Neurology Central

Aducanumab: Biogen to seek US FDA approval

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Biogen (MA, USA) and Eisai Co. (Tokyo, Japan) have announced plans to pursue regulatory approval for aducanumab as a treatment for early Alzheimer’s disease (AD) after consultation with the US FDA. If approved, aducanumab would be the first line of therapy to reduce the clinical decline of AD and the first therapy to demonstrate the clinical benefit of removing amyloid beta.

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