RecruitingPhase 1Phase 2NCT06625190

Alpha/Beta T and B Cell Depletion With Zoledronic Acid for Solid Tumors

Allogeneic Stem Cell Transplantation Utilizing Alpha/Beta T Cell and CD19+ B Cell Depletion With Zoledronic Acid in Combination to Treat Pediatric, Adolescent, and Young Adult Patients With Relapsed/Refractory Solid Tumors


Sponsor

University of Florida

Enrollment

27 participants

Start Date

Feb 11, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Hematopoietic stem cell transplantation can cure patients with blood cancer and other underlying diseases. αβ-T cell and B cell depletion has been introduced to decrease GVHD and PTLD and has demonstrated effectiveness for hematologic malignancies and non-malignant diseases additionally increasing the donor pool as to allow for haploidentical transplant to safely occur. While solid tumors can be highly chemotherapy sensitive, many remain resistant and require multimodalities of treatment. Immunotherapy has been developed to harness the immune system in fighting solid tumors, though not all have targeted effects. Some solid tumors are treated with autologous transplants; however, they do not always demonstrate an improved event free survival or overall survival. There has been evidence of the use of allogeneic stem cell transplants to provide a graft versus tumor effect, though studies remain limited. By utilizing αβ-T cell and B cell depletion for stem cell transplants and combining with zoledronic acid, the immune system may potentially be harnessed and enhanced to provide an improved graft versus tumor effect in relapsed/refractory solid tumors and promote an improved event-free survival and overall survival. This study will investigate the safety of treatment with a stem cell graft depleted of αβ-T cell and CD19+ B cells in combination with zoledronic acid in pediatric and young adult patients with select solid tumors, as well as whether this treatment improves survival rates in these patients.


Eligibility

Min Age: 6 MonthsMax Age: 25 Years

Plain Language Summary

Simplified for easier understanding

This trial tests a stem cell transplant approach for children and young adults with hard-to-treat solid tumors. It uses a donor's stem cells (from a partially matched family member) along with a bone-strengthening drug called zoledronic acid, aiming to harness the donor's immune system to fight the cancer. **You may be eligible if...** - You are between 6 months and 25 years old - You have a relapsed or treatment-resistant solid tumor such as neuroblastoma, rhabdomyosarcoma, osteosarcoma, Ewing sarcoma, or other high-risk tumors - A standard stem cell transplant using your own cells failed or is not an option - You have a partially matched family donor available - Your heart, lungs, and kidneys are functioning at adequate levels **You may NOT be eligible if...** - You have an active uncontrolled infection - You received an unrelated donor transplant within the last 6 months - Your life expectancy is less than 3 months - You are of childbearing potential and unwilling to use contraception Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEMiltenyi CliniMACS Prodigy ® system

Subjects will receive an allogeneic stem cell transplant that has been depleted of ⍺/β T-cells and CD19+ B-cells using the Miltenyi CliniMACS Prodigy® system.

DRUGZoledronic acid

All subjects will receive zoledronic acid intravenously on days +28, +56, +84, +112, and +140. Dosing in the phase Ib portion of the study will follow a 3 + 3 design where the first 3 subjects will receive the expected phase II dose of 1.25 mg/m2 (dose level 1). If no dose-limiting toxicities (DLTs) occur in these subjects, dose level 1 will be the maximum tolerated dose. However, if at least 1 DLT is observed in the first 3 patients, 3 additional subjects will be enrolled at dose level 1. If more than 2 DLTs are observed in these 6 subjects, then dose de-escalation to 0.8 mg/m2 (dose level 0) will occur and 3-6 additional subjects may be enrolled. All subjects in the phase II portion of the study will receive the maximum tolerated dose determined in the phase Ib portion.


Locations(1)

University of Florida

Gainesville, Florida, United States

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NCT06625190


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