Condition: Acute Myelogenous Leukemia · Acute Lymphocytic Leukemia · Biphenotypic Acute Leukemia · Sponsor: Masonic Cancer Center, University of Minnesota
This is a Phase II study following subjects proceeding with our Institutional non-myeloablative cyclophosphamide/ fludarabine/total body irradiation (TBI) preparative regimen followed by a related, unrelated, or partially matched family donor stem cell infusion using post-transplant cyclophosphamide (PTCy), sirolimus and MMF GVHD prophylaxis.
This description comes directly from the study's public registry record.
Mark Juckett · 6126255469 · juck0001@umn.edu
Always discuss trial participation with your own doctor first.
| Masonic Cancer Center at University of Minnesota | Minneapolis, Minnesota, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05805605