News
The U.S. Food and Drug Administration is planning to ask Sarepta Therapeutics to voluntarily stop all shipments of its gene ...
Shares of Sarepta Therapeutics plunged more than 30% on Friday as the future of its approved gene therapy appeared at risk.
The Food and Drug Administration plans to ask Sarepta Therapeutics Inc. to pause shipments of its Elevidys treatment after ...
The death will likely further stoke safety concerns around Sarepta's gene therapies, as well as raise questions around the ...
The company had previously halted shipments to certain older patients following the deaths of two teenagers treated with the ...
Investors showed growing mistrust of the Sarepta team, repeatedly asking why the Cambridge company had not disclosed the ...
1d
MedPage Today on MSNDuchenne Gene Therapy Will Undergo Changes After Patient DeathsAt the FDA's request, delandistrogene moxeparvovec (Elevidys), the only approved gene therapy for Duchenne muscular dystrophy ...
Sarepta Therapeutics (NASDAQ:SRPT) shares plummeted on Friday following reports of a third patient death linked to its gene ...
GlobalData on MSN8h
Sarepta share price drops again after third gene therapy deathSarepta Therapeutics was approached for comment by Clinical Trials Arena but did not respond before publication. This comes ...
The FDA will request Sarepta Therapeutics stop all shipments of Elevidys, its gene therapy for Duchenne muscular dystrophy, ...
The patient, who was being treated with an investigational gene therapy for limb-girdle muscular dystrophy, died of acute ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results