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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Acute Lymphocytic Leukemia
  • Acute Myelogenous Leukemia
  • Anemia, Refractory, with Excess of Blasts
  • Biphenotypic Acute Leukemia
  • Burkitt Lymphoma
  • Chronic Myelogenous Leukemia
  • Follicular Lymphoma
  • Hematologic Diseases
  • Leukemia
  • Leukemia, Biphenotypic, Acute
  • Leukemia, Lymphocytic, Chronic, B-Cell
  • Leukemia, Lymphoid
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive
  • Leukemia, Myeloid
  • Leukemia, Myeloid, Acute
  • Leukemia, Plasma Cell
  • Leukemia, Prolymphocytic
  • Lymphoma
  • Marginal Zone Lymphoma
  • Myelodysplastic Syndrome With Excess Blasts-1
  • Myelodysplastic Syndromes
  • Myelofibrosis
  • Myeloproliferative Disorders
  • Myeloproliferative Neoplasm
  • Plasma Cell Leukemia
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma
  • Preleukemia
  • Prolymphocytic Leukemia
  • Relapsed Chronic Lymphocytic Leukemia
  • Relapsed T-Cell Lymphoma
  • Small Lymphocytic Lymphoma
  • Syndrome
  • Undifferentiated Leukemia

NCT number NCT05805605
Study type Interventional
Source Masonic Cancer Center, University of Minnesota
Contact Mark Juckett
Phone 6126255469
Email juck0001@umn.edu
Status Recruiting
Phase Phase 2
Start date May 1, 2023
Completion date October 22, 2028

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