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Sarepta is facing a number of issues currently, including platform-level safety concerns, management credibility issues, etc.
After deaths and FDA setbacks, Sarepta abandoned LGMD gene therapy, leaving families desperate and patients without ...
Sarepta Therapeutics has provided additional safety data on its gene therapy Elevidys as a Duchenne muscular dystrophy ...
4 lá
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 ...
Sarepta Therapeutics Inc. landed a deal with investors to restructure around $700 million of debt, giving the company a ...
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.
A refinancing deal will delay the maturity of $700 million in debt until 2030, allowing the company to “fully fund” its ...
Kriya is advancing a host of gene therapies for a wide variety of chronic diseases, including geographic atrophy, trigeminal ...
Gene therapy biotech Kriya Therapeutics has secured $313 million in a new series fundraise. | Gene therapy biotech Kriya ...
2 láon MSNOpinion
Benefits outweigh risks. FDA right to greenlight Columbus company's treatment | Opinion
The FDA’s shift on Elevidys sends a message: boldness, scientific rigor and urgency are essential in confronting rare ...
The drug, based on Nobel Prize-winning gene-editing technology CRISPR-Cas9, reaches the liver cells and splices out the ...
The CDMO will be cutting 350 jobs at its Baltimore gene therapy site after a major client’s demand shift, less than a year ...
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