Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
A radiolabeled antibody drug, 64Cu-DOTA-TLX592 is a radioimmunoconjugate composed of a humanized, engineered monoclonal antibody (HuX592r) targeting the tumor-associated antigen prostate-specific membrane antigen (PSMA), which is highly expressed in prostate cancer cells. The antibody is conjugated with the chelator DOTA and labeled with the positron-emitting isotope copper-64 (^64Cu), enabling detection by PET imaging. It is primarily developed as a diagnostic and dosimetry agent to predict therapeutic behavior for future use with therapeutic radionuclides such as actinium-225 (^225Ac). The drug demonstrates rapid blood clearance and hepatic elimination, favorable for targeted alpha therapy applications. Developed by Telix Pharmaceuticals, it is being investigated in Phase I clinical trials for metastatic prostate cancer[1][2][3][4][5].
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-DOTA-TLX592.