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).
Treatment: Super CAR-T — This study was a phase I safety and tolerability clinical trial conducted in a single-center, open-label, 3+3 design with dose escalation.
Check if I qualifyExtracted eligibility criteria
Treatments studied
Other
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
Prior therapy
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.
Check if I qualifyRelated pages