Drug intelligence / Profile preview

florquinitau F 18

Development stage
Approved
Lead developer
Lantheus
Modality
Small Molecules, Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

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.

Brand names
TAUKLARIFY
Other names
florquinitau F 18 injection
02

Targets

MAOA (Monoamine oxidase A)Amyloid-beta aggregate (N-terminal epitope)Tau (Microtubule-associated protein tau (aggregated))

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