Ipamorelin

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Also known as: NNC 26-0161

A selective growth hormone secretagogue with minimal side effects.

Overview

Ipamorelin is a pentapeptide growth hormone secretagogue that stimulates GH release from the pituitary with high selectivity. Unlike other GHRPs, it does not significantly affect cortisol or prolactin levels.

Mechanism of Action

Binds to ghrelin/GHS receptors in the pituitary, triggering GH release. Does not affect ACTH, cortisol, or prolactin secretion, making it highly selective for GH pathway.

Pharmacokinetics

Peak GH release 30-40 minutes post-injection. Half-life approximately 2 hours. Effects last 3-4 hours.

Dosing Protocols

Note: These are research protocols from literature. This is not medical advice.

1

Standard

Dose

200-300 mcg

Frequency

1-3x daily

Duration

8-12 weeks

Before bed and/or post-workout

2

Anti-Aging

Dose

100-200 mcg

Frequency

Once daily at bedtime

Duration

Ongoing

Lower maintenance dose

Stacking Recommendations

Peptides that may be combined based on complementary mechanisms in research settings.

Rationale: Synergistic GH release

Synergy: GHRH + GHRP combination amplifies GH pulse

Rationale: Enhanced body composition

Synergy: Dual pathway GH stimulation

Research Areas

Growth Hormone DeficiencyAnti-AgingBody CompositionBone Health

Key Research Findings

  • 1Dose-dependent GH release without cortisol or prolactin increase
  • 2Improved body composition in clinical studies
  • 3Enhanced sleep quality and recovery
  • 4Favorable safety profile compared to other secretagogues

Side Effects & Contraindications

Reported Side Effects

  • Headache
  • Flushing
  • Dizziness (rare)

Contraindications

  • Active malignancy
  • Pregnancy

Safety Considerations

Well-tolerated with minimal side effects. No significant impact on glucose metabolism at standard doses.

Storage Requirements

Store lyophilized at -20C. Reconstituted stable at 2-8C for 30 days.

Scientific References

Quick Reference

Sequence
Aib-His-D-2-Nal-D-Phe-Lys-NH2
Molecular Weight
711.85 g/mol
Half-Life
~2 hours
Bioavailability
High (SC)
Research Stage
clinical phase 2
Administration
Subcutaneous injection