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Tesamorelin Dosage: 1mg/Day, 5 On/2 Off Protocol (2026)

Tesamorelin is a synthetic GHRH analog that stimulates endogenous growth hormone production. It is the only FDA-approved treatment for reducing visceral fat in HIV-associated lipodystrophy, with Phase III trial data showing both visceral fat reduction and incr

Tesamorelin is a synthetic GHRH analog that stimulates endogenous growth hormone production. It is the only FDA-approved treatment for reducing visceral fat in HIV-associated lipodystrophy, with Phase III trial data showing both visceral fat reduction and increased lean body mass.

Research-context information only. Tesamorelin is the active ingredient in an FDA-approved product for HIV-associated lipodystrophy; research-peptide and compounded forms are not FDA-approved and are sold for research purposes only. Protocols, doses, and reactions reported below come from published clinical trials and self-reported community sources. This article reports what has been documented, not what should be done. Consult a licensed physician for personal medical decisions.

FDA-approved for HIV lipodystrophy. Off-label community use is growing but lacks equivalent clinical evidence. This is not medical advice.

Tesamorelin Dosing Table

Match your vial size below — reconstitution and dose math update automatically.

1 mg

40 units

0.4 mL

Daily SubQ (5-on/2-off)Community

2 mg

80 units

0.8 mL

Daily SubQFDA-approved dose

Math assumes U-100 insulin syringes (1 mL = 100 units). Verify your syringe matches before injecting. Round half-units to the nearest visible mark.

20 units

0.2 mL

10 units

0.1 mL

Daily SubQ (5-on/2-off)

Running Tesamorelin? Share your protocol

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Quick Reference: Standard Protocol

Dose

1 mg (20 units on insulin syringe)

Route

Subcutaneous injection

Timing

AM or PM

Frequency

5 days on, 2 days off

Cycle

8 weeks on, 8 weeks off

Vial size

10 mg

Reconstitution

2 mL bacteriostatic water → 5 mg/mL

Draw amount

20 units on insulin syringe

Storage

Refrigerate, use within 28 days

Standard protocol: 1 mg subcutaneous, 5 days on / 2 days off, for 8 weeks on / 8 weeks off. For the full tesamorelin profile, vendor pricing, and stacking options, see our tesamorelin peptide page.

Cycling Details

The 5on/2off schedule gives receptors periodic rest while maintaining consistent GH stimulation throughout the work week. The 8-week cycle length balances efficacy with cost management and receptor sensitivity.

Community protocols describe morning or evening dosing interchangeably; consistent timing is the documented standard approach. Fasted injection is commonly described in community sources as slightly optimizing GH response. Tesamorelin does not use a loading phase; documented protocols describe a direct 1 mg starting dose with no loading phase.

Continuous use versus cycling: what the trials documented

The community 8-on/8-off pattern is one approach; the clinical record describes another. In the Phase 3 program, tesamorelin was dosed at 2 mg subcutaneously every day for 52 continuous weeks with no scheduled breaks. IGF-1 reached its elevated plateau by week 26 and was maintained at that level through week 52, and visceral-fat reduction was sustained across the full year — the trials documented no tachyphylaxis (no loss of response over time) on continuous daily dosing (Falutz et al., 2007; 52-week extension, 2010). Trial data also documented that visceral fat re-accumulated after dosing stopped.

Community sources therefore describe two documented paths. Cycled use (commonly 8 weeks on, 8 weeks off) is typically described in the context of cost management and letting IGF-1 normalize between blocks. Continuous use mirrors the FDA-approved protocol, where the trial evidence for a sustained, non-attenuating response is strongest. In the trials, IGF-1 was monitored against the laboratory reference range, and published protocols described dose reduction when IGF-1 rose above it.

Enhanced Protocol (Clinical/FDA)

Note: The standard protocol above reflects the common community protocol at 1 mg. The FDA-approved protocol below uses the higher clinical dose.

2 mg daily

Every day (continuous)

Continuous under medical supervision

Indication

HIV-associated lipodystrophy

Evidence

Phase III RCT: 18% visceral fat reduction at 26 weeks

The FDA protocol runs continuously at 2 mg/day. Community protocols use 1 mg with cycling to manage cost and receptor sensitivity while still achieving meaningful GH elevation. Discontinuation leads to visceral fat regain regardless of dose. To estimate your total spend per cycle, see our tesamorelin cycle cost calculator. When you're ready to source, the tesamorelin buying guide covers which 4 of 7 vendors publish COA with mass spec verifying the 5,196 Da identity, plus vial-size selection (5mg vs 10mg).

Routes of Administration

Subcutaneous (only route): Trial protocols and FDA labeling describe rotating injection sites between left and right abdomen, with documented avoidance of scar tissue and the navel area. Community reconstitution guides note 27–30 gauge, ½ inch needle use.

Reconstitution Quick Reference

2 mL

5 mg/mL

10 mg vial + 2 mL BAC water = 5 mg/mL. At that dilution, a 1 mg dose corresponds to 20 units on an insulin syringe. One vial lasts 10 doses.

Community protocols describe gentle swirling — not shaking — to avoid degradation, with storage at 2–8°C and use within 28 days.

Ready to buy? Compare verified vendors on our best tesamorelin sources page (affiliate links — we earn a commission at no cost to you), or browse all coupon codes for up to 50% off.

CONNECTED / MODULES

Post-session references

Selected from shared article topics. Source links are retained where available.

01

Handling & safety lane

Source-derived education, not individual medical guidance or an instruction to dose.

STORAGE

Proper Storage: Protecting Your Investment

Peptide integrity doesn't stop after reconstitution. In fact, they are even more fragile in liquid form. Proper storage is absolutely essential. Before Reconstitution (Lyophilized Powder): The powder is stable at room temperature for short periods (like during shipping), but for long-term storage, it should be kept in a refrigerator (2°C to 8°C or 36°F to 46°F). For even longer-term storage (many months to years), it can be frozen. After Reconstitution (Liquid Solution): The vial must be refrigerated immediately. Never freeze a reconstituted peptide, as the freeze-thaw cycle can destroy its structure. It should also be stored in the dark (in its box or wrapped in foil) to protect it from light degradation. Once reconstituted with bacteriostatic water, Tesamorelin is typically stable for up to 4 weeks when properly refrigerated. Using sterile water without the bacteriostatic agent dramatically shortens this window to just a few days. This is a crucial distinction.
03

Evidence cooldown

Research context and source excerpts for a slower second read.

RESEARCH

Is tesamorelin FDA-approved and what does that mean for research?

Yes. Tesamorelin (brand name Egrifta, later EGRIFTA WR) is the only FDA-approved GHRH peptide analog. Initial approval came in 2010 for HIV-associated lipodystrophy; the updated EGRIFTA WR formulation received FDA approval in March 2025. This regulatory status means the 2mg daily tesamorelin dosage has undergone Phase III safety and efficacy evaluation — providing a level of adverse event characterization, pharmacokinetic data, and dosing validation that non-approved GHRH peptides lack. For research purposes, this documented safety profile is one of the primary reasons researchers select this compound over alternatives like Sermorelin or CJC-1295. See the full Tesamorelin vs CJC-1295/Ipamorelin comparison.

05

Product & matchup locker

Linked catalog and comparison files.

Comparison

Tesamorelin Dosage vs Other GHRH Analogs

Tesamorelin 2mg daily FDA-approved (2010) Phase III, 806 participants From $59.99 Sermorelin 200-300mcg daily Previously approved (withdrawn) Phase III (historical) $44.99-$79.99 …

Comparison

Egrifta SV® vs Egrifta WR™: What’s Changed

In 2024, the manufacturer Theratechnologies introduced a new formulation called Egrifta WR™, designed for more convenient dosing. Formulation Daily Dose Volume Reconstitution Adva…