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Fat loss

Tesa / Ipa Blend

Tesamorelin and ipamorelin in one blended vial. The vial ratio determines what one draw contains.

At a glance

What is in it
Sold as
One blended vial
The evidence
The two compounds separately are the best-documented pair in this file: tesamorelin has FDA approval and Phase 3 visceral-fat data, ipamorelin has Phase 2 studies of selective GH release and remains a 503B Category 2 substance. The pre-blended vial has neither. There is no trial of the combination, no stability data for the two sharing a solution, and no published composition anybody stands behind. Everything about the vial itself is a vendor claim.Combination-specific research is limited. Treat each compound’s evidence as separate unless a study of the combination itself is named here, and review the complete plan with a qualified clinician.
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Running this stack, with the schedule, the vials it takes and a log of what you took, happens in the app: Claritide for iPhone.

Context

Why people explore it

Common reasons for exploring it

  • Adults 35+ with stubborn midsection fat despite consistent training and nutrition, which is what the tesamorelin half is used for
  • People who want the growth hormone axis worked through their own pituitary rather than by injecting growth hormone
  • People willing to measure by DEXA, CT or waist circumference rather than the bathroom scale
  • People who would otherwise run these two as separate vials and want one injection instead of two
  • Anyone who already owns a tesamorelin/ipamorelin vial and wants to know what a draw actually delivers

Where clinician input matters

  • Anyone who has not run these compounds individually. One barrel removes your ability to attribute a result or a side effect to either one.
  • Anyone with active cancer or a cancer history
  • Pituitary pathology, including prior pituitary surgery or irradiation. This is a label contraindication, not a caution
  • Anyone acutely critically ill
  • Diabetic retinopathy
  • Pregnant or nursing, under 25
  • Drug-tested athletes
Mechanism

The science

Each compound's mechanism, in plain English. The rationale for combining them is pharmacologic, not proven.
Read the compound mechanisms
TesamorelinThe GH Optimizer

Tesamorelin is a secretagogue, not a hormone replacement. It binds GHRH receptors on the anterior pituitary and tells the gland to produce and release your own growth hormone, which then travels to the liver and tissues and drives IGF-1 production. Because it works through the pituitary, the body's natural pulsatile release pattern and its somatostatin feedback brake stay intact, which is the central difference from injecting growth hormone directly, and the reason the insulin resistance risk is lower. The fat-loss effect runs through GH-mediated lipolysis: growth hormone activates hormone-sensitive lipase in fat cells, breaking stored triglycerides into free fatty acids. Visceral fat responds preferentially because those cells carry a higher density of beta-adrenergic receptors and are more metabolically active than subcutaneous fat. GH production declines roughly 14% per decade after age 30, which is the rationale for off-label use.

IpamorelinThe Clean Pulse

Ipamorelin activates the ghrelin receptor (GHS-R) on the pituitary. Ghrelin is the hunger hormone, and its receptor also sits on the GH release pathway, which is why this class works at all. The functional effect is suppression of somatostatin, the hormone that normally brakes GH release. Pairing it with a GHRH analog produces a larger pulse than either alone, because one compound is signalling for release while the other removes the restraint. Ipamorelin's distinguishing feature is selectivity: it hits the GH pathway without the cortisol, prolactin and appetite effects that older ghrelin mimetics produce.

No standard dose publishedRead the COA, not the name. This is a name printed on a vial rather than a protocol, and the composition changes by vendor. We publish no dose for it and the builder will not prefill one. Enter your own vial’s composition and derive each figure from it.

What vendors sell

Components

A vendor SKU has no protocol to publish. These are the compounds the name covers; the amounts come from your own vial, not from us.
  • Tesamorelin

    The GHRH half: it tells the pituitary to release your own growth hormone

    • 10 mg · Vendor listings, unattributed
    Prescription
  • Ipamorelin

    The ghrelin-receptor half: it suppresses somatostatin, the brake on that same release

    • 3 mg · Vendor listings, unattributed
  • Tesamorelin: The GHRH half of the pair. Tesamorelin is a secretagogue rather than a hormone replacement: it binds GHRH receptors on the anterior pituitary and tells the gland to produce and release your own growth hormone, which drives IGF-1 and, through GH-mediated lipolysis, the loss of visceral fat specifically. Because the signal runs through the pituitary, the natural pulsatile pattern and the somatostatin feedback brake stay intact. It is the only compound in this library with an FDA approval aimed at visceral fat, and that approval is for the single-agent product rather than for anything blended. Our 2026 fact-check recorded a 10 mg / 3 mg pre-blend still being sold, which puts tesamorelin at 10 mg of a 13 mg vial. Worth knowing about the approved product for comparison, and only for comparison: the EGRIFTA labels dose tesamorelin at 1.28–1.4 mg daily, and they state that their own two formulations are not substitutable with each other. A figure from a label is not a figure for a blended vial.
  • Ipamorelin: The ghrelin-receptor half, and the brake release. Ipamorelin activates GHS-R on the pituitary, which suppresses somatostatin, the hormone that normally stops growth hormone release. That is why the pair is sold together: one compound signals for release while the other removes the restraint, producing a larger pulse than either alone. Our sources describe ipamorelin as the most selective compound in its class, hitting the GH pathway without the cortisol, prolactin and appetite effects older ghrelin mimetics produce. Recorded at 3 mg of the same 13 mg vial. The ratio is what decides your ipamorelin dose, not you: at 10 mg / 3 mg in 2 mL of bacteriostatic water the vial holds tesamorelin 5 mg/mL and ipamorelin 1.5 mg/mL, so 20 units draws 1 mg tesamorelin and 300 mcg ipamorelin together. Change the draw to fix one and the other moves with it.
Duration
No cycle length is published for the blend by any source we can stand behind. The cadence sold alongside it (once daily in the evening, 5 days on and 2 off, 8 weeks on and 8 off) is vendor-tier and is not reproduced here as a schedule.
What vendors sell

Reported compositions

Every composition we have actually seen under this name, each attributed to the vendor who publishes it. Agreement between affiliate pages is common-source copying, not corroboration, so we render the disagreement rather than resolving it.

None of these is “the” composition. Switching vendors at the same product name and the same total milligrams can change a single component by 2×, with nothing on either label to tell you. That is why the only figure worth trusting here is the one on your own vial’s certificate of analysis.

Vendor listings, unattributed
13 mg total

The 10 mg / 3 mg pre-blend our 2026 fact-check recorded as still sold. No single vendor page is cited behind those figures, so read them as one reported composition and not as the composition. Check your own COA before you draw anything.

Reconstitution

Mixing each compound

Concentration (mg/mL) = vial mg ÷ BAC water mL. Never mix two peptides in the same syringe: we found no study showing it is safe, and mixed drugs can lose activity even when they look unchanged.
Tesamorelin
2 mg + 0.5 mL BAC = 4 mg/mL
  • 35 units = 1.4 mg
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Ipamorelin

Not established in available literature. Use the figures printed on your own vial.

Expectations

Week by week

What our material describes people reporting for each compound. Nobody has published a timeline for the combination itself.

Tesamorelin

  1. Week 1–2

    Adaptation. Possible mild joint stiffness or water retention, signs the GH axis is responding. These typically resolve by week 3.

  2. Week 3–4

    Sleep quality and recovery begin to improve, usually the first noticeable effect. Some report better skin quality.

  3. Month 2–3

    Measurable visceral fat reduction begins. Body composition shifts become visible; waist circumference drops. Total scale weight may not move much, since fat loss is offset by lean tissue gain.

  4. Week 16–26

    Full clinical effect as demonstrated in trials: maximum visceral fat reduction by week 26, around 15–18%. Bloodwork may show improved fasting glucose and lipids.

  5. Beyond 26 weeks

    Benefits maintained with continued use. LIPO-011 showed fat reduction maintained through 52 weeks.

  6. After stopping

    In LIPO-011, patients switched to placebo at week 26 saw visceral fat return to baseline. Ongoing treatment is needed to maintain the reduction.

Ipamorelin

  1. Early weeks

    Improved sleep and recovery are the first effects our sources describe, driven by amplified GH pulses during deep sleep.

  2. Week 4–8

    Our tesamorelin page describes stack users reporting significant fat reduction beginning in this window.

Budget

What it costs

Combined, where our sources publish a figure
$300–$500
per month
  • Tesamorelin: $300–500 per month
  • Ipamorelin: Not established in available literature

The combined figure excludes Ipamorelin, for which our sources publish no price.

Before you start

Cautions

  • Read the COA, not the name. This vial has no brand and no standard, so the ratio inside it is whatever your vendor mixed. Enter that composition and derive both doses from it.
  • The ratio is the dose. In one barrel you cannot raise tesamorelin without raising ipamorelin by the same multiple, so the draw that puts one where you want it puts the other wherever the vendor decided.
  • The tesamorelin label contraindications are hard, not cautions, and they do not soften because it arrived in a blend: disruption of the hypothalamic-pituitary axis (hypophysectomy, hypopituitarism, pituitary tumour or surgery, head irradiation, head trauma), active malignancy, hypersensitivity, and pregnancy.
  • Both EGRIFTA labels state plainly: not indicated for weight loss management, and long-term cardiovascular safety is not established.
  • The quantified label numbers are worth reading before starting. At 26 weeks, 47% of patients had IGF-1 above 2 standard deviations and 36% above 3. HbA1c reached 6.5% or higher in 5% of patients versus 1% on placebo. The intention-to-treat hazard odds ratio for developing diabetes was 3.3 (95% CI 1.4–9.6).
  • FDA cites literature reports of serious adverse events including death when ipamorelin was given intravenously for gastric motility.
  • This is two GH-axis compounds firing at once, in one injection. The Playbook warns explicitly against combining GH-modulating peptides without medical guidance.
  • No stability study exists for these two peptides sharing a solution. Anyone telling you what a colour change means in this vial is telling you something nobody measured.
  • Tesamorelin is a prescription compound. A blend is not a way around that.
  • Both are on the WADA prohibited list under S2.

Absence from this list does NOT mean safety. It means lack of research.

Every stack here is free to read, and it stays free. Your own schedule, vials and log live in the app: Claritide for iPhone.