Notwithstanding a three-month delay in a US Food and Drug Administration verdict, Biogen, Inc. is including the Alzheimer’s disease drug aducanumab in its 2021 guidance as dampened sales of its approved multiple sclerosis (MS) and spinal muscular atrophy (SMA) drugs have weighed on revenues. And if the amyloid-beta-targeting drug is not approved, the company maintains it still has a deep pipeline beyond aducanumab.
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