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Effects of exenatide twice daily versus sitagliptin on 24-h glucose, glucoregulatory and hormonal measures: a randomized, double-blind, crossover study
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This enhanced potency reflects a higher GHS-R1a binding affinity resulting from GHRP-2s optimised hexapeptide structure incorporating D-Nal in place of GHRP-6s D-Trp, and positions GHRP-2 as the reference compound of choice when maximal GHS-R1a activation is the research objective
Diagnostic criteria applied across the included studies varied by disorder
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