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A few weeks after Sarepta Therapeutics confirmed a patient died after receiving its drug Elevidys, research published April 3 ...
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Investor's Business Daily on MSNSarepta Dives On 'Another Unfortunate Development' For Its Gene TherapySarepta stock plunged Thursday after European officials put all studies of the company's gene therapy, Elevidys, on hold.
Sarepta and Roche paused Elevidys trials in the EU after a patient death. Analysts warn of potential sales declines as safety ...
One day after the European Medicines Agency requested that three clinical trials of Elevidys be placed on hold after the ...
16d
Zacks Investment Research on MSNSRPT Stock Down After EMA Places Clinical Hold on DMD Gene TherapyShares of Sarepta Therapeutics SRPT dropped more than 6% yesterday after the EMA placed a clinical hold on all studies evaluating Elevidys, its one-shot gene therapy for Duchenne muscular dystrophy ...
Just a few weeks after closing a $155 million series B, RNA editing biotech AIRNA is bringing an experienced gene therapy ...
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GlobalData on MSNSarepta and Roche aim to resume paused Elevidys trials following patient deathSarepta Therapeutics and Roche are looking to get approval to continue clinical trials of their Duchenne muscular dystrophy ...
Explore Solid Biosciences’ potential with promising SGT-003 trial results for DMD, strong financials, and market recovery ...
Multidisciplinary coordination across prescribing teams, nursing, laboratory medicine, finance, and infusion centers is crucial for gene therapy delivery in Duchenne muscular dystrophy (DMD).
In March, Sarepta Therapeutics, Inc. (NASDAQ:SRPT) shared an update on Elevidys (delandistrogene moxeparvovec-rokl), the only approved gene therapy in patients with Duchenne muscular dystrophy.
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