AAVrh10-PCCA Gene Therapy for Propionic Acidemia

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
AAVrh10-PCCA Gene Therapy for Propionic Acidemia	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, inborn disorder of amino acid metabolism, inborn errors of metabolism, metabolic disease, propionic acidemia	Recruiting	Phase 1	2026-08-21		NCT07643844

1 results · Page 1 of 1

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Organizations	Linked trials
Mayo Clinic	970

1 results · Page 1 of 1

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Research sites	City	Country	Linked trials
Mayo Clinic	Rochester	United States	664

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