Biogen, Inc.’s push to bring Aduhelm (aducanumab-avwa) to market as the first disease-modifying Alzheimer’s therapy seems to have backfired one year later. Instead of changing the lives of millions of patients and boosting the company’s profile and profits, the success of gaining accelerated approval from the US Food and Drug Administration was followed by commercial failure.
How Biogen’s Aduhelm Bet Became A Commercial Bust
Biogen caught a lucky break in getting the first FDA approval for a potentially disease-modifying Alzheimer’s therapy, but doubt over clinical benefit and commercial missteps have left Biogen in a precarious position a year later.
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Pipeline Watch is a weekly snapshot of selected late-stage clinical trial events and approvals announced by pharmaceutical and biotech companies at medical and industry conferences, in financial and company presentations, and in company releases and statements.
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