Biogen Announces Detailed Results From The Phase 2/3 DEVOTE Study, Highlighting The Safety And Efficacy Of A Higher Dose Nusinersen Regimen In SMA
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Biogen has announced positive results from its Phase 2/3 DEVOTE study, demonstrating the safety and efficacy of a higher dose nusinersen regimen for treating spinal muscular atrophy (SMA). The study showed clinical benefits and a more rapid slowing of neurodegeneration. Biogen plans to seek regulatory approval globally for this higher dose regimen.
October 08, 2024 | 11:54 am
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Biogen's Phase 2/3 DEVOTE study results indicate that a higher dose of nusinersen is both safe and effective for SMA treatment, showing clinical benefits and slowing neurodegeneration. Biogen plans to submit for regulatory approval worldwide.
The positive results from the DEVOTE study suggest that Biogen's higher dose nusinersen regimen could become a new standard for SMA treatment, potentially increasing market share and revenue. The planned regulatory submissions indicate confidence in the product's approval, which could drive stock prices up.
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