Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
64Cu-NODAGA-CANF is a novel positron emission tomography (PET) radiopharmaceutical imaging agent developed by the Washington University School of Medicine. It consists of the positron-emitting radioisotope copper-64 (64Cu) chelated by NODAGA (1,4,7-triazacyclononane-1-glutaric acid-4,7-diacetic acid) and conjugated to C-type atrial natriuretic factor (CANF), a selective peptide ligand for the natriuretic peptide receptor C (NPR-C). NPR-C is upregulated in atherosclerotic plaques, particularly in vulnerable, unstable lesions. 64Cu-NODAGA-CANF is designed for non-invasive PET-MR or PET-CT imaging of carotid atherosclerosis to identify high-risk plaques and predict stroke risk. It is currently being evaluated in Phase 1 clinical trials for dosimetry, safety, and biodistribution in healthy volunteers.
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-NODAGA-CANF.