Genetic Variation in IgG in Alpha 1 Antitrypsin Deficiency
Genetic Variation in IgG in Alpha 1 Antitrypsin Deficiency
Recruiting · NCT07135427 · Registry updated 2025-11-10Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Genetic Variation in IgG in Alpha 1 Antitrypsin Deficiency | Chronic Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Disease Attributes, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Subcutaneous Emphysema, alpha 1-antitrypsin deficiency, chronic obstructive pulmonary disease, hereditary disease, liver disorder, lung disorder, obstructive lung disease, pulmonary emphysema, respiratory system disorder | Recruiting | Phase 4 | 2025-11-10 | NCT07135427 |
2 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Alpha-1 Foundation | 6 |
| University of Alabama at Birmingham | 467 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| University of Alabama at Birmingham | Birmingham | United States | 247 |