Eli Lilly has announced that the US FDA has approved a label update with a new recommended dosing regimen for Kisunla, its bimonthly treatment for adults with early symptomatic Alzheimer's disease.

The new recommended regimen has significantly reduced rates of ARIA-E (amyloid imaging abnormalities with edema/effusion) compared to the initial dosing regimen, further strengthening the treatment's established safety profile.

By significantly reducing the risk of ARIA-E, we can offer patients and caregivers greater confidence in the safety of Kisunla while maintaining its ability to reduce amyloid, the Irvine Center for Clinical Research said.


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