The ASI Responds to FDA Approval of Lecanemab

The Alzheimer Society of Ireland (The ASI) welcomes the positive decision by the US Food & Drug Administration (FDA) to approve the Lecanemab antibody, which will be marketed as Leqembi, under their accelerated approval pathway. Leqembi targets a harmful protein called amyloid beta in the brain, and data indicates that it has the potential to slow down the progression of Alzheimer’s Disease.*

Leqembi’s accelerated approval was based on Phase II trial data, but in recent months further data from a large Phase III trial was presented by the Japanese Pharmaceutical Company Eisai at the annual Clinical Trials in Alzheimer’s Disease (CTAD) conference in San Francisco. This data supported the earlier results and provided more information on the potential benefits of the drug.

There are currently an estimated 64,000 people with dementia in Ireland, and by 2045, that number is anticipated to increase to 150,000.

Responding to this promising news, The ASI Research and Policy Manager, Dr Laura O’Philbin, said:

“The FDA’s decision to grant accelerated approval of Leqembi is a hugely positive and significant step closer to a credible treatment option for Mild Cognitive Impairment and early Alzheimer’s Disease.

‘In Europe, we expect Eisai to file for marketing approval with the European Medicines Agency by March this year. The world is watching and waiting, and there is no denying that we have entered into a hugely exciting time in the treatment of Alzheimer’s Disease, with news of other drug therapies also expected this year”.

It’s important to remember that we still have a way to go as Leqembi will need to go through the FDA’s full traditional process and that this drug will not be suitable for everyone and carries some safety concerns. The Alzheimer Society of Ireland looks forward to continuing to support all people affected by dementia”.

To read the FDA’s Full Statement, please follow this link.