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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Surrogate Markers of Response to New Therapies in Cystic Fibrosis PatientsCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Infant, Newborn, Diseases, cystic fibrosis, hereditary disease, lung disorder, pancreas disorder, respiratory system disorderRecruitingNot applicable2024-03-12NCT02965326