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OncoMatch/Clinical Trials/NCT07493044

An Open-Label, Phase I Clinical Trial of Super CAR-T With GPC3-Positive Advanced Hepatocellular Carcinoma

Is NCT07493044 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies Super CAR-T for advanced hepatocellular carcinoma (hcc).

Phase 1RecruitingGuangzhou FineImmune Biotechnology Co., LTD.NCT07493044Data as of May 2026

Treatment: Super CAR-TThis study was a phase I safety and tolerability clinical trial conducted in a single-center, open-label, 3+3 design with dose escalation.

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Extracted eligibility criteria

Cancer type

Hepatocellular Carcinoma

Biomarker criteria

Required: GPC3 positive expression (positive)

Disease stage

Required: Stage IIA, IIB, IIIA, IIIB

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 2 prior lines

Must have received: standard systemic therapy

Previous failure of or intolerance to at least two lines of standard systemic therapy

Cannot have received: radiotherapy

Exception: within 2 weeks prior to apheresis

Received radiotherapy...within 2 weeks prior to apheresis

Cannot have received: systemic chemotherapy

Exception: within 2 weeks prior to apheresis

Received...systemic chemotherapy...within 2 weeks prior to apheresis

Cannot have received: immune checkpoint inhibitor

Exception: within 2 weeks prior to apheresis

Received...immune checkpoint inhibitors for the study disease within 2 weeks prior to apheresis

Cannot have received: small-molecule targeted therapy (sorafenib, regorafenib, lenvatinib)

Exception: within 1 week prior to apheresis

received small-molecule targeted therapies such as sorafenib, regorafenib, or lenvatinib within 1 week prior to apheresis

Cannot have received: systemic glucocorticoid therapy

Exception: within 7 days prior to single-plasma donation; inhaled/topical/physiological-dose replacement therapy permitted

Received systemic glucocorticoid therapy within 7 days prior to single-plasma donation; patients currently using or who have recently used inhaled or topical glucocorticoids, as well as those on physiological-dose replacement therapy, are eligible for enrollment

Lab requirements

Blood counts

ANC ≥1.0×10⁹/L; PLT ≥75×10⁹/L; Hb ≥ 75 g/L

Kidney function

Creatinine clearance ≥ 60 mL/min

Liver function

AST ≤ 5×ULN; ALT ≤ 5×ULN; TBIL ≤ 3×ULN; Child-Pugh liver function score ≤ 7

Cardiac function

Echocardiography showing a left ventricular ejection fraction (LVEF) ≥50%

Child-Pugh liver function score ≤ 7; ANC ≥1.0×10⁹/L; PLT ≥75×10⁹/L; Hb ≥ 75 g/L; Creatinine clearance ≥ 60 mL/min; AST ≤ 5×ULN; ALT ≤ 5×ULN; TBIL ≤ 3×ULN; Echocardiography showing a left ventricular ejection fraction (LVEF) ≥50%

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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