CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 69 enrolled / 69 target
Drug / intervention
Cyclophosphamide +11 moredrug
Likely dose
60 mg/kgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03849651
NCT03849651Phase 2ActiveUpdate Overdue (0.8/mo)Completion was 22mo ago

TCRαβ-depleted Progenitor Cell Graft With Additional Memory T-cell DLI, Plus Selected Use of Blinatumomab, in Naive T-cell Depleted Haploidentical Donor Hematopoietc Cell Transplantation for Hematologic Malignancies

St. Jude Children's Research Hospital·interventional·Posted Feb 21, 2019·Updated Jun 3, 2026

In Brief

A Phase 2 clinical trial evaluating Cyclophosphamide, Fludarabine, and 10 other interventions for Acute Lymphoblastic Leukemia (ALL) and 7 related conditions. Active but no longer recruiting, targeting 69 participants across 1 site.

Signals

Enrollment appears stalled

Detailed Summary

Patients less than or equal to 21 years old with high-risk hematologic malignancies who would likely benefit from allogeneic hematopoietic cell transplantation (HCT). Patients with a suitable HLA matched sibling or unrelated donor identified will be eligible for participation ONLY if the donor is not available in the necessary time. The purpose of the study is to learn more about the effects (good and bad) of transplanting blood cells donated by a family member, and that have been modified in a laboratory to remove the type of T cells known to cause graft-vs.-host disease, to children and young adults with a high risk cancer that is in remission but is at high risk of relapse. This study will give donor cells that have been TCRαβ-depleted. The TCR (T-cell receptor) is a molecule that is found only on T cells. These T-cell receptors are made up of two proteins that are linked together. About 95% of all T-cells have a TCR that is composed of an alpha protein linked to a beta protein, and these will be removed. This leaves only the T cells that have a TCR made up of a gamma protein linked to a delta protein. This donor cell infusion will be followed by an additional infusion of donor memory cells (CD45RA-depleted) after donor cell engraftment. This study will be testing the safety and effects of the chemotherapy and the donor blood cell infusions on the transplant recipient's disease and overall survival.

Study Details

Timeline

Phase 2ActiveOverdue
20192020202120222023202420252026
First PostedFeb 21, 2019
Enrollment StartJan 31, 2019
Primary CompletionAug 7, 2024
Study CompletionJun 7, 2026
TodayJul 2, 2026
Enrollment to primary: 5.5 yearsPosted 7.4 years ago

Arms & Interventions

Transplant participantsexperimental

Participants receive a conditioning regimen of ATG (rabbit),Cyclophosphamide 60 mg/kg intravenous once daily, mesna, fludarabine, thiotepa, melphalan, followed by HPC,A Infusion(TCRα/β+ and CD19+ depleted),HPC, A infusion (if needed to achieve goal CD34+ cell dose.CD45RA-depleted DLI will be given at least two weeks after engraftment. Blinatumomab will be given at least one week post-DLI, and only to patients with CD19+ malignancies. G-csf 5mcg/kg subcutaneous or intravenous daily until ANC \>2000 for 2 consecutive days. Cells for infusion are prepared using the CliniMACS system.

Drug: CyclophosphamideBiological: FludarabineDrug: ThiotepaDrug: MelphalanBiological: G-csfDrug: MesnaDevice: CliniMACSBiological: ATG (rabbit)Drug: BlinatumomabBiological: TCRα/β+Biological: CD19+Biological: CD45RA-depleted DLI

Interventions

Cyclophosphamidedrug

Cyclophosphamide is a nitrogen mustard derivative. It acts as an alkylating agent that causes cross-linking of DNA strands by binding with nucleic acids and other intracellular structures, thus interfering with the normal function of DNA. intravenously (IV) once daily (QD) on day -9

Fludarabinebiological

Fludarabine phosphate is a synthetic purine nucleoside analog. It acts by inhibiting DNA polymerase, ribonucleotide reductase and DNA primase by competing with the physiologic substrate, deoxyadenosine triphosphate, resulting in inhibition of DNA synthesis. fludarabine phosphate IV QD on days -8 to -4

Thiotepadrug

Thiotepa is a cell-cycle nonspecific polyfunctional alkylating agent.

Melphalandrug

Melphalan, a derivative of nitrogen mustard, is a bifunctional alkylating agent. Melphalan is active against tumor cells that are actively dividing or at rest. melphalan IV QD on days -2 to -1

G-csfbiological

G-csf (granulocytic colony stimulating factor), is a biosynthetic hematopoietic agent that is made using recombinant DNA technology in cultures of Escherichia coli. G-CSF stimulates production, maturation and activation of neutrophils. In addition, endogenous G-CSF enhances certain functions of mature neutrophils, including phagocytosis, chemotaxis and antibody--dependent cellular cytotoxicity.

Mesnadrug

Mesna is a synthetic sulfhydryl (thiol) compound. Mesna contains free sulfhydryl groups that interact chemically with urotoxic metabolites of oxaza-phosphorine derivatives such as cyclophosphamide and ifosfamide. Following glomerular filtration, mesna disulfide is rapidly reduced in the renal tubules back to mesna, the active form of the drug.

CliniMACSdevice

Cells for infusion are prepared using the CliniMACS

ATG (rabbit)biological

Anti-thymocyte globulin is a purified, pasteurized, gamma immune globulin, obtained by immunization of rabbits with human thymocytes. rabbit anti-thymocyte globulin IV daily over 6 hours on days -5 to -3,

Blinatumomabdrug

Blinatumomab is a bispecific CD19-directed CD3 T-cell engager that mediates formation of a synapse between T cells and the CD19+ target cell, resulting in lysis of that CD19+ cell.Blinatumomab will be given to patients with a history of CD19+ malignancy as determined by St. Jude hematopathologist review of current and historical specimens and reports. blinatumomab IV for 28 days beginning at least 1 week post-DLI

TCRα/β+biological

IV on day 0 and may receive an additional dose on day 1

CD19+biological

IV on day 0 and may receive an additional dose on day 1

CD45RA-depleted DLIbiological

infusion IV