House committees claim concern at apparent anomalies in FDA's Aduhelm review
A stern letter has been written to the US Food and Drug Administration (FDA) by the chairs of two US congressional committees, demanding answers in relation to the approval of Biogen (Nasdaq: BIIB) and Eisai’s (TYO: 4523) Alzheimer’s drug, Aduhelm (aducanumab).
Energy and Commerce chairman Frank Pallone and Oversight and Reform chairwoman Carolyn Maloney sent a letter to the FDA’s Acting Commissioner Janet Woodcock seeking information regarding the review process and accelerated approval.
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