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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Observational Study for Patients With Hemoglobinopathies and Rare Inherited Anemia and Covid 19Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, hematologic disorder, hereditary disease, inherited hemoglobinopathyRecruitingNot stated2022-05-05NCT04746066

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