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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Study About the Diagnosis and Management of Hereditary Angioedema (HAE) in EgyptCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Hereditary Complement Deficiency Diseases, Hypersensitivity, Immediate, Primary Immunodeficiency Diseases, Skin and Connective Tissue Diseases, angioedema, cardiovascular disorder, hereditary angioedema, hereditary disease, immune system disorder, inborn error of immunity, skin disorder, skin vascular disease, urticaria, vascular disorderNot yet recruitingNot stated2026-06-18NCT07218393

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OrganizationsLinked trials
Takeda163

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