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Specimen Atlas of Research Peptides30 plates · MIT
Side-by-side · Research reference

GHRP-2vsTesofensine

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

APhase 2Reviewed15/42 cited
BPhase 3Draft10/40 cited
GHRP-2
Hexapeptide GHRP · Phase 2 (clinical diagnostic)
100–300 mcgPer doseBowers 1990
Phase 2Evidence levelBowers 1990Sigalos 2018
~30 minHalf-lifeMalagón 1999
SQ · Multiple sites · 1–3×/day
Tesofensine
SNDRI · Phase 3 obesity candidate
0.25–0.5 mgDaily doseAstrup 2008
9.2 kgWeight ↓ (24 wk)Astrup 2008
Phase 3Evidence levelAstrup 2008
Oral · Once daily morning

01Mechanism of Action

Parameter
GHRP-2
Tesofensine
Primary target
Ghrelin receptor (GHS-R1a) on anterior pituitaryBowers 1990
Serotonin / norepinephrine / dopamine transporters (SERT / NET / DAT)Astrup 2008
Pathway
GHS-R1a → Gαq → Ca²⁺ → GH vesicle exocytosisBowers 2002
Triple monoamine reuptake inhibition → ↑synaptic 5-HT, NE, DA → appetite suppression + thermogenesisAstrup 2008
Downstream effect
Strong GH pulse + IGF-1 elevation; appetite increase via ghrelin agonismBowers 2002
Strong appetite suppression, mild thermogenic effect, weight lossAstrup 2008
Feedback intact?
Yes, with somatostatin feedback active
Origin
Synthetic hexapeptide; developed by Bowers/Tulane group in the 1980sBowers 1990
Small molecule developed by NeuroSearch (Denmark) for CNS indications, repurposed for obesityAstrup 2008
Antibody development

02Dosage Protocols

Parameter
GHRP-2
Tesofensine
Standard dose
100–300 mcg per injectionBowers 1990
0.25–0.5 mg / dayAstrup 2008
Frequency
1–3× per day
Once daily, morning
Lower / starter dose
50 mcg per dose
0.125 mg / day
Evidence basis
Phase 2 + clinical diagnostic useBowers 1990
Phase 2b + ongoing Phase 3Astrup 2008
Duration
8–12 weeks on / 4 off (anecdotal)
24 weeks per studied cycle
Reconstitution
Bacteriostatic water
Timing
Pre-sleep + fasted preferred
Morning to avoid sleep disruption
Half-life
~9 days (very long)
Form
Oral capsule

04Side Effects & Safety

Parameter
GHRP-2
Tesofensine
Cortisol elevation
Mild but measurableBowers 1990
Prolactin elevation
Mild but measurable
Hunger
Strong appetite increase
Injection site reaction
Mild erythema
IGF-1 elevation
Strong; monitor with chronic high-dose use
Cancer risk
Contraindicated in active malignancy
Pregnancy / OB
Avoid
Contraindicated
Heart rate / BP
Dose-dependent ↑ HR + BPAstrup 2008
Insomnia
Dose-related; mitigate with morning timing
Dry mouth
Common
Nausea
Common
Mood changes
Anxiety / agitation possible
Cardiovascular events
Phase 3 trial monitoring; not yet FDA-cleared
Absolute Contraindications
GHRP-2
  • ·Active malignancy
  • ·Pregnancy / breastfeeding
Tesofensine
  • ·Pregnancy / breastfeeding
  • ·Severe cardiovascular disease
  • ·Concurrent MAOI use
Relative Contraindications
GHRP-2
  • ·Untreated diabetes
Tesofensine
  • ·Hypertension
  • ·Anxiety disorder
  • ·Insomnia

05Administration Protocol

Parameter
GHRP-2
Tesofensine
1. Reconstitution
Add 2 mL bacteriostatic water to 5 mg vial → 2.5 mg/mL.
Oral capsule (investigational; not commercial).
2. Injection site
SQ — abdomen or thigh. Rotate sites.
Swallow whole with water, morning only.
3. Timing
Pre-sleep + fasted preferred.
Morning to mitigate insomnia. Do not dose evening.
4. Storage
Lyophilised: room temp, light-protected. Reconstituted: refrigerate ≤30 days.
Room temp ≤25 °C, dry place.
5. Needle
29–31G, 4–8 mm insulin syringe.
Monitor BP + HR + mood. Avoid stimulants + MAOIs.

06Stack Synergy

GHRP-2
+ CJC-1295 (no DAC)
Strong
View CJC-1295 (no DAC)

GHRP-2 + CJC-1295-no-DAC is a higher-amplitude alternative to the ipamorelin + CJC-1295 stack. GHRP-2 produces a stronger pulse but with cortisol + prolactin signal — choose when maximum GH amplitude is the goal and the side-effect tolerance is acceptable.

GHRP-2
100–200 mcg SQ · pre-sleep
CJC-1295 (no DAC)
100 mcg SQ · same injection
Primary benefit
High-amplitude GH pulse, body composition
Tesofensine
— no documented stacks