The search for effective Alzheimer’s treatments has recently accelerated, marked by significant progress from medical institutions and pharmaceutical companies. Alzheimer’s disease, characterized by memory and cognitive decline, affects millions worldwide. Recent developments offer new hope in the fight against this debilitating condition.
NIH Grant Supports Genetic Research at Banner Alzheimer's Institute
The Banner Alzheimer's Institute in Phoenix has been awarded a $74.5 million grant from the National Institutes of Health (NIH). This five-year funding will support research focused on treating Alzheimer's linked to hereditary genetic mutations, specifically the presenilin 1 (PSEN1) E280A mutation prevalent among certain Colombian families. The study aims to understand how this genetic anomaly influences the onset of Alzheimer's.
Dr. Eric Reiman, executive director of Banner Alzheimer's Institute, emphasized the importance of this collaboration with the University of Antioquia, highlighting the global effort required to address the complexities of Alzheimer's. The research will investigate the formation of amyloid plaques, a hallmark of Alzheimer's, and evaluate whether their removal can halt or alter cognitive impairment. The initial phase will treat participants with donanemab, an FDA-approved medication for Alzheimer’s.
The second phase, starting in fall 2025, will enroll approximately 200 individuals, both cognitively unimpaired and mildly impaired, from the Colombian cohort. Researchers also plan to include around 40 non-carriers on placebo to comprehensively assess treatment effectiveness.
EMA Approves Lecanemab (Leqembi) for Use in Europe
In Europe, lecanemab, marketed as Leqembi, has been approved by the European Medicines Agency (EMA). This marks the first Alzheimer’s drug licensed for use in Great Britain that has demonstrated tangible slowing of the disease's progression.
Lecanemab works by targeting amyloid protein production to reduce its accumulation around brain cells. Following clinical trials, the EMA approved the medication for early-stage Alzheimer’s. However, safety concerns remain, as the drug may cause severe side effects, including potential brain hemorrhages, particularly in individuals with specific genetic risks.
The EMA initially hesitated to approve lecanemab due to concerns about the balance of risks and benefits. Approval was granted after re-evaluation, focusing on patients with lower genetic predispositions for severe side effects. Specifically, patients with one or no copies of the ApoE4 gene, linked to higher Alzheimer’s risks, are considered eligible for treatment.
Leqembi has been available in the US since January. British health authorities are working to integrate this treatment responsibly, emphasizing controlled programs to ensure appropriate patient selection.
Expert Perspectives and Future Directions
Experts express cautious optimism about these developments. Hilary Evans-Newton, CEO of Alzheimer’s Research UK, noted that lecanemab represents progress, even though it is not a cure. Dr. Mercè Rovira from the Ace Alzheimer Center emphasized the urgent need for continued research and development, highlighting the importance of balancing aggressive research with patient safety.
These parallel paths—genetic research and pharmacological advancements—share the goal of improving the lives of those affected by Alzheimer’s. Collaborative efforts and cutting-edge research offer the potential to develop effective treatment options, addressing both symptoms and underlying mechanisms of the disease. With continued dedication and investment, the paradigm of Alzheimer's care may shift significantly, offering brighter futures for individuals and families facing this challenging disorder.
