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It is not an FDA-approved drug with a prescribing label

The structures, together with mutagenesis studies, revealed distinct features of the CCK1R and CCK2R ligand-binding pockets that determine CCK1R selectivity for sulfated CCK-8 and SR146131, and CCK2R selectivity for gastrin-17, and thus highlighted the activation mechanism for both CCK1R and CCK2R

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Bone, lung, liver, and brain are the most frequent metastatic sites, and each sites possess different microenvironments to favor survival of metastasizing cancer cells [ Figure 3I ] (186, 187)