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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Alpha/Beta TCD HCT in Patients With Inherited BMF DisordersBone Marrow Failure, Bone Marrow Failure Disorders, Congenital Abnormalities, Congenital Bone Marrow Failure Syndromes, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA repair disease, Fanconi anemia, Hemic and Lymphatic Diseases, Nutritional and Metabolic Diseases, Skin Abnormalities, Skin and Connective Tissue Diseases, X-linked disease, anemia, aplastic anemia, bone marrow disorder, dyskeratosis congenita, hematologic disorder, hereditary disease, hereditary skin disorder, inherited aplastic anemia, metabolic disease, myelodysplastic syndrome, skin disorderRecruitingPhase 22026-01-30NCT03579875

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Research sitesCityCountryLinked trials
Masonic Cancer Center at University of MinnesotaMinneapolisUnited States12