Sarepta Therapeutics Inc

NASDAQ: SRPT
$126.66
-$2.14 (-1.7%)
Closing price April 30, 2024
Sarepta Therapeutics Inc is a pioneering biopharmaceutical company dedicated to developing unique treatments for rare diseases, with a strong focus on RNA-targeted therapies, gene therapies, and genetic therapeutic modalities. It is known for producing EXONDYS 51, VYONDYS 53, AMONDYS 45, and ELEVIDYS, targeting duchenne muscular dystrophy among other conditions. The company is actively working on advancing its pipeline, including SRP-5051 and SRP-9003 for muscular dystrophies. Founded in 1980 and based in Cambridge, Massachusetts, Sarepta collaborates with leading institutions to push the boundaries of genetic medicine.
The top analyst upgrades, downgrades and other research calls from Friday included AMC, Alkermes, Echostar, Kohls, L Brands, US Bancorp and Sarepta Therapeutics.
These four top Suntrust biotech picks for 2018 all have the potential for big upside moves if they do indeed exceed first-quarter expectations.
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The top analyst upgrades, downgrades and other research calls from Wednesday include Callaway Golf, Capital One, Sarepta Therapeutics, Tesla, UnitedHealth and Wayfair.
A new RBC report is reasonably positive on the biotech sector for the coming year. These eight top picks for 2018 all have the potential for big upside moves.
Sarepta Therapeutics saw its shares hit a new multiyear high on Friday after the firm announced that it received a key approval from the FDA.
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Sarepta Therapeutics, Inc. (NASDAQ: SRPT) saw its shares make a handy gain on Monday after the firm received an upgrade from Morgan Stanley. The driving force behind this upgrade is Sarepta’s...
Source: courtesy of Jon OggStocks were indicated to open higher on Monday after hitting all-time highs the prior week. The one trend that has been proven time after time in this eight-year bull...
24/7 Wall St. has collected several catalysts that are coming up in October for biotech and pharmaceutical companies.
Sarepta Therapeutics saw its shares make a handy gain on Wednesday after the firm announced muscle biopsy results from its mid-stage study for the treatment of Duchenne muscular dystrophy.
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