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OncoMatch/Clinical Trials/NCT07473167

Study of Safety and Efficacy of TC011 in the Relapsed/Refractory Large B Cell Non-Hodgkin Lymphoma Patients

Is NCT07473167 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies TC011 for relapsed large b-cell lymphoma.

Phase 1/2RecruitingTICAROS Co., Ltd.NCT07473167Data as of Jun 2026Location: South Korea

Treatment: TC011This is a multi-center, phase I/II study to determine the safety and efficacy of TC011(CD19 Targeted CAR-T) in adult patients with relapsed or refractory large B-cell non -hodgkin lymphoma.

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Extracted eligibility criteria

Treatments studied

Other

TC011

Cancer type

Diffuse Large B-Cell Lymphoma

Non-Hodgkin Lymphoma

Performance status

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

Demographics

Ages ≥ 19

Prior therapy

Min 2 prior lines

Must have received: systemic chemotherapy

Relapsed/refractory after ≥2 prior lines of systemic chemotherapy

Cannot have received: anti-CD19 agent

Prior therapies such as anti-CD19 agents

Cannot have received: adoptive T-cell therapy

Prior therapies such as ... adoptive T-cell therapy

Cannot have received: gene therapy

Prior therapies such as ... gene therapy

Cannot have received: allogeneic HSCT

Prior therapies such as ... allogeneic HSCT

Lab requirements

Blood counts

adequate organ function

Kidney function

adequate organ function

Liver function

adequate organ function

Cardiac function

LVEF ≥40%; significant cardiac disease within 6 months [excluded]

Adequate organ, and pulmonary function; LVEF ≥40%; Significant cardiac disease within 6 months [excluded]

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

Frequently asked questions

Is NCT07473167 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior anti-CD19 agent, adoptive T-cell therapy, gene therapy disqualifies patients from 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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