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To provide a tool for direct assessment of occupancy at the GCGR we recently developed the Positron Emission Tomography (PET) radioligand [ 68 Ga]Ga-DO3A-Tuna-2 (also known as [ 68 Ga]Ga-DO3A-S01-GCG) 7 that displayed suitable affinity and selectivity for the GCGR in rat, non-human and human liver, in combination and with negligible cross-activity on the GLP1R

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Its extreme potency means tiny doses suffice, which partially offsets the higher per-milligram cost