Overview

Study of HLA-Haploidentical Stem Cell Transplantation to Treat Clinically Aggressive Sickle Cell Disease

Status:
Recruiting
Trial end date:
2024-09-12
Target enrollment:
Participant gender:
Summary
The study is a Phase II clinical trial. Patients will receive intensity modulated total body irradiation (TBI) at a dose of 3 Gy with standard fludarabine/ i.v. cyclophosphamide conditioning prior to human leukocyte antigen (HLA)-haploidentical hematopoietic stem cell transplant (HSCT). The primary objective of the study is to determine the engraftment at Day +60 following HLA-haploidentical hematopoietic stem cell transplant protocol using immunosuppressive agents and low-dose total body irradiation (TBI) for conditioning and post-transplant cyclophosphamide in patients with sickle cell disease.
Phase:
Phase 2
Details
Lead Sponsor:
University of Illinois at Chicago
Treatments:
Cyclophosphamide
Everolimus
Fludarabine
Fludarabine phosphate
Mycophenolate mofetil
Mycophenolic Acid
Sirolimus
Thymoglobulin