University Hospital Birmingham NHS Foundation Trust

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
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
AAV Gene Therapy Study for Subjects with PKU	Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, brain disorder, central nervous system disorder, hereditary disease, inborn disorder of amino acid metabolism, inborn errors of metabolism, metabolic disease, nervous system disorder, phenylketonuria	Active, not recruiting	Phase 1 / Phase 2	2024-12-12		NCT04480567

Clinical trials