guidesApril 25, 2026·6 min read

Tesamorelin + Ipamorelin: 1mg/300mcg Blend Dosage

FDA-studied GHRH + selective ghrelin-mimetic in one vial. 10mg/3mg blend protocol, PM timing, and why this beats sermorelin for fat loss.

Tesamorelin + Ipamorelin Blend: 1mg/300mcg Stack Dosing

Tesamorelin is a synthetic analog of growth-hormone-releasing hormone (GHRH) with the strongest human evidence for reducing visceral fat — 15-18% reductions in HIV-associated lipodystrophy trials (Falutz et al., NEJM 2007). Ipamorelin is a selective ghrelin receptor agonist that amplifies GH release without the cortisol, prolactin, or hunger spikes of older GHRPs. Combining the two activates GHRH and ghrelin receptors simultaneously — a 2-3x greater GH pulse than either alone (Bowers et al., JCEM 1991). The blend is typically sold as 10mg tesamorelin + 3mg ipamorelin in a single vial for convenience. This is not medical advice.

Research-context information only. Tesamorelin is the active ingredient in FDA-approved products 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 clinical trials and community sources. This article reports what has been documented, not what should be done. Consult a licensed physician for personal medical decisions.

Tesamorelin / Ipamorelin Blend Dosing Table

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

Reconstitute: add 2 mL of bacteriostatic water to the 13 mg vial. Resulting concentration: 6.5 mg/mL.

Vials are labeled "10/3" — 10 mg tesamorelin + 3 mg ipamorelin (13 mg total). Doses below are split at that same 10:3 ratio.

0.5 mg + 150 mcg10 units · 0.1 mL
Daily PM SubQ
Lower
1 mg + 300 mcg20 units · 0.2 mL
Daily PM SubQ (5-on/2-off)
Standard

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

Quick Reference: Standard Protocol

Parameter Value
Total dose per injection 1 mg tesamorelin + 300 mcg ipamorelin
Frequency Once daily, evening before bed
Schedule 5 days on / 2 days off
Cycle length 8 weeks on / 8 weeks off
Route Subcutaneous (abdomen rotation)
Vial 10mg / 3mg blend, reconstituted in 2 mL BAC water
Units per dose 20 units on a U-100 insulin syringe

For reconstitution step-by-step, see the Tesamorelin Reconstitution Guide. For ipamorelin's safety profile as a standalone, see Ipamorelin Benefits.

Cycling Details

The 5-on/2-off weekly pattern and 8-on/8-off cycle structure both respect the pulsatile biology of the GH axis. Continuous dosing downregulates both receptor systems — the off periods maintain sensitivity. Expect gradual body composition shifts starting week 3-4, with visceral fat changes most visible by week 8.

Typical goal timing:

  • Fat loss focus — PM pre-bed dosing, 8-week cycle, optional second AM injection in weeks 4-8 for aggressive protocols (split the total — 0.5 mg tesa + 150 mcg ipa per dose)
  • Recovery/anti-aging — PM only, 8-week cycles, standard 1mg/300mcg
  • Body recomposition with resistance training — PM + post-workout on training days (split dose)

Routes of Administration

Subcutaneous is the standard. Abdomen sites (avoiding the 2" navel radius) absorb most consistently. Trial protocols describe rotating injection sites daily to prevent lipoatrophy at any one location. Intramuscular is possible but unnecessary — SC delivers equivalent GH pulses with less injection pain.

Reconstitution Quick Reference

Vial Size BAC Water Concentration 1mg/300mcg Dose
10mg / 3mg blend 2 mL 5 mg/mL + 1.5 mg/mL 20 units

Community reconstitution protocols document the following dilution math: 10mg / 2mL = 5mg/mL = 5,000mcg/mL. For 1mg tesamorelin: 1,000 / 5,000 = 0.2 mL = 20 units. The ipamorelin at 3mg/2mL = 1.5mg/mL rides along at 300mcg per 20-unit dose — the same draw delivers both. Ratio is fixed by the vial — users seeking higher ipamorelin dosing buy standalone ipamorelin separately.

Community protocols describe swirling gently (not shaking), followed by refrigeration at 2–8°C; vials are typically used within 28 days. For step-by-step reconstitution with photos, see the Tesamorelin Reconstitution Guide.

Top Tesamorelin + Ipamorelin Vendors

Ranked by price, COA availability, and reputation

Affiliate disclosure: vendor links in this article are affiliate links — The Peptide Catalog may earn a commission if you buy through them, at no additional cost to you.

Ready to buy? Compare the top vendors on our best Tesamorelin + Ipamorelin blend sources page. For standalone options see best tesamorelin vendors or best ipamorelin vendors.

Where These Numbers Come From

Tesamorelin's dosing rationale comes from the HIV lipodystrophy trials (Falutz et al., 2007; Stanley et al., 2014) where 2mg daily SC for 26 weeks produced the 15-18% visceral fat reduction. Ipamorelin dosing at 200-300 mcg comes from Bowers' dose-response work in the 1990s and subsequent phase-I/II trials showing reliable GH pulses at that range.

Trial evidence:

Community protocols extend this evidence base with cycling patterns that weren't studied in the original trials — the 5-on/2-off rhythm and 8-week cycles are empirical community consensus, not clinically validated.

Tesamorelin + Ipamorelin vs CJC-1295 + Ipamorelin

Both are GHRH + GHRP blends. Core differences:

Feature Tesa + Ipa CJC-1295 + Ipa (no DAC)
GHRH half-life ~25 min ~30 min
Strongest human evidence Visceral fat (FDA-studied) None specific (community use)
Dosing cadence Daily PM Daily AM/PM or 2-3x daily
Off-label fit Body recomposition, stubborn abdominal fat Anti-aging, sleep, recovery
Typical blend 10mg / 3mg 5mg / 5mg
Cost per mg Higher (tesamorelin is pricier) Lower

For visceral fat specifically, tesamorelin has the strongest case. For general anti-aging, CJC-1295 is the more-used pick. See the CJC-1295 + Ipamorelin dosing guide for the other half of this comparison.

Side Effects & Safety

Typical first-cycle side effects:

  • Weeks 1-2: mild water retention, vivid dreams, light head/warmth after injection
  • Weeks 3-4: occasional joint stiffness, improved sleep quality, slight appetite increase overnight
  • Weeks 5-8: adaptation phase — most side effects fade, body composition changes visible

Clinical discontinuation signals (trial-reported): Clinical participants in tesamorelin studies were discontinued upon experiencing:

  • Persistent headaches with visual changes (intracranial pressure marker in trial monitoring protocols)
  • Sustained fasting glucose elevation of ~15 mg/dL above baseline
  • Unusual peripheral swelling persisting beyond weeks 1-2
  • Carpal tunnel symptoms unresponsive to dose titration in community-reported protocols

Tesamorelin has been studied at 2mg/day for 6+ months without notable safety signals at therapeutic doses. Ipamorelin's clean profile (no cortisol/prolactin) makes the blend one of the better-tolerated GHRH+GHRP combinations.

mg to Units Conversion

On a standard 100-unit insulin syringe, each "unit" equals 0.01 mL (so 100 units = 1 mL). Because this is a pre-mixed blend, a single draw delivers both peptides together — but at different amounts, since the vial holds 10 mg tesamorelin and 3 mg ipamorelin (a fixed 10:3 ratio).

At the standard reconstitution from the Quick Reference above (10 mg / 3 mg vial + 2 mL BAC water, 5 mg/mL tesamorelin + 1.5 mg/mL ipamorelin), each draw delivers:

Units (insulin syringe) Volume (mL) Tesamorelin Ipamorelin
10 units 0.1 mL 0.5 mg 150 mcg
20 units 0.2 mL 1 mg 300 mcg
30 units 0.3 mL 1.5 mg 450 mcg
40 units 0.4 mL 2 mg 600 mcg

These conversions reflect the dilution documented in community reconstitution protocols. They report how the math is described, not a recommended dosing schedule.

Frequently Asked Questions

What is the Tesamorelin + Ipamorelin blend?
A pre-mixed vial containing tesamorelin (GHRH analog) and ipamorelin (selective ghrelin receptor agonist) — most commonly sold as 10mg tesamorelin + 3mg ipamorelin in a single vial. The two peptides activate different receptors that converge on growth hormone release, producing 2-3x greater GH pulses than either alone.
What is the standard Tesamorelin + Ipamorelin dose?
The community protocol is 1 mg tesamorelin + 300 mcg ipamorelin subcutaneously, once daily in the evening before bed, 5 days on / 2 days off, for 8 weeks on / 8 weeks off. Community protocols describe reconstituting the 10mg/3mg vial with 2 mL bacteriostatic water; each dose is drawn at 20 units on a U-100 insulin syringe.
What injection timing do protocols describe for this blend?
Evening before bed is the dominant protocol because it amplifies the natural nocturnal GH surge (which peaks ~90 minutes into deep sleep). Morning dosing on an empty stomach also works and is sometimes chosen for workout synergy, but PM is preferred for body-composition goals.
Why pair tesamorelin with ipamorelin specifically?
Tesamorelin (GHRH) tells the pituitary to release GH; ipamorelin (ghrelin mimetic) amplifies the pulse by activating a second pathway. Critically, ipamorelin is selective for growth hormone release — unlike GHRP-2 or GHRP-6 it doesn't spike cortisol, prolactin, or hunger. The pairing gives you a stronger pulse without the hormonal side effects other GHRPs bring.
How does this compare to CJC-1295 + Ipamorelin?
Tesamorelin + Ipamorelin is the FDA-studied version — tesamorelin has published trial data showing 15-18% reduction in visceral fat. CJC-1295 + Ipamorelin is more popular for general anti-aging and recovery, with a wider cycle flexibility (daily non-DAC or weekly DAC). For stubborn abdominal fat specifically, tesamorelin has the strongest human evidence. For lean-mass/sleep/recovery goals, CJC-1295 is the more common pick.
How long does tesamorelin stay in the body?
Tesamorelin's plasma half-life is ~25 minutes, but its downstream effect on GH is amplified by the ipamorelin pulse and persists longer. The 5-on/2-off rhythm respects this pulsatile biology — longer or more frequent dosing increases receptor desensitization without meaningful gain.
What are the side effects of this blend?
Most common: mild injection site reactions (redness, bruising), temporary flushing or warmth after injection, vivid dreams during the night-dose phase, mild water retention in weeks 1-2. Less common: joint stiffness (usually resolves), carpal tunnel symptoms at higher doses, mild fasting glucose elevation. Trials and community sources report subjects consulting physicians or discontinuing upon experiencing sustained headaches, significant visual changes, or unusual swelling.
How do I reconstitute the 10mg/3mg blend?
Community reconstitution protocols describe adding 2 mL of bacteriostatic water to the vial, directing the stream toward the glass wall rather than the lyophilized powder, and swirling gently — shaking is avoided. The resulting concentration is 5mg/mL tesamorelin + 1.5mg/mL ipamorelin. A 20-unit dose on a U-100 insulin syringe delivers 1mg tesamorelin + 300mcg ipamorelin. The solution is stored at 2-8°C and typically used within 28 days.
Do women respond differently to this blend?
GH secretagogues don't affect sex hormone levels. Women use the same protocol. The visceral fat reduction mechanism is the same for both sexes; body composition response is gender-neutral based on trial data.
Is tesamorelin FDA-approved?
Tesamorelin (brand name removed intentionally — use the generic) has FDA approval for HIV-associated lipodystrophy. Ipamorelin has no FDA approval. The combination blend has no human trial data — protocols are derived from single-compound studies plus community practice.
Do I need PCT after this cycle?
No. GH secretagogues don't suppress endogenous testosterone or other sex hormones. The pituitary GH axis recovers naturally during the 8-week off-cycle. PCT is unnecessary.
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References

  1. Falutz J, et al. "Metabolic effects of a growth hormone-releasing factor in patients with HIV." NEJM 2007. PMID 17699044
  2. Stanley TL, et al. "Effect of tesamorelin on visceral fat and liver fat in HIV-infected patients with abdominal fat accumulation." JAMA 2014. PMID 25387188
  3. Raun K, et al. "Ipamorelin, the first selective growth hormone secretagogue." EJE 1998. PMID 9539826
  4. Bowers CY, et al. "On the regulation of growth hormone secretion in man: GHRH + GHRP synergy." JCEM 1991. PMID 2004615
  5. Stanley TL, et al. "Reduction in visceral adiposity is associated with an improved metabolic profile in HIV-infected patients receiving tesamorelin." Clin Infect Dis 2012. PMID 22570272