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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Long-term Follow-up Study in Participants Who Received CTX001Congenital, 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 32026-08-11NCT04208529