Newcastle Upon Tyne Hospitals

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
A Clinical Study of PGN-EDODM1 in People With Myotonic Dystrophy Type 1	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular disease	Recruiting	Phase 2	2026-07-29		NCT06667453

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