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Eisai’s Etalanetug Shows Promise in Targeting Alzheimer’s Tau Pathology

Experimental anti-tau antibody etalanetug significantly reduced levels of the plasma biomarker eMTBR-tau243 in patients with dominantly inherited Alzheimer’s disease, according to new data presented at the 2026 Alzheimer’s Association International Conference in London. The findings suggest a potential shift toward less invasive diagnostic and monitoring tools for the neurodegenerative condition.

Eisai’s Etalanetug Shows Promise in Targeting Alzheimer’s Tau Pathology

Eisai Co., Ltd. reported that its investigational compound, etalanetug (E2814), demonstrated a robust impact on tau tangle pathology, a hallmark of Alzheimer’s disease. In the Phase Ib/II Study 103, the antibody reduced plasma eMTBR-tau243 levels by 78% after three months and over 90% after nine months of treatment. These results closely mirror changes observed in cerebrospinal fluid, positioning the plasma assay as a viable, non-invasive alternative to traditional lumbar punctures or PET scans.

Unlike other tau species that increase in plasma due to peripheral tissue stabilization, eMTBR-tau243 is largely absent in healthy individuals and specifically tracks brain-based tau pathology. The study also marked the first time an anti-tau therapy has been shown to reduce p-tau205 in the cerebrospinal fluid of patients with dominantly inherited Alzheimer's disease, a key marker for late-stage pathology. Etalanetug, discovered in collaboration with University College London, is designed to bind to the microtubule-binding region of the tau protein, effectively preventing the seeding and propagation of tangles throughout the brain. The drug is currently undergoing further evaluation in the Tau NexGen Phase II/III trial and a global study for early sporadic Alzheimer's, both in combination with lecanemab.

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