Drug intelligence / Profile preview

[18F] SPAL-T-06

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

Overview

[18F] SPAL-T-06 is a second-generation Positron Emission Tomography (PET) radiopharmaceutical tracer developed by Eisai Co., Ltd. for the detection and quantification of tau protein aggregates in the human brain. Tau pathology, characterized by the formation of neurofibrillary tangles, is a core feature of Alzheimer's disease and other tauopathies, correlating more closely with cognitive decline than amyloid-beta plaques. SPAL-T-06 was designed to offer improved sensitivity and higher selectivity for tau aggregates compared to first-generation tracers, with significantly reduced off-target binding to sites such as monoamine oxidase-B (MAO-B). It serves as a critical biomarker tool in clinical research to facilitate early diagnosis, patient stratification, and the monitoring of therapeutic response in trials for neurodegenerative disease-modifying therapies.

Other names
18F-SPAL-T-06
02

Targets

aggregated α-syn (Alpha-synuclein (α-syn))

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