RecruitingPhase 1NCT06313957

A Study of LUCAR-20SP in Subjects With Relapsed/Refractory B-cell Non-Hodgkin Lymphoma

A Phase I Clinical Study to Evaluate the Safety, Tolerability, and Efficacy of LUCAR-20SP, an Allogenic Chimeric Antigen Receptor(CAR)-T Cell Therapy Targeting CD20 in Subjects With Relapsed/Refractory B-cell Non-Hodgkin Lymphoma


Sponsor

Peking University Cancer Hospital & Institute

Enrollment

42 participants

Start Date

Mar 14, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This is a prospective, single-arm, open-label, exploratory clinical study of LUCAR-20SP in adult subjects with relapsed/refractory B-cell non-Hodgkin lymphoma.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new CAR-T cell therapy called LUCAR-20SP for patients with B-cell non-Hodgkin lymphoma that has returned or stopped responding to previous treatments. CAR-T therapy involves taking a patient's own immune cells, engineering them in a lab to recognize and attack cancer cells, and infusing them back into the patient. **You may be eligible if...** - You are 18 years or older - You have been diagnosed with large B-cell lymphoma, follicular lymphoma, mantle cell lymphoma, or indolent lymphoma that has transformed — all confirmed by biopsy - Your cancer cells are CD20-positive (a protein on the surface of the cancer cells that the therapy targets) - Your cancer has returned or stopped responding to previous treatment - You have at least one measurable tumor on imaging - Your general health is good (ECOG 0–1) and your life expectancy is at least 3 months **You may NOT be eligible if...** - You have recently received other cancer treatments without an adequate washout period - You have previously received CAR-T or other gene/cell therapy (with some exceptions) - You have active uncontrolled infection or poor organ function Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BIOLOGICALLUCAR-20SP cells

Prior to infusion of the LUCAR-20SP, subjects will receive a conditioning premedication regimen consisting of cyclophosphamide and fludarabine.


Locations(3)

Beijing GoBroad Boren Hospital

Beijing, Beijing Municipality, China

Peking University Cancer Hospital & Institute

Beijing, Beijing Municipality, China

Henan Cancer Hospital

Zhengzhou, China

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NCT06313957


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