And Then There Were Three: Woodcock Offers Another Explanation For Aduhelm’s Labeling Fiasco
Acting US FDA Commissioner says it is standard for the Office of Neuroscience to issue broad labels like the one originally granted to Biogen’s new Alzheimer’s drug, but the agency declined to answer follow-up questions on such a policy. Woodcock continued to defend Aduhelm’s accelerated approval but conceded that the process might have been improved in an unusually tense public appearance.
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Survey of advisory committee members finds many believe an overwhelmingly negative vote should prevent a product approval. Survey was prompted by FDA accelerated approval of Alzheimer’s disease treatment Aduhelm despite overwhelming committee rejection.
A survey of advisory committee members finds many believe that an overwhelmingly negative vote should prevent a product approval.
Woodcock again defends the decision, saying Congress intended accelerated approval for those situations.