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)
SQ · Multiple sites · 1–3×/day
Tesofensine
SNDRI · Phase 3 obesity candidate
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
Frequency
1–3× per day
Once daily, morning
Lower / starter dose
50 mcg per dose
0.125 mg / day
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
Form
—
Oral capsule
04Side Effects & Safety
Parameter
GHRP-2
Tesofensine
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
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)
StrongGHRP-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