drugset / Trial / NCT03244306

A Phase 1 Study of CD22-CAR TCell Immunotherapy for CD22+ Leukemia and Lymphoma

NCT03244306 ↗

Phase 1 Completed 4 enrolled Seattle Children's Hospital
NaSingle-groupOpen-labelTreatment

Summary

Patients with relapsed or refractory leukemia often develop resistance to chemotherapy and some patients who relapse following CD19 directed therapy relapse with CD19 negative leukemia. For this reason, the investigators are attempting to use T-cells obtained directly from the patient, which can be genetically modified to express a chimeric antigen receptor (CAR) to CD22, a different protein from CD19, expressed on the surface of the leukemic cell in patients with CD22+ leukemia. The CAR enables the T-cell to recognize and kill the leukemic cell through the recognition of CD22, a protein expressed on the surface of the leukemic cell in patients with CD22+ leukemia. This is a Phase 1 study designed to determine the safety and feasibility of the CAR+ T - cells and the feasibility of making enough to treat patients with CD22+ leukemia.

Timeline

Start
2017-07-27
Primary completion
2018-11-14
Completion
2024-04-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Patient-derived CD22-specific CAR T-cells also expressing an EGFRt Cell therapy — —

Indications