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Sarepta shares gained even though the U.S. Food and Drug Administration said late Friday that it was probing the death of an ...
Brazilian authorities said the death was unlikely to have been caused by Elevidys and was instead more in line with severe ...
The U.S. Food and Drug Administration (FDA) announced on Friday, after market close, that it is investigating the death of an ...
2don MSN
The U.S. Food and Drug Administration said on Friday it was investigating the death of an eight-year-old boy who received ...
U.S. regulators asked Sarepta Therapeutics on Friday to voluntarily halt shipments of its Elevidys gene therapy after a ...
Sarepta Therapeutics is pausing shipments of its gene therapy for muscular dystrophy following several patient deaths that ...
Sarepta Therapeutics (SRPT) shares dropped sharply on Monday following news that the FDA is investigating a patient death potentially connected to its gene therapy, Elevidys.
The Food and Drug Administration is investigating Sarepta’s gene therapy products following reports of a third death from acute liver failure.
In this week’s edition of InnovationRx, we look at Moderna’s use of quantum computers, a new top drug regulator at the FDA, ...
CBER is unanimously against Elevdiys’ return to the market without additional evidence, according to media reports citing an ...
As the controversy over the safety of Sarepta Therapeutics’ gene therapies comes to a head, the biotech is standing firm ...
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