Tesamorelin

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Also known as: Egrifta, TH9507

An FDA-approved GHRH analog for reducing visceral adipose tissue.

Overview

Tesamorelin is a synthetic GHRH analog approved for treatment of HIV-associated lipodystrophy. It specifically targets visceral fat reduction while stimulating natural GH pulsatility.

Mechanism of Action

Binds pituitary GHRH receptors to stimulate physiological GH release. The resulting GH and IGF-1 elevation promotes lipolysis, particularly in visceral adipose tissue.

Pharmacokinetics

Peak GH release within 30-60 minutes. Effects on body composition require weeks of treatment. Half-life approximately 26 minutes.

Dosing Protocols

Note: These are research protocols from literature. This is not medical advice.

1

Standard

Dose

2 mg

Frequency

Once daily

Duration

24+ weeks

FDA-approved dosing

Stacking Recommendations

Peptides that may be combined based on complementary mechanisms in research settings.

Rationale: Enhanced GH release

Synergy: GHRH + GHRP amplification

Rationale: Body composition

Synergy: Visceral fat from multiple mechanisms

Research Areas

LipodystrophyVisceral FatNAFLDCognitive Function

Key Research Findings

  • 1FDA-approved for HIV lipodystrophy with significant VAT reduction
  • 2Reduced liver fat in NAFLD studies
  • 3Potential cognitive benefits in aging populations
  • 4Maintains pulsatile GH pattern

Side Effects & Contraindications

Reported Side Effects

  • Injection site reactions
  • Joint pain
  • Peripheral edema
  • Paresthesia

Contraindications

  • Active malignancy
  • Disrupted hypothalamic-pituitary axis
  • Pregnancy

Safety Considerations

May cause joint pain, peripheral edema. Monitor glucose in diabetic patients. Contraindicated in active malignancy.

Storage Requirements

Refrigerate at 2-8C

Scientific References

Quick Reference

Sequence
Trans-3-hexenoic acid-Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-NH2
Molecular Weight
5135.9 g/mol
Half-Life
26-38 minutes
Bioavailability
High (SC)
Research Stage
approved
Administration
Subcutaneous injection