Drug intelligence / Profile preview

SAR-bisFAP

Development stage
Preclinical
Lead developer
Clarity Pharmaceuticals
Modality
Small Molecules, Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

SAR-bisFAP is a novel dimeric radiopharmaceutical targeting fibroblast activation protein (FAP), developed by Clarity Pharmaceuticals. It is designed to overcome the low tumor uptake and retention seen with earlier FAP-targeted agents by combining an industry-leading FAP inhibitor (bisFAP) with Clarity’s proprietary SAR chelator technology. This allows for labeling with copper isotopes—copper-64 for diagnostic imaging and copper-67 for targeted radiotherapy of cancers. Preclinical studies have demonstrated that SAR-bisFAP exhibits significantly higher tumor uptake and prolonged retention compared to monomeric FAP agents and first-generation compounds such as FAPI-46, making it a promising candidate for next-generation cancer theranostics[5][6][8].

Brand names
SAR-bisFAP
Other names
64Cu-SAR-bisFAP67Cu-SAR-bisFAP
02

Targets

FAP (Fibroblast activation protein alpha)

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