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Reviewed against editorial standards · Updated 2026-05-13

Hexarelin: Dosage & Administration

Part of the Hexarelin Complete Guide

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Dosage Protocols by Application

Hexarelin (examorelin) is a synthetic hexapeptide GH secretagogue. Italian endocrinology trials by the Ghigo group and others established the dose ranges below.[1]

ApplicationDoseFrequencyRouteNotes
GH release (research)100–200 mcg1–3× dailySCFasted; standard protocol
Cardiac research100–200 mcg1–2× dailySCCD36-mediated cardioprotection; GH-independent
Clinical stimulation testing1.5–2 mcg/kgSingle doseIV bolusPituitary diagnostic; not for chronic use
Older / GH-deficient adults1.5 mcg/kgTwice dailySCLower weight-scaled dose

The most-published research dose is 2 mcg/kg SC twice daily (approximately 150 mcg/dose for a 75 kg adult). At higher doses, the GH pulse plateaus while cortisol and prolactin continue to rise, which is one reason most protocols stay near the 2 mcg/kg range.[2]

Cycling for Receptor Desensitization (Critical)

This is the single most important practical fact about hexarelin: GH response diminishes substantially with continuous daily dosing. Published studies have characterized the time course:[2]

  • Week 1–2: Robust GH pulse (full effect)
  • Week 3–4: Begins to diminish (~70% of initial response)
  • Week 5–8: Substantially blunted (~40–50%)
  • Week 8+: Minimal GH response despite continued dosing

This distinguishes hexarelin from ipamorelin, GHRP-2, and GHRP-6, which largely maintain GH response with chronic dosing.

Standard cycling protocol

  • 4 weeks on / 2 weeks off is the most commonly cited research protocol.
  • During the off period, GHSR-1a receptor expression and sensitivity recover.
  • If GH support is needed during the off period, switch to ipamorelin or GHRP-2 (which do not cross-desensitize hexarelin).
  • Some protocols use longer 6 weeks on / 4 weeks off cycles; both work.

The cardiac CD36-mediated effects may persist even after GHSR-1a desensitization — they operate through a separate receptor system.[3]

Reconstitution Math

Hexarelin typically ships as lyophilized powder in 2 mg or 5 mg vials.

  • 2 mg vial + 1 mL BAC water = 2 mg/mL (2,000 mcg/mL) — 0.1 mL (10 units on insulin syringe) = 200 mcg.
  • 2 mg vial + 2 mL BAC water = 1 mg/mL (1,000 mcg/mL) — 0.1 mL (10 units) = 100 mcg.
  • 5 mg vial + 2.5 mL BAC water = 2 mg/mL — 0.05 mL (5 units) = 100 mcg.
  • 5 mg vial + 5 mL BAC water = 1 mg/mL — 0.1 mL (10 units) = 100 mcg.

Use the peptide calculator for exact units for your specific vial. See the reconstitution guide for technique.

Fasted Timing (Critical for GH Response)

Like all GH secretagogues, hexarelin's GH-releasing effect is dramatically reduced by food. Carbohydrates blunt GH most; protein also dampens. The standard rule: no food for 2 hours before dose, 30 minutes after.

Best dosing times:

  • Morning fasted — first thing on waking, before breakfast.
  • Pre-workout — at least 2 hours after last meal.
  • Bedtime — at least 2 hours after dinner; pairs with natural overnight GH pulse.

The cardiac CD36 effects appear less food-dependent than GH release, so cardiac-focused protocols are less strict on fasting.

Stacking with GHRH Analogs

Hexarelin works synergistically with GHRH analogs (sermorelin, CJC-1295 Mod GRF 1-29, tesamorelin) because the two molecule families activate complementary signaling pathways. Combined GH release exceeds either alone.

  • Hexarelin 100–150 mcg + CJC-1295 (no DAC) 100 mcg, SC, before bed: a common research stack for short cycles.
  • Avoid combining with other GHRPs (ipamorelin, GHRP-2, GHRP-6) — these compete for the same GHSR-1a receptor and combining produces no additive effect, just additive side effects.

The desensitization issue still applies — the hexarelin component will lose efficacy over 4–8 weeks even in a stack.

Storage

  • Lyophilized vials: -20°C for long-term, or 2–8°C (refrigerator) short-term.
  • Reconstituted: refrigerate at 2–8°C. Use within 28 days; clarity should remain.
  • Protect from light: use opaque containers or store in original box.
  • Avoid freeze-thaw cycles with reconstituted solution.

For broader storage rules, see the peptide storage guide.

FAQ

Frequently Asked Questions

References

  1. [1] Ghigo E, Arvat E, Gianotti L, et al.. Growth hormone-releasing activity of hexarelin, a new synthetic hexapeptide, after intravenous, subcutaneous, intranasal, and oral administration in man. Journal of Clinical Endocrinology & Metabolism, 1994.
  2. [2] Rahim A, O'Neill PA, Shalet SM. Growth hormone status during long-term hexarelin therapy. Journal of Clinical Endocrinology & Metabolism, 1998.
  3. [3] Locatelli V, Rossoni G, Schweiger F, et al.. Growth hormone-independent cardioprotective effects of hexarelin in the rat. Endocrinology, 1999.
  4. [4] Imbimbo BP, Mant T, Edwards M, et al.. Growth hormone-releasing activity of hexarelin in humans. A dose-response study. European Journal of Clinical Pharmacology, 1994.

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Reviewed against Peptides Insider editorial standards · Last reviewed 2026-05-13.