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:
-
Medical University of South Carolina
- Principal Investigator, Alexander, Jonathan, at alexjon@musc.edu .
- Study Coordinator, Baker, Hana, at bakerhan@musc.edu .
Trial opened at the following institutions:
Medical University of South Carolina