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TAUKLARIFY (florquinitau F 18) is an F18-labeled small molecule radiopharmaceutical developed by Enigma Biomedical USA in collaboration with Lantheus for use in positron emission tomography (PET) imaging. It is specifically indicated for the visualization of tau neurofibrillary tangles (NFTs) in the brains of adult patients with cognitive impairment who are being evaluated for Alzheimer's disease. By binding to aggregated tau protein deposits, a hallmark of Alzheimer's pathology, TAUKLARIFY provides clinicians with a diagnostic tool to assess the presence and density of tau pathology. The agent received FDA approval on August 14, 2026, following Fast Track designation.
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