Treatment studies
tested GH, TSH, LH secretion and metabolic markers
result Combined GHRP-2+TRH+GnRH reactivated GH, TSH, LH axes and reduced ureagenesis (P=0.01) and increased serum osteocalcin (P=0.03), effects not seen with GHRP-2 alone.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GH secretion (pulsatile GH, GH regularity, IGF‑I, IGFBP‑3, IGFBP‑1, GH mass after GHRP‑2 infusion)
result Testosterone increased serum Te from 0.87 to 5 and 7.3 nmol/L (P<0.001) but did not change pulsatile GH (29, 32, 27 µg/L/12h), GH regularity (0.52‑0.57), IGF‑I (126‑141 µg/L), or GH mass after GHRP‑2 (123‑147 µg/L/3h).
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested food intake
result GHRP-2 increased ad libitum food intake by 10.2 ± 3.9% at low dose (p=0.011) and 33.5 ± 5.8% at high dose (p<0.001) versus placebo.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GH secretion response to GHRP-2
result GHRP-2–stimulated GH secretion was unchanged after GnRH agonist–induced short‑term hypogonadism (no significant difference reported).
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested cortisol concentrations and pulsatile cortisol secretion
result GHRP-2 raised peak cortisol to 616±42 nmol/L, higher than saline/GHRH/SS (≈420±21 nmol/L).
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Treatment studies
tested change in height SD score (growth) after 48 weeks
result Mean height SD change: placebo 0.07 SD, low‑dose GHRP‑2 0.03 SD, high‑dose GHRP‑2 0.02 SD; no significant differences among groups.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested synchronization of GH, TSH and prolactin secretion
result GHRP-2 infusion (1 µg/kg/h) markedly synchronized serum GH, TSH and PRL profiles (all P≤0.007), whereas placebo showed no synchrony.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GH secretion (peak level and AUC)
result Peak GH to GHRP-2 was 80.8±21.2 µg/L before prednisone and 71.3±18.4 µg/L during prednisone (no significant change); AUC decreased significantly (P=.04).
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GH response; sensitivity 78.6%, specificity 100%
result Using a cut‑off of 17 mU/L, the GHRH/GHRP‑2 test showed 78.6% sensitivity and 100% specificity for diagnosing adult GHD compared with ITT.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested pulsatile GH secretion and IGF‑I, IGFBP‑3, IGFBP‑5 concentrations
result 30‑day GHRP‑2 infusion (1 µg/kg·h) increased pulsatile GH >3‑fold on day 1 and >1.8‑fold on days 14/30 (P<0.001 vs saline) and raised IGF‑I to a stable plateau (P<0.025).
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested plasma growth hormone (GH) peak levels
result Pralmorelin markedly increased plasma GH in healthy subjects; GH response was significantly lower in GH‑deficient patients, with a diagnostic cut‑off GH peak of 15.0 µg/L.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GH secretory burst mass, frequency, and irregularity
result Octreotide (1 µg/kg) reduced fasting GH from 0.27±0.07 to 0.12±0.02 µg/L (P=0.020) and GH burst mass from 2.7±0.65 to 0.55±0.11 µg/L (P=0.013); in GHRP-2‑stimulated setting, burst mass fell from 28±3.2 to 18±2.0 (P=0.045).
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GH secretory-burst mass
result E2 clamp increased mean fasting GH (P=0.032), GH burst mass (P=0.037), and maximal stimulation by l-arginine/GHRP-2 (P=0.028).
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested pulsatile GH secretion
result L-arginine/GHRP-2 induced 2.2‑fold greater burst‑like GH release in women vs men (P=0.015); fasting GH 7.6‑fold higher in women (P<0.001).
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested percentage feedback inhibition (GH autofeedback)
result Feedback inhibition correlated negatively with age after rhGH/saline infusion (R²=0.42, P=0.005) and with IGF‑I after rhGH/GHRP‑2 infusion (R²=0.40, P=0.009).
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GH and IGF‑I secretion
result Testosterone raised fasting GH (~7.5‑fold) and IGF‑I, but did not alter maximal GH response to GHRP‑2 infusion (no‑change).
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GH secretory burst duration/shape
result GHRP-2 stimulation lengthened GH secretory bursts regardless of estradiol presence.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested basal and pulsatile growth hormone secretion
result Te/placebo raised testosterone 2.8‑fold, DHT 2.6‑fold, estradiol 1.9‑fold; Te/dutasteride reduced DHT 89% and Te/anastrozole reduced estradiol 86%; testosterone positively predicted GH peak (P<0.001) and GHRP‑2‑stimulated pulsatile GH (P<0.001).
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested pulsatile growth hormone secretion
result GHRP-2 stimulated GH more than GHRH (P<0.001) under both low and high estradiol; postmenopausal women had lower GH responses to GHRP-2 (P<0.001).
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested Rec/Pit ratio (GH isoform ratio)
result GHRP-2 (100 µg IV) reduced the rhGH‑induced Rec/Pit ratio to 39.9‑43.9% of the elevated level, masking detection of rhGH doping.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GH nadir, peak concentrations and integrated GH recovery
result Dual‑peptide infusion increased nadir GH (P=0.001) and peak GH (P<0.001) versus saline, with greater peak response in women (P=0.016).
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GH recovery (integrated, nadir, peak)
result GHRP-2 enhanced nadir and peak GH during feedback (P<0.001 for both)
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested detection window of approximately 4.5 h for GHRP‑2 in urine
result Detection window of approximately 4.5 h for GHRP‑2 in urine
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested urinary detection window of GHRP-2 and its metabolites
result GHRP-2 free acid and GHRP-2 (1-3) free acid detected in urine up to 47 h post‑nasal dose.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Treatment studies
tested body weight increase of 6.7 kg and improved hypoglycemia
result Body weight increased by 6.7 kg (21.1 kg→27.8 kg) over 14 months; hunger and food intake increased, early satiety decreased, hypoglycemia improved.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GH secretion (peak) after GHRP‑2 stimulation
result GH peak correlated negatively with BMI (r=-0.59, p=0.001) and increased after LSG in the two obese patients.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Treatment studies
tested serum IGF-1 level
result IGF-1 rose from 159.5 ± 26.7 ng/mL to 239.0 ± 54.6 ng/mL after ~134 days (p < .0001).
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GHRP-2 test showed preserved GH response, confirming isolated ACTH deficiency
result GHRP-2 test indicated normal GH secretion, supporting isolated ACTH deficiency in the patient
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested poor ACTH response to GHRP-2 load test
result GHRP-2 load test failed to elicit an ACTH response, indicating ACTH deficiency.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GHRP-2 detectable in DBS up to 4 h post‑dose
result A single 100 µg IV dose of GHRP‑2 was detectable in DBS for up to 4 h; limit of detection 50 pg/ml; long‑term stability >2 years.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GHRP-2 assay showed excessive basal GH response; hypoglycemia resolved after dexamethasone treatment
result GHRP-2 assay revealed an excessive basal GH reaction, confirming NICTH; hypoglycemia was corrected with dexamethasone
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GH deficiency identified via GHRP-2 test
result A GHRP-2 provocation test revealed GH deficiency in the patient; subsequent GH replacement therapy improved his muscle pain and depression.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested peak GH response to GHRP‑2 / prevalence of severe GHD
result 45/104 (43%) had severe GHD; overweight odds ratio 3.86 (95% CI 1.02‑14.66); postoperative severe GHD 100% vs 48% (P<0.001).
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested diagnostic accuracy of ACTH response in GHRP2 test for secondary adrenal insufficiency
result ACTH response cutoff 1.55‑fold achieved 83% sensitivity, 88% specificity; combined with cortisol >10 µg/dL gave 100% specificity and accuracy 0.94 for diagnosing pituitary‑AI.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GH peak level after GHRP-2 stimulation
result GH response was preserved with a mean peak of 35.5 ng/mL after GHRP-2 stimulation in 15 long COVID patients.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GH peak response (µg/L)
result All 15 children given intranasal GHRP-2 (5–20 µg/kg) had significant GH response; mean peak GH 31.3 µg/L at 15 µg/kg. Responses to GHRP-2 comparable to iv GHRH and superior to arginine, L‑dopa, insulin.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Diagnostic & mechanistic studies
tested GH response
result additive to synergistic GH response
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
Preclinical / mechanistic research
tested rat · A 6-day intracerebroventricular infusion of the growth hormone-releasing peptide KP-102 stimulates food intake in both non-stressed and intermittently-stressed rats. (PMID 10713408 · DOI 10.1016/s0304-3940(00)00882-x)
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested rabbit · Endocrine and metabolic effects of growth hormone (GH) compared with GH-releasing peptide, thyrotropin-releasing hormone, and insulin infusion in a rabbit model of prolonged critical illness.
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested rat · Anti-inflammatory effect of the ghrelin agonist growth hormone-releasing peptide-2 (GHRP-2) in arthritic rats.
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested rat · ACTH releasing activity of KP-102 (GHRP-2) in rats is mediated mainly by release of CRF.
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested mouse · Effects of long-term treatment with growth hormone-releasing peptide-2 in the GHRH knockout mouse.
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested mouse · Growth hormone releasing peptide 2 reverses anorexia associated with chemotherapy with 5-fluoruracil in colon cancer cell-bearing mice.
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested rat · Ghrelin receptor agonist, GHRP-2, attenuates burn injury-induced MuRF-1 and MAFbx expression and muscle proteolysis in rats.
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested rat · Growth hormone releasing peptide-2, a ghrelin agonist, attenuates lipopolysaccharide-induced acute lung injury in rats.
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested mouse · Ghrelin receptor agonist, GHRP-2, produces antinociceptive effects at the supraspinal level via the opioid receptor in mice.
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested rat · [Effect of newly developed analogue of growth hormone releasing peptide [D-Ala-D-beta Nal-Ala-Trp-D-Phe-Lys-NH2 (KP-102)] on growth hormone secretion in adult male rats].
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested rat · Effect of D-Ala-D-beta Nal-Ala-Trp-D-Phe-Lys-NH2 (KP-102) on GH secretion in urethan-anesthetized rats. (PMID 7846295 · DOI 10.1016/0167-0115(94)90168-6)
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested rat · Effects of the synthesized growth hormone releasing peptide, KP-102, on growth hormone release in sodium glutamate monohydrate-treated low growth rats. (PMID 8761023 · DOI 10.1016/0024-3205(96)00356-6)
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested Differential regulation of GHRH-receptor and GHS-receptor expression by long-term in vitro treatment of ovine pituitary cells with GHRP-2 and GHRH.
result In-vitro publication captured from PubMed/Europe PMC; assay details require paper-level extraction.