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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Gene Therapy for Alpha 1- Antitrypsin DeficiencyCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Subcutaneous Emphysema, alpha 1-antitrypsin deficiency, hereditary disease, liver disorder, lung disorder, pulmonary emphysema, respiratory system disorderRecruitingPhase 12026-09-25NCT06996756

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Research sitesCityCountryLinked trials
WCMC Department of Genetic MedicineNew YorkUnited States2