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OncoMatch/Clinical Trials/NCT02508038

Alpha/Beta CD19+ Depleted Haploidentical Transplantation + Zometa for Pediatric Hematologic Malignancies and Solid Tumors

Is NCT02508038 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies Zoledronate for acute myeloid leukemia.

Phase 1RecruitingUniversity of Wisconsin, MadisonNCT02508038Data as of May 2026

Treatment: ZoledronateThis phase I trial studies the safety of transplantation with a haploidentical donor peripheral blood stem cell graft depleted of TCRαβ+ cells and CD19+ cells in conjunction with the immunomodulating drug, Zoledronate, given in the post-transplant period to treat pediatric patients with relapsed or refractory hematologic malignancies or high risk solid tumors.

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Extracted eligibility criteria

Cancer type

Acute Myeloid Leukemia

Acute Lymphoblastic Leukemia

Hodgkin Lymphoma

Non-Hodgkin Lymphoma

Myelodysplastic Syndrome

Rhabdomyosarcoma

Sarcoma

Glioblastoma

Osteosarcoma

Neuroblastoma

Prior therapy

Must have received: hematopoietic stem cell transplant — auto-HSCT ineligible or failed

Patients with hematologic malignancy must have no HLA identical sibling or suitable unrelated donor OR time needed to find an acceptable unrelated donor match would likely result in disease progression such that the patient may become ineligible for any type of potentially curative transplant

Must have received: hematopoietic stem cell transplant — auto-HSCT ineligible or failed

Patients with solid tumor must have failed or have been ineligible to receive auto-HSCT or if auto-HSCT would not offer > 20% chance of cure

Lab requirements

Kidney function

Glomerular Filtration Rate (GFR) ≥ 60 ml/min/1.73m2

Liver function

Total bilirubin < 3 mg/dL; ALT (alanine aminotransferase, SCPT) ≤ 5 x Upper Limit of Normal (ULN) for age

Cardiac function

Ejection fraction of > 40% by Multigated Acquisition Scan (MUGA) or echocardiogram

Total bilirubin < 3 mg/dL; ALT (alanine aminotransferase, SCPT) ≤ 5 x Upper Limit of Normal (ULN) for age; Glomerular Filtration Rate (GFR) ≥ 60 ml/min/1.73m2; Ejection fraction of > 40% by Multigated Acquisition Scan (MUGA) or echocardiogram

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • University of Wisconsin Carbone Cancer Center · Madison, Wisconsin

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