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Alzheimer’s disease and the clinical stage sigma-1 agonist blarcamesine

The sigma-1 receptor was initially mistaken for an opioid receptor but was later identified as a chaperone protein that regulates cellular stress and calcium balance, playing a role in neurodegenerative diseases. Blarcamesine is an oral drug that targets the sigma-1 and muscarinic receptors to restore brain cell function, reduce harmful protein buildup, and promote waste clearance, which may help slow disease progression. In a Phase 2b/3 trial for early Alzheimer’s disease, blarcamesine significantly improved cognitive decline on the ADAS-Cog13 scale and reduced brain volume loss but did not achieve statistical significance on a key functional measure. The ongoing ATTENTION-AD trial is evaluating its long-term effects, with early findings suggesting that starting treatment sooner leads to better cognitive and functional outcomes.

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The debate over Alzheimer’s diagnosis

The field of Alzheimer’s disease (AD) is seeing a heated debate about the best way to diagnose this devastating condition. On one side, the Alzheimer Association (AA) proposed new criteria that rely solely on biological markers—such as proteins seen in brain scans or found in the liquid bathing the brain and spine, called cerebrospinal fluid (CSF)—even in individuals who show no symptoms. These biomarkers, which include amyloid and tau proteins, are widely associated with the risk of developing AD. However, a group of international experts, known as the International Working Group (IWG), has proposed an alternative approach, suggesting that the disease should be diagnosed based on biological markers and clinical symptoms, rather than biomarkers alone.

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