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FDA advisers narrowly vote in favor of experimental gene therapy for rare muscle disease - CNN
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5/12/23 at 11:24pm
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CNN
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Meg Tirrell
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SRP-9001, an experimental gene therapy that aims to slow or stop the progression of Duchenne muscular dystrophy, is being considered for accelerated approval by the FDA.
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https://www.cnn.com/2023/05/12/health/duchenne-muscular-dystrophy-therapy-fda/index.html
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