Tesamorelin: the GHRH analog, explained
Tesamorelin is a stabilized GHRH analog — and the only FDA-approved drug of its class, sold as Egrifta. It raises your own growth hormone to preferentially reduce visceral (deep abdominal) fat. But the approval is narrow: it's licensed only for HIV-associated lipodystrophy, and everything else is off-label. This page is the honest version: what it does, what the trials showed, the IGF-1 monitoring and side effects that matter, the short half-life, the reconstitution math, the anti-doping status, and how to track it. It is not dosing or sourcing advice.
- • Tesamorelin is a stabilized GHRH analog — the only FDA-approved one (Egrifta) — that raises your own GH/IGF-1 to cut visceral fat.
- • Approved only for HIV-lipodystrophy. General fat-loss / anti-aging use is off-label; never approved in the EU.
- • It raises IGF-1 — monitor it. Side effects: joint pain, edema, glucose effects; benefit reverses on stopping.
- • Once-daily SC; ~10–40 min half-life (effect outlasts it); WADA-banned (S2.2). This page is honest facts + math + tracking.
What it is
Tesamorelin is a synthetic, stabilized analog of growth-hormone-releasing hormone (GHRH) — a GHRH(1–44) analog with a trans-3-hexenoic acid group added to resist enzymatic breakdown. It's a GHRH-receptor agonist: it acts on the pituitary to stimulate release of your own (endogenous) growth hormone in a pulsatile, physiologic pattern, which in turn raises IGF-1. It's made by Theratechnologies. Importantly, it's the approved member of the GHRH-analog family — unlike the gray-market GHRH peptides CJC-1295 and sermorelin. (Note: ipamorelin is a different class — a ghrelin-receptor GHRP, not a GHRH analog.)
Approval & what the trials showed
Tesamorelin is FDA-approved as Egrifta (November 2010), with reformulations Egrifta SV and the newer Egrifta WR (2025), for the reduction of excess abdominal fat in HIV-infected adults with lipodystrophy. The label is explicit that it's not for weight-loss management — the effect is on visceral fat specifically, and it's weight-neutral.
The pivotal evidence is the Phase 3 HIV-lipodystrophy program (Falutz et al., NEJM 2007, and LIPO-010/011): over 26 weeks, visceral adipose tissue fell ~15% on tesamorelin versus a ~5% increase on placebo. There's also genuine research interest in liver fat (NAFLD/NASH) in HIV (a 2019 Lancet HIV trial reduced hepatic fat), but that and any anti-aging/general-fat-loss use remain investigational and off-label. And the benefit is not durable: visceral fat re-accumulates after the drug is stopped.
The math
The approved Egrifta products are reconstituted by the patient per their instructions. The arithmetic on this page is for the gray-market lyophilized powder route — reconstituted with bacteriostatic water, dosed in milligrams — the same math the peptide reconstitution calculator does. Worked example, purely as arithmetic:
| Vial label | 10 mg lyophilized powder |
| Add | 2 mL bacteriostatic water |
| Concentration | 10 mg ÷ 2 mL = 5 mg/mL |
| Per 0.1 mL | 0.5 mg — i.e. 10 units on a U-100 syringe = 0.5 mg |
| So a 2 mg dose would be | 0.4 mL = 40 units |
Concentration is just milligrams divided by millilitres, and units are just hundredths of a millilitre on a U-100 insulin syringe. The reconstitution calculator converts vial size + water + target into exact syringe units. The milligrams above are illustrative arithmetic, not a recommended dose — the approved doses are 1.28–2 mg daily depending on the formulation; off-label use is commonly reported around 1–2 mg/day but no validated off-label dose exists.
Half-life & daily dosing
Tesamorelin's plasma half-life is very short — the current Egrifta WR label cites ~11 minutes, while older sources cite ~26–38 minutes, so call it roughly 10–40 minutes, source-dependent. It's dosed once daily anyway, because the downstream GH/IGF-1 effect lasts far longer than the drug — the peptide triggers a GH pulse and then clears, but the IGF-1 elevation persists. You can see how a short half-life behaves with daily dosing in the half-life visualizer.
IGF-1 monitoring, side effects & storage
The defining safety point: tesamorelin raises IGF-1, so the label requires monitoring IGF-1 and discontinuing if it stays elevated (sustained high IGF-1 is the GH-axis safety concern). Other documented effects:
- Most common: joint pain (arthralgia), injection-site reactions, swelling (peripheral edema), muscle pain.
- Glucose: can impair glucose tolerance / raise blood sugar — monitor, especially with diabetes risk.
- Fluid retention: edema and, occasionally, carpal-tunnel-type symptoms.
- Contraindicated in active malignancy, disruption of the hypothalamic-pituitary axis, and pregnancy.
- Storage: approved Egrifta per its label; gray-market powder kept cold/dark, reconstituted in bacteriostatic water and refrigerated at 2–8°C, used within about four weeks. Gray-market purity is not guaranteed.
Tracking tesamorelin in OptiPin
If you're tracking a GH-axis protocol, OptiPin treats it like any other entry — without endorsing off-label use:
- Daily dose log + reminders — record the once-daily injection and get reminded on the due day, with site rotation.
- IGF-1 & glucose tracking — log bloodwork (IGF-1, fasting glucose/HbA1c) over your dose timeline — IGF-1 is the monitoring that actually matters here.
- Waist & body metrics — log waist circumference and weight, since the effect is on visceral fat specifically (and weight-neutral).
- OptiInsight analysis — OptiPin's AI reads the full record (doses, labs, measurements) and surfaces what moved with what.
- Built-in reconstitution math — the same calculator covered above is one tap in the app.
Log doses, IGF-1 & waist in OptiPin
Daily reminders, IGF-1/glucose-over-dose charts, waist & weight tracking, vial runout warnings, built-in reconstitution math, and OptiInsight analysis — all on-device.
Download on the App StoreFAQ
Is tesamorelin FDA-approved?
Yes — the only approved GHRH analog (Egrifta / Egrifta SV / Egrifta WR), but only for visceral fat in HIV-associated lipodystrophy. General fat-loss/anti-aging use is off-label. Never approved in the EU (application withdrawn 2012).
What does it actually do?
Stimulates your own GH release → raises IGF-1 → preferentially reduces visceral (deep abdominal) fat (~15% over 26 weeks in trials). It's weight-neutral, and the benefit reverses after stopping.
Half-life and dosing?
Once-daily SC (approved 1.28–2 mg by formulation). Plasma half-life is short (~10–40 min, source-dependent), but the GH/IGF-1 effect lasts much longer, so daily dosing works.
Side effects?
Joint pain, injection-site reactions, edema, muscle pain. It raises IGF-1 (must be monitored), can affect blood sugar and cause fluid retention; contraindicated in active malignancy/pituitary disruption/pregnancy.
Is it banned in sport?
Yes — a GHRH analog under WADA S2.2 (growth-hormone-releasing factors), prohibited at all times.
Sources
- FDA / DailyMed — Egrifta WR (tesamorelin) prescribing information
- Falutz et al. — Tesamorelin for visceral fat in HIV-lipodystrophy (NEJM, 2007)
- Stanley et al. — Tesamorelin & NAFLD/liver fat in HIV (Lancet HIV, 2019)
- EMA — Egrifta EU marketing-authorisation application withdrawn (2012)
- WADA Prohibited List (S2.2 GHRH and analogues)
Related
Ipamorelin + CJC-1295 · MK-677 · Peptides guide · Peptide reconstitution calculator · Half-life visualizer · Bloodwork