Sarepta: Coming FDA talks will determine fastest path toward eteplirsen approval The company said, "We look forward to our upcoming meetings with the FDA to discuss our eteplirsen data and to determine the fastest path toward potential approval, along with our plans to supply the market in the event of an early approval." The company said additional drugs for Duchenne Muscular Dystrophy, or DMD, continue to progress through preclinical development.
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