Donanemab Alzheimer’s Approval: A New Era in Treatment

By João L. Carapinha

August 8, 2025

The EMA granted marketing authorization for donanemab, a monoclonal antibody targeting beta-amyloid plaques. It treats early symptomatic Alzheimer’s disease (mild cognitive impairment or mild dementia with confirmed amyloid pathology). This approval highlights donanemab’s role in Alzheimer’s treatment. It followed a re-evaluation of phase 3 data showing a 35% reduction in cognitive decline compared to placebo at 18 months. Patients with low-to-moderate tau levels benefited most. The therapy will be distributed through a controlled access program, and restrictions apply for ApoE4 homozygotes to mitigate risks like amyloid-related imaging abnormalities (ARIA).

Key Insights

Donanemab’s efficacy aligns with newer Alzheimer’s paradigms prioritizing biomarker-driven treatment. The EMA imposed strict controls, including mandatory amyloid confirmation via PET scans or CSF testing. This balances therapeutic access with safety with updated dosing regimens that aim to reduce ARIA-E risk. The TRAILBLAZER-ALZ 6 trial found a 13.7% ARIA-E incidence with titration versus 23.7% with standard dosing.

Biomarkers like beta-amyloid and tau are central to modern Alzheimer’s diagnosis. FDA-approved imaging agents (e.g., amyvid®, tavid®) and CSF tests enable precise patient stratification. Symptomatic treatments like cholinesterase inhibitors and memantine remain widely used. Many early-stage patients remain untreated, highlighting unmet needs in disease-modifying therapies. The FDA prioritizes early intervention, as seen with accelerated approvals for drugs like dordaviprone, which targets tau-related pathologies.

Implications

Donanemab‘s approval marks a shift toward precision medicine in Alzheimer’s. Implementation challenges include equitable access to biomarker testing and controlled distribution logistics. Higher upfront costs for the drug and diagnostics may be offset by savings from delaying institutionalization and caregiver burden. For the latest details on donanemab’s approval, check the full article here.

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