Growth-hormone response
Human endocrine studies show acute GH release.4
Growth-hormone secretagogue
Investigational; no FDA-approved hexarelin product identified.
6 residues · N → C3
H–dMeW–A–W–dF–KdMeW = D-2-methyltryptophan; dF = D-phenylalanine. C-terminal amide.
Amidated hexapeptide; parent mass excludes salt counterions.
This value is reported by a secondary reference. The stated attribution has not been independently verified as a route- and formulation-matched human PK measurement.
Illustrative scenario using an unverified reference estimate.
Five half-lives in this estimated model. This is not a prediction of when effects stop.
Population: Not established by the reference estimate
Source’s stated attribution: Imbimbo et al. 1994
Source’s reported peak time: 30 min. This has not been independently confirmed and is not used in the elimination curve.
100 × 2−time / half-life. Time zero is a reference level, not the moment of administration. Absorption, repeated dosing, metabolites and clinical effects are not modeled. Five half-lives leaves 3.125%, not zero. This curve cannot determine a dosing interval.
A 12-man placebo-controlled dose-response study observed GH peaks around 30 minutes after IV dosing. This measures hormone response, not recovery.4
After 16 weeks, fat mass, lean mass, bone density and IGF-I did not significantly change in the cited study.1
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| Route | Dose | Frequency | Goal / evidence | Duration | References |
|---|---|---|---|---|---|
| SubQSubcutaneous injection | 1.5 μg/kg | Twice daily | Assess sustained GH-axis effectsAdults; participant count not stated in the indexed abstractHuman study | 16 weeks, with reassessment 4 weeks after stopping | 1 |
Population Adults; participant count not stated in the indexed abstract Context GH response attenuated during treatment and recovered after withdrawal. | |||||
| SubQ | 100 mcg | 3x daily (morning, midday, evening) | GH OptimizationReference report | 8-16 weeks maximum | 23 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. WADA prohibition and desensitization claims do not make community cycles clinically established. Interaction labels are source claims. Source tabs Injectable / Nasal | |||||
| SubQ | 100-200 mcg | 2x daily | Cardioprotection ResearchReference report | 8-16 weeks maximum | 23 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. WADA prohibition and desensitization claims do not make community cycles clinically established. Interaction labels are source claims. Source tabs Injectable / Nasal | |||||
| SubQ | 100 mcg | 2x daily (morning and bedtime) | Recovery/Anti-AgingReference report | 8-16 weeks maximum | 23 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. WADA prohibition and desensitization claims do not make community cycles clinically established. Interaction labels are source claims. Source tabs Injectable / Nasal | |||||
| SubQ | 100 mcg hexarelin + 100 mcg CJC-1295 | 2-3x daily | With GHRH (Synergistic)Reference report | 8-16 weeks maximum | 23 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. WADA prohibition and desensitization claims do not make community cycles clinically established. Interaction labels are source claims. Source tabs Injectable / Nasal | |||||
No protocols match these filters.
Study and label doses retain their study context. Reference reports are unvalidated practices, not personal treatment instructions. Ranges remain ranges; escalation stages are labeled.
Reported use periods and breaks. These do not establish a safe cycle or prove that breaks prevent tolerance.
Morning upon waking, midday (optional), and 30 minutes before bed. Administer on empty stomach.
Human testing found ACTH and cortisol stimulation as well as GH release; responses differed in people with Cushing’s disease.
2The GH response decreased during 16 weeks of repeated dosing and recovered after withdrawal.
1Short endocrine experiments and a 16-week study do not establish long-term safety for community recovery regimens.
41Cortisol/prolactin elevation, edema, glucose disruption and possible hypogonadism; active cancer requires particular caution.
Hand numbness/joint pain, persistent edema, breast symptoms, fatigue, hyperglycemia, headache/vision changes or allergy.
Not a complete safety screen. Discuss health decisions with a qualified clinician.
Check cautions and reported pairings. A compatibility claim does not establish that a combination is safe.
Overlapping hormonal action.23
Reference report · Pep-Pedia label: Use CautionOverlapping hormonal action.23
Reference report · Pep-Pedia label: Use CautionProlonged exposure concern.23
Reference report · Pep-Pedia label: Use CautionOverlapping receptor stimulation.23
Reference report · Pep-Pedia label: Monitor CombinationExcess GH concern.23
Reference report · Pep-Pedia label: Avoid CombinationComplementary receptor action.23
Reference report · Pep-Pedia label: SynergisticGH-response research.23
Reference report · Pep-Pedia label: SynergisticClaim of softened side effects unproven.23
Reference report · Pep-Pedia label: CompatibleGHRH-class extrapolation.23
Reference report · Pep-Pedia label: SynergisticSafety unestablished.23
Reference report · Pep-Pedia label: CompatibleSingle-compound studies do not validate community stacking. The long-term study also shows that response can attenuate with repeated exposure.1
Research contextNo matching interactions. Try another name or filter.
Enter your peptide amount and container size. Get a volume and a simple measurement scale.
For dry powder, assuming negligible volume displacement. Use bacteriostatic water only if the formulation specifies it.
Amounts below are total blend mass. Ingredient amounts are listed separately.
| Pen units | Amount | Volume |
|---|
Enter an amount to calculate its volume and device setting.
The suggestion favors a simple 1, 2, or 5 × power-of-ten amount per unit, then the largest final volume that fits. It does not choose a dose or a biologically suitable concentration.
The water estimate applies only to dry powder and assumes negligible powder displacement. Final solution volume, specified diluent, solubility, stability, sterility, cartridge compatibility, and working fill limits must be established separately. No allowance is made for priming or transfer losses.
V2 measurement specification ↗Bacteriostatic water: formulation instructions ↗No formulation-specific human reconstitution instructions were verified for this research powder.1
A compatible solvent, concentration, preservative and beyond-use period cannot be inferred from vial mass. The cited source does not validate a universal bacteriostatic-water recipe.1
Reported handling information, not a validated formulation or instruction to prepare an injectable product.
Pep-Pedia provides two vial concentration examples.
The source describes gentle mixing and avoiding vigorous shaking.
The nasal tab repeats the injectable vial and syringe examples.
The source describes gentle mixing and avoiding vigorous shaking.
It does not establish nasal formulation compatibility or pump delivery volume.
Appearance and a purity certificate cannot establish sterility, identity, or suitability for injection.
Packaging examples, not a market survey. Approved and research products are not interchangeable.
Pep-Pedia reports these handling limits after mixing. They are not validated stability or sterility limits for your vial.
Refrigerate at 2-8°C immediately after reconstitution. Use within 4 weeks.
Storage depends on the formulation, diluent, container, and handling. Follow the specific product label or pharmacist’s instructions.
Device units measure volume. Concentration determines the amount in mg.
Documented 1-unit V2 models
Use the numbered dose window. Whole-unit settings only; confirm the specification for your exact model.
100 units = 1 mL
Read the printed unit scale. A small line may represent 0.5, 1, or 2 units depending on the syringe.
mL syringes and calibrated pipettes
Drops, sprays and other pen clicks need their own verified volume per increment. They have no universal conversion.
3 mL is cartridge capacity. It does not mean you must prepare or load 3 mL. The original vial and the pen cartridge are different containers. This reference compares measurement scales; it does not establish product or route compatibility.
Clinically meaningful recovery, strength, cardiovascular, or longevity benefit.1
5 distinct primary sources or abstracts checked. Evidence may concern a parent compound, individual blend ingredient, animal, or cell model; it does not necessarily establish a benefit for this exact product.
Evidence definitions →WADA prohibition and desensitization claims do not make community cycles clinically established. Interaction labels are source claims.
Hexarelin is a growth-hormone secretagogue studied in small human endocrine experiments. It can raise GH, but repeated administration can blunt the response, and a longer study did not show significant lean-mass or fat changes.
Other names: Examorelin · HEX · Hexarelin (Examorelin)
Investigational; no FDA-approved hexarelin product identified.
Examorelin / hexarelin: His-D-2-methyl-Trp-Ala-Trp-D-Phe-Lys-NH2.3
6 amino acids · 887.04 Da
His-D-2-methyl-Trp-Ala-Trp-D-Phe-Lys-NH2Reference description; checked chemical identity takes precedence when available.23
GHS-R1a stimulation plus CD36-related cardiac signaling; nasal exposure is less predictable than injection.23
After 16 weeks of twice-daily administration, the GH response to a challenge was lower and recovered after four weeks off. IGF-I, total fat, lean mass, and bone mineral density did not significantly change.
1A human endocrine study found increases in ACTH and cortisol after intravenous hexarelin. The compound is not exclusively a GH signal.
2A 2025 hepatocyte study identified hexarelin as an alexamorelin metabolite. It informs analytical detection, not hexarelin effectiveness or a human dosing schedule.
7Growth-hormone response research. Human endocrine studies show acute GH release.4
GH/IGF-1. Hormone release, not demonstrated general anti-aging benefit.23
Cardiac protection. Ischemia and fibrosis models.23
Brain protection. Neurogenesis, oxidative injury and ALS cell-model research.23
Recovery and metabolism. Muscle-preservation, lipid/glucose and exercise claims require clinical confirmation.23
PepPedia discusses GH, recovery, and cardioprotection goals; these should not be read as established patient benefits.8
PepPedia's editorial protocol summary, not measured community consensus. Benefits, product identity, and safety are not independently verified; these reported practices are not recommendations.
Added a 2025 hepatocyte metabolite-detection paper; it is not a new human hexarelin treatment trial.
AI-prepared summaries. Independent medical editorial review is pending.
Voluntary, unverified reports. These percentages do not measure effectiveness or safety.
Number of responses to this question: not disclosed.
Number of responses to this question: not disclosed.
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Number of responses to this question: not disclosed.
The source displays “11 responses” for this profile. This is not a confirmed participant count or a denominator for individual questions.
Original sources and review status. Open a reference to read its summary.
Sixteen weeks of repeated treatment produced reversible attenuation of GH response without significant IGF-I or body-composition changes.
After 16 weeks of twice-daily administration, the GH response to a challenge was lower and recovered after four weeks off. IGF-I, total fat, lean mass, and bone mineral density did not significantly change.
A monitored endocrine study found significant ACTH and cortisol increases in healthy subjects after intravenous hexarelin.
A human endocrine study found increases in ACTH and cortisol after intravenous hexarelin. The compound is not exclusively a GH signal.
Defines hexarelin’s six-residue sequence, parent formula and average molecular weight 887.0 g/mol.
Twelve men received escalating IV hexarelin and placebo. GH peaked at about 30 minutes; the reported 55-minute half-life concerns GH, not the administered peptide.
Twelve men received escalating IV hexarelin and placebo. GH peaked at about 30 minutes; the reported 55-minute half-life concerns GH, not the administered peptide.
Pep-Pedia bibliography · Checked 2026-10-12
Twelve men received escalating IV hexarelin and placebo. GH peaked at about 30 minutes; the reported 55-minute half-life concerns GH, not the administered peptide.
Pep-Pedia bibliography · Checked 2026-10-12
Examorelin, also called hexarelin, was identified as an alexamorelin metabolite in hepatocyte incubations. This analytical study is not a clinical hexarelin treatment trial.
A 2025 hepatocyte study identified hexarelin as an alexamorelin metabolite. It informs analytical detection, not hexarelin effectiveness or a human dosing schedule.
Additional research · Checked 2026-10-12
Secondary editorial account of discussed practices; not a clinical trial or representative survey.
Lists a 5 mg lyophilized research vial. Quantity examples only; vendor quality and suitability are not endorsed.
Pep-Pedia reports: Infarcted mice had better ventricular function and about 53% less ventricular collagen, with lower inflammatory markers.
Reported population / model
Mouse model
Reported study details
0.3 mg/kg/day SubQ · 21 days · LAD ligation
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: Mutant-SOD1 neuroblastoma cells showed less peroxide injury and DNA-damage signaling; this was not an ALS patient study.
Reported population / model
In vitro
Reported study details
1 μM · Human neuroblastoma cells · SOD1-G93A mutation
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: The review describes CD36-mediated cardiac effects independent of GH and limited human cardiac measurements; clinical outcome benefit is unproven.
Reported population / model
Review
Reported study details
Multiple studies · CD36 receptor mechanism
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: GH response declined during 16 weeks in 12 older people and returned toward baseline four weeks after stopping.
Reported population / model
Human
Reported study details
SubQ twice daily · 16 weeks · 12 elderly subjects
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: Rat IV half-life was reported as 75.9 minutes; clearance and accumulation results cannot be assumed for human subcutaneous use.
Reported population / model
Rat model
Reported study details
IV and SubQ · Multiple doses · PK analysis
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: Infarcted mice had better ventricular function and about 53% less ventricular collagen, with lower inflammatory markers.
Reported population / model
Mouse model
Reported study details
0.3 mg/kg/day SubQ · 21 days · LAD ligation
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Reference retained from Pep-Pedia’s bibliography; findings and bibliographic accuracy have not been independently verified.
Pep-Pedia bibliography · Checked 2026-10-12
Reference retained from Pep-Pedia’s bibliography; findings and bibliographic accuracy have not been independently verified.
Pep-Pedia bibliography · Checked 2026-10-12
Reference retained from Pep-Pedia’s bibliography; findings and bibliographic accuracy have not been independently verified.
Pep-Pedia bibliography · Checked 2026-10-12
Reference retained from Pep-Pedia’s bibliography; findings and bibliographic accuracy have not been independently verified.
Pep-Pedia bibliography · Checked 2026-10-12
Reference retained from Pep-Pedia’s bibliography; findings and bibliographic accuracy have not been independently verified.
Pep-Pedia bibliography · Checked 2026-10-12
Reference retained from Pep-Pedia’s bibliography; findings and bibliographic accuracy have not been independently verified.
Pep-Pedia bibliography · Checked 2026-10-12
Lists a half-life of 1 hr and a peak time of 30 min. Stated attribution: Imbimbo et al. 1994. This value is reported by a secondary reference. The stated attribution has not been independently verified as a route- and formulation-matched human PK measurement. Five half-lives is not complete clearance, and the source’s “cleared” value is not used as a measured endpoint.
Secondary reference page checked; the underlying quantitative claim is not independently confirmed. · Checked 2026-10-12
Source page checked across available routes. Protocols, cycles, storage, mechanisms and pairing claims are secondary reports; checking the page does not independently validate those claims. Original concise summaries are used here.
Content coverage audit · Checked 2026-10-12