An experimental Alzheimer’s drug outperforms one just approved by the FDA

The experimental Alzheimer’s drug donanemab slowed progression of the disease by about 35% in a recent study, outperforming the just approved drug Leqembi.

Reported findings: The study involved over 1,700 individuals and the findings suggest that donanemab is as effective, if not more, than Leqembi which has been shown to reduce progression by about 27%.
* The experimental drug has been described as “the biggest effect that’s ever been seen in an Alzheimer’s trial for a disease-modifying drug”.

Explaining the drugs: Donanemab, like Leqembi, is a monoclonal antibody designed to remove beta-amyloid, a substance which forms sticky plaques in the brains of Alzheimer’s patients, from the brain.
* The donanemab study focused on patients with early Alzheimer’s that exhibited only mild cognitive symptoms.
* The researchers found that patients with advanced stages of the disease saw less benefit from the drug, suggesting the importance of early intervention.

Administration process: The study also implies that patients might not require monthly intravenous infusions of donanemab for life.
* Once most of the plaques in their brains were gone, generally within a year, treatment was ceased and the plaques did not re-appear during the 18-month study period.
* This finding may give donanemab an edge over Leqembi which requires ongoing treatment, but the longevity of donanemab’s effects years after treatment ends remains unclear.

Safety concerns: Both donanemab and Leqembi can cause dangerous swelling or bleeding in the brain.
* In the donanemab study, brain scans revealed this side effect in approximately 25% of patients with about 6% showing related symptoms like headache, nausea, and confusion.
* Three patient deaths were reported during the study.

Not a cure: It is important to underscore that donanemab is not a cure for Alzheimer’s, but its benefits equate to about a seven-month delay in memory and cognitive loss.
* The manufacturer of donanemab, Eli Lily, has submitted the results of the study to the FDA and a decision is expected by the end of the year.

View original article on NPR

This summary was created by an AI system. The use of this summary is subject to our Terms of Service.

Contact us about this post

Posted

in

by

Tags:

Comments

Leave a Reply

Your email address will not be published. Required fields are marked *