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

SermorelinvsTesofensine

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

APhase 3Reviewed14/43 cited
BPhase 3Draft10/40 cited
Sermorelin
GHRH 1-29 fragment · Short-acting
100–500 mcgPer doseMolteno 2013
Phase 3Evidence levelWalker 1994Molteno 2013
~12 minHalf-lifeMolteno 2013
SQ · Pre-sleep · 1×/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
Sermorelin
Tesofensine
Primary target
Pituitary GHRH receptorWalker 1994
Serotonin / norepinephrine / dopamine transporters (SERT / NET / DAT)Astrup 2008
Pathway
GHRH-R → Gαs → cAMP → PKA → GH vesicle exocytosisWalker 1994
Triple monoamine reuptake inhibition → ↑synaptic 5-HT, NE, DA → appetite suppression + thermogenesisAstrup 2008
Downstream effect
Pulsatile GH release; subsequent IGF-1 elevationMolteno 2013
Strong appetite suppression, mild thermogenic effect, weight lossAstrup 2008
Feedback intact?
Yes — short pulse preserves feedback
Origin
Unmodified active 29-AA fragment of human GHRH (1-44)Walker 1994
Small molecule developed by NeuroSearch (Denmark) for CNS indications, repurposed for obesityAstrup 2008
Antibody development

02Dosage Protocols

Parameter
Sermorelin
Tesofensine
Standard dose
100–500 mcg per injectionMolteno 2013
0.25–0.5 mg / dayAstrup 2008
Frequency
Once daily, pre-sleep
Once daily, morning
Lower / starter dose
100 mcg per dose
0.125 mg / day
Evidence basis
Phase 3 (Geref pediatric); clinical practiceWalker 1994Molteno 2013
Phase 2b + ongoing Phase 3Astrup 2008
Duration
8–12 weeks per cycle
24 weeks per studied cycle
Reconstitution
Bacteriostatic water
Timing
Pre-sleep, fasted preferred
Morning to avoid sleep disruption
Half-life
~12 min (plasma)Molteno 2013
Shorter than tesamorelin (~26 min) — simpler GHRH analogue.
~9 days (very long)
Form
Oral capsule

04Side Effects & Safety

Parameter
Sermorelin
Tesofensine
Injection site reaction
Mild erythema, transient pain
Flushing / headache
Common transient effect
IGF-1 elevation
Modest at standard doses
Cancer risk
Contraindicated in active malignancy (GH/IGF-1 axis)
Pregnancy / OB
Avoid
Contraindicated
Glucose handling
Generally neutral
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
Sermorelin
  • ·Active malignancy
  • ·Pregnancy / breastfeeding
  • ·Disrupted hypothalamic-pituitary axis
Tesofensine
  • ·Pregnancy / breastfeeding
  • ·Severe cardiovascular disease
  • ·Concurrent MAOI use
Relative Contraindications
Sermorelin
  • ·Untreated diabetes
Tesofensine
  • ·Hypertension
  • ·Anxiety disorder
  • ·Insomnia

05Administration Protocol

Parameter
Sermorelin
Tesofensine
1. Reconstitution
Add 2 mL bacteriostatic water to 5 mg vial → 2.5 mg/mL = 250 mcg per 0.1 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.
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

Sermorelin
+ Ipamorelin
Strong
View Ipamorelin

Sermorelin (GHRH analogue) and ipamorelin (selective GHRP) form the prototypical GHRH+GHRP dual-axis stack at the lowest cost. Both peak within 30 min and produce a sharp physiological GH pulse without cortisol/prolactin elevation.

Sermorelin
200–300 mcg SQ · pre-sleep
Ipamorelin
200–300 mcg SQ · same injection
Primary benefit
Pulsatile GH stimulation, recovery, body composition
Tesofensine
— no documented stacks