Eli Lilly and Company has announced that the European Medicines Agency's Committee for Medicinal Products for Human Use $(CHMP)$ has issued a positive opinion recommending donanemab for the treatment of early symptomatic Alzheimer's disease. This recommendation is aimed at adults with confirmed amyloid pathology who are apolipoprotein E ε4 (ApoE4) heterozygotes or non-carriers. The European Commission is expected to make a final regulatory decision on donanemab in the coming months. This development is based on encouraging clinical trial data demonstrating donanemab's potential to slow cognitive and functional decline, marking a significant milestone in Alzheimer's treatment efforts across Europe.
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