News

Sarepta shares gained even though the U.S. Food and Drug Administration said late Friday that it was probing the death of an ...
The Trump FDA tries to kill a therapy that has helped boys with a deadly diagnosis.
The U.S. Food and Drug Administration said on Friday it was investigating the death of an eight-year-old boy who received ...
In this week’s edition of InnovationRx, we look at Moderna’s use of quantum computers, a new top drug regulator at the FDA, ...
Sarepta Therapeutics is pausing shipments of its gene therapy for muscular dystrophy following several patient deaths that ...
The U.S. Food and Drug Administration (FDA) announced on Friday, after market close, that it is investigating the death of an ...
After the FDA request, Cambridge, Massachusetts-based Sarepta said in a statement that it will continue to ship the therapy ...
In its own communique issued shortly after the FDA’s, Sarepta elaborated on the situation and confirmed a Roche statement to ...
Brazilian authorities said the death was unlikely to have been caused by Elevidys and was instead more in line with severe ...
Arrowhead said it has met both of these conditions in a July 28 release and now expects to receive the $100 million within 60 days. The company also said it plans on reaching the second enrollment ...
CBER is unanimously against Elevdiys’ return to the market without additional evidence, according to media reports citing an ...