A rare genetic condition, Spinal Muscular Atrophy (SMA) affects one in 7,000 people in India. It mostly affects children and ...
Speakers from the Muscular Dystrophy Association (MDA) highlighted 75 years of progress in understanding and treating ...
Evrysdi is the third treatment approved for SMA, an ultra-rare muscle wasting disease that can begin in early childhood, after Biogen’s Spinraza (nusinersen) and Novartis’ Zolgensma ...
Along with Zolgensma – which made its debut in 2019 – Biogen has had approval to market its antisense-based therapy Spinraza (nusinersen) since 2016, while Roche got a green light for its ...
RNA-based therapeutics are gaining traction due to advancements in delivery technologies, despite historical challenges with ...
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Treatment with Spinraza (nusinersen) can help stabilize or improve motor function in adults with SMA, according to a new ...
A higher dose of Spinraza may be more effective than the currently approved dosing schedule for maintaining motor function in ...
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