The development and pharmacology of a new potent growth hormone (GH) secretagogue, ipamorelin, is described. Ipamorelin is a pentapeptide (Aib-His-D-2-Nal-D-Phe-Lys-NH 2 ), which displays high GH releasing potency and efficacy in vitro and in vivo. As an outcome of a major chemistry programme, ipamorelin was identified within a series of compounds lacking the central dipeptide Ala-Trp of growth hormone-releasing peptide (GHRP)-1.In vitro, ipamorelin released GH from primary rat pituitary cells with a potency and efficacy similar to GHRP-6 (EC 50 ¼ 1.3Ϯ0.4 nmol/l and E max ¼ 85Ϯ5% vs 2.2Ϯ0.3 nmol/l and 100%). A pharmacological profiling using GHRP and growth hormone-releasing hormone (GHRH) antagonists clearly demonstrated that ipamorelin, like GHRP-6, stimulates GH release via a GHRP-like receptor.In pentobarbital anaesthetised rats, ipamorelin released GH with a potency and efficacy comparable to GHRP-6 (ED 50 ¼ 80Ϯ42 nmol/kg and E max ¼ 1545Ϯ250 ng GH/ml vs 115Ϯ36 nmol/kg and 1167Ϯ120 ng GH/ml).In conscious swine, ipamorelin released GH with an ED 50 ¼ 2.3Ϯ0.03 nmol/kg and an E max ¼ 65Ϯ0.2 ng GH/ml plasma. Again, this was very similar to GHRP-6 (ED 50 ¼ 3.9Ϯ1.4 nmol/kg and E max ¼ 74Ϯ7 ng GH/ml plasma). GHRP-2 displayed higher potency but lower efficacy (ED 50 ¼ 0.6 nmol/kg and E max ¼ 56Ϯ6 ng GH/ml plasma).The specificity for GH release was studied in swine. None of the GH secretagogues tested affected FSH, LH, PRL or TSH plasma levels. Administration of both GHRP-6 and GHRP-2 resulted in increased plasma levels of ACTH and cortisol. Very surprisingly, ipamorelin did not release ACTH or cortisol in levels significantly different from those observed following GHRH stimulation. This lack of effect on ACTH and cortisol plasma levels was evident even at doses more than 200-fold higher than the ED 50 for GH release.In conclusion, ipamorelin is the first GHRP-receptor agonist with a selectivity for GH release similar to that displayed by GHRH. The specificity of ipamorelin makes this compound a very interesting candidate for future clinical development.