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OncoMatch/Clinical Trials/NCT07306156

GP350 CAR-T for Relapse/Refractory and Epstein-Barr Virus Infection Associated Lymphoid Neoplasms

Is NCT07306156 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies GP350 CAR-T for ebv associated lymphoid neoplasms.

Phase 1/2RecruitingZhimin ZhaiNCT07306156Data as of Jun 2026Location: China

Treatment: GP350 CAR-TThis is a Phase 1/Phase 2 open-label, single-arm clinical study of GP350 CAR-T for Relapse/Refractory and Epstein-Barr virus infection associated lymphoid neoplasms. Each participant will undergo leukapheresis after enrolment, receive treatment of the conditioning chemotherapy, and an intravenous infusion of CAR-T cells. Each participant will proceed through the following study procedures: * Screening * Enrollment/Leukapheresis * Conditioning chemotherapy * CAR T treatment * Post-treatment assessment * Long-term follow-up

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Extracted eligibility criteria

Treatments studied

Other

GP350 CAR-T

Biomarker criteria

Required: GP350 positivity (≥10% of tumor cells) (≥10% of tumor cells)

Tumor cell GP350 positivity (≥10% of tumor cells by immunohistochemistry or flow cytometry)

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Ages ≤ 70

Lab requirements

Blood counts

ANC ≥1.0×10⁹/L; Hemoglobin >60 g/L; CD3+ T-cell count >0.5×10⁹/L; Platelet count >30×10⁹/L

Kidney function

Creatinine clearance ≥60 mL/min

Liver function

ALT/AST ≤2× ULN; Total bilirubin ≤2× ULN

Cardiac function

LVEF ≥50%, no pericardial effusion, no clinically significant ECG abnormalities; NYHA Class III or IV congestive heart failure [excluded]; Myocardial infarction or coronary artery bypass grafting within the past 6 months [excluded]; Clinically significant ventricular arrhythmia or unexplained syncope [excluded]; History of severe non-ischemic cardiomyopathy [excluded]; Cardiac insufficiency (LVEF <45%) within 8 weeks prior to apheresis [excluded]

Creatinine clearance ≥60 mL/min; ALT/AST ≤2× ULN; Total bilirubin ≤2× ULN; LVEF ≥50%, no pericardial effusion, and no clinically significant ECG abnormalities; Minimal or no pleural/ascitic fluid; Oxygen saturation ≥95%

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

Frequently asked questions

Is NCT07306156 currently recruiting?

Yes, this trial is currently recruiting patients.

Does this trial require GP350?

Yes, GP350 positivity (≥10% of tumor cells) is a required biomarker for enrollment.

Is there an age limit?

Yes. Patients must be 70 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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