News
Treatment with salanersen slowed neurodegeneration and improved motor function in children with SMA in a Phase 1 trial, ...
New data from Biogen reveals higher Spinraza doses may enhance motor function in SMA patients. Read more here.
Biogen plans to advance an experimental treatment for the neuromuscular disease spinal muscular atrophy, or SMA, into registrational studies following encouraging results from an early-stage trial.
The cumulative data from the Phase 1 study indicate that salanersen has a generally well tolerated safety profile at both the 40 mg and 80 mg doses, with most adverse events (AEs) mild to moderate in ...
Many SMA patients continue to see gains in motor function with long-term Spinraza treatment, a real-world study from ...
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Talker on MSNGirl diagnosed with rare muscle condition after she stopped crawlingShe dreams that she’s not in a wheelchair. She dreams that she can run." The post Girl diagnosed with rare muscle condition ...
For the first time in India, a newborn diagnosed with Spinal Muscular Atrophy (SMA) received pre-symptomatic treatment within days of birth in Kerala, marking a significant milestone in the treatment ...
DataM Intelligence | competitive Intelligence Spinal Muscular Atrophy treatment is evolving fast, with gene therapy, oral drugs, and next-g ...
Spinal muscular atrophy, a progressive neurodegenerative disorder set in motion before birth, could be treated in utero. News . Published: February 21, 2025 . ... The parents in this case were both ...
Spinal muscular atrophy (SMA), a #geneticdisorder caused by a lack of survival motor neuron protein, affects about 1 in every 11,000 births in the United States. #pregnancy #medindia ’ Advertisement ...
In a hopeful step for medicine, a 2-and-a-half-year-old child born with spinal muscular atrophy (SMA) has shown no symptoms of the genetic condition, all thanks to a gene-targeting drug that the ...
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