Fondazione Serena Onlus - Centro Clinico NeMO Milano | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Estab Biomarkers and Clinical Endpoints in Myotonic Dystrophy Type 1 (END-DM1)	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 dystrophy type 1, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular disease	Recruiting	Not stated	2026-06-10		NCT03981575
ALS/MND Natural History Study Data Repository	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Kennedy disease, Nutritional and Metabolic Diseases, TDP-43 proteinopathy, X-linked disease, amyotrophic lateral sclerosis, central nervous system disorder, hereditary disease, inherited neurodegenerative disorder, metabolic disease, motor neuron disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, progressive bulbar palsy, proteostasis deficiencies, spinal cord disorder, spinal muscular atrophy	Recruiting	Not stated	2026-05-20		NCT05966038
Transition to Adulthood in People With Muscular Dystrophy	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne muscular dystrophy, Muscular Disorders, Atrophic, X-linked disease, hereditary disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular disease	Not yet recruiting	Not applicable	2025-08-03		NCT07101185