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RAD 402

Development stage
Phase 2
Lead developer
Radiopharm Theranostics, Ltd
Modality
Alpha Emitters → Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Beta Emitters → Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

RAD 402 is an investigational radiopharmaceutical being developed for the treatment of advanced prostate cancer. It consists of the radioactive isotope Terbium-161 (Tb-161) linked to a proprietary monoclonal antibody that targets Kallikrein-related peptidase 3 (KLK3), a protein highly expressed in prostate cancer cells but with limited expression in healthy tissue. This targeted approach aims to deliver cytotoxic radiation directly to tumor cells while sparing normal tissues. The mechanism leverages both the specificity of monoclonal antibody targeting and the therapeutic effects of beta-emitting Tb-161, which may offer advantages over existing radiotherapeutics such as reduced kidney toxicity and improved efficacy against micrometastatic disease. Developed by Radiopharm Theranostics, with isotope supply from TerThera, RAD 402 is expected to enter Phase I clinical trials for advanced prostate cancer[1][3][4][6].

Other names
RAD-402RAD402RAD 402
02

Targets

PSA (Puromycin-sensitive aminopeptidase)

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