Drug intelligence / Profile preview

FTX-TATEs

Development stage
Preclinical
Modality
Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Peptides
Administration
Intravenous
01

Overview

FTX-TATEs is a somatostatin receptor (SSTR)-targeted radioligand theranostic program being developed by Fuzionaire Theranostics for the diagnosis and treatment of neuroendocrine tumors (NETs). Developed using the proprietary HetSiFA® platform, FTX-TATEs are designed as 'chemical twin' analogs to the FDA-approved 177Lu-DOTA-TATE (Lutathera). The platform enables the creation of theranostic pairs that combine fluorine-18 (18F) for high-resolution PET imaging with therapeutic radionuclides such as lutetium-177 (177Lu), terbium-161 (161Tb), or actinium-225 (225Ac). By targeting SSTR-expressing cells, the drug delivers ionizing radiation directly to tumor sites for therapy or allows for precise localization via PET imaging for companion diagnostics.

Other names
SSTR-targeted radioligandchemical twin analog to 177Lu-DOTA-TATE
02

Targets

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