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Study · Non-randomized trial · n = 10 · 1998

4 results

Pharmacokinetics and pharmacodynamics of growth hormone-releasing peptide-2: a phase I study in children.

Pihoker C, Kearns GL, French D, Bowers CY

The Journal of clinical endocrinology and metabolism1 Apr 1998Cited by 17 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study4

4 results from studies that gave the peptide. 4 results from people.

  1. 01HumanNon-randomized trialPharmacokinetics

    In prepubertal children with short stature, a single intravenous 1 microg/kg dose of GHRP‑2 gave a terminal half-life of 0.55 h, Cmax of 7.4 ng/mL and clearance of 0.66 L/h x kg.

    In plain wordsIn short children, GHRP‑2 given into a vein was cleared from the blood quickly, with a half-life of about half an hour.

    Peptide
    GHRP-2
    Outcome
    Not applicableGHRP-2 pharmacokinetics
    Study

    n = 10

    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    1 microg/kg · intravenous · single dose over 1 minAs given in this study (human).

    Measurements

    alpha
    13.4 h(-1)
    GHRP-2
    beta
    1.3 h(-1)
    GHRP-2
    t1/2beta
    0.55 h
    GHRP-2
    AUC(0-infinity)
    2.02 ng/mL x h
    GHRP-2
    Cmax
    7.4 ng/mL
    GHRP-2
    plasma clearance
    0.66 L/h x kg
    GHRP-2
    apparent volume of distribution
    0.32 L/kg
    GHRP-2

    Source sentences

    Summary
    GHRP-2 PK parameters (mean +/- SD) were: alpha = 13.4 +/- 9.7 h(-1), beta = 1.3 +/- 0.3 h(-1), t(1/2beta) = 0.55 +/- 0.14 h, AUC(0-infinity) = 2.02 +/- 1.37 ng/mL x h, Cmax = 7.4 +/- 3.8 ng/mL, plasma clearance = 0.66 +/- 0.32 L/h x kg, and apparent volume of distribution = 0.32 +/- 0.14 L/kg.
    1 context sentence
    Summary · context
    Ten prepubertal children (nine boys and one girl; 7.7 +/- 2.4 yr old) received a single 1 microg/kg i.v. dose of GHRP-2 over 1 min, followed by repeated (n = 9) blood sampling over 2 h.
  2. 02HumanNon-randomized trialPharmacokinetics

    After a single intravenous GHRP‑2 dose in children with short stature, plasma GH reached a Cmax of 50.7 ng/mL at a Tmax of 0.42 h.

    In plain wordsIn short children, one GHRP‑2 dose raised growth hormone in the blood to a peak within the first hour.

    Peptide
    GHRP-2
    Outcome
    Not applicableGH pharmacokinetics after GHRP-2
    Study

    n = 10

    Outcome group
    Pharmacokinetics · Endocrine and hormones
    Studied dose
    1 microg/kg · intravenous · single dose over 1 minAs given in this study (human).

    Measurements

    appearance rate constant
    5.9 h(-1)
    GH
    elimination t1/2
    0.37 h
    GH
    lag time
    0.05 h
    GH
    Cmax
    50.7 ng/mL
    GH
    Tmax
    0.42 h
    GH
    AUC(0-infinity)
    47.9 ng/mL x h
    GH

    Source sentences

    Summary
    PK parameters for GH were: appearance rate constant = 5.9 +/- 3.1 h(-1), elimination t(1/2) = 0.37 +/- 0.15 h, lag time = 0.05 +/- 0.01 h, Cmax = 50.7 +/- 17.2 ng/mL, Tmax = 0.42 +/- 0.16 h, and AUC(0-infinity) = 47.9 +/- 26.1 ng/mL x h.
    1 context sentence
    Summary · context
    Ten prepubertal children (nine boys and one girl; 7.7 +/- 2.4 yr old) received a single 1 microg/kg i.v. dose of GHRP-2 over 1 min, followed by repeated (n = 9) blood sampling over 2 h.
  3. 03HumanNon-randomized trialActivity measurement

    A sigmoid Emax model of plasma GH after GHRP‑2 in children with short stature gave an EC50 of 1.09 ng/mL and an Emax of 67.5 ng/mL.

    In plain wordsIn short children, a model linked the GHRP‑2 level in blood to the growth hormone rise it caused.

    Peptide
    GHRP-2
    Outcome
    Not applicableGHRP-2 pharmacodynamic parameters for GH
    Study

    n = 10

    Outcome group
    Growth hormone and IGF-1 · Endocrine and hormones
    Studied dose
    1 microg/kg · intravenous · single dose over 1 minAs given in this study (human).

    Measurements

    Ke0
    1.13 h(-1)
    GHRP-2
    gamma
    13.15
    GHRP-2
    E0
    6.63 ng/mL
    GH
    Emax
    67.5 ng/mL
    GH
    EC50
    1.09 ng/mL
    GHRP-2

    Source sentences

    Summary
    PD parameters for GHRP-2 were: Ke0 = 1.13 +/- 0.94 h(-1), gamma = 13.15 +/- 9.44, E0 = 6.63 +/- 4.86 ng/mL (GH), Emax = 67.5 +/- 23.5 ng/mL (GH), and EC50 = 1.09 +/- 0.59 ng/mL.
    2 context sentences
    Summary · context
    PD parameters were generated using the sigmoid Emax model.
    Summary · context
    Ten prepubertal children (nine boys and one girl; 7.7 +/- 2.4 yr old) received a single 1 microg/kg i.v. dose of GHRP-2 over 1 min, followed by repeated (n = 9) blood sampling over 2 h.
  4. 04HumanNon-randomized trialEfficacy outcome

    In children with short stature, GHRP‑2 produced a significant increase in plasma GH concentrations compared with pretreatment values.

    In plain wordsIn short children, GHRP‑2 raised growth hormone in the blood compared with before treatment.

    Peptide
    GHRP-2
    Outcome
    IncreasePlasma GH increase after GHRP-2
    Study

    n = 10

    Comparator
    Pretreatment values
    Outcome group
    Growth hormone and IGF-1 · Endocrine and hormones
    Studied dose
    1 microg/kg · intravenous · single dose over 1 minAs given in this study (human).

    Source sentences

    Summary
    GHRP-2 produced a predictable and significant (i.e. compared to pretreatment values) increase in plasma GH concentrations
    1 context sentence
    Summary · context
    Ten prepubertal children (nine boys and one girl; 7.7 +/- 2.4 yr old) received a single 1 microg/kg i.v. dose of GHRP-2 over 1 min, followed by repeated (n = 9) blood sampling over 2 h.

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Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    13 Oct 2026, 21:44 UTC

    Study results updated

  2. Version 1

    13 Oct 2026, 16:31 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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