Rare CFTR Mutation Cell Collection Protocol (RARE)

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Rare CFTR Mutation Cell Collection Protocol (RARE)	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Infant, Newborn, Diseases, cystic fibrosis, hereditary disease, lung disorder, pancreas disorder, respiratory system disorder	Recruiting	Not stated	2026-05-29		NCT03161808

2 results · Page 1 of 1

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Organizations	Linked trials
Cystic Fibrosis Foundation	42
George Solomon	2

1 results · Page 1 of 1

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Research sites	City	Country	Linked trials
University of Alabama at Birmingham	Birmingham	United States	193

Clinical trials