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Reporter sues FDA for documents related to Sarepta drug approval

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A journalist has filed a federal lawsuit against the FDA seeking documents related to the agency’s controversial approval last year of Exondys 51, a Duchenne muscular dystrophy treatment developed by Cambridge-based Sarepta Therapeutics. Charles Seife, a journalist and professor at New York University, filed a complaint Thursday in Manhattan federal court challenging the FDA’s decision not to disclose records that he requested under the Freedom of Information Act. The documents relate to the…

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