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Primary, Booster and Consolidation Multi-CAR-T Cell Therapy for the Treatment of Refractory B Cell Lymphomas

Who is this study for? Child to adult patients with Primary B Cell Lymphoma
What treatments are being studied? 4S-Engineered CD19/CD20/CD22/CD70/PSMA/CD13/CD79b/GD2-Positive CAR-T Cells
Status: Recruiting
Location: See all (2) locations...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

This study aims to evaluate safety and efficacy of a combination of 4th generation chimeric antigen receptor gene-modified T cells targeting B cell surface molecules including CD19 and alternative CARTs as booster and consolidation treatment for patients with highly resistant B cell lymphomas, including primary mediastinal B cell lymphoma (PMBCL) and BCL involving central nervous system (CNS-BCL). Clinical response and development of a simplified and standardized lentiviral vector and cell production protocol will be investigated. This is a phase I/II trial enrolling patients from multiple clinical centers.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 6 months
Maximum Age: 75
Healthy Volunteers: f
View:

• Age older than 6 months.

• Primary B cell lymphoma surface expression of CD19 and/or CD22/CD70/PSMA/ CD13/CD79b/GD2 molecules.

• The KPS score over 80 points, and survival time is more than 1 month.

• Greater than Hgb 80 g/L.

• No contraindications to blood cell collection.

Locations
Other Locations
China
Shenzhen Geno-Immune Medical Institute
RECRUITING
Shenzhen
The Seventh Affilliated Hospital, Sun Yat-Sen University
RECRUITING
Shenzhen
Contact Information
Primary
Lung-Ji Chang, Ph.D
c@szgimi.org
+86 0755 86573763
Time Frame
Start Date: 2026-06-01
Estimated Completion Date: 2030-12-31
Participants
Target number of participants: 11
Treatments
Experimental: 4SCAR19 and 4SCAR20/22/70/PSMA/13/79b/GD2
Patients who have relapsed and refractory B cell lymphoma (BCL) after chemotherapy will be treated with a combination of 4SCAR gene-engineered T cells.
Related Therapeutic Areas
Sponsors
Collaborators: The Seventh Affiliated Hospital of Sun Yat-sen University
Leads: Shenzhen Geno-Immune Medical Institute

This content was sourced from clinicaltrials.gov

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