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Sarepta soars

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FDA takes U-turn on Sarepta's Elevidys, backing Duchenne gene therapy again in ambulatory patients
Monday, the FDA said Sarepta may resume treating ambulatory DMD patients with Elevidys. The recommendation comes just 10 days after the agency requested that the company halt all shipments of the one-time treatment following reports of three deaths among patients who had received a Sarepta gene therapy, including two on Elevidys.

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Sarepta soars after FDA says some patients can get Elevidys
Sarepta resumes shipping of gene therapy Elevidys to patients who can walk
Sarepta Shares Rise After Company Says It Will Resume Elevidys Shipments
Shares of Sarepta surged Tuesday, a day after the FDA said the company could lift a voluntary pause on shipments of its Elevidys drug, which had been linked to three patient deaths this year.

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FDA allows Sarepta to resume some Elevidys shipments
Sarepta shares rebound after shipments of gene therapy Elevidys resume in US
Sarepta's FDA woes raise questions for future of gene therapy treatments
While Sarepta’s challenges could push some away from investing in gene therapies, it could also lead to interest in different approaches.

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FDA recommends lifting voluntary hold on Elevidys in ambulatory patients
Parents call on FDA for path forward after Duchenne's gene therapy pause | Morning in America
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Sarepta Stock On the Rise Following Resumption of Elevidys Shipments in US
While MSN reports that Sarepta’s stock price began to rise on Monday on the heels of the announcement, 5 the company is still facing challenges. Shipments of the gene therapy for non-ambulatory patients are still halted, and other incidents are still being investigated.
Sarepta Therapeutics stock sinks further Tuesday after halting shipment of bestselling drug Elevidys
Sarepta stock tanked Friday after a new patient death was uncovered, spurring an FDA request to halt shipments of an unrelated drug.
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