Eisai and Biogen begin application process for second Alzheimer's drug

Lecanemab, which is being developed as a treatment for Alzheimer's disease by Eisai and Biogen, has been sent to the FDA through a "rolling submission" process under an accelerated approval pathway.

BY ELIZABETH MØNSTED JOHANSEN, TRANSLATED BY DANIEL PEDERSEN

Eisai and Biogen are now making another attempt to tackle Alzheimer's disease, initiating a "rolling submission" process at the US Food and Drug Administration (FDA) of the drug lecanemab, the companies inform in a press release.

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