Protocol Overview
| Field | Value |
|---|---|
| Name | Tesamorelin / Ipamorelin Combination |
| Reference Code | PHOENIX |
| Category | Growth Hormone Secretagogue Combination (GHRH + GHSR Agonist) |
| Example Strength | 12 mg / 2 mg (compounded formulation; varies by pharmacy) |
| Reference Range | Half blend dose for initial tolerance assessment → Full blend dose once daily (investigational use) |
| Frequency | Once daily |
| Key Safety Warning | Compounded combination. Not FDA-approved as a fixed-dose blend. Contraindicated in active malignancy, pituitary dysfunction, and pregnancy. May increase IGF-1 levels. Monitor for fluid retention and glucose intolerance. |
Mechanism of Action (Educational)
Tesamorelin is a synthetic growth hormone–releasing hormone (GHRH) analog that stimulates endogenous growth hormone secretion from the anterior pituitary.
Ipamorelin is a selective ghrelin receptor (GHSR-1a) agonist that promotes pulsatile GH release without significant stimulation of cortisol or prolactin.
When administered together, the combination produces synergistic stimulation of endogenous growth hormone through complementary hypothalamic–pituitary signaling pathways.
Growth hormone pulses are typically observed within 30 minutes following administration. Body composition changes may develop gradually over several months.
Indications (Investigational / Off-Label)
| Body composition research |
| Visceral adiposity investigations |
| Recovery optimization frameworks |
| IGF-1 modulation protocols |
Administration (Protocol-Based)
| Parameter | Details |
|---|---|
| Route | Subcutaneous |
| Frequency | Once daily |
| Injection Site | Abdomen (rotate sites) |
| Timing | Bedtime preferred; empty stomach recommended |
Pharmacokinetics (Component-Dependent)
Tesamorelin has a half-life of approximately 26–38 minutes. Ipamorelin has an approximate half-life of ~2 hours.
GH pulse typically occurs within 30 minutes following administration.
High glucose intake may blunt GH response. Monitoring of IGF-1 is recommended in structured protocols.
Titration Schedule (Protocol Example)
| Weeks 1–2 | Half blend dose once daily (tolerance assessment) |
| Week 3+ | Full blend dose once daily |
Dose escalation is guided by tolerability, fluid balance, and IGF-1 response.
Reconstitution & Concentration (Compounded Formulation Example)
| Parameter | Value |
|---|---|
| Diluent | Bacteriostatic water |
| Example Reconstitution | 12 mg Tesamorelin + 2 mg Ipamorelin + 2 mL diluent |
| Resulting Concentration | Tesamorelin: 6 mg/mL Ipamorelin: 1 mg/mL |
| Stability | Up to 28 days refrigerated (2–8°C; varies by compounding standards) |
This section is provided for arithmetic and formulation reference only.
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
Safety & Contraindications (Summary)
Contraindications
| Active malignancy |
| Pituitary dysfunction |
| Pregnancy or breastfeeding |
Drug Interactions
| Food intake may blunt GH response; fasted administration recommended |
Adverse Events
| Injection site reactions |
| Flushing |
| Headache |
| Water retention |
Higher-Dose Risks
| Significant edema |
| Glucose intolerance |
Monitoring (Protocol-Based)
| IGF-1 levels |
| Fasting glucose |
| Body composition metrics |
| Assessment of fluid retention |
Disclaimer
Tesamorelin/Ipamorelin combination products are compounded formulations and are not FDA-approved as fixed-dose combinations. This content is provided for educational and professional reference purposes only. It does not constitute medical advice or prescribing guidance.
Reference Sources
1. Falutz J, et al. Tesamorelin and visceral fat reduction in HIV.
N Engl J Med. 2010; PMID: 20159903.
2. Raun K, et al. Ipamorelin: Selective GH secretagogue.
Eur J Endocrinol. 2003; PMID: 12829766.
3. Smith RG, et al. Growth hormone secretagogues: Physiology and mechanism.
Endocr Rev. 1999; PMID: 10637194.