Drug intelligence / Profile preview

NU101

Development stage
Unknown
Lead developer
Nuclidium
Modality
Beta Emitters → Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Alpha Emitters → Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

NU101 (also known as NuriPro) is a copper-based theranostic radiopharmaceutical program developed by Nuclidium AG for the management of metastatic castration-resistant prostate cancer (mCRPC). The program consists of a diagnostic component, 61Cu-NuriPro (Cu-61-NU101), and a therapeutic component, 67Cu-NuriPro (Cu-67-NU101). Both agents utilize the PSMA I&T ligand conjugated via a NODAGA chelator to target the Prostate-Specific Membrane Antigen (PSMA) expressed on prostate cancer cells. The diagnostic agent leverages the 3.3-hour half-life of Copper-61 to provide high-resolution PET imaging with a broader distribution window than traditional imaging agents. The therapeutic agent uses Copper-67 to deliver targeted beta-particle radiation to tumor sites, aiming to minimize off-target effects while maximizing anti-tumor efficacy. The diagnostic component is currently in Phase 1 clinical trials, while the therapeutic component is expected to enter clinical development in early 2026.

Brand names
NuriPro
Other names
61Cu-NuriPro67Cu-NuriPro61Cu-PSMA67Cu-PSMA
02

Targets

1C metabolism (One-carbon metabolism)

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