Drug intelligence / Profile preview

F-18 3F4AP

Development stage
Phase 1
Lead developer
Massachusetts General Hospital
Modality
Small Molecules, Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

**F-18 3F4AP** is a radiolabeled small molecule positron emission tomography (PET) tracer developed for imaging demyelination in the central nervous system. It is a fluorinated analog of the FDA-approved multiple sclerosis drug 4-aminopyridine (fampridine), specifically labeled with fluorine‑18 for PET imaging. The compound binds to exposed voltage-gated potassium channels that become accessible when myelin sheaths are lost due to demyelinating diseases such as multiple sclerosis (MS), Alzheimer's disease, and traumatic brain injury. By targeting these potassium channels, F‑18 3F4AP enables visualization and quantification of demyelinated lesions in vivo. The tracer has demonstrated metabolic stability and high specificity for demyelinated regions in preclinical models and early human studies[1][6][8]. Its primary use is investigational as a diagnostic tool to assess myelin integrity in neurological disorders.

Other names
F18-3F4APF-18-3F4APF 18-3F4AP[^18F]3-fluoro-4-aminopyridine
02

Targets

Kir (Inward-rectifier potassium channels)

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