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Patient or parent\u002Flegal guardian is willing and able to provide written informed consent once the nature of the registry has been explained and prior to the start of any registry-related procedures.\n2. Patient and\u002For parent\u002Fguardian are willing and able to complete QoL questionnaires.\n3. Male patients at least 2 years old.\n4. Confirmed diagnosis of DMD (via genetic testing or muscle biopsy with absent dystrophin staining to anti- dystrophin antibodies 3, 1, or 2, or dystrophin immunohistochemistry or western blot).\n5. Patient has a current, active prescription for, or is on, AGAMREE®.\n\nExclusion Criteria:\n\n1\\. Any contraindication to AGAMREE® or medical condition, which, in the opinion of the Investigator, would affect registry participation, performance, or interpretation of registry assessments.","MALE","2 Years",{"count":453,"type":454},250,"ESTIMATED","5 Years","OBSERVATIONAL","The goal of this study is to collect additional information on the safety of long-term treatment with AGAMREE® and to explore long-term clinical impact of AGAMREE® on quality of life, as assessed by standardized patient-reported outcome measures (QoL questionnaires) in male patients aged 2 years and older with Duchenne muscular dystrophy (DMD).",[459],"Duchenne Muscular Dystrophy",[459,461,14,11,462,463],"Neuromuscular","DMD","Muscular Dystrophy","2026-02-23",{"date":466,"type":467},"2026-02-27","ACTUAL",{"date":469,"type":467},"2024-09-25",{"date":471,"type":454},"2032-02",{"name":5,"class":6},27]