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Biogen Plans Regulatory Filing for Aducanumab in Alzheimer's Disease Based on New Analysis of Larger Dataset from Phase 3 Studies

Written by ACN Newswire - Press Releases

TOKYO, Oct 23, 2019 - (JCN Newswire) - Biogen (Nasdaq: BIIB) and Eisai, Co., Ltd. (Tokyo, Japan) has announced that, after consulting with the U.S. Food and Drug Administration (FDA), Biogen plans to pursue regulatory approval for aducanumab, an investigational treatment for early Alzheimer's disease (AD). The Phase 3 EMERGE Study met its primary

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Starter's gun goes off on new phase of media concentration as Nine-Fairfax lead the way

It is necessary to worry about health, but pessimism about the economy will hurt us

I chose the electricity retailer offering the best deal for my home. That's not what I got

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