Universitair Medisch Centrum Utrecht - PPDS

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
A Study to Assess the Long-term Safety and Clinical Activity of mRNA-3927 in Participants Previously Enrolled in the mRNA-3927-P101 Study	Acid-Base Imbalance, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, acidosis disorder, hereditary disease, inborn disorder of amino acid metabolism, inborn errors of metabolism, metabolic disease, propionic acidemia	Recruiting	Phase 1 / Phase 2	2026-03-23		NCT05130437
Open-Label Study of mRNA-3927 in Participants With Propionic Acidemia	Acid-Base Imbalance, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, acidosis disorder, hereditary disease, inborn disorder of amino acid metabolism, inborn errors of metabolism, metabolic disease, propionic acidemia	Recruiting	Phase 1 / Phase 2	2026-01-22		NCT04159103

Clinical trials