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Preparing for disease-modifying dementia therapies in the UK

Although lecanemab has been licensed for use in the UK, the systems to deliver this or similar disease-modifying therapies do not exist. These systems need to be developed urgently, but not at the expense of post-diagnostic care.

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Correspondence to Claudia Cooper.

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Competing interests

C.R.M. has consulted for Roche and is NHS (London) Clinical Director for dementia. J.M.S. has consulted for AVID, Biogen, Eli Lilly, GE, Merck and Roche and is Chief Medical Officer for Alzheimer’s Research UK. He is supported by the NIHR UCL/H Biomedical Research Centre. S.B. has held the following positions: Non-Executive Director Somerset NHS Foundation Trust, Trustee of the Alzheimers Society, Executive Dean of the University of Plymouth, and Pro-Vice Chancellor of the University of Nottingham. He has acted as a consultant and in an educational role for Lilly and Lundbeck. C.C. is Chief investigator of the Alzheimer’s society NIDUS programme.

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Cooper, C., Marshall, C.R., Schott, J.M. et al. Preparing for disease-modifying dementia therapies in the UK. Nat Rev Neurol 20, 641–642 (2024). https://doi.org/10.1038/s41582-024-01022-1

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