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Activates melanocortin receptors through sublingual absorption to support desire and arousal

The first three measurements were used to establish a baseline rate

doi: 10.1530/EJE-14-0712 65 SistiECocoBMenconiFLeoMRocchiRLatrofaFet al

To improve the pharmacokinetic profile and further explore the therapeutic potential of such an endogenously based GLP-1R/GcgR co-agonist, a DPP-IV-resistant OXM analogue was developed by adding a d-stereoisomer of serine at position 2 and a cholesterol moiety to the C-terminal domain

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