Hospital Universitario Infanta Sofia

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Study of SRP-1003 in Participants With Type 1 Myotonic Dystrophy	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	Enrolling by invitation	Phase 1 / Phase 2	2026-10-05		NCT06138743

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