Today’s approval of lecanemab (Leqembi®) from the Medicines and Healthcare products Regulatory Agency is a great step in the right direction for the treatment of Alzheimer’s disease. It’s heartening to see progress, and while the decision from NICE - National Institute for Health and Care Excellence not to make the drug available on the NHS is difficult, we hope more people will have access to this potentially life-changing drug over time. We’re proud of our contributions to the humanisation of lecanemab, and while it signifies a significant breakthrough in the future treatment of Alzheimer's and similar diseases, we acknowledge that early diagnosis remains a crucial challenge. This is why we are committed to advancing our efforts with partners like the UK Dementia Research Institute and continue to invest in innovative research to improve early detection and intervention.
📣 We have approved a product licence for Lecanemab (Leqembi) for use in the early stages of Alzheimer’s disease Lecanemab is the first treatment for Alzheimer’s disease licensed for use in Great Britain that targets the underlying pathology and shows some evidence of efficacy in slowing the decline including in quality of life and independence for those suffering from the disease. 💡 Lecanemab is approved to treat adults in the early stages of Alzheimer’s disease who have one or no copies of the apolipoprotein E4 gene (APOE4). Julian Beach, our Interim Executive Director, said: “Licensing medicines which meet acceptable standards of safety, quality and efficacy is a key priority for us. “We’re assured that, together with the conditions of the licence approval, the appropriate regulatory standards for this medicine have been met. “As with all medical products, we will keep its safety under close review, and with a controlled access programme and safety studies we will ensure that the benefit risk of Lecanemab in clinical use is closely followed up.” To learn more, visit ➡️ https://bit.ly/46Z862T