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MT2023-20: Hematopoietic cell transplant with reduced intensity conditioning and post-transplant cyclophosphamide for severe aplastic anemia and other forms of acquired bone marrow failure.

Status: Recruiting

Although allogeneic hematopoietic cell transplant (HCT) is standard treatment for severe aplastic anemia, the use of the lower intensity conditioning drugs with a personalized dosing strategy, low dose total body irradiation (TBI) with dosing based on age and bone marrow abnormalities, and use of the drug cyclophosphamide early after transplant is a newer approach. We are studying whether this new approach is safer and more effective than our previous approach.

I'm interested

Sex: Male or Female
Age Group: Not specified
This study is NOT accepting healthy volunteers
Inclusion Criteria:

• 0 to 75 years old
• diagnosis of Idiopathic Severe Aplastic Anemia (SAA)
• see link to clinicaltrials.gov for complete inclusion and exclusion criteria
Exclusion Criteria:

• women who are pregnant, breastfeeding or intending to become pregnant during the study
• uncontrolled infection
Interventions:

Biological: Cell Infusion, Drug: Cyclophosphamide, Drug: Fludarabine, Drug: Mycophenolate Mofetil, Drug: Post-Transplant G-CSF, Drug: Rabbit ATG, Drug: Rituximab, Drug: Tacrolimus, Radiation: Total Body Irradiation

Conditions:

Blood Disorders

Keywords:

Clinics and Surgery Center (CSC), Acquired Amegakaryocytic Thrombocytopenia, Aplastic Anemia, Paroxysmal Nocturnal Hemoglobinuria, SA

Study Contact: Christen Ebens - ebens012@umn.edu
Principal Investigator: Christen Ebens
Phase: PHASE2
IRB Number: STUDY00021781
See this study on ClinicalTrials.gov

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