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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Gene Editing For Sickle Cell DiseaseCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, anemia, familial hemolytic anemia, hematologic disorder, hemolytic anemia, hereditary disease, inherited hemoglobinopathy, sickle cell diseaseRecruitingPhase 12026-05-05NCT06506461

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Research sitesCityCountryLinked trials
St. Jude Children's Research HospitalMemphisUnited States194