Déjà Vu In England: Lilly’s Alzheimer’s Drug Kisunla Gets MHRA Yes, But NICE Says No

Lilly’s Kisunla has hit the same barrier as its competitor, Eisai/Biogen’s Leqembi, in England.

The UK’s drug regulator has approved Eli Lilly’s early Alzheimer’s drug Kisunla, but England’s health technology assessment agency NICE said that the product “does not currently demonstrate value” for the National Health Service.

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Eli Lilly’s early-stage Alzheimer’s disease therapy Kisunla (donanemab) has secured marketing approval in Great Britain from the Medicines and Healthcare products Regulatory Agency, but has been provisionally deemed too expensive for use on the National Health Service in England.

NICE, the health technology assessment (HTA) organization for England and Wales, said on 23 October that Kisunla demonstrated a “relatively small benefit” for patients that did not justify its price...

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