Compound Reference Overview
| Field | Value |
|---|---|
| Name | Tesamorelin |
| Reference Code | TESA |
| Category | Growth Hormone–Releasing Hormone (GHRH) Analog |
| Example Strength | 10 mg vial (commercial formulation) |
| Reference Dose | 2 mg once daily (FDA-approved dosing for HIV-associated lipodystrophy) |
| Frequency | Once daily (subcutaneous) |
| Key Safety Warning | Contraindicated in active malignancy and disrupted hypothalamic–pituitary axis. May increase IGF-1 levels. Effects reverse upon discontinuation. |
Mechanism of Action (Educational)
Tesamorelin is a synthetic analog of growth hormone–releasing hormone (GHRH). It stimulates the anterior pituitary to increase endogenous growth hormone secretion in a physiologic pulsatile pattern.
The resulting increase in GH leads to elevated insulin-like growth factor 1 (IGF-1) levels, which contributes to reduction in visceral adipose tissue.
Unlike exogenous growth hormone administration, tesamorelin acts upstream at the hypothalamic–pituitary level.
Indications (Literature)
- FDA-approved: HIV-associated lipodystrophy (reduction of excess abdominal visceral fat)
- Investigational: Visceral adiposity modulation in other metabolic contexts
Administration (Literature)
| Parameter | Details |
|---|---|
| Route | Subcutaneous |
| Frequency | Once daily |
| Injection Site | Abdomen (rotate sites) |
| Timing | Administered consistently at the same time daily; empty stomach preferred in some protocols |
Pharmacokinetics (Literature)
Tesamorelin has a half-life of approximately 26–38 minutes.
GH secretion increases within minutes of administration. Reduction in visceral adipose tissue is typically observed after 3–6 months of consistent therapy.
Titration Schedule (FDA-Approved)
No titration required. Therapy is initiated at the full dose of 2 mg once daily.
Reconstitution & Concentration (Commercial Formulation)
Commercially manufactured tesamorelin is supplied with sterile diluent and should be reconstituted according to manufacturer instructions.
| Parameter | Value |
|---|---|
| Diluent | Sterile water (commercial kit) or bacteriostatic water in compounded settings |
| Example Reconstitution | 10 mg vial + 2 mL diluent → 5 mg/mL |
| Stability | Use immediately if sterile water; up to 28 days refrigerated if bacteriostatic water (varies by formulation) |
Safety & Contraindications (Summary)
Contraindications
- Active malignancy
- Disrupted hypothalamic–pituitary axis
- Pregnancy
Drug Interactions
- Glucocorticoids (e.g., prednisone) may reduce effectiveness
Adverse Events
- Injection site reactions
- Arthralgia
- Peripheral edema
- Myalgia
Serious Risks
- Fluid retention
- Carpal tunnel syndrome
- Glucose intolerance
Monitoring (Literature)
- IGF-1 levels
- Fasting glucose / HbA1c
- Body composition (visceral fat assessment)
Mathematical Calculation Tool
The calculator below allows mathematical concentration and volume calculations using variable vial strengths and reconstitution volumes. This tool is provided strictly for arithmetic reference.
Peptide Reconstitution Calculator
For Educational & Professional Reference Only
Disclaimer
Tesamorelin is FDA-approved for HIV-associated lipodystrophy. All other uses are investigational. This content is provided for educational and professional reference purposes only.
Reference Sources
1. Falutz J, et al. Effects of tesamorelin on visceral fat in HIV patients.
N Engl J Med. 2010; PMID: 20159903.
2. Stanley TL, et al. Long-term safety and efficacy of tesamorelin.
J Clin Endocrinol Metab. 2011; PMID: 21098711.
3. Biller BMK, et al. Growth hormone–releasing hormone analog pharmacology.
Endocr Rev. 2007; PMID: 17339510.