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ACTIVE NOT RECRUITING
NCT03620058
PHASE1

CART22 Alone or in Combination With huCART19 for ALL

Sponsor: University of Pennsylvania

View on ClinicalTrials.gov

Summary

This is a single center, open-label, phase 1 study to determine the safety and feasibility of infusing CART22-65s with or without huCART19 after administration of lymphodepleting chemotherapy in adult patients with relapsed or refractory B-ALL.

Official title: Phase 1 Study of Autologous Anti-CD22 Chimeric Antigen Receptor Redirected T Cells (CART22-65s) Alone and When Co-administered With Humanized Anti-CD19 Chimeric Antigen Receptor Redirected T Cells (huCART19) In Patients With Chemotherapy Resistant Or Refractory Acute Lymphoblastic Leukemia

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

23

Start Date

2018-09-27

Completion Date

2036-01

Last Updated

2025-10-14

Healthy Volunteers

No

Interventions

BIOLOGICAL

CART22-65s cells

Autologous T cells transduced with a lentiviral vector to express anti-CD22 scFv TCRz:41BB

BIOLOGICAL

huCART19 Cells

Autologous T cells transduced with lentiviral vector to express anti-CD19 scFv TCRζ:4-1BB

Locations (1)

University of Pennsylvania

Philadelphia, Pennsylvania, United States