Longevity News

ADDF Statement: FDA Approval of Subcutaneous Starting Dose for Leqembi Advances Alzheimer

Source: PR Newswire • Published: 13 Jul 2026, 23:03

ADDF Statement: FDA Approval of Subcutaneous Starting Dose for Leqembi Advances Alzheimer

Look at the shift toward weekly at-home subcutaneous initiation for anti-amyloid Alzheimer's therapy and its implications for treatment delivery models.

Key Takeaways
  • FDA approved a weekly subcutaneous starting dose enabling at-home administration
  • Clinical data presented at AAIC showed similar performance and safety to IV initiation
  • Previously patients had an 18-month IV initiation period before switching to maintenance dosing
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