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Biogen granted marketing authorization for Qalsody by EC

Biogen announced the European Commission, or EC, has granted marketing authorization under exceptional circumstances and maintained orphan designation for Qalsody for the treatment of adults with amyotrophic lateral sclerosis, or ALS, associated with a mutation in the superoxide dismutase 1 gene, or SOD1-ALS. Qalsody is the first treatment approved in the European Union to target a genetic cause of ALS, also known as motor neuron disease, or MND.

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