Allogeneic HSCT With Low-Dose Post-Transplant Cyclophosphamide for GVHD Prevention

PHASE2Not yet recruitingINTERVENTIONAL
Enrollment

41

Participants

Timeline

Start Date

November 1, 2025

Primary Completion Date

August 1, 2030

Study Completion Date

August 1, 2031

Conditions
Graft-versus-Host Disease (GVHD)Hematologic MalignanciesAllogeneic Stem Cell Transplantation
Interventions
DRUG

Cyclophosphamide (primary intervention for GVHD prophylaxis)

This study evaluates the use of low-dose (25 mg/kg) post-transplant cyclophosphamide (PTCy) for prophylaxis of Graft-versus-Host Disease (GVHD) following allogeneic stem cell transplantation. The intervention involves administering PTCy on days +3 and +4 post-transplant, in combination with tacrolimus and mycophenolate mofetil (MMF) for GVHD prevention. The goal is to assess the safety and efficacy of this regimen in patients undergoing reduced-intensity or non-myeloablative conditioning using peripheral blood stem cells from matched sibling, matched unrelated, and haploidentical donors

Trial Locations (1)

17033

Penn State Cancer Institute, Hershey

All Listed Sponsors
lead

Milton S. Hershey Medical Center

OTHER

NCT06926595 - Allogeneic HSCT With Low-Dose Post-Transplant Cyclophosphamide for GVHD Prevention | Biotech Hunter | Biotech Hunter