OncoMatch

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 (Jun 2026). This Phase 1 trial studies Super CAR-T for advanced hepatocellular carcinoma (hcc).

Phase 1RecruitingGuangzhou FineImmune Biotechnology Co., LTD.NCT07493044Data as of Jun 2026Location: China

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

Treatments studied

Other

Super CAR-T

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)

Demographics

Ages ≤ 75

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.

Frequently asked questions

Is NCT07493044 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior radiotherapy, systemic chemotherapy, immune checkpoint inhibitor disqualifies patients from enrollment.

Does this trial require GPC3?

Yes, GPC3 positive expression is a required biomarker for enrollment.

What disease stage is eligible?

Stage IIA or IIB or IIIA or IIIB is required.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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