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FDA's Reversal on Gene Therapy Helps My Son

FDA's Reversal on Gene Therapy Helps My Son

Thank you for your editorial 'On Sarepta, a Welcome FDA Reversal' (Review & Outlook, July 30). As a parent of an 11-year-old son with Duchenne muscular dystrophy, I know the devastation this diagnosis brings. I also know the hope that gene therapy such as Elevidys can bring. Such therapies have helped my son, Andrew, fight back against a disease that once offered no chance to do so.
I'm concerned about the recent debate surrounding Elevidys and gene therapies like it. The death of any patient participating in a clinical trial is heartbreaking. Such tragedies and regulatory reactions to them risk casting a shadow over therapies like Elevidys.
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