Did The FDA Make A Mistake? Sarepta’s Elevidys Approval Under Scrutiny

FDA is investigating Sarepta’s Elevidys after two deaths from liver failure in non-ambulatory DMD patients, raising safety and regulatory concerns.

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DateFirmActionFromTo Mar 2022Morgan StanleyMaintainsEqual-Weight Mar 2022RBC CapitalMaintainsOutperform Feb 2022Morgan StanleyMaintainsEqual-Weight

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