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OncoMatch/Clinical Trials/NCT07284927

Clinical Study of LV009 Injection for the Treatment of Hematologic and Lymphoid Malignancies

Is NCT07284927 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies LV009 for non-hodgkin lymphoma.

Phase 1RecruitingPersonGen BioTherapeutics (Suzhou) Co., Ltd.NCT07284927Data as of May 2026

Treatment: LV009This clinical trial is designed as a single-arm, open-label, single-center, investigator-initiated, early-phase study. Its primary objective is to evaluate the safety of LV009 Injection in subjects with relapsed/refractory CD19-positive hematolymphoid malignancies.

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Extracted eligibility criteria

Cancer type

Non-Hodgkin Lymphoma

Acute Lymphoblastic Leukemia

Biomarker criteria

Required: CD19 overexpression (positive)

confirmed diagnosis of CD19-positive hematolymphoid malignancy

Performance status

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

Prior therapy

Must have received: relapsed or refractory disease

Meets the National Comprehensive Cancer Network (NCCN) criteria for relapsed or refractory disease

Cannot have received: CAR-T cell therapy

Patients who have received CAR-T therapy or other genetically modified cell therapies prior to screening.

Lab requirements

Blood counts

ALC ≥ 0.5 × 10⁹/L; Platelet count ≥ 50 × 10⁹/L; CD3-positive T-cell count ≥ 150 cells/μL

Kidney function

adequate renal function

Liver function

adequate hepatic function

Cardiac function

adequate cardiopulmonary function

Adequate hepatic, renal, and cardiopulmonary function; ALC ≥ 0.5 × 10⁹/L; Platelet count ≥ 50 × 10⁹/L; CD3-positive T-cell count ≥ 150 cells/μL

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

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