Biogen And Eisai Co., Announced That The US Food And Drug Administration Has Extended The Review Period By Three Months For The Supplemental Biologics License Application For A Once-weekly Lecanemab-irmb Subcutaneous Injection As A Starting Dose F...

Biogen Inc.

Biogen Inc.

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Biogen And Eisai Co., Announced That The US Food And Drug Administration Has Extended The Review Period By Three Months For The Supplemental Biologics License Application For A Once-weekly Lecanemab-irmb Subcutaneous Injection As A Starting Dose For The Treatment Of Early Alzheimer's Disease
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