What are the dosing guidelines for Ipamorelin (growth hormone secretagogue) for growth hormone stimulation?

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Dosing Guidelines for Ipamorelin for Growth Hormone Stimulation

Ipamorelin should be administered at a dose of 0.045-0.05 mg/kg body weight per day by subcutaneous injection in the evening for optimal growth hormone stimulation. 1

Mechanism of Action and Efficacy

  • Ipamorelin is a synthetic pentapeptide (Aib-His-D-2-Nal-D-Phe-Lys-NH2) that functions as a growth hormone secretagogue, stimulating the release of growth hormone from the anterior pituitary gland 2
  • It acts through a GHRP-like receptor mechanism similar to other growth hormone-releasing peptides, but with higher selectivity for GH release 2
  • In animal studies, ipamorelin has demonstrated dose-dependent increases in longitudinal bone growth rate and body weight gain 3
  • Unlike other growth hormone secretagogues, ipamorelin shows high specificity for GH release without significantly affecting ACTH or cortisol levels, making it potentially safer for clinical use 2

Dosing Protocol

  • Subcutaneous administration is the recommended route for ipamorelin 1
  • Evening administration is preferred to mimic the natural circadian pattern of growth hormone release 1
  • For children with growth hormone deficiency, the recommended dosage range is 0.045-0.05 mg/kg body weight per day 1
  • Injections should be given consistently at the same time each day to maintain stable hormone levels 1

Monitoring and Follow-up

  • Clinic visits should be scheduled every 3-6 months (more frequently for young patients) to monitor 1:

    • Stature and height velocity
    • Pubertal development
    • Skeletal maturation via wrist radiography
    • Thyroid hormone levels (TSH and free T3)
    • Serum glucose, calcium, phosphate, bicarbonate, and parathyroid hormone levels
  • An adequate growth response is indicated by a height velocity increase of at least 2 cm per year over baseline during the first year of treatment 1

Treatment Duration and Discontinuation

  • Treatment should be discontinued in the following circumstances 1:
    • When epiphyseal closure is demonstrated
    • If height velocity drops below 2 cm per year in late-pubertal adolescents
    • When the patient reaches their genetic target height
    • In cases of severe adverse effects
    • If there is evidence of accelerated bone maturation
    • When there is an inadequate response despite optimal dosing and adherence

Special Considerations

  • For non-responders (height velocity increase <2 cm/year over baseline), evaluate 1:

    • Patient adherence to therapy
    • Serum IGF-1 levels
    • Weight-adjusted dosage
    • Nutritional and metabolic factors
  • Higher doses are not more effective than the recommended range and should not be used in non-responders 1

  • Yearly assessment of pubertal stages (Tanner stages) is recommended for children older than 10 years of age to monitor for potential accelerated pubertal development 1

  • Yearly assessment of bone age by radiography of the left wrist should be performed to exclude accelerated bone maturation 1

Safety Profile

  • Ipamorelin has shown a favorable safety profile in animal studies with minimal side effects 2
  • The most commonly reported adverse events with similar growth hormone secretagogues include transient facial flushing and pain at the injection site 4
  • Regular monitoring of bone age and pubertal development is essential to detect potential accelerated maturation 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Ipamorelin, the first selective growth hormone secretagogue.

European journal of endocrinology, 1998

Research

Ipamorelin, a new growth-hormone-releasing peptide, induces longitudinal bone growth in rats.

Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society, 1999

Research

Sermorelin: a review of its use in the diagnosis and treatment of children with idiopathic growth hormone deficiency.

BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy, 1999

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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