A Study to Learn About the C1-Inhibitor Function as Diagnosis for Hereditary Angioedema
A Study to Learn About the C1-Inhibitor Function as Diagnosis for Hereditary Angioedema
Recruiting · NCT07293364 · Registry updated 2026-05-19Clinical trials
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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 |
2 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| CRO Axelys Santé DZ | 1 |
| Takeda | 163 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| EPH de Rouiba (Etablissement Public Hospitalier) | Algiers | Algeria | 1 |