A Study of Immune Suppression Treatment for People With Sickle Cell Disease or β-Thalassemia Who Are Going to Receive an Allogeneic Hematopoietic Cell Transplantation (HCT)
Pre-Transplant Immune Suppression With Hematopoietic Cell Transplantation From Haploidentical Donors for Adults and Children With Sickle Cell Disease or ß-Thalassemia (Haplo PTCy)
Phase
PHASE2
Enrollment
24 (est.)
Age range
2 Years to 50 Years
Sex
ALL
Summary
Hematopoietic Cell Transplantation/HCT involves receiving healthy blood-forming cells (stem cells) from a donor to replace the diseased or damaged cells in participants' bone marrow. The researchers think giving participants treatment with fludarabine and dexamethasone, drugs that lower the activity of the body's immune system (immune suppression), before standard conditioning therapy and HCT may help prevent serious side effects, including graft failure and GvHD. In this study, depending on how participants' body responds to the fludarabine and dexamethasone, the study doctor may decide participants should receive another drug, called cyclophosphamide, instead of fludarabine. In addition, depending on the results of participants' routine blood tests, participants may receive the drugs bortezomib and rituximab, which also help with immune suppression.
Conditions studied
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Feb 9, 2023 – est. completion Feb 9, 2027
Sponsors
Study locations
Memorial Sloan Kettering at Basking Ridge (Consent only)
Basking Ridge, New Jersey
Memorial Sloan Kettering Monmouth (Consent only)
Middletown, New Jersey
Memorial Sloan Kettering Bergen (Consent only)
Montvale, New Jersey
Memorial Sloan Kettering Suffolk - Commack (Consent only)
Commack, New York
Memorial Sloan Kettering Westchester (Consent only)
Harrison, New York
Memorial Sloan Kettering Nassau (All protocol activities)
Rockville Centre, New York