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A Pediatric and Young Adult Trial of Genetically Modified T Cells Directed Against CD19 for Relapsed/Refractory CD19+ Leukemia

Active, not recruiting · Phase 1, Phase 2 · NCT02028455

Conditions: CD19+ Acute Leukemia

At a glance

Research payments reported, 2025
$4.3M
U.S. investigators named
14
Sites paid
12
Planned or actual enrollment
167

About the trial

Sponsor
Seattle Children's Hospital
Tested
Patient Derived CD19 specific CAR T cells also expressing an EGFRt (biological)
Dates
Started 2014-02-11; completion 2036-07
Results posted
Yes

Patients with relapsed or refractory leukemia often develop resistance to chemotherapy. For this reason, we are attempting to use T cells obtained directly from the patient, which can be genetically modified to express a chimeric antigen receptor (CAR). The CAR enables the T cell to recognize and kill the leukemic cell through the recognition of CD19, a protein expressed of the surface of the leukemic cell in patients with CD19+ leukemia. This is a phase 1/2 study designed to determine the maximum tolerated dose of the CAR+ T cells as well as to determine the efficacy. The phase 1 cohort is restricted to those patients who have already had an allogeneic hematopoietic cell transplant (HCT)…

From ClinicalTrials.gov, last updated 2026-08-06. Full record, eligibility and contacts (opens in a new tab)

Industry funding

E.r. Squibb & Sons, L.l.c. reported $4.3M in research payments for this study in 2025 (15 payments).

Products named: Breyanzi

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.