EMA Refuses Marketing Authorization for Alzheimer’s Drug

AI Summary

This article discusses how the EU has refused to grant marketing authorization for Leqembi, a drug for Alzheimer's, due to concerns about its risk of serious adverse events outweighing its ability to delay cognitive decline.

Leqembi’s EU-wide marketing authorization was refused because the drug’s effect on delaying cognitive decline does not counterbalance the risk for serious adverse events.
Medscape Medical News

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