RecruitingPhase 1NCT06395870

Targeting CD19/CD20 Dual-targeted Cell in Patients With Relapsed/Refractory B-cell Non-Hodgkin Lymphoma

A Phase I, Open-label Clinical Study to Evaluate the Safety, Tolerability, and Efficacy of LUCAR-G39D, a Dual-targeted Cell Preparation Targeting CD19/CD20, in Patients With Relapsed/Refractory B-cell Non-Hodgkin Lymphoma


Sponsor

Tianjin Medical University Cancer Institute and Hospital

Enrollment

33 participants

Start Date

May 9, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

A phase I, open-label clinical study to evaluate the safety, tolerability, and efficacy of LUCAR-G39D, a dual-targeted cell preparation targeting CD19/CD20, in patients with relapsed/refractory B-cell non-Hodgkin lymphoma.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This study tests a new CAR-T cell therapy that targets two proteins at once — CD19 and CD20 — on cancer cells in patients with B-cell lymphoma or leukemia that has come back or stopped responding to other treatments. **You may be eligible if...** - You have been diagnosed with relapsed or refractory B-cell lymphoma or B-cell acute lymphoblastic leukemia - Your cancer expresses CD19, CD20, or both proteins - You have received at least two prior lines of treatment - You are at least 18 years old with adequate organ function **You may NOT be eligible if...** - You have active brain involvement from your lymphoma - You have serious active infections (including untreated HIV or hepatitis) - You have received prior CAR-T cell therapy targeting CD19 or CD20 recently - You are pregnant or breastfeeding - You have serious heart, liver, or kidney problems 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-G39D cells product

Prior to infusion of the LUCAR-G39D, subjects will receive a conditioning premedication regimen consisting of cyclophosphamide and fludarabine.


Locations(2)

Oncology Department, The First Affiliated Hospital of USTC west district

Hefei, Anhui, China

Tianjin Cancer Hospital

Tianjin, China

View Full Details on ClinicalTrials.gov

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NCT06395870


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