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Research compound · not FDA-approved

AOD-9604

Also written AOD 9604.

AOD-9604 is the tail end of human growth hormone — residues 176 to 191, with one extra amino acid added on the front.

What matters first

Why people look it up
It is sold for fat loss, on the idea that this fragment carries the hormone’s fat-mobilizing part and leaves the rest behind.
What the evidence shows
That idea was tested properly and it did not hold. An Australian company ran controlled human obesity trials, the larger ones did not separate it from placebo on weight, and development stopped there. The 10 mg group lost less than the 1 mg group, and the doses were swallowed rather than injected.
Dose status
AOD-9604 is not FDA-approved, so no dosing label exists for it. The sections below explain what researchers tested and what remains unknown.

Evidence snapshot

Foreign approval or limited human data

The fastest way to see what kind of evidence this page is built on.

Regulation
Not FDA-approvedNo US prescribing label
Dose source
Reported range only2 circulating ranges · not established
Safety evidence
5 listed safety findingsCommon and serious effects shown apart
Sources
3 cited sourcesMedical review complete · 2026-08-12
AOD-9604 at a glance: foreign approval or limited human data, dosing basis, regulatory status, safety coverage, and cited-source count. These details summarize the available sources; they are not treatment recommendations.

Further down: research and dosing details · how good the evidence is · questions

Medically reviewed by Jennifer Montecillo, MD · non-practicing medical reviewerReviewed 2026-08-12open the primary sources

What is known about AOD-9604

AOD-9604 is the tail end of human growth hormone: residues 176 to 191, with a tyrosine added. Researchers cut it out on the theory that the fat-mobilizing activity sat in that fragment. The growth-promoting and glucose effects, they thought, belonged to the rest of the hormone. An Australian company developed it as an anti-obesity drug and ran controlled human trials. The larger trials did not separate it from placebo on weight, and development stopped.

AOD-9604 research and regulatory details: evidence quality, approval status, doses, handling, and presentation.
TopicValue
Strongest sourcelimited human data
FDA approvalNot FDA-approved
Reported range1–10 mg once daily over 12 weeks — the trials did not inject it, the 1 mg group lost 2.6 kg against 0.8 kg on placebo, the 10 mg group lost less than the 1 mg group, and the primary trial reports were never published reported in the literature
What people report using250–500 mcg a day, split over two or three injections under the skin; the human trials swallowed this compound rather than injecting it, and at roughly ten times the quantity no trial has tested this quantity
Typical vials5 mg

Every row links back to a source listed below. These facts are for reference, not a personal recommendation.

The row headed “what people report using” is not evidence. No trial produced that quantity. It is printed because it is what circulates, and because it is better read here, beside what the studies actually did, than on a page that is selling the vial. It describes a practice. It is not a starting point.

What the evidence for AOD-9604 is

People have received this compound in a documented setting, or it has approval outside the United States. The available human evidence is still too limited to show a clear dose-and-result pattern for US use.

limited human data
What it establishes
It shows that people have received it and that some human information exists.
What it does not establish
It does not prove that the same dose is appropriate in the United States or that uncommon and long-term risks are known.

Check the country, study size and reason it was used. Do not treat limited human data as an FDA-approved schedule.

Where AOD-9604 is in clinical trials

No trial of this compound is registered on ClinicalTrials.gov.

That is worth sitting with. Nobody has registered a study to find out whether AOD-9604 works in people, so no result is coming and no date is worth waiting for. Sellers are not waiting for that work either.

A registered study means a sponsor filed a plan and started enrolling. It is not evidence the drug works, and most drugs tested in people never reach a pharmacy. Sponsors write and update these sources themselves; the National Library of Medicine publishes them without checking them.

ClinicalTrials.gov · retrieved 2026-08-23

Every compound we track, and what stage each one has reached →

Regulatory status

This compound has an unusual regulatory footprint for a research peptide.

It failed as a drug candidate, then found a second life as a food and supplement ingredient. It later became publicly contentious in Australia, in a sports-supplements investigation. The question there was whether it counted as a prohibited substance.

Anti-doping authorities concluded that it was not. None of that shows it works: a substance can be legal, on sale and useless at once.

Full regulatory tracker →

Where to go next on AOD-9604

The schedule, the side effects and the mixing math each have their own page.

Safety notes

  • Controlled human obesity trials did not separate this fragment from placebo on weight. Development stopped there
  • Nobody published the trials as primary papers. The quantities here come from a peer-reviewed review of a company market announcement. This record therefore frames them as reported, not studied
  • The trial doses were swallowed, not injected. They carry no arithmetic across to a reconstituted vial
  • The 10 mg group lost less weight than the 1 mg group. The range on this record is not a ladder: more did not work better
  • Anti-doping authorities did not prohibit it. That is a classification decision, not evidence of benefit
  • Oral and nasal presentations are also sold. Their absorption differs so completely that quantities do not transfer between formats

Questions about AOD-9604

Is AOD-9604 FDA-approved?

No. There is no prescribing label for it, so no approved dose exists — the regulatory status section above has the detail.

How is AOD-9604 taken?

Trials study it both by mouth and by injection under the skin. The table above keeps each route and schedule separate.

How does AOD-9604 differ from the other compounds in this class?

AOD-9604 has been studied in people, but it works through a different system from GLP-1 and amylin drugs. Its doses and results are not directly comparable with theirs.

What is not known about AOD-9604?

It does not prove that the same dose is appropriate in the United States or that uncommon and long-term risks are known.

Is there a AOD-9604 dosing schedule on this site?

Not a schedule — there is no approved schedule to publish here. What you get instead is the trial dosing program: the doses each arm received and how the protocol worked up to them. See what the trials tested.

3primary sources, each with the day we read it — open the documents used on this page