★ Growth Hormone

Tesamorelin

Growth Hormone · 5mg × 10 vials

In plain terms: Tesamorelin is a research compound - oral, fast-acting and well studied.

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Quick Start
🧪
Format
Injectable (reconstituted) · 5mg × 10 vials
🎯
Who it's for
visceral fat focus
💉
How it's run
1 mg subcutaneous daily, pre-bed
When you'll notice
6-12 weeks visceral fat
Pricing
$190from · kit of 10
US: 2-5 day · Intl: 7-14 day
+ $40 ship · singles $20 · free over $1k per tier
5mg × 10 vials$190
10mg × 10 vials$325
Order / Consult on Telegram →
0 min
Half-life
continuous
Cycling
6-12 weeks visceral fat
First effects
growth-hormone
Class
Overview

What Is Tesamorelin?

Tesamorelin is a stabilized synthetic analog of growth hormone-releasing hormone (GHRH(1-44)). It binds the GHRH receptor on the anterior pituitary and triggers pulsatile release of the body's own growth hormone, which in turn raises circulating IGF-1. The key engineering trick is an N-terminal trans-3-hexenoyl modification that protects the molecule from dipeptidyl peptidase IV degradation, giving it enough plasma stability to actually reach the pituitary (native GHRH has a half-life of a couple minutes; tesamorelin's plasma half-life is around 26 minutes, longer in HIV patients). Because it works upstream of the pituitary rather than replacing GH directly like exogenous HGH does, tesamorelin preserves the body's natural feedback loop (IGF-1 negative feedback still throttles output), which is why side-effect profile is cleaner than HGH and why visceral fat is selectively burned without wrecking subcutaneous fat or muscle. The downstream effect is that hepatic and visceral adipose tissue (the dangerous deep belly fat that wraps organs) becomes the preferred fuel substrate, with mean VAT reductions of 15-18% over 26 weeks in pivotal trials.

Protocols

Typical dose ranges by experience level - educational reference. Message us and we tailor it to you.

Protocol1 mg subcutaneous daily, pre-bed
Frequency1x daily (short ~26 min half-life means daily dosing is required; the metabolic effect runs through IGF-1 which stays elevated longer)
Duration12 weeks minimum before assessing visceral fat response; meaningful body comp change typically shows at the 6-12 week mark

Trial protocol used 2 mg daily from day one in HIV patients, but for non-HIV research the 1 mg start is the community standard. It cuts the early water retention and tingling/numbness signal in half. Reconstitute 10 mg vial with 2 ml BAC = 5 mg/ml, so 1 mg = 0.20 ml = 20 IU on a U-100 syringe. Inject subQ into the lower abdomen pre-bed.

Protocol2 mg subQ daily, pre-bed
Frequency1x daily
DurationContinuous through the body comp goal window (12-26 weeks typical). Pivotal trials ran 26 weeks then a 26-week safety extension; both phases showed sustained VAT reduction with no plateau through 52 weeks.

Most users hit their peak visceral fat response at 2 mg daily over 16-26 weeks. Above 2 mg there's no efficacy data and the IGF-1 elevation becomes harder to keep in physiological range. If joint pain or carpal tunnel symptoms emerge, pull back to 1 mg rather than stopping cold.

Protocol2 mg daily continuous, optionally split-dose (1 mg AM + 1 mg PM) or stacked with CJC+Ipa for double GH pulse
Frequency1x or 2x daily
Duration6-12 month continuous runs are common in the longevity / AAS-recomp community. Some users cycle 12 weeks on / 4 weeks off to reset receptor sensitivity, but the continuous schedule is what the pivotal trials validated and what most non-HIV researchers run.

Bodybuilders and AAS users running tesa specifically for "HGH gut" / palumboism reversal often pair with low-dose HGH (1-2 IU) at the same pre-bed window. Monitor IGF-1 quarterly if running long-term, target middle to upper end of age-adjusted normal range, pull back if it crests above the reference range. Watch for HbA1c drift on a 12-month run, the pivotal data shows a small +0.1% bump that can compound on top of GLP-1 stacks.

What To Expect
6-12 weeks visceral fat
noticeable change
Side Effects

Straight talk - what people actually report, and what the studies measured.

What users report
From forums, Discord & TikTok
  • Water retention / "puffy face" weeks 1-2: most-reported sensation, resolves by week 3-4 as body adapts
  • Numbness/tingling in fingers (mild carpal-tunnel-like): common at 2 mg, resolves on 1 mg dose drop
  • Joint stiffness in the morning: reported across forums, especially in users running tesa with HGH or CJC+Ipa
  • Vivid dreams / improved sleep: positive AE, very commonly reported because the GH pulse hits during sleep
  • Hunger increase: tesa doesn't suppress appetite (unlike GLP-1s), and the GH pulse can mildly elevate hunger; some users report stronger appetite at the 2 mg dose
  • Belly measurement drop before scale weight drop: classic visceral-specific signal, users report waistline tightening at 6-8 weeks before total weight moves
  • Reasons people stop: cost (tesa is one of the pricier daily peptides on a per-month basis), wanted faster visible result and switched to a GLP-1 instead, finished a 6-month cycle and rotated off
  • - Divergence: RCT injection-site reaction rate is ~8% but community reports closer to 15-20% during the first 4 weeks, mostly driven by users not rotating sites within the abdomen panel. Resolves with proper rotation.
What the studies show
Measured in clinical trials
  • Injection site erythema: 8.5% vs 2.7% placebo (Falutz/Stanley pooled Phase 3) - mild, resolves with site rotation
  • Injection site pruritus (itching): 7.6% vs 0.8% placebo - mild
  • Peripheral edema (fluid retention in hands/ankles): 6.1% vs 2.3% placebo - mild to moderate, typically resolves weeks 2-4 as body adjusts to elevated IGF-1
  • Arthralgia (joint pain): 5-13% across trials - usually mild, related to fluid shift, resolves with continued use or dose reduction
  • Hypoesthesia / paresthesia (numbness, tingling, carpal-tunnel-like): 4-7% - IGF-1 driven, dose-dependent, resolves on dose reduction
  • Mean IGF-1 increase: ~80% from baseline at 26 weeks; ~47% of treated patients exceeded age-adjusted upper limit at some point during treatment
  • Glucose tolerance: HbA1c bumped a mean +0.1% in trials; 5% of tesa group hit HbA1c ≥6.5% vs 1% placebo. Fasting glucose unchanged at 26 weeks in non-diabetic cohort. In the dedicated T2D trial, no significant glucose worsening over 12 weeks at 2 mg/day.
  • Anti-tesamorelin IgG antibodies: ~50% develop them, did not affect efficacy or safety in the majority
The Research

Peer-reviewed studies and clinical guidelines - tap any to read the source.

PubMed / NEJMFalutz et al, NEJM 2007 - Metabolic Effects of a Growth Hormone-Releasing Factor in HIV (NCT00123345)

](https://www.nejm.org/doi/full/10.1056/NEJMoa072375) - landmark pivotal trial, 412 patients, 15-18% VAT reduction at 26 weeks on 2 mg/day SC

Read study ↗
PubMedFalutz et al, 2010 - randomized trial with safety extension (PMID 20101189)

](https://pubmed.ncbi.nlm.nih.gov/20101189/) - 52-week safety/efficacy data

Read study ↗
PubMedFalutz et al, 2010 - pooled Phase 3 analysis (PMID 20554713)

](https://pubmed.ncbi.nlm.nih.gov/20554713/) - combined two Phase 3 trials, AE rates and IGF-1 data

Read study ↗
PubMedStanley et al, Lancet HIV 2019 - Tesamorelin on NAFLD in HIV

32% liver fat reduction at 12 months, fibrosis prevention

Read study ↗
PubMedStanley et al, JCI Insight 2020 - hepatic transcriptomic effects

mechanism of liver fat reduction

Read study ↗
PubMedReduction in visceral adiposity associated with improved metabolic profile (PMID 22495074)

](https://pmc.ncbi.nlm.nih.gov/articles/PMC3348954/) - metabolic profile improvements paralleling VAT loss

Read study ↗
+ 9 more studies & references
From The Community

Aggregated sentiment from public forums & socials - real-world reports, not individual endorsements.

SSwolverine - Tesamorel

Water retention / "puffy face" weeks 1-2: most-reported sensation, resolves by week 3-4 as body adapts

SSpartan Peptides - Tes

Numbness/tingling in fingers (mild carpal-tunnel-like): common at 2 mg, resolves on 1 mg dose drop

TThe Peptide Catalog -

Joint stiffness in the morning: reported across forums, especially in users running tesa with HGH or CJC+Ipa

PPeptide Protocol Wiki

Vivid dreams / improved sleep: positive AE, very commonly reported because the GH pulse hits during sleep

PParahealth - Tesamorel

Hunger increase: tesa doesn't suppress appetite (unlike GLP-1s), and the GH pulse can mildly elevate hunger; some users report stronger appetite at the 2 mg dose

PPerfect B - Tesamoreli

Belly measurement drop before scale weight drop: classic visceral-specific signal, users report waistline tightening at 6-8 weeks before total weight moves

Common Questions
SubQ. 1 mg subcutaneous daily, pre-bed
6-12 weeks visceral fat
Yes - baseline labs before starting and a recheck a few weeks in is the standard advice. We can walk you through which markers to watch.
A popular pairing is Tesa + Retatrutide (visceral focus). See the Protocols section, or ask us for a stack built around your goal.
Yes. Every batch is third-party lab tested - request the COA on Telegram and we send it over.
Safety & Contraindications

Hard stops

  • Active malignancy (GH/IGF-1 axis stimulation is contraindicated in active cancer)
  • Pituitary gland disorders, pituitary tumors, hypopituitarism from surgery/radiation/trauma
  • Pregnancy or actively trying to conceive
  • Severe untreated diabetic retinopathy (IGF-1 can worsen)
  • Hypersensitivity to mannitol (Egrifta excipient)

Caution flags

  • Diabetes or pre-diabetes (HbA1c drift signal, monitor quarterly)
  • History of carpal tunnel syndrome (IGF-1 can re-trigger)
  • Severe renal impairment (no dosing data)
  • Severe hepatic impairment
  • Elevated baseline IGF-1 (already at upper end of normal, tesa will push above range)

Stacking conflicts

  • Do NOT stack tesamorelin with sermorelin or CJC-1295 with DAC alone - both are GHRH analogs hitting the same receptor, no additive benefit and increased risk of supraphysiological IGF-1. CJC-1295 *without DAC* + ipamorelin pairs cleanly because it hits a different receptor (GHS-R, the ghrelin pathway).
  • Caution with high-dose HGH stacks, additive IGF-1 elevation can push past physiological range fast.
  • Insulin and sulfonylureas, GH-driven counter-regulation may need dose adjustment.
Is It Right For You?

✓ Good fit

  • visceral fat focus
  • menopausal weight resistance
  • post-bariatric layering
  • AAS users with belly creep
  • GLP-1 plateau breakers
  • longevity-oriented
  • recomp goals
  • "stubborn midsection" complainers

✗ Not a fit

  • active cancer history
  • pituitary disorders
  • severe diabetic
  • want fast scale weight movement
  • can't commit to daily injection
  • restrictive budget
  • planning pregnancy

Administration & Storage

Route: SubQ

Injection site: abdomen, rotate within the abdominal panel daily to avoid injection site reactions (this is the most common AE in the Phase 3 trials)

Storage: refrigerated, 28 days after reconstitution. Unreconstituted vials refrigerated (lyophilized form is more forgiving but keep cold).

Notes: Inject pre-bed on an empty stomach (2-3 hours post-meal). Eating right before/after blunts the GH pulse because insulin suppresses GH release. Pre-bed timing also stacks with the body's natural overnight GH pulse for an amplified effect. Do not shake the vial, swirl gently to mix. Allow vial to reach room temp before injecting once mixed. Use a fresh insulin syringe per draw.

All products sold for research purposes only. Not for human or animal consumption. Must be 21 or older to purchase. By placing an order you confirm compliance with all applicable local laws and regulations.