July 17, 2026
5 min read
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The FDA has approved a subcutaneous dose for initiation of lecanemab treatment in adults with Alzheimer’s disease, according to a press release from the administration. Previously, patients had to begin treatment with an intravenous dose. Researchers conducting a real-world study, presented at the Alzheimer’s Association International Conference, found that most patients remained stable over an
July 17, 2026
5 min read
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Outcomes following subcutaneous and intravenous treatment with lecanemab for Alzheimer’s disease were comparable, according to a…

ADDF Statement: FDA Approval of Subcutaneous Starting Dose for Leqembi Advances Alzheimer's Care Toward Combination Therapy Future

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