Reported Earlier, Eisai And Submit LEQEMBI BLA For Subcutaneous Alzheimer's Treatment To FDA, Targeting Early Disease Stages
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Eisai and Biogen have submitted a Biologics License Application (BLA) to the FDA for a subcutaneous version of LEQEMBI, targeting early-stage Alzheimer's. The application is based on data from the Clarity AD study. If approved, the LEQEMBI autoinjector could be used at home or in medical facilities, offering a more convenient administration method.
November 01, 2024 | 7:29 am
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Biogen, in collaboration with Eisai, has submitted a BLA for a subcutaneous version of LEQEMBI to the FDA. This could lead to a new, more convenient treatment option for early-stage Alzheimer's patients.
The submission of the BLA for a subcutaneous version of LEQEMBI represents a significant development for Biogen, as it could lead to a new product offering in the Alzheimer's treatment market. This could positively impact Biogen's stock if approved, due to the potential for increased market share and convenience for patients.
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