The US Food and Drug Administration (FDA) and European Medicines Agency (EMA) have accepted Biogen’s applications for a higher dose regimen of spinal muscular atrophy (SMA) treatment Spinraza (nusinersen).
The proposed higher dose regimen includes two 50mg doses administered 14 days apart, followed by a maintenance dose of 28mg every four months. This is fewer doses compared to the existing regimen, which involves four loading doses of 12mg over 60 days and a maintenance dose of 12mg every four months.
Biogen previously announced that it was planning regulatory approval for the investigational dose regimen in September 2024, alongside data from the Phase II/III DEVOTE study which has supported these regulatory filings.
The three-part study (NCT04089566) enrolled 145 patients of various ages across various SMA types. In a key cohort of 75 treatment-naïve children with infantile-onset SMA, the higher-dose regimen of Spinraza demonstrated statistically significant improvements in motor function at six months, as measured by the CHOP-INTEND scale. The results were compared to a prespecified untreated control group from the earlier ENDEAR trial, which supported Spinraza’s standard dose approval.
Secondary outcomes from the DEVOTE trial showed favourable trends for the higher-dose version in biomarker and efficacy measures compared to the 12mg dose. Safety data indicated that adverse events were consistent with SMA and Spinraza’s established profile. Notably, the incidence of serious adverse events was lower in the higher dose group at 60%, compared to the 72% incidence seen in the 12mg group.
Spinraza – approved in the US in 2016 and Europe in 2017 – was the first disease-modifying therapy for SMA. It is an antisense oligonucleotide (ASO) designed to increase the production of survival motor neurone (SMN) protein, addressing the underlying cause of motor neuron loss. The treatment is administered directly into the central nervous system to target motor neurons.

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