| Summary: | Broad availability and cost-effectiveness of <sup>99</sup>Mo/<sup>99m</sup>Tc generators worldwide support the use, and thus the development, of novel <sup>99m</sup>Tc-labelled radiopharmaceuticals. In recent years, preclinical and clinical developments for neuroendocrine neoplasms patient management focused on somatostatin receptor subtype 2 (SST<sub>2</sub>) antagonists, mainly due to their superiority in SST<sub>2</sub>-tumour targeting and improved diagnostic sensitivity over agonists. The goal of this work was to provide a reliable method for facile preparation of a <sup>99m</sup>Tc-labelled SST<sub>2</sub> antagonist, [<sup>99m</sup>Tc]Tc-TECANT-1, in a hospital radiopharmacy setting, suitable for a multi-centre clinical trial. To ensure successful and reproducible on-site preparation of the radiopharmaceutical for human use shortly before administration, a freeze-dried three-vial kit was developed. The final composition of the kit was established based on the radiolabelling results obtained during the optimisation process, in which variables such as precursor content, pH and buffer, as well as kit formulations, were tested. Finally, the prepared GMP-grade batches met all predefined specification parameters together with long-term kit stability and stability of the product [<sup>99m</sup>Tc]Tc-TECANT-1. Furthermore, the selected precursor content complies with micro-dosing, based on an extended single-dose toxicity study, where histopathology NOEL was established at 0.5 mg/kg BW, being more than 1000 times higher than the planned human dose of 20 µg. In conclusion, [<sup>99m</sup>Tc]Tc-TECANT-1 is suitable to be advanced into a first-in-human clinical trial.
|
|---|