Human growth hormone: injecting it, or stimulating your own
Last checked August 24, 2026. Compounding rules in this area are actively contested — verify before relying on any of it.
Growth hormone is made in your pituitary and released in pulses, mostly during deep sleep. It drives tissue repair, lean mass, fat metabolism, bone density and skin. Output peaks in adolescence and falls steadily from your twenties — by sixty, most people produce a small fraction of what they once did.
That decline is the entire premise of this market, and it is a real decline. The question everything below turns on is whether reversing the number reverses what people attribute to it — and there are two fundamentally different ways of trying.
Read this before the rest: the two approaches do not combine.
You can inject growth hormone, or you can use a peptide to prompt your own pituitary to release more. People sometimes do both, reasoning that two inputs must beat one. They cancel out, and the reason is the feedback loop.
Injected GH raises IGF-1. Rising IGF-1 tells your hypothalamus to stop sending GHRH and to start sending somatostatin — the stop signal. Your pituitary goes quiet. Measured directly: raising IGF-1 suppresses natural GH output by roughly 85%, mostly by flattening the pulses.
So a secretagogue taken alongside injected GH is prodding a gland that is being actively told to shut up. You are paying for the second thing to do almost nothing, while stacking whatever risk it carries on top of the first. It is one or the other.
Approach one: injecting growth hormone
Somatropin — recombinant human growth hormone
This is the hormone itself, manufactured, injected. Not a signal or a prompt — the finished molecule, delivered directly. It works, in the sense that it unambiguously raises GH and IGF-1. Everything else about it is a question of what for, and at what cost.
The medical uses, which are real and well established
Somatropin is approved in Canada and the US for growth hormone deficiency in adults and children, several paediatric growth disorders (Turner syndrome, Prader-Willi, small-for-gestational-age children who do not catch up), HIV-associated wasting, and short bowel syndrome. In genuine deficiency it is transformative rather than incremental — this is replacing something a body actually cannot make.
Diagnosing adult deficiency is deliberately rigorous: stimulation testing, not a single low reading, because GH is pulsatile and a random draw between pulses looks like deficiency in a healthy person. That distinction — a diagnosed deficiency versus an age-related decline everyone has — is the line the rest of this section sits on.
Why people use it without that diagnosis
The longevity case is that age-related decline is itself a deficiency, just a universal one, and that restoring youthful levels restores youthful tissue. It traces largely to a small 1990 study in older men that reported gains in lean mass and losses in fat — a paper that launched an industry and whose own journal later published an editorial cautioning against exactly the use it was being cited for.
Alongside that: athletes and bodybuilders for recovery and body composition, and a broader group chasing sleep quality, skin, and the general sense of resilience that fades. Body composition does genuinely change. What is much less established is whether the things people actually want — feeling better, functioning better, living longer — follow, and there is a real counter-argument in the other direction: lower IGF-1 signalling is associated with longer life across a number of species, which is an awkward fact for the longevity pitch.
The legal position is stricter than people expect
In the US, human growth hormone is not a controlled substance — it sits outside that schedule entirely, which sounds permissive and is not. It has its own dedicated provision instead: distributing HGH for any purpose other than an approved indication is a federal felony carrying up to five years, doubling for distribution to a minor.
The detail that surprises people: the FDA reads "distribution" as including writing the prescription. The ordinary off-label latitude that covers most of medicine does not apply here in the same way. This is the single biggest reason anti-aging clinics offer peptides instead — not better evidence, just a statute that does not name them.
Canada has no equivalent HGH-specific criminal provision; somatropin is a prescription drug under the ordinary rules. Buying it online from outside that system is a different problem — unverified product, no recourse, and counterfeit GH is common enough to be the default assumption rather than the exception.
Approach two: prompting your own pituitary
Secretagogues — GHRH analogues and ghrelin mimetics
The rationale, stated fairly — because it is a good one
Rather than supplying the hormone, these send the signal that makes your pituitary release its own. The argument for it is genuinely sound in principle: your release comes in natural pulses, mostly overnight, with the feedback loop intact — so there is a ceiling your body still controls. Injected GH overrides that and holds a flat level the system never sees naturally.
More physiological, self-limiting, and in principle safer. That is a mechanistic argument, and it is where most of these part company with the evidence: a good reason to expect something is not the same as a demonstration that it happened.
There are two different switches, which is why some get sold in pairs
Your pituitary responds to two separate signals. GHRH, from the hypothalamus, is the accelerator. Ghrelin — the same hormone involved in hunger — acts on a different receptor and also triggers release, partly by suppressing the brake. They are independent inputs, so hitting both at once produces a larger pulse than either alone.
That is the whole logic behind "CJC-1295 + ipamorelin" being sold as a unit: one from each column. It is a sound piece of physiology. It is also the point at which two unapproved compounds become one unstudied combination.
GHRH analogues — the accelerator
Tesamorelin (Egrifta)
Approved in Canada — for HIV lipodystrophy onlyThe same kind of signal your hypothalamus sends, prompting a natural pulse. A stabilised GHRH analogue.
Who takes it: In its approved use: people with HIV-associated lipodystrophy, prescribed by an HIV specialist and usually covered because it is a genuine treatment for a genuine complication. Almost nobody gets Egrifta prescribed for body composition or training — it is expensive, the indication does not fit, and no Canadian or US physician is writing it for the gym. The tesamorelin bought from peptide vendors is not Egrifta.
Status: APPROVED — for one thing. Health Canada issued a Notice of Compliance in April 2014; the FDA approved it earlier. The indication is reducing excess visceral abdominal fat in HIV patients with lipodystrophy, on two trials in 816 patients. It is NOT approved for weight loss, body composition, athletic performance or aging, in either country.
Sermorelin
Not approved — compounding grey zoneThe original of this class, and the shortest-acting — a brief signal that produces a single sharp pulse.
Who takes it: Largely superseded. Its half-life is minutes, so it needs frequent injection to do much, and CJC-1295 was built specifically to solve that. Some anti-aging clinics still offer it, partly because it once had an approval and so sounds more legitimate than the alternatives. Rarely anyone's first choice now.
Status: Was approved as Geref, then withdrawn from the market — for commercial reasons, not a safety finding. Now supplied through US compounding pharmacies. Not an approved product in Canada.
CJC-1295
Not approved — compounding grey zoneA longer-acting GHRH analogue. The DAC version binds to albumin and persists for days rather than minutes.
Who takes it: The workhorse of US anti-aging clinics, almost always paired with ipamorelin. Note that two different things are sold under this name: WITH DAC (lasts days — convenient, but holds a signal meant to be pulsatile permanently on, which is the main objection to it) and WITHOUT DAC, also sold as mod-GRF 1-29 (lasts minutes, needs frequent injection, preserves the pulse). People arguing about CJC-1295 online are often arguing about different drugs.
Status: Not approved anywhere. Supplied by US compounding pharmacies on prescription, but its standing on the FDA's 503A bulk substances lists is genuinely contested — sources in 2026 place it in different categories. Nothing equivalent exists in Canada.
Ghrelin mimetics — the other switch
Ipamorelin
Not approved — compounding grey zoneNot a GHRH analogue at all — it acts on the ghrelin receptor, the other switch that triggers a GH pulse.
Who takes it: The default in this class, and it displaced its predecessors on tolerability rather than potency. GHRP-6, GHRP-2 and hexarelin came first and are now largely abandoned: they also raised cortisol and prolactin and provoked severe hunger, which made them unpleasant and, for anything long-term, counterproductive. Ipamorelin is the selective one that mostly does not. If you see the older three offered, that is a vendor selling old stock, not a considered choice.
Status: Not approved anywhere. It was investigated as a real drug candidate and abandoned in development — the pharmaceutical interest was genuine and it did not finish. Supplied by US compounding pharmacies; 503A standing contested, same as CJC-1295. Not available in Canada.
MK-677 (ibutamoren)
Rejected for compoundingThe same receptor as ipamorelin, but orally active and very long-acting — a pill rather than an injection.
Who takes it: Taken almost entirely by people who will not inject, which is a real constraint and the whole basis of its popularity. Sold openly as a 'research chemical' rather than through clinics. The two things that make people stop are the hunger — substantial, unlike ipamorelin — and the water retention, which is often mistaken for the muscle gain it was taken for.
Status: Not approved — and uniquely on this page, that is a considered NO rather than silence. In October 2024 an FDA advisory committee examined it directly and voted 13–1 AGAINST allowing it to be compounded, naming fluid retention, raised blood glucose and congestive heart failure. Everything else here is merely unstudied; this was looked at and refused, which is far more informative.
What tesamorelin proves about the whole category
This is the most useful thing on the page, even if tesamorelin itself is irrelevant to you. It is mechanistically the same class as sermorelin and CJC-1295 — a GHRH analogue prompting your own pituitary. The difference is not the mechanism, the molecule type, or anything intrinsic. The difference is that somebody ran the trials: 816 patients, a defined endpoint, a regulator that read the data.
So "it's only a peptide, it just nudges your own hormone" is not a reason something cannot be studied and approved. One of them was. The others have not been — and that is a statement about evidence, not about the category.
The corollary cuts the other way too, and it is the part most worth being clear about: tesamorelin is approved for visceral fat in HIV-associated lipodystrophy. Not for aging, not for body composition in healthy adults, not for recovery, not for training. An approval for one indication is not a general endorsement, and no Canadian or US physician is prescribing Egrifta for the gym — it does not fit the indication and it is expensive enough that nobody would try.
Which leads to the thing that actually matters here: the tesamorelin people buy from peptide vendors is not Egrifta. It is unregulated material with the same name. The approval belongs to a specific manufactured product that went through trials — it does not transfer to a vial from a research-chemical site any more than a trial result transfers to it. So tesamorelin's presence on this page is an argument about what the category could be if studied, not a green light on what is being sold.
"But a clinic prescribed it"
People genuinely are prescribed CJC-1295, ipamorelin and sermorelin by licensed practitioners. In the US the route is 503A compounding — a real regulated channel, but an exemption FROM the approval process rather than a form of it. Canada is stricter and Health Canada has named CJC-1295 and ipamorelin in its unauthorised-peptide warning. Either way, a prescription is a practitioner's decision, not a finding that anything was assessed. The full picture is on its own page: how unapproved drugs get prescribed in Canada.
There is one tell worth recognising here specifically. If a clinic offers you secretagogues but will not prescribe growth hormone itself, that is not a clinical judgement that the peptides are better — it is the statute. HGH carries a federal criminal provision covering exactly these uses; the peptides do not. The choice is being made by legal exposure, not by evidence — and the evidence for the peptides is thinner than for the hormone. A clinic that explains it that honestly is worth more of your trust than one presenting it as the superior protocol.
Sermorelin causes particular confusion because it was once an approved drug, which makes it sound more legitimate than its shelf-mates. It was withdrawn commercially, and the version compounded today is not the approved product any more than vendor tesamorelin is Egrifta.
Whichever route: the measurement problem
GH is released in pulses and is nearly undetectable between them, so a single blood draw tells you almost nothing — this is the same fact that makes diagnosing real deficiency require stimulation testing. What gets tracked instead is IGF-1, which is stable enough to measure. It is a downstream proxy, not the thing itself.
Practically: if you are on any of this, "is it doing anything?" is genuinely hard to answer from how you feel, and the honest approach is a baseline IGF-1 before starting and a repeat after. Anyone prescribing this without measuring is not running an experiment — and neither are you.
Everything on this page, in one table
| What | Class | Route | In Canada |
|---|---|---|---|
| SomatropinThe hormone itself. Overrides your own production entirely. | Recombinant HGH | Injection | Approved — for deficiency and specific conditions, not aging |
| TesamorelinThe only approved secretagogue — but the vendor version is not the approved product. | GHRH analogue | Injection | Approved for HIV lipodystrophy ONLY — not weight loss or training |
| SermorelinLargely superseded — minutes-long half-life meant frequent injections. | GHRH analogue | Injection | Not available |
| CJC-1295Long-acting. The DAC version holds a signal meant to be pulsatile. | GHRH analogue | Injection | Not approved |
| IpamorelinThe selective one — little cortisol, prolactin or hunger. Abandoned in development. | Ghrelin mimetic | Injection | Not approved |
| MK-677Oral, long-acting, raises hunger. Explicitly rejected 13–1 for compounding. | Ghrelin mimetic | Oral | Not approved |
Everything below the first row is either unapproved or approved only for something other than what it is usually taken for.
What the table adds up to
Read down that first column and the sorting is not really by molecule. One is a genuine treatment for a genuine deficiency. One was studied properly and approved — for a condition you almost certainly do not have. The rest share a mechanism with those two and have no outcome data at all.
What separates them is not the category. It is whether anyone ran the trial. Tesamorelin is the same class of molecule as sermorelin and CJC-1295; the difference is 816 patients and a regulator who read the file. So "it is only a peptide" is not a defence of the unstudied ones, and it is not a criticism of the studied one either. It is simply not the relevant question.
Two things are worth carrying away. Whichever row you pick, pick one column — injected hormone and secretagogues suppress each other, so taking both is paying for one of them to do very little. And measure IGF-1 before and after, because on a pulsatile hormone your own sense of whether it is working is close to worthless. Without a baseline you are not running an experiment; you are running a subscription.
If you are on one of these, what is worth having is your own before-and-after across months rather than an impression. Titr logs what you took and when, and plots it against your own measurements. Mixing from a vial? The reconstitution calculator handles the arithmetic.
General information, not medical advice, and not a recommendation to use anything described here. Most of what is on this page is not approved for the uses people seek it for. Growth hormone raises blood glucose, interacts with several conditions, and is contraindicated in active malignancy — this is a conversation for a physician who knows your history.