- Conditions
- Acquired Bone Marrow Failure Syndromes, Acute Leukemia, Acute Lymphoblastic Leukemia, Acute Myeloid Leukemia, Biphenotypic/Undifferentiated/Prolymphocytic Leukemias, Burkitt Lymphoma, Chronic Lymphocytic Leukemia, Chronic Myelogenous Leukemia, Diffuse Large Cell Non Hodgkins Lymphoma, Follicular Lymphoma, High Grade Non-Hodgkin's Lymphoma, Adult, High Risk Anemia, Juvenile Myelomonocytic Leukemia, Lymphoblastic Lymphoma, Lymphoma, Lymphoplasmacytic Lymphoma, MRD Positive Leukemia, Mantle-Cell Lymphoma, Marginal Zone B-Cell Lymphoma, Multiple Myeloma, Myelodysplasia, Myelofibrosis, Myeloproliferative Neoplasms, Natural Killer Cell Malignancies, Plasma Cell Leukemia, Prolymphocytic Leukemia, Refractory Anemia, Small Lymphocytic Lymphoma
- Interventions
- HSCT with Non-TBI Regimen, HSCT with TBI Regimen
- Biological
- Lead sponsor
- Masonic Cancer Center, University of Minnesota
- Other
- Eligibility
- Up to 60 Years
- Enrollment
- 300 participants
- Healthy volunteers
- Healthy volunteers not accepted
- Timeline
- 2018 – 2027
- U.S. locations
- 1
- States / cities
- Minneapolis, Minnesota
Source: ClinicalTrials.gov public record
Updated Jun 23, 2025 · Synced May 21, 2026, 12:56 AM EDT