up to 2 years
Duration of response (DOR)
Timeframe: Throughout the duration of the study; up to 2 years