RecruitingPhase 1Phase 2NCT07523555

Adaptive Dual-Target CAR-T Cells for Relapsed or Refractory Hematologic Malignancies

A Phase 1/2, Open-Label, Nonrandomized, Multi-arm Umbrella Study of Biomarker-Selected Dual-Target CAR-T Cell Modules in Adults With Relapsed or Refractory Hematologic Malignancies


Sponsor

Beijing Biotech

Enrollment

96 participants

Start Date

Mar 2, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Phase 1/2 umbrella study evaluates biomarker-selected dual-target CAR-T cell modules for adults with relapsed or refractory hematologic malignancies. After central antigen co-expression screening, participants are assigned to the most appropriate active dual-target module: CD19/CD22, CD19/CD20, BCMA/CD19, BCMA/CD38, BCMA/GPRC5D, CD33/CD123, CD33/CLL1, or CD5/CD7. Phase 1 determines safety, dose-limiting toxicities, and the recommended phase 2 dose for each module; phase 2 estimates preliminary antitumor activity, including overall response rate and MRD-negative response. Lymphodepletion with fludarabine/cyclophosphamide precedes infusion. The design is intended to reduce antigen escape by matching disease biology and target co-expression to a rational dual-target strategy.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a biological treatment called Autologous BCMA/CD19 dual-target CAR-T module, a biological treatment called Autologous BCMA/CD38 dual-target CAR-T module, and others for people with bpdcn; relapsed/refractory t-cell acute lymphoblastic leukemia, peripheral t cell lymphoma, and other related conditions. The study is currently recruiting participants at 1 location.

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

BIOLOGICALAutologous CD19/CD22 dual-target CAR-T module

Biological: Autologous CD19/CD22 dual-target CAR-T module after lymphodepletion with fludarabine/cyclophosphamide.

BIOLOGICALAutologous CD19/CD20 dual-target CAR-T module

Biological: Autologous CD19/CD20 dual-target CAR-T module after lymphodepletion with fludarabine/cyclophosphamide.

BIOLOGICALAutologous BCMA/CD19 dual-target CAR-T module

Biological: Autologous BCMA/CD19 dual-target CAR-T module after lymphodepletion with fludarabine/cyclophosphamide.

BIOLOGICALAutologous BCMA/CD38 dual-target CAR-T module

Biological: Autologous BCMA/CD38 dual-target CAR-T module after lymphodepletion with fludarabine/cyclophosphamide.

BIOLOGICALAutologous BCMA/GPRC5D dual-target CAR-T

Biological: Autologous BCMA/GPRC5D dual-target CAR-T module after lymphodepletion with fludarabine/cyclophosphamide

BIOLOGICALAutologous CD33/CD123 dual-target CAR-T module

Biological: Autologous CD33/CD123 dual-target CAR-T module (simultaneous or planned sequential paired infusion, module-specific) after lymphodepletion.

BIOLOGICALAutologous CD33/CLL1 dual-target CAR-T module

Biological: Autologous CD33/CLL1 dual-target CAR-T module after lymphodepletion with fludarabine/cyclophosphamide.

BIOLOGICALAutologous CD5/CD7 dual-target CAR-T module

Biological: Autologous CD5/CD7 dual-target CAR-T module (including sequential paired infusion if needed for manufacturing/safety) after lymphodepletion.


Locations(1)

Peking University Shenzhen Hospital

Shenzhen, Guangdong, China

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NCT07523555


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