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EU Blow For Alzheimer’s Drug Leqembi; Eisai To Appeal

 
• By Neena Brizmohun

The EMA says the benefits of treatment with Leqembi are not large enough to outweigh its risks. Meanwhile, Alzheimer Europe is hoping that real-world findings from the US-mandated patient registry or from ongoing trials will help persuade the EU regulator to reconsider its position.

The Alzheimer’s disease drug Leqembi is already approved in the US, Japan, China, South Korea, Hong Kong and Israel • Source: Shutterstock

Eisai and Biogen are to appeal against the European Medicines Agency’s recommendation to refuse EU marketing approval for their Alzheimer’s disease (AD) drug Leqembi (lecanemab), which is already approved in the US, Japan, China, South Korea, Hong Kong and Israel.

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