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The U.S. Food and Drug Administration (FDA) announced on Friday, after market close, that it is investigating the death of an ...
A recent FDA investigation has paused further distribution of Elevidys, following reports of at least three patient deaths.
In its own communique issued shortly after the FDA’s, Sarepta elaborated on the situation and confirmed a Roche statement to ...
The FDA is investigating the death of an 8-year-old boy who received Elevidys, a gene therapy developed by Sarepta Therapeutics to treat Duchenne muscular dystrophy. The child died June 7, prompting ...
Note that some links may require registration or subscription. HHS Secretary Robert F. Kennedy Jr. is facing new questions ...
The Food and Drug Administration is investigating Sarepta’s gene therapy products following reports of a third death from acute liver failure.
Brazilian authorities said the death was unlikely to have been caused by Elevidys and was instead more in line with severe ...
7h
TipRanks on MSNFDA probing death of 8-year-old boy who received Sarepta’s ElevidysThe U.S. Food and Drug Administration is investigating the death of an 8-year-old boy who received Elevidys, a Sarepta (SRPT) Therapeutics gene ...
The US Food and Drug Administration (FDA) issued a press release late Friday announcing an investigation into the death of an ...
Sarepta Therapeutics now trades at book value with strong cash and cost-cutting plans, while ELEVIDYS may regain broader use.
When Pasadena-based Arrowhead Pharmaceuticals Inc. signed a huge licensing and collaboration deal with Cambridge, ...
14h
Stocktwits on MSNRetail Bulls Stick With Sarepta After 8-Year-Old Patient’s Death Deemed Unrelated To DMD Gene TherapyRetail sentiment around Sarepta Therapeutics remained upbeat on Monday after the company said Friday that the death of an ...
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