Comparison

Tesamorelin vs Sermorelin

Two GHRH analogs with approval histories. Which one still earns the price?

Reviewed by the amino101 editorial team. , first published .

TesamorelinSermorelin
Typical dosage1 to 2 mg200 to 500 mcg
Frequencyonce dailyonce daily
RouteSubcutaneousSubcutaneous
Half-life26 to 38 minutes in plasma10 to 20 minutes in plasma
Cycleongoing; reassess at 3 to 6 months with IGF-1 and waist measurements3 to 6 months
Research levelExtensively studiedExtensively studied
Human trialsApproved drugApproved drug
StatusFDA approved (Egrifta) for HIV-associated lipodystrophy; off-label otherwiseFormerly FDA approved (Geref, withdrawn 2008); widely available via compounding pharmacies
Effects timelineIGF-1 rise 2 to 4 weeks, waist and visceral fat change 12 to 26 weekssleep quality 1 to 2 weeks, IGF-1 rise on bloodwork 4 to 6 weeks, body composition and skin 2 to 3 months if at all

Key differences

Sequence
Tesamorelin
Full GHRH 1-44 with a trans-3-hexenoic acid cap
Sermorelin
GHRH 1-29, no modifications
Half-life
Tesamorelin
26 to 38 minutes
Sermorelin
10 to 20 minutes
Approval
Tesamorelin
FDA approved as Egrifta (2010), current
Sermorelin
FDA approved as Geref 1997 to 2008, withdrawn for commercial reasons; now compounded
Reported dose
Tesamorelin
1 to 2 mg once daily
Sermorelin
200 to 500 mcg once daily at bedtime
Fat loss evidence
Tesamorelin
Visceral fat down about 15 to 18 percent over 26 weeks in phase 3
Sermorelin
None specific; a 16 week trial in older adults showed modest lean mass gain
Side effects
Tesamorelin
Injection site reactions, joint pain, fluid retention, possible glucose rise
Sermorelin
Injection site reactions, flushing, drowsiness; mild water retention
Cost
Tesamorelin
High, milligram doses
Sermorelin
Low, microgram doses

Tesamorelin vs Sermorelin dosage

Dosage patterns reported in research and community protocols, by goal. Taken from each compound page. Not a prescription.

Tesamorelin1 to 2 mg
GoalDosageFrequency
Approved dose2 mgonce daily
Reduced dose for cost or side effects1 mgonce daily
Stacked with a GHRP1 to 2 mgonce daily before bed, with 100 mcg ipamorelin
Maintenance after fat loss1 mgonce daily, or 2 mg on alternating days
Sermorelin200 to 500 mcg
GoalDosageFrequency
Clinic standard200 to 300 mcgonce daily before bed
Higher single dose500 mcgonce daily before bed
Stacked with a GHRP200 mcgonce daily before bed, with 100 mcg ipamorelin
5 on 2 off variant300 mcgonce daily, weekdays only

Convert any of these to syringe units in the dosage calculator.

Side effects compared

Tesamorelin
  • ▲Injection site redness, itching, bruising, or irritation
  • ▲Joint pain and stiffness
  • ▲Swelling in the hands and feet, carpal tunnel symptoms
  • ▲Elevated blood glucose in susceptible people
  • ▲Headache or flushing
Full safety section
Sermorelin
  • ▲Injection site redness, itching, or small lumps
  • ▲Flushing or warmth shortly after a dose
  • ▲Headache or dizziness
  • ▲Mild water retention
  • ▲Drowsiness, which is why bedtime dosing is preferred
Full safety section

Which should you choose?

Pick Tesamorelin if
Pick Sermorelin if
Verdict

Stacking: Not stacked with each other; they hit the same receptor and adding one to the other does little. Either is paired with ipamorelin before bed.

Tesamorelin vs Sermorelin: frequently asked

Is tesamorelin stronger than sermorelin?
Can you take tesamorelin and sermorelin together?
Which is better for fat loss, tesamorelin or sermorelin?
Why do clinics prescribe sermorelin instead of tesamorelin?
Do tesamorelin and sermorelin raise blood sugar?

Sources

  1. Tesamorelin, a growth hormone-releasing factor analog, in HIV-infected patients with excess abdominal fat: pooled analysis of two Phase 3 trials. Journal of Acquired Immune Deficiency Syndromes, 2010
  2. Effects of nightly GHRH 1-29 administration in healthy older men and women. Journal of Clinical Endocrinology and Metabolism, 1997
  3. Egrifta (tesamorelin for injection) prescribing information. US Food and Drug Administration, 2010
Educational only. Dose ranges describe what appears in published research and community protocols. This is not medical advice and most of these compounds are not approved for human use. Talk to a clinician who knows your history.