News
The FDA’s shift on Elevidys sends a message: boldness, scientific rigor and urgency are essential in confronting rare ...
Discover the challenges and opportunities for Keros Therapeutics, Inc., including FDA designations, partnerships, and ...
Certain Sarepta Therapeutics Inc. insiders were accused in a stockholder lawsuit of reaping a combined $6.2 million selling ...
Sarepta is facing a number of issues currently, including platform-level safety concerns, management credibility issues, etc.
The drug, based on Nobel Prize-winning gene-editing technology CRISPR-Cas9, reaches the liver cells and splices out the ...
The debt refinancing follows the firm's recent trouble with the FDA and efforts to refocus its pipeline priorities, preserve resources, and meet financial obligations.
Morning. Today, we see fallout from the FDA’s rejection of Replimune’s melanoma drug affecting another biotech, learn how ...
Sarepta Therapeutics Inc. landed a deal with investors to restructure around $700 million of debt, giving the company a ...
A refinancing deal will delay the maturity of $700 million in debt until 2030, allowing the company to “fully fund” its ...
After deaths and FDA setbacks, Sarepta abandoned LGMD gene therapy, leaving families desperate and patients without ...
Detailed price information for Sarepta Therapeutics (SRPT-Q) from The Globe and Mail including charting and trades.
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Stocktwits on MSNCiti Believes FDA May Closely Watch Sarepta’s Safeguards For Gene Therapy In Non-Ambulatory DMD Patients
Citi said on Wednesday that the U.S. Food and Drug Administration may take a “more comprehensive look” at the level of ...
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