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A cell therapy preserves muscle structure and function in laboratory mice with a type of disease similar to Duchenne muscular ...
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InvestorsHub on MSNDyne Therapeutics Shares Rise 3.6% After FDA Grants Breakthrough Therapy StatusDyne Therapeutics Inc (NASDAQ:DYN) stock climbed 3.6% following the announcement that the U.S. Food and Drug Administration ...
Precision BioSciences Inc., a clinical-stage company developing gene editing therapies for diseases with high unmet need, has ...
Dyne Therapeutics' DYNE-251 receives FDA breakthrough status for Duchenne muscular dystrophy treatment. Read more here.
An alternative to using standard glucocorticoids is the synthetic dissociative steroid vamorolone (Agamree), which was ...
Targeted rewriting of the epigenome promises to overcome several challenges in direct gene editing in patient therapies.
Parents of boys with Duchenne muscular dystrophy weigh in on drug innovation and medical regulation.
REGENXBIO Inc. (NASDAQ:RGNX) is one of the biotech stocks to buy according to Wall Street analysts. On July 10, REGENXBIO ...
Furious competition in GLP-1 drugs rebuts the anti-pharma crowd.
Prasad, a longtime critic of the FDA’s leniency in drug approvals, joined the agency in May. WASHINGTON — The Food and Drug ...
The FDA greenlit multiple new drugs this month and issued some notable label expansions, including for Eli Lilly’s Kisunla.
Shipment of delandistrogene moxeparvovec, a gene therapy for Duchenne muscular dystrophy (DMD), will resume following a ...
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