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OncoMatch/Clinical Trials/NCT06589089

Autologous Hematopoietic Stem Cell Boost Study After CAR-T Therapy

Is NCT06589089 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies autologous hematopoietic stem cell for diffuse large b cell lymphoma.

Phase 2RecruitingRuijin HospitalNCT06589089Data as of Jun 2026Location: China

Treatment: autologous hematopoietic stem cellThis is a prospective, single-arm, open study to observe the efficacy and safety of the CART-SCB regimen (Clinical Regimen for the Prospective Study of Autologous Hematopoietic Stem Cell Boost for the Improvement of Bone Marrow Suppression in Patients with High-Risk Immunohematologic Toxicity Lymphoma After Chimeric Antigen Receptor T (CAR-T)-Cell Immunotherapy Therapy) . After the patient has completed CAR-T therapy, if the patient has unrelieved hematologic toxicity, consider infusing a reserve of stem cells; if myelosuppression has not been significantly relieved, stem cell infusion can be performed again.

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Extracted eligibility criteria

Treatments studied

Other

autologous hematopoietic stem cell

Cancer type

Diffuse Large B-Cell Lymphoma

Non-Hodgkin Lymphoma

Prior therapy

Must have received: CAR-T cell therapy

Prior CAR-T cell immunotherapy

Cannot have received: allogeneic hematopoietic stem cell transplantation

History of allogeneic hematopoietic stem cell transplantation

Lab requirements

Blood counts

Myelosuppression as determined by the investigator has occurred after CAR-T therapy

Cardiac function

Severe cardiovascular disease: grade II or greater myocardial ischemia or myocardial infarction, poorly controlled arrhythmias; grade III-IV cardiac insufficiency according to NYHA criteria, or cardiac ultrasound suggestive of a left ventricular ejection fraction (LVEF) <50%

Adequate organ function; Myelosuppression as determined by the investigator has occurred after CAR-T therapy; Suffering from severe cardiovascular disease: grade II or greater myocardial ischemia or myocardial infarction, poorly controlled arrhythmias; grade III-IV cardiac insufficiency according to New York Heart Association (NYHA) criteria, or cardiac ultrasound suggestive of a left ventricular ejection fraction (LVEF) <50%

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

Frequently asked questions

Is NCT06589089 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior allogeneic hematopoietic stem cell transplantation 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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