open-label trial of an allogeneic dual-target CAR-NK product directed against GPC3 and B7-H3 for adults with advanced hepatocellular carcinoma. The design intentionally uses GPC3 as the primary target anchor because GPC3 is the dominant HCC cell-therapy antigen in current clinical development, while adding B7-H3 to reduce antigen escape and to broaden coverage across tumor and tumor-microenvironment compartments. The study first evaluates safety and dose-limiting toxicities, then expands at the recommended phase 2 dose.
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Incidence of dose-limiting toxicities (DLTs)
Timeframe: 28 Days
Incidence, type, and severity of treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs)
Timeframe: 12 months