Abstract Prostate-specific membrane antigen (PSMA) is a transmembrane glycoprotein highly expressed on prostate cancer cells, making it an ideal target for novel prostate cancer therapies. Currently, there are several actinium-225 (225Ac)-PSMA-targeting small molecules (SMOL) in clinical development for treating patients with metastatic castration-resistant prostate cancer. 225Ac-PSMA-Trillium (BAY 3563254), is a novel PSMA-targeting molecule which comprises a highly specific PSMA-binding motif, an albumin-binding domain to optimize tumor uptake and retention, and a Macropa™ chelator complexed with the alpha-emitter 225Ac. Here, we compared 225Ac-PSMA-Trillium with three other 225Ac-PSMA-SMOLs, i.e., 225Ac-PSMA-617, 225Ac-PSMA-R2 and 225Ac-PSMA-I Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 7202.
Building similarity graph...
Analyzing shared references across papers
Loading...
Urs B. Hagemann
Maria Spelling
Shankari Nair
Cancer Research
Corlife (Germany)
Building similarity graph...
Analyzing shared references across papers
Loading...
Hagemann et al. (Fri,) studied this question.
www.synapsesocial.com/papers/69d1fceba79560c99a0a2aaa — DOI: https://doi.org/10.1158/1538-7445.am2026-7202