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Clinical Trial Summary

The study participant has one of the following blood cancers: acute myelogenous leukemia (AML)/myelodysplastic syndrome (MDS), acute lymphoblastic leukemia (B-ALL, T-ALL) or Lymphoma. Your cancer has been difficult to treat (refractory) or has come back after treatment (relapse). Primary Objective To determine the safety and maximum tolerated dose of intravenous infusions of escalating doses of CD70-CAR T cells in patients (≤21 years) with recurrent/refractory CD70+ hematological malignancies after lymphodepleting chemotherapy. Secondary Objectives To evaluate the antileukemic activity of CD70-CAR T cells. We will determine the anti- leukemic activity of the CD70-CAR T cells in the bone marrow and in the treatment of extramedullary disease.


Clinical Trial Description

The primary interventions are a lymphodepleting chemotherapy regimen (fludarabine and cyclophosphamide), followed by a single autologous infusion of CD70-CAR T cells. Phase I study evaluating three (3) dose levels of CD70-CAR T cells. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06326463
Study type Interventional
Source St. Jude Children's Research Hospital
Contact Swati Naik, MBBS
Phone 866-278-5833
Email referralinfo@stjude.org
Status Recruiting
Phase Phase 1
Start date July 2024
Completion date July 1, 2031

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