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OncoMatch/Clinical Trials/NCT03050190

A Phase I/II Multiple Center Trial of 4SCAR19 Cells in the Treatment of Relapsed and Refractory B Cell Malignancies

Is NCT03050190 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies non-drug interventions for b-cell malignancies.

Phase 1/2RecruitingShenzhen Geno-Immune Medical InstituteNCT03050190Data as of Jun 2026Location: China

The study will evaluate safety and efficacy of a 4th generation chimeric antigen receptor gene-modified T cells targeting CD19 (4SCAR19) for patients with B cell malignancies. Clinical response and development of a standardized lentiviral vector and cell production protocol will be investigated. This is a phase I/II trial enrolling patients from multiple clinical centers.

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Extracted eligibility criteria

Biomarker criteria

Required: CD19 surface expression

malignant B cell surface expression CD19 molecules

Demographics

Ages ≥ 0

Prior therapy

Cannot have received: CAR-T cell therapy

Exception: if previously used CAR-T but was invalid

confirmed before used CAR - but invalid

Lab requirements

Blood counts

hgb > 80 g/l

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

Frequently asked questions

Is NCT03050190 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior CAR-T cell therapy disqualifies patients from enrollment.

Does this trial require CD19?

Yes, CD19 surface expression is a required biomarker for enrollment.

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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