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Drug intelligence / Profile preview
211At-AstraTate
- Development stage
- Preclinical
- Lead developer
- TetraKit Technologies
- Modality
- Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Alpha Emitters → Radiopharmaceuticals, Peptide-Drug Conjugates → Peptide Conjugates → Peptides
- Administration
- Intravenous
01
Overview
211At-AstraTate (also known as AstraTate or OCT-TBD) is a preclinical-stage targeted alpha-particle therapy (TAT) being developed by TetraKit Technologies, a spin-off from the University of Copenhagen, for the treatment of neuroendocrine tumors (NETs). The radiopharmaceutical consists of the somatostatin receptor type 2 (SSTR2)-targeting peptide octreotate labeled with the alpha-emitting radionuclide astatine-211 (211At) using TetraKit's proprietary tetrazine-based radiolabeling platform. By targeting SSTR2, which is highly overexpressed on neuroendocrine tumor cells, the drug delivers highly localized, high-energy alpha radiation directly to the tumor site, causing lethal double-strand DNA breaks while minimizing damage to surrounding healthy tissues.
- Other names
- AstraTate
02
Targets
DNASSTR2 (Somatostatin receptor type 2)
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