Status and phase
Conditions
Treatments
Study type
Funder types
Identifiers
About
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.
Full 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.
Enrollment
Sex
Ages
Volunteers
Inclusion and exclusion criteria
Inclusion Criteria
Age ≤21 years old
Relapsed/refractory CD70+ hematological malignancy
Relapsed disease: Patients developing recurrent disease after a prior complete remission (CR)
Refractory disease: Patients with persistent disease despite 3 cycles of induction chemotherapy.
Relapsed/refractory CD70+ AML or MDS:
Relapsed/refractory CD70+ B-cell ALL:
Relapsed/refractory CD70+ T-cell ALL:
Mixed Phenotype Acute Leukemia (MPAL):
Relapsed/refractory CD70+ lymphoma:
Estimated life expectancy of >12 weeks
Karnofsky or Lansky (age- dependent) performance score ≥50
Patients with a history of prior allogeneic HCT must be clinically recovered from prior HCT therapy, have no evidence of active GVHD and have not received a donor lymphocyte infusion (DLI) within the 28 days prior to apheresis
Patient must have an identified HCT donor
For females of childbearing age:
i. Not lactating with intent to breastfeed
ii. Not pregnant with negative serum or urine pregnancy test within 7 days prior to enrollment
Exclusion Criteria
Primary purpose
Allocation
Interventional model
Masking
18 participants in 1 patient group
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Central trial contact
Swati Naik, MBBS
Data sourced from clinicaltrials.gov
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