Purpose <p>In recent years, copper-61 has attracted considerable attention from both physicists and radiochemists due to its favorable physical decay properties for PET imaging and its ease of production at any cyclotron center producing [¹⁸F]FDG. The aim of this study was to evaluate the potential of ⁶¹Cu-based radiopharmaceuticals for PET imaging of NETs, as an alternative to the commonly used gallium-68.</p> Methods <p>Copper-61 was produced by irradiation of natural zinc liquid targets, followed by post-processing. In vitro evaluation of ⁶¹Cu- and ⁶⁸Ga-labeled SST analogues was performed in SSTR positive AR42J tumor cells. PET/MRI was carried out in mice bearing AR42J subcutaneous tumors.</p> Results <p>High molar activity [⁶¹Cu]Cu-DOTA-TATE and [⁶¹Cu]Cu-NOTA-TATE were successfully prepared with a radiochemical purity of over 95% and were shown to be stable for at least 6&#xa0;h after the EOS. Both ⁶¹Cu- and ⁶⁸Ga-labeled SST analogues exhibited high cellular uptake, with residual uptake when blocked with an excessive amount of peptide precursor. [⁶¹Cu]Cu-NOTA-TATE showed the highest tumor uptake at 1&#xa0;h p.i. (13.25 ± 1.86%ID/g) and the tumor-to-non-tumor ratio increased from 1&#xa0;h to 4&#xa0;h p.i. At the later time point, tumor visualization improved compared to 1&#xa0;h p.i. Moreover, preclinical PET/MR images demonstrated that [⁶¹Cu]Cu-NOTA-TATE has a more favorable biodistribution and imaging properties than [⁶¹Cu]Cu-DOTA-TATE, with the extended PET imaging window providing a clear advantage of [⁶¹Cu]Cu-NOTA-TATE over its gallium-68 analogues.</p> Conclusion <p>[⁶¹Cu]Cu-NOTA-TATE showed similar biodistribution and pharmacokinetics to [⁶⁸Ga]Ga-DOTA-TATE at 1&#xa0;h p.i., while demonstrating superior imaging characteristics for late PET imaging. These findings demonstrate that [⁶¹Cu]Cu-NOTA-TATE holds promising characteristics for improving the detection of NETs with increased translational potential.</p>