September 2, 2025
Source: drugdu
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On August 29th local time, Japan's Eisai Co., Ltd. and the US Biogen Inc. announced that the US FDA (U.S. Food and Drug Administration) has approved the weekly maintenance dose of lencanelumab subcutaneous automatic injection (SC-AI) for the treatment of early Alzheimer's disease (AD).
Comment: As of now, there are limited AD treatment drugs approved worldwide. This approval makes Lencaneluzumab the first AD treatment drug that can be administered subcutaneously at home using an automatic injector. The entire injection process takes an average of only 15 seconds, which further consolidates the company's market position in this field.
https://finance.eastmoney.com/a/202509013500390220.html
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