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Hope for boys with Duchenne Muscular Dystrophy (DMD) has arrived with SRP-9001, the first FDA-approved gene therapy for this challenging condition. But what exactly is SRP-9001 (Delandistrogene moxeparvovec), and how does it work? Discover how this innovative treatment works at the genetic level, potentially offering a life-altering solution for those affected by this debilitating condition. Take a look at the findings from the latest clinical trial, and the promising results that have sparked excitement within the medical community. References: 1. Manini A, Abati E, Nuredini A, Corti S, Comi GP. Adeno-Associated Virus (AAV)-Mediated Gene Therapy for Duchenne Muscular Dystrophy: The Issue of Transgene Persistence. Front Neurol. 2022;12:814174. Published 2022 Jan 5. doi:10.3389/fneur.2021.814174 2. Sarepta Therapeutics announces FDA approval of Elevidys, the first gene therapy to treat Duchenne muscular dystrophy. News release. June 22, 2023. Accessed February 13, 2024. https://www.businesswire.com/news/hom... 3. https://www.fda.gov/news-events/press... 4. Sarepta Therapeutics announces topline results from EMBARK, a global pivotal study of ELEVIDYS gene therapy for Duchenne muscular dystrophy. News release. Sarepta Therapeutics. October 30, 2023. Accessed February 13, 2024. https://investorrelations.sarepta.com... 5. https://www.musculardystrophyuk.org/n... Disclaimer: This YouTube video is not intended to provide diagnosis, treatment, or medical advice. The content provided in this video is for informational purposes only. Please consult with a physician or other healthcare professional regarding any medical or health-related diagnosis or treatment options. Information on this video should not be considered as a substitute for advice from a healthcare professional. The statements made about specific products are not to diagnose, treat, cure, or prevent disease. #Elevidys #SRP9001 #DuchenneMuscularDystrophy #MedicalBreakthroughs #HopeForDMD #genetherapy #healthtech #biotechnology #DelandistrogeneMoxeparvovec