CRO Axelys Santé DZ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
A Study to Learn About the C1-Inhibitor Function as Diagnosis for Hereditary Angioedema	Congenital, 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 disorder	Recruiting	Not applicable	2026-05-19		NCT07293364

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