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Barbara McGowan et al

in the U.K

Therefore, multi-targeting or unimolecular peptides possessing combinatorial agonism at GIPR, GLP-1R and GCGR have been extensively explored and more than a dozen peptides including two GIPR/GLP-1R dualagonists, ten GLP-1R/GCGR dualagonists and five GIPR/GLP-1R/GCGR triagonists have entered into clinical development (Fig

In short, triple agonist peptides are backed by published results, which open grant and protocol opportunities

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