Immediate response
Growth-hormone release follows administration within the pulse window.

Protocol / Research Dosing Guide
A source-gated Ipamorelin reference covering the community-derived schedule, vial arithmetic and the boundary where published evidence stops.
Ipamorelin is a pentapeptide growth-hormone secretagogue known for releasing growth hormone without meaningfully raising cortisol or prolactin. Published human work used other routes and formulations for different endpoints. No human trial has tested ipamorelin for growth-hormone optimization, body composition or anti-aging outcomes, so the schedule below is community-derived.
Why researchers care
Growth-hormone pulse research, body composition and recovery discussion
Class
Selective growth-hormone secretagogue acting at the ghrelin (GHS-R1a) receptor
Route reported
Subcutaneous after reconstitution
Cycle length
Community reported 8–12 weeks on, 4 weeks off
Regulatory status
Not FDA approved
The supplied source reports a titration from 100 mcg per day in week one to 200–300 mcg per day through weeks four to twelve, one to three administrations daily, then a four-week off period. It states plainly that this is community-derived rather than trial-derived.
| Phase or study | Amount | Frequency / evidence |
|---|---|---|
| Week 1 | 100 mcg per day, once at bedtime, fasted | Community reported titration |
| Weeks 2–3 | 200 mcg per day, once at bedtime or split morning and evening | Community reported |
| Weeks 4–8 | 200–300 mcg per day, one to two administrations | Community reported |
| Weeks 9–12 | 200–300 mcg per day, continued if tolerated | Community reported |
| Off cycle | 4 weeks at zero | Community reported |
No human trial has validated these amounts, this titration, the block length or the off period. Reported practice describes roughly 300 mcg per administration as a practical ceiling because the growth-hormone response is said to flatten above it.
Neutral research-material planning only. This does not establish an appropriate amount or route.
Research planning item
Exact labeled research vial
Research planning item
Bacteriostatic water, roughly 3 mL per 10 mg vial in the source example
Research planning item
U-100 insulin syringes, 0.3 mL barrel preferred for small draws
Research planning item
Alcohol prep swabs
Research planning item
Sharps container
Research planning item
Refrigeration for the prepared vial
Research planning item
Written concentration label
Concentration
3.333 mg/mL
Draw volume
0.06 mL
U-100 units
6
Mathematical draws
50
Arithmetic only. The entered amount is not a recommendation and does not establish suitability.
Community practice favors bedtime because growth hormone surges during deep sleep.
Reported practice describes an empty stomach, commonly one to two hours after food and twenty to thirty minutes before eating, because insulin blunts the growth-hormone pulse.
One to three administrations per day appear in reported schedules; three is described as the maximum.
Reported practice resumes at the next scheduled time rather than doubling.
| Format | What is reported | Evidence limit |
|---|---|---|
| Subcutaneous | The route used in community schedules | No trial for these endpoints |
| Intravenous (published studies) | Used in published human pharmacology | Different route and formulation; do not transfer the schedule |
| Oral | Not viable | Digestion degrades the peptide |
Routes and amounts are not interchangeable unless a verified study explicitly establishes a conversion.
| Measure | Finding | Evidence limit |
|---|---|---|
| Reported half-life | About two hours | Published pharmacology |
| Why frequency varies | The short half-life is the reason schedules range from one to three administrations daily | Reported rationale |
| Pulse coverage | One administration gives one clean pulse; two or three extend coverage | Reported rationale |
| Duration of effect | Not established for the community endpoints | No trial |
| Route | Amount | Frequency | Source | Human validation |
|---|---|---|---|---|
| Subcutaneous | 100 mcg | Once daily | Community report | No |
| Subcutaneous | 100 mcg | Twice daily (200 mcg per day) | Community report | No |
| Subcutaneous | 200 mcg | Once daily | Community report | No |
| Subcutaneous | 300 mcg | Up to three times daily (900 mcg per day) | Community report | No |
Published study values describe those studies. Community-reported values are not validated dosing recommendations.
Concentration: 3.333 mg/mL
| Entered amount | Volume | U-100 units |
|---|---|---|
| 0.2 mg | 0.06 mL | 6 units |
| 0.4 mg | 0.12 mL | 12 units |
| 0.6 mg | 0.18 mL | 18 units |
Reconstitution does not establish identity, purity, sterility, stability, or an appropriate amount.
Ipamorelin is a selective agonist at the ghrelin receptor, GHS-R1a.
Current status · verified September 16, 2026
Not FDA approved
This is an evidence-gap and precaution list, not an approved prescribing label.
Active or prior cancer
Growth-hormone axis stimulation is not evaluated for safety in this setting
Pregnancy or breastfeeding
No safety data
Children or adolescents
Growth-axis effects are not characterized for this use
Diabetes or impaired glucose tolerance
Growth hormone can reduce insulin sensitivity
Untreated endocrine disease
Requires diagnosis and clinical management first
Important limitation: No controlled incidence data.
Important limitation: Commonly reported after administration.
Important limitation: Consistent with growth-hormone effects but not quantified.
Important limitation: Ghrelin-receptor activity makes this mechanistically plausible.
Important limitation: Growth hormone can reduce insulin sensitivity.
Important limitation: No follow-up evidence.
Growth-hormone release follows administration within the pulse window.
Sleep and recovery reports appear within weeks in community accounts; these are anecdotal.
Eight to twelve weeks on, four weeks off, per reported practice.
No validated monitoring schedule exists; IGF-1 testing is discussed in communities without trial support.
| Claim | Evidence level | What research shows | Important limitation |
|---|---|---|---|
| Growth-hormone release | Established pharmacology | Level 2 | Not an outcome claim |
| Body composition | Not established | Community reported | No human trial |
| Sleep quality | Not established | Anecdotal | No controlled data |
| Recovery | Not established | Anecdotal | No controlled data |
Follow the product label; keep cool, dry and out of light.
Refrigerate and protect from light; follow the product label for the use window.
Repeated freeze-thaw cycles are avoided for peptide solutions.
Cloudiness, discoloration or particles mean the solution should not be used.
Concentration depends on the liquid volume you added; recompute from your own vial.
Mechanistically consistent with ghrelin-receptor activity; it is not a validated dosing signal.
Stop and seek qualified product guidance.
Reported practice resumes at the next scheduled time without doubling.
Seek licensed clinical review; no validated safety protocol exists.
| Compound | Class or mechanism | Evidence | FDA status |
|---|---|---|---|
| Ipamorelin | Selective GHS-R1a agonist | Minimal cortisol and prolactin rise reported | Not approved |
| CJC-1295 without DAC | GHRH analogue | Different receptor and pulse profile | Not approved |
| MK-677 | Orally active secretagogue | Longer exposure and different side-effect profile | Not approved |
A pentapeptide growth-hormone secretagogue acting at the ghrelin receptor.
No.
No. It is community-derived.
About two hours in published pharmacology.
Growth hormone naturally surges during deep sleep, and food raises insulin, which blunts the pulse.
Reported practice describes about 300 mcg per administration as the practical ceiling before side effects rise without more growth hormone.
No sex-specific amount is established; some community sources describe 100–200 mcg per administration for women, which already sits inside the general range.
About 3,333 mcg/mL, so 200 mcg is 6 units on a U-100 syringe.
At 200 mcg per day it covers roughly 50 administrations before priming losses.
It is characterized as selective, with minimal cortisol and prolactin effect compared with older secretagogues.
Concentration and volume arithmetic only.
Coverage source
Supplied coverage source for the community schedule, supply planning and vial arithmetic.
Open direct sourcePublished pharmacology
Original pharmacology describing selectivity and growth-hormone release.
Open direct sourcePublished research
Receptor-level context for secretagogue activity.
Open direct source