Drug intelligence / Profile preview

Cu-FBP8

Development stage
Unknown
Lead developer
Massachusetts General Hospital
Modality
Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Peptides
Administration
Intravenous
01

Overview

Cu-FBP8 (also known as [64Cu]FBP8) is a novel fibrin-targeted radiopharmaceutical developed for positron emission tomography (PET) imaging. It consists of a cyclic disulfide peptide (FBP8) with high affinity and specificity for fibrin, conjugated to a copper-64 (64Cu) radioisotope via a chelator (such as NODAGA). By selectively binding to fibrin, a major component of blood clots and pathological tissue deposits, Cu-FBP8 enables the non-invasive detection and characterization of arterial and venous thrombosis, pulmonary embolism, left atrial appendage thrombi, and pathological fibrin deposition in diseases like multiple sclerosis and cardiac amyloidosis.

Other names
64Cu-FBP8[64Cu]FBP8copper Cu 64 FBP8copper Cu 64-FBP8copper-64 fibrin-binding peptide 8copper64 fibrin-binding peptide 8copper 64 fibrin-binding peptide 8copper-64 fibrin-binding probe 8copper64 fibrin-binding probe 8copper 64 fibrin-binding probe 8fibrin-binding probe 8
02

Targets

Fibrin (Factor Ia)

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