27 June 2025
The decision cites high treatment costs, limited clinical benefits, and insufficient long-term evidence. NICE also noted the significant burden on NHS resources and potential displacement of more effective treatments. Expert comments included concerns that the modest benefits observed in trials were unlikely to be noticeable to patients, especially given the risks and substantial monitoring required. Stakeholders can appeal NICE’s decision by 8 July 2025. The draft recommendation contrasts with recent European approval of lecanemab.