Drug intelligence / Profile preview

18F-fallypride

Development stage
Phase 2
Lead developer
University of California, Irvine
Modality
Small Molecules, Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

18F-fallypride is a high-affinity radiopharmaceutical PET imaging agent that targets dopamine D2 and D3 receptors (D2/D3R). Developed and extensively studied by researchers at the University of California, Irvine, it is a small molecule radiotracer labeled with the radioisotope fluorine-18. It is primarily utilized in clinical research to visualize both striatal and extrastriatal dopamine receptors in the brain, facilitating the study of various neurological and psychiatric disorders such as schizophrenia, Parkinson's disease, Alzheimer's disease, and substance addiction. Beyond neuroimaging, 18F-fallypride has been investigated as a non-invasive tool for monitoring pancreatic beta-cell mass in patients with Type 1 Diabetes Mellitus, as these cells also express D2 receptors. It is used as a diagnostic research tool rather than a therapeutic agent.

Other names
fallyprideFluorine-18 fallyprideFluorine18 fallyprideFluorine 18 fallypride(S)-N-[(1-allyl-2-pyrrolidinyl)methyl]-5-(3-[18F]fluoropropyl)-2,3-dimethoxybenzamide
02

Targets

DRD3 (Dopamine receptor D3)DRD4 (Dopamine D4 Receptor)DRD2 (Dopamine D2 Receptor)

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