Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
[64Cu]Cu-SAR-FAP is a diagnostic radiopharmaceutical imaging agent developed by Clarity Pharmaceuticals for the detection and visualization of solid tumors. It consists of a fibroblast activation protein (FAP) inhibitor, derived from the small molecule UAMC1110, conjugated to a sarcophagine (SAR) chelator and radiolabeled with the positron-emitting isotope copper-64 (64Cu). FAP is a cell-surface protease that is highly overexpressed on cancer-associated fibroblasts (CAFs) within the tumor microenvironment of most epithelial cancers, while remaining nearly undetectable in healthy adult tissues. The SAR chelator provides exceptional stability for the copper radioisotope, preventing transchelation and ensuring high-contrast PET imaging with prolonged tumor retention. This agent is part of Clarity's Targeted Copper Theranostic (TCT) platform, designed to be paired with copper-67 for therapeutic applications.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on [64Cu]Cu-SAR-FAP.