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Specimen Atlas of Research Peptides81 plates · MIT
Side-by-side · Research reference

IpamorelinvsVesugen

Side-by-side comparison across mechanism, dosage, evidence, side effects, administration, and stack synergies. Citations on every claim where available.

APhase 1HUMAN-REVIEWED21/57 cited
BAnimal-MechanisticHUMAN-REVIEWED5/43 cited
Ipamorelin
Selective GHRP · Ghrelin Mimetic
200–300 mcgPer doseRaun 1998
Phase 1Evidence levelRaun 1998Sigalos 2018
~2 hrHalf-lifeRaun 1998
SQ · Multiple sites · 1–3×/day
Vesugen
Bioregulatory Tripeptide · Vascular Endothelium
3 AATripeptide
Endothelin-1 ↓Atherosclerotic tissue
Ki-67 ↑Aged endothelium
SQ / IM · Protocol varies

01Mechanism of Action

Parameter
Ipamorelin
Vesugen
Primary target
Ghrelin receptor (GHS-R1a) on anterior pituitaryRaun 1998
Vascular endothelial cell nucleus — MKI67 gene promoter
Pathway
GHS-R1a binding → Gαq/11 → ↑intracellular Ca²⁺ → GH vesicle exocytosisRaun 1998Bowers 1991
KED → MKI67 promoter interaction (CATC binding motif -14 to +12 bp) → Ki-67 proliferation protein ↑
Downstream effect
GH pulse amplification, IGF-1 elevation, recovery and lipolytic effectsBowers 2002
Normalised endothelin-1 expression in atherosclerotic/restenotic endothelium, restored connexin expression for cell-cell communication, enhanced proliferative capacity in senescent endothelial culturesKozlov 2016Khavinson 2014
Feedback intact?
Yes — pulsatile pattern preserved; somatostatin feedback activeBowers 2002
Not applicable — does not operate via hormone axis
Origin
Pentapeptide H-Aib-His-D-2-Nal-D-Phe-Lys-NH₂; rationally designed for ghrelin-receptor selectivityRaun 1998
Khavinson bioregulatory peptide school — designed as tissue-specific (vascular) cytomodulator
Antibody development
Not reported in short-term studies

02Dosage Protocols

Parameter
Ipamorelin
Vesugen
Standard dose
200–300 mcg per injectionRaun 1998
Anecdotal community range; clinical doses 1–3 mg IV in trials.
Frequency
1–3× per day
Once daily pre-sleep is most common; twice or thrice for advanced users.
Not specified in available literature
Lower / starter dose
100 mcg per dose
Evidence basis
Phase 1 + clinical practiceRaun 1998Sigalos 2018
Animal models (atherosclerosis, restenosis, aging) · Russian case series
Duration
8–12 weeks on / 4 weeks off (anecdotal)
GHS-R desensitisation reported with continuous dosing.
Case series report treatment courses in elderly arterial insufficiency
Reconstitution
Bacteriostatic water; typical 2 mL per 5 mg vial
Timing
Pre-sleep + fasted preferred; 30 min away from food
Half-life
~2 hoursRaun 1998
Longer than GHRP-6 (15 min); shorter than CJC-1295-DAC (~8 days).
Not reported
Tripeptides typically cleared rapidly.
Standard dose (reported)
Not standardised — Russian clinical case series
Protocols vary; no FDA-approved regimen.
Route
Subcutaneous or intramuscular

04Side Effects & Safety

Parameter
Ipamorelin
Vesugen
Cortisol elevation
Negligible vs other GHRPsRaun 1998
Prolactin elevation
NegligibleRaun 1998
Hunger
Mild appetite increase via ghrelin-receptor crosstalk
Injection site reaction
Mild irritation possible
GH excess (overdose)
Joint pain, edema, insulin resistance
IGF-1 elevation
Dose-dependent; monitor with chronic high-dose use
Cancer risk
Theoretical via GH/IGF-1 axis; contraindicated in active malignancy
Pregnancy / OB
Avoid
Reported adverse events
None documented in available abstracts
Injection site
Assumed minimal — typical for small peptides
Long-term safety
Unknown — no long-term RCT data
Epigenetic mechanism risk
Theoretical concern: direct gene promoter interaction — proliferative effects in non-target tissues not characterised
Absolute Contraindications
Ipamorelin
  • ·Active malignancy or cancer history
  • ·Pregnancy / breastfeeding
  • ·Disrupted hypothalamic-pituitary axis
Vesugen
Relative Contraindications
Ipamorelin
  • ·Untreated diabetes
  • ·Severe insulin resistance
  • ·Concurrent corticosteroid use (theoretical desensitisation)
Vesugen
  • ·Active malignancy — proliferative mechanism (Ki-67 upregulation) untested in oncologic context

05Administration Protocol

Parameter
Ipamorelin
Vesugen
1. Reconstitution
Add 2 mL bacteriostatic water to 5 mg vial → 2.5 mg/mL. Roll gently. Solution should be clear.
Lyophilised powder reconstituted with sterile water or bacteriostatic water per supplier protocol. No standardised formulation.
2. Injection site
Subcutaneous, abdomen or thigh. Rotate sites. Pinch fat for shallow SQ delivery.
Subcutaneous (abdomen, thigh) or intramuscular. Rotate sites if multi-dose protocol.
3. Timing
Pre-sleep optimal — aligns with natural GH pulse. Some protocols add a morning fasted dose.
No reported circadian or fasting requirement. Russian protocols typically integrated into geroprotective regimens.
4. Storage
Lyophilised: room temp, protected from light. Reconstituted: refrigerate 2–8 °C, use within 30 days.
Lyophilised: refrigerate 2–8 °C, light-protected. Reconstituted: use immediately or refrigerate per supplier guidance (typically <7 days).
5. Needle
29–31G, 4–8 mm insulin syringe.

06Stack Synergy

Ipamorelin
+ Tesamorelin
Strong
View Tesamorelin

Ipamorelin (GHRP) + tesamorelin (GHRH analogue) is the textbook dual-axis GH stack. They activate two distinct pituitary receptors — the ghrelin receptor and the GHRH receptor — producing a synergistic GH pulse larger than either alone. Ipamorelin's selectivity (no cortisol/prolactin spike) makes it the ideal GHRP partner for long-term protocols.

Ipamorelin
200–300 mcg SQ · pre-sleep
Tesamorelin
2 mg SQ · same injection · pre-sleep
Primary benefit
Maximal GH pulsatility, fat loss, recovery, sleep depth
+ CJC-1295 (no DAC)
Strong
View CJC-1295 (no DAC)

CJC-1295 (no DAC) is a short-acting GHRH analogue. Combined with ipamorelin (GHRP), the pulse is amplified across both receptor systems with timing similar to native physiology. Without the DAC modification, the stack maintains sharp peaks rather than the sustained elevation seen with CJC-1295-DAC + ipamorelin.

Ipamorelin
200–300 mcg SQ · pre-sleep
CJC-1295 (no DAC)
100 mcg SQ · same injection
Primary benefit
Pulsatile GH stimulation matching physiological pattern
Vesugen
+ Thymalin
Multi-pathway
View Thymalin

Both from Khavinson bioregulatory school. Thymalin targets thymic/immune axis, Vesugen targets vascular endothelium. Rationale: multi-system geroprotection in elderly — immune senescence + vascular aging. Documented in Khavinson-tradition protocols combining tissue-specific peptides for poly-organ rejuvenation. No direct synergy study; combinatorial logic based on distinct target tissues.

Vesugen
Per protocol (SQ/IM)
Thymalin
Per protocol (SQ/IM)
Frequency
Sequential or concurrent per geroprotective protocol
Primary benefit
Multi-system age-related decline mitigation (vascular + immune)