FDA accepts Eisai's subcutaneous Leqembi filing, sets January 25 decision date

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via About a month after Eisai initiated a rolling FDA application for its subcutaneous form of Leqembi, the U.S. agency has accepted the filing.

And with that rubber stamp, Eisai's SC form of its much-hyped Alzheimer's drug has a date with FDA destiny: January 25, 2025, according to a Monday release.

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