A short piece of the growth hormone molecule, marketed almost entirely on one statistic. The mechanism is real and the statistic is not what people think it is — and the difference between those two sentences is most of what is worth knowing here.
Regulatory status. Research compound — no FDA approval. Legal gray area in most jurisdictions. That is the app’s own field, reproduced here rather than summarised. It means no regulator has reviewed a manufacturer’s evidence for identity, purity, potency or safety in people for this compound, so nothing below is a marketing claim about a product you can buy.
Purity, identity and concentration are therefore unverified by anyone but whoever made the vial. The storage rule in the fact box below is general practice for this formulation rather than a specification for a particular product: General handling practice for this formulation. Your supplier’s own insert or COA overrides anything here.
This page names no vendor, no clinic and no testing service, and there is no discount code anywhere on this site — the moment a page like this recommends where to buy, it stops being information.
Human growth hormone is 191 amino acids. Animal-only or theoretical Work in the 1990s identified the C-terminal region as carrying the lipolytic activity independently of the rest of the molecule, and fragment 176-191 is that region synthesised on its own. The claim that follows is appealing: fat metabolism without the growth-promoting and insulin-desensitising effects that come with whole growth hormone, because the fragment does not bind the growth hormone receptor and does not raise IGF-1.
That last part is testable and is the one genuinely useful monitoring instruction in the app’s entry: IGF-1 should not move. If it does, the vial contains something other than what the label says. For a compound with no reference standard and no approved product, a marker that detects mislabelling is worth more than a marker of effect.
The app models the half-life at about thirty minutes and flags it as an estimate. That is why the dosing rows describe one to two injections daily rather than a single dose, and like every estimated figure here, anything derived from it inherits the uncertainty.
Animal-only or theoretical Nearly every description of this peptide reports that it is 12.5 times more potent than growth hormone for fat burning. The app’s own entry repeats it. It traces back to animal work — obese rodent models comparing the fragment against whole growth hormone on lipolytic endpoints — and not to any human study. It is a real finding about mice, presented for two decades as though it were a fact about people.
What exists in humans is much thinner: no published randomised controlled trial of this fragment for fat loss at all. Compare that with AOD-9604, a modified version of the same region that was taken into phase IIb trials in humans and did not separate from placebo on its primary endpoint. That is the closest thing to a human test this mechanism has had, and it is not an encouraging one.
None of that makes the mechanism wrong. It makes the confidence unwarranted, and it makes the specific number a marketing artefact rather than a result.
The app records a row describing injection near a target fat area. Animal-only or theoretical It is reproduced above because this site publishes what the app holds, and it is worth saying plainly that the idea behind it — that injecting subcutaneously near a fat depot produces a local rather than systemic effect — has no controlled human evidence behind it. Spot reduction is one of the more thoroughly examined claims in exercise science and has not held up in other contexts.
There is no approved product. Identity, purity and concentration rest entirely with whoever made the vial, and this fragment is a case where a mislabelled product is particularly plausible: the aka field in the app’s own reference overlaps with AOD-9604’s, and the two are frequently sold under each other’s names. This site names no vendor and no testing service.
There is no meaningful bloodwork to follow here beyond the IGF-1 check described above and a fasting glucose that should stay put. Assessment is body composition over months, which means an honest record of diet and training alongside it or the result means nothing. Anything experienced while using it belongs with a clinician who knows the whole picture.
pkCurve function.
The vertical axis is relative: the shape carries across people, the absolute
concentration does not. This compound’s half-life is flagged as an estimate in the app, so read the curve as the right shape rather than the right numbers.Try other intervals on the half-life and steady-state calculator, which runs the same function against whatever cadence you type.
Animal-only or theoretical Reproduced from the app’s reference so you can see what it holds, not as a recommendation. Which row applies to a particular person, if any, is a clinical decision this page does not make — and rows describing supraphysiological or post-cycle use are filtered out before this table is built, so what you see here is a subset.
| Label | Amount | Route and frequency | Duration recorded |
|---|---|---|---|
| Fat loss | 500mcg | SubQ 1-2x daily fasted | 8-12 weeks |
| Local and Spot | 250-500mcg | SubQ near target fat area | 8 weeks |
The panel below is the app’s own monitoring note for HGH Fragment 176-191, verbatim. The analytes in it that have a page here are linked; those pages cover what each one measures, which assay produced it and how to read a trend.
From the app’s own entry. The first item and the fourth are the load-bearing ones, and the sixth — that it does not build muscle — is a useful corrective to how it is usually sold.
It is a real finding in animal models and it has never been demonstrated in people. Treating it as a human fact is the single most common error in writing about this compound.
That is exactly why it matters. The fragment should leave IGF-1 unchanged; a rise suggests the vial contains growth hormone or something else. It is a mislabelling detector rather than an efficacy marker.
AOD-9604 is a modified version of the same C-terminal region and is the one that went into human trials, where it did not separate from placebo on its primary obesity endpoint. That is the closest human evidence this mechanism has.
No controlled human evidence supports it. The app records the practice because it is in the reference; this page reports that the idea is untested rather than endorsing it.
Named rather than linked. Publisher URLs move, and a citation that resolves to a 404 two years from now is worse than one you can search for by name — every entry below is findable from the title and year alone.
A compound assessed on body composition over months needs the months recorded alongside it. TherapyLog keeps the doses dated.
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