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flag European agency recommends approval for Alzheimer's drug lecanemab, reversing earlier decision.

flag The European Medicines Agency (EMA) has recommended approval for lecanemab, a treatment for early Alzheimer's disease, for adult patients without or with one copy of the ApoE ε4 gene. flag This positive recommendation reverses an earlier negative assessment and, if finalized by the European Commission within 67 days, will make the drug available in the EU. flag Lecanemab is already approved in the U.S. and several other countries.

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