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S2CID 2873101

Importantly, this relationship did not hold up for prostate cancer

Unlike selective GLP-1 receptor agonists, GLP2s unique dual-action mechanism activates both incretin pathways simultaneously, representing a novel therapeutic class often referred to as twincretins. The peptides strategic design includes lipidation with a C20 fatty diacid moiety attached via a hydrophilic linker, which enables albumin binding and extends its half-life to approximately 5 days, permitting convenient once-weekly dosing

This program helps make regenerative medicine more accessible for out-of-state and international patients