A Randomized, Multicenter, Phase III Trial of Tacrolimus/Methotrexate/Ruxolitinib versus Post-Transplant Cyclophosphamide/Tacrolimus/Mycophenolate Mofetil in Non-Myeloablative/Reduced Intensity Conditioning Allogeneic Peripheral Blood Stem Cell Transplantation

Sponsor:
BMT CTN
Sponsor Study ID:
2203/INCB 18424-370
CTO #:
104014
NCT Number:
NCT06615050
Phase:
III
Protocol Type:
Treatment
Age Group:
Adults
Disease Sites:
Myeloid and Monocytic Leukemia; Non-Hodgkin's Lymphoma; Other Hematopoietic
Study Objectives:
The primary objective of the Phase Ill portion of the trial is to compare GVHD-free survival (GFS) up to 24 months after hematopoietic cell transplantation (HCT) between the two GVHD prophylaxis regimens. An event for this time-to-event outcome is defined as Grade Ill-IV acute GVHD, chronic GVHD requiring systemic immune suppression, or death by any cause.
eConsent:
Not available
Study Documents:
Open Study Documents
(MUSC NetID required for document access)

For more information about this trial please contact the study team:

Trial opened at the following institutions:

Medical University of South Carolina