Recruiting studies: Merosin Deficient Congenital Muscular Dystrophy

Studies currently listed as recruiting on the public registry for this search term. Each page explains the study in plain language, with locations and the study team's contact details. Clinicians: generate a printable list for your patient →

A 5-year Natural History Study in LAMA2-related Muscular Dystrophy and SELENON-related Myopathy.
Phase N/A · 1 location(s) · Radboud University Medical Center · NCT06132750 Characterization of the Natural History of LAMA2-RD and Identification of Novel Disease Biomarkers
Phase N/A · 1 location(s) · Università Vita-Salute San Raffaele · NCT07125040 Natural History Study of Children With LAMA2-related Dystrophies
Phase N/A · 4 location(s) · Institut de Myologie, France · NCT06354790 Observation Study in Patients Age 0-5 Years With LAMA2-related Congenital Muscular Dystrophy
Phase N/A · 14 location(s) · Nationwide Children's Hospital · NCT06503367 Spanish Natural History Study for LAMA2 Muscular Dystrophy
Phase N/A · 1 location(s) · Hospital Universitari Vall d'Hebron Research Institute · NCT06924125 Congenital Muscle Disease Study of Patient and Family Reported Medical Information
Phase N/A · 1 location(s) · Cure CMD · NCT01403402

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This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.