FDA Accepts Biogen’s New Drug Application and Grants Priority Review of Tofersen for SOD1 MND

Biogen is seeking approval of tofersen under the FDA’s accelerated approval pathway, based on the use of neurofilament as a surrogate biomarker. Decision expected 25 Jan 2023. Results from their phase 1 up to most recent phase 3 VALOR and OLE studies is included. Tofersen targets subtype of MND caused by SOD1 mutation. Click link to read news release.

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