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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
European Rare Blood Disorders Platform (ENROL)Bone Marrow Failure, Bone Marrow Failure Disorders, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, Neoplasms by Histologic Type, Neoplasms by Site, Nutritional and Metabolic Diseases, anemia, bone marrow disorder, cardiovascular disorder, familial hemolytic anemia, hematologic disorder, hematopoietic and lymphoid system neoplasm, hemolytic anemia, hemorrhagic disease, hereditary disease, inherited hemoglobinopathy, iron metabolism disease, leukemia, lymphoid neoplasm, metabolic disease, neoplasm, plasma cell neoplasm, sickle cell disease, thalassemia, vascular disorder, vascular hemostatic diseaseRecruitingNot stated2024-02-09NCT06250595