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The logo of Eisai Co Ltd is displayed at the company headquarters in Tokyo, Japan on March 8 2018. File Picture: REUTERS/Issei Kato
The logo of Eisai Co Ltd is displayed at the company headquarters in Tokyo, Japan on March 8 2018. File Picture: REUTERS/Issei Kato

Alzheimer's patients in Britain’s state-run health service are unlikely to get access to Eisai and Biogen’s new Leqembi drug, after it was approved on Thursday by the country’s regulator but deemed too expensive for wide use.

The Medicines and Healthcare products Regulatory Agency said the drug, also known as Lecanemab, is the first treatment for Alzheimer’s licensed for use in the country “that shows some evidence of efficacy in slowing progression of the disease”.

But in its draft guidance published simultaneously, the National Institute for Health and Care Excellence said the medicine's high cost and need for intensive monitoring for side effects “means it cannot be considered good value for the taxpayer”.

The UK cost effectiveness body’s findings mark the latest blow faced by the drugmakers amid slow take-up of the drug in the US It also highlights the complexities of a new class of drugs that benefit early-stage Alzheimer patients but could cause rare and serious side effects.

The therapy for early Alzheimer’s disease has been approved in the US, China, Hong Kong, Israel, Japan, South Korea and the UAE.

But last month the EU’s drugs regulator rejected the drug, saying the risk of serious brain swelling did not outweigh its small impact on slowing cognitive decline.

The companies said then that they will seek re-examination of the recommendation, but did not disclose what information they would provide the regulator.

Reuters

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