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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Open-Label Extension Study to Pioneer Study 6058-SCD-101Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, anemia, beta thalassemia, familial hemolytic anemia, hematologic disorder, hemolytic anemia, hereditary disease, inherited hemoglobinopathy, sickle cell disease, thalassemiaEnrolling by invitationPhase 22026-04-14NCT07401823