News
FDA is investigating Sarepta's Elevidys after two deaths from liver failure in non-ambulatory DMD patients, raising safety ...
21h
Fintel on MSNHC Wainwright & Co. Downgrades Sarepta Therapeutics (SRPT)Fintel reports that on June 25, 2025, HC Wainwright & Co. downgraded their outlook for Sarepta Therapeutics (NasdaqGS:SRPT) ...
In one of the first major tests of the new FDA leadership’s regulatory philosophy toward gene therapies for rare diseases, ...
The FDA said yesterday that it is investigating the deaths from liver failure of two non-ambulatory boys with Duchenne ...
Sarepta Therapeutics, Inc. (NASDAQ:SRPT) is one of the 10 Worst Aggressive Growth Stocks to Buy According to Short Sellers.
17h
Stocktwits on MSNSarepta Stock Slumps After FDA Opens Probe Into Patient Death, Analyst Sounds AlarmBrokerage H.C. Wainwright on Wednesday opined that there will be” little intrinsic value” in Sarepta Therapeutics (SRPT) if ...
Elevidys has been given full approval to treat ambulatory patients with DMD, with an accelerated approval in non-ambulatory ...
Writing in JAMA, four former governmental officials warn that the Trump administration’s involvement in delaying the approval ...
Here are the five things you need to know in Boston business news to start your busy workday, including Beth Israel's DEI shift, Hao's successor, Sarepta FDA investigation, and welcome back, Lucy CFO ...
20h
MedPage Today on MSNFDA Probes Gene Therapy After Two DeathsDuchenne muscular dystrophy is characterized by a mutation in the DMD gene that leads to a lack of dystrophin and muscle loss ...
HC Wainwright & Co. analyst Mitchell Kapoor downgraded Sarepta Therapeutics, Inc. SRPT from Neutral to Sell and lowered the ...
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