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The U.S. Food and Drug Administration said on Tuesday that it is investigating reports of two deaths due to acute liver ...
The FDA is investigating two deaths in non-ambulatory Duchenne muscular dystrophy patients who received a Sarepta gene ...
Shares of Sarepta Therapeutics closed down as much as 42% to hit a nine-year low of $18.30 on Monday after a second death of ...
A second patient receiving its experimental gene therapy Elevidys has died from liver failure, raising serious questions on ...
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GlobalData on MSNSarepta and Roche halt DMD gene therapy’s use in certain patients after second deathShares in both companies were down following news of the second death, casting fresh safety concerns over Elevidys.
The FDA is assessing the need for “further regulatory action” on Sarepta's Duchenne muscular dystrophy gene therapy in the ...
The FDA said yesterday that it is investigating the deaths from liver failure of two non-ambulatory boys with Duchenne ...
Shares of Sarepta Therapeutics have plunged again after the drugmaker reported a second death in connection with its gene ...
The death of a boy with Duchenne muscular dystrophy, tied to a gene therapy, is above all a tragedy. But it is also ...
FDA is investigating Sarepta's Elevidys after two deaths from liver failure in non-ambulatory DMD patients, raising safety ...
Cambridge-based Sarepta Therapeutics said it was halting shipments of its Duchenne muscular dystrophy gene therapy for ...
In one of the first major tests of the new FDA leadership’s regulatory philosophy toward gene therapies for rare diseases, ...
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