Tesamorelin
Also known as: Egrifta, TH9507
Tesamorelin is a GHRH analog that specifically reduces visceral adipose tissue. It is FDA-approved for HIV-associated lipodystrophy and has cognitive and metabolic benefits.
Research Status
FDA-approved for HIV-associated lipodystrophy
For research purposes only. Not approved for human use. Not medical advice.
Research Areas
Side Effects
Localised redness, swelling, or itching at the injection site typically resolves within hours to days. Rotate injection sites to minimise recurrence. Apply ice if needed for comfort. Ensure proper injection technique and allow solution to reach room temperature before injection.
GH-induced fluid retention can compress the median nerve in the wrist, causing pain, numbness, or tingling in the hand. Reported in approximately 5–10% of tesamorelin users in clinical trials. Symptoms typically appear after 4–12 weeks of therapy. Manage with wrist splinting, NSAIDs, or dose reduction. Discontinue if symptoms are severe or progressive. Resolves within weeks of stopping therapy.
GH-induced fluid retention and metabolic changes can cause joint pain, particularly in the knees, hips, and shoulders. Usually mild and self-limiting. Manage with NSAIDs, stretching, and adequate hydration. Typically resolves within 4–8 weeks as the body adapts.
Muscle soreness or mild weakness may occur early in therapy, likely due to metabolic shifts and increased protein turnover. Usually resolves within 2–4 weeks. Ensure adequate protein intake and hydration.
GH stimulates sodium and water retention, potentially causing mild swelling in the hands, feet, or face. More common in patients with pre-existing hypertension or renal impairment. Manage with sodium restriction and adequate hydration. Typically mild and self-limiting. Monitor blood pressure regularly.
GH has anti-insulin effects and can transiently elevate fasting glucose or impair glucose tolerance, particularly in patients with pre-existing insulin resistance or diabetes. Monitor fasting glucose and HbA1c at baseline and during therapy. Usually mild and reversible. Tesamorelin's visceral fat reduction may improve insulin sensitivity over time, offsetting acute GH-induced effects.
Mild to moderate headaches reported in approximately 5–8% of users, possibly related to fluid retention or metabolic changes. Usually self-limiting. Manage with analgesics and hydration. Discontinue if severe or persistent.
Mild nausea, bloating, or changes in appetite may occur early in therapy. Usually transient and resolves within 1–2 weeks. Take with food if tolerated; ensure adequate hydration.
GH can increase blood pressure through fluid retention and increased cardiac output. Monitor blood pressure regularly, especially in patients with pre-existing hypertension. Manage with sodium restriction, weight loss, and antihypertensive medication if needed. Discontinue if blood pressure becomes uncontrolled.
GH can affect thyroid function and increase the risk of autoimmune thyroiditis in susceptible individuals. Monitor TSH and free T4 at baseline and annually during therapy. Manage with levothyroxine if hypothyroidism develops. More common in patients with pre-existing thyroid disease or autoimmune conditions.
GH-induced changes in sex hormone metabolism or increased aromatisation of androgens to oestrogen may rarely cause breast tissue growth in males. Usually mild and reversible. Discontinue if bothersome or progressive.
Theoretical concern with long-term GH elevation, though clinical evidence in tesamorelin trials is reassuring. Tesamorelin is contraindicated in patients with active malignancy or a history of malignancy within 5 years. Monitor for signs of malignancy during therapy. Discuss risk–benefit ratio with your healthcare provider, especially if you have a personal or family history of cancer.
Chronic peptide therapy can trigger antibody formation, potentially reducing efficacy over time. Reported in <5% of tesamorelin users in clinical trials. If efficacy wanes after initial improvement, antibody testing may be warranted. Discontinuation and rechallenge after a washout period may restore responsiveness.
Dosing Reference
| Parameter | Value |
|---|---|
| Dose range | 2 mg |
| Frequency | Daily |
| Timing | Morning, subcutaneous in abdomen |
| Route | Subcutaneous |
Rotate injection sites. Specifically targets visceral fat. Prescription required.
Research disclaimer
Figures drawn from published research literature and community logs. Not clinical recommendations. Consult a qualified professional. Research use only.
Reconstitution Guide
Do not use saline or bacteriostatic saline — use only bacteriostatic water for reconstitution
Do not shake the vial vigorously; gentle swirling prevents peptide degradation
Discard immediately if the solution appears cloudy, discolored, or contains visible particles
Use within 30 days of reconstitution when stored at 2–8°C
Do not freeze the reconstituted solution; freezing may denature the peptide
Use the PeptideVolt reconstitution calculator for your exact concentration
Molecular and Pharmacological Data
| Molecular weight | 5136 Da |
| Half-life | 26–40 minutes (endogenous GH half-life is 15–20 minutes; tesamorelin extends GH elevation) |
| Sequence | H-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-Gln-Gln-Gly-Glu-Ser-Asn-Gln-Glu-Arg-Gly-Ala-Arg-Ala-Arg-Leu-NH2 |
Tesamorelin is a synthetic analog of growth hormone-releasing hormone (GHRH) that binds to GHRH receptors on the anterior pituitary gland, stimulating the release of endogenous growth hormone (GH). This increased GH secretion enhances lipolysis (fat breakdown) and preferentially reduces visceral adipose tissue (deep abdominal fat) while preserving or increasing lean muscle mass. The mechanism is particularly effective at targeting visceral fat depots, which are metabolically active and associated with insulin resistance and cardiovascular risk.
GHRH Receptor Signalling
Tesamorelin activates GHRH receptors on somatotroph cells in the anterior pituitary, triggering cAMP-mediated signalling that stimulates GH synthesis and secretion into the bloodstream.
Growth Hormone-Mediated Lipolysis
Elevated GH levels activate lipolysis through GH receptor signalling in adipose tissue, promoting the breakdown of triglycerides and mobilisation of free fatty acids, with preferential effects on visceral fat depots.
Insulin-Like Growth Factor-1 (IGF-1) Axis
Increased GH stimulates hepatic and peripheral production of IGF-1, which mediates anabolic effects including increased protein synthesis, lean body mass accretion, and metabolic improvements.
Metabolic and Cognitive Effects
GH elevation improves insulin sensitivity, reduces hepatic steatosis, and enhances cognitive function through both direct GH receptor signalling and IGF-1-mediated neuroprotection.
- Tesamorelin is a 44-amino acid peptide that is a synthetic analog of naturally occurring GHRH, differing by substitution of the first amino acid (tyrosine for alanine) to increase receptor binding affinity and resistance to enzymatic degradation.
- FDA-approved specifically for HIV-associated lipodystrophy, a condition characterised by abnormal fat redistribution and visceral adiposity that increases metabolic and cardiovascular complications.
- Clinical studies demonstrate preferential reduction of visceral adipose tissue (VAT) by 20–30% over 6 months, with minimal effects on subcutaneous fat, making it unique among GH secretagogues.
- Tesamorelin increases endogenous GH secretion rather than providing exogenous GH, preserving the body's natural pulsatile GH release pattern and feedback regulation.
- Cognitive benefits including improved memory and executive function have been documented in clinical trials, attributed to GH and IGF-1 effects on hippocampal and prefrontal cortex function.
- The peptide does not directly bind to GH receptors; its effects are entirely dependent on stimulating the pituitary to release endogenous GH, which then acts systemically.
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