CalcMyPeptide
Growth HormoneAlso known as: Egrifta

Tesamorelin

Tesamorelin is an intensely potent, FDA-approved Growth Hormone Releasing Hormone (GHRH) analog utilized medically under the brand name Egrifta. Unlike traditional secretagogues that induce generalized systemic effects, Tesamorelin displays an extraordinary, highly specific affinity for annihilating deep visceral adipose tissue (VAT). Originally designed to combat severe lipodystrophy in HIV patients, it is the premier clinical choice for aggressively reversing visceral fat accumulation, reversing hepatic steatosis (fatty liver), and drastically improving systemic lipid profiles without causing severe insulin resistance.

Reviewed by CalcMyPeptide Editorial Team
Last updated: April 2026Evidence: High1 peer-reviewed citation

Quick Stats

Half-Life~26 minutes (SC)
Dose Range1-2 mg/day
Frequency1× daily
Vial Sizes2 mg
BioavailabilitySubcutaneous injection
Year Developed2010 (FDA approval)

Scientific Data

Molecular Formula
C221H366N72O67S1
Molecular Weight
5135.8 g/mol
CAS Number
PubChem ID

Mechanism of Action

Tesamorelin is a synthetic analog of GHRH(1-44) with a trans-3-hexenoic acid modification at the N-terminal for enhanced stability. It is the only FDA-approved GHRH analog (Egrifta), approved for HIV-associated lipodystrophy (excess visceral and truncal fat).

Tesamorelin binds GHRH receptors in the pituitary, stimulating pulsatile Growth Hormone release. Unlike exogenous GH, it preserves the natural pulsatile GH rhythm and hypothalamic feedback loop. It specifically reduces visceral adipose tissue (VAT) and has shown improvements in cognitive function, cardiovascular markers, and body composition in both HIV+ and general populations.

Source: FDA Label (Egrifta), PMID: 20947872

Background & History

Tesamorelin (Egrifta) is an FDA-approved synthetic GHRH analog developed by Theratechnologies for lipodystrophy in HIV patients. It is the only GHRH analog approved for human use in the United States. A modified version of native GHRH with the addition of a trans-3-hexenoic acid group for protease stability, it has a longer half-life (~30 min) than native GHRH (~7 min). Clinical trials showed 15–18% reduction in visceral adipose tissue — the most consistent pharmacological reduction of visceral fat demonstrated in clinical trials.

Research Use Cases

  • HIV-associated lipodystrophy (FDA approved, Egrifta)
  • Visceral adiposity reduction independent of HIV status (off-label research)
  • GH/IGF-1 elevation with physiological pulsatile pattern preservation
  • Cognitive benefits in mild cognitive impairment (Phase II trial data)

Dosing Protocol

Typical Dose1-2 mg/day
Frequency1× daily
Half-Life~26-38 minutes
Common Vial Sizes2 mg

Dosing Protocols

FDA-Approved (Lipodystrophy)

Dose
2 mg
Frequency
Daily SC injection
Note: FDA-approved dose for HIV-associated lipodystrophy. Clinically proven reduction in VAT.

Longevity / Body Composition

Dose
1 - 2 mg
Frequency
Daily SC injection
Note: Off-label use for visceral fat reduction and GH optimization. Often cycled to minimize IGF-1 elevation.

Body-Weight Dosing Reference

Estimated doses extrapolated from the published research range of 10002000 mcg/day (referenced to 70 kg / 154 lb). These are approximations — consult a qualified healthcare provider for personalised guidance.

WeightLowTargetHigh
120 lb(54 kg)771 mcg1157 mcg1543 mcg
140 lb(63 kg)900 mcg1350 mcg1800 mcg
160 lb(73 kg)1043 mcg1564 mcg2086 mcg
180 lb(82 kg)1171 mcg1757 mcg2343 mcg
200 lb(91 kg)1300 mcg1950 mcg2600 mcg
220 lb(100 kg)1429 mcg2143 mcg2857 mcg
250 lb(113 kg)1614 mcg2421 mcg3229 mcg

💉 For exact syringe units based on your vial concentration, use the Tesamorelin Reconstitution Calculator →

Administration

Route
Subcutaneous injection
Timing
Once daily, preferably at bedtime on an empty stomach.
Fasting Required?
Yes — inject on an empty stomach

Expected Timeline

Week 1-4
Increased GH pulse amplitude. Improved sleep quality and recovery.
Month 2-6
Measurable reduction in visceral adipose tissue (VAT). Improved body composition.
Month 6+
Sustained VAT reduction. Cognitive and cardiovascular marker improvements in clinical studies.

Who Is It For?

Visceral Fat / Lipodystrophy

High

FDA-approved for HIV lipodystrophy. RCT data shows 15-20% VAT reduction in 26 weeks.

GH Optimization / Body Composition

Moderate

Off-label use. Preserves pulsatile GH rhythm vs. exogenous GH. Favorable safety profile.

Cognitive Enhancement

Moderate

Clinical studies show improved cognitive function in older adults with abdominal obesity.

Reconstitution Example

Vial
2 mg
Water
2 mL
Concentration
1 mg/mL
Per Unit (100u syringe)
10 mcg
Dose of 1000 mcg = 100 units on a 100-unit insulin syringe

Safety & Considerations

FDA-approved (Egrifta). Generally well-tolerated. Injection site reactions are common. Monitor IGF-1 levels — discontinue if levels exceed normal range. Contraindicated in active malignancy or hypersensitivity.

Regulatory & Legal Status

FDA Status (US)
Approved

FDA-approved as Egrifta® for HIV-associated lipodystrophy

WADA Status (2026)
Prohibited (S2)

Competitive athletes subject to anti-doping controls should not use Tesamorelin.

Classification

Prescription Drug

US Compounding: Not eligible / not available

⚠️ This information is for educational purposes only and may not reflect the most current regulatory updates. Always verify with official FDA, WADA, and jurisdiction-specific sources before use.

Interactions & Contraindications

GH/IGF-1 elevation affects glucose metabolism — monitor blood glucose. Contraindicated with active malignancy. Not for use in pregnancy. Simvastatin and other glucocorticoids may reduce efficacy.

Synergies & Common Stacks

Tesamorelin (GHRH analog) + Ipamorelin (GHRP) creates the same synergistic mechanism as Mod GRF + Ipamorelin, with tesamorelin's longer half-life offering slightly more convenience.

Tesamorelin reduces visceral fat via GH stimulation; AOD-9604 directly targets adipose tissue lipolysis. Complementary fat loss mechanisms.

Tesamorelin vs. Sermorelin

AttributeTesamorelinSermorelin
FDA StatusFDA-approved (Egrifta® — HIV lipodystrophy)Not FDA-approved (was revoked)
Half-Life~26 minutes~11–13 minutes
PotencyStronger — engineered GHRH analogModerate — native GHRH fragment
Best ForVisceral fat + GH deficiency protocolAnti-aging GH optimization
CostHigher (Rx only)Lower (compounded)

Verdict: Tesamorelin is the clinically superior GHRH analog with proven visceral fat reduction and FDA medical validation. For users specifically targeting body composition and clinical evidence, tesamorelin is the preferred choice.

Dosing Quick Reference

Tesamorelin— Dosing Guide
Dose Range
1-2 mg/day
Half-Life
~26-38 minutes
Frequency
1× daily
Route
Subcutaneous
2 mg vial
💧 2 mL BAC water📐 1 mg/mL concentration💉 10 mcg/unit (100u syringe)
Growth Hormonecalcmypeptide.com

Frequently Asked Questions

What makes tesamorelin different from CJC-1295?
Both are GHRH analogs but tesamorelin is the full GHRH(1-44) sequence with an added modification, making it FDA-approved with extensive clinical data. CJC-1295 (with DAC) has a much longer half-life due to albumin binding but lacks FDA approval and clinical trial record.
How does tesamorelin reduce visceral fat?
By stimulating pulsatile GH release, tesamorelin increases lipolysis (fat breakdown) specifically in visceral adipose tissue, which is highly GH-sensitive. Clinical trials show 15-20% reduction in VAT after 6 months of daily use.

References

  1. Falutz J et al. "Tesamorelin (Egrifta) for HIV-Associated Lipodystrophy".” NEJM (2010). PMID: 20427810
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