Background: Cardiac sympathetic nervous system molecular imaging has demonstrated prognostic value. Compared with meta-[C]hydroxyephedrine, [F]flubrobenguane (FBBG) facilitates reliable estimation of SNS innervation using similar analytical methods and possesses a more convenient physical half-life. The aim of this study was to evaluate pharmacokinetic and metabolic properties of FBBG in target clinical cohorts.
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