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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Correction of Nonsense Mutations in Cystic FibrosisCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Infant, Newborn, Diseases, cystic fibrosis, hereditary disease, lung disorder, pancreas disorder, respiratory system disorderRecruitingNot stated2026-05-22NCT03670472

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