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116 CR has been shown to shape the TME in several ways, including through the specific reduction in the number of TAMs, increase in the formation of CD8 + cytotoxic T cells and memory T cells, and negative modulation of immunosuppressive Treg cell activity and immunosuppressive cytokine levels

As an investigational triple receptor agonist targeting GLP-1, GIP, and glucagon receptors, it has shown considerable promise in Phase 2 clinical trials for obesity and type 2 diabetes

[4] The result is a GHRH-receptor agonist that survives slightly longer in circulation than the unmodified hormone while still producing the same fundamental action: stimulation of the somatotroph cells of the anterior pituitary to release GH in a pulsatile, physiologic pattern, which in turn raises IGF-1