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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 ...
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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 ...
Just a few weeks after closing a $155 million series B, RNA editing biotech AIRNA is bringing an experienced gene therapy ...
The determination comes after recruitment and dosing in certain trials were paused after a young patient died due to acute ...
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).
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Zacks.com on MSNSRPT Provides Pipeline Updates on Rare Muscular Disorder TherapiesSarepta Therapeutics SRPT announced updates from its clinical programs, which focus on targeting different subtypes of limb-girdle muscular dystrophy (LGMD), a group of rare genetic disorders marked ...
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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