Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
61Cu-NU101 (also known as 61Cu-noDAGa-PSMA I&T) is an investigational radiopharmaceutical diagnostic imaging agent developed by Hoag Memorial Hospital Presbyterian for the detection of prostate cancer metastases. It consists of the positron-emitting radioisotope copper-61 (61Cu) complexed with the chelator noDAGa and conjugated to the PSMA I&T ligand. This agent targets Prostate-Specific Membrane Antigen (PSMA), a protein highly expressed on the surface of prostate cancer cells. By binding to PSMA, 61Cu-NU101 allows for high-resolution Positron Emission Tomography (PET) imaging of primary and metastatic prostate cancer lesions. The use of 61Cu, which has a half-life of approximately 3.3 hours, may offer logistical advantages over other PSMA-targeted tracers like 68Ga-PSMA-11 or 18F-DCFPyL (Pylarify) by allowing for centralized production and longer imaging windows. It is currently being evaluated in Phase 2 clinical trials to compare its diagnostic performance against FDA-approved PSMA PET agents.
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 61Cu-NU101.