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Lexicon

AOD-9604

A modified, more stable variant of the lipolytic GH fragment, meant for fat loss without the other GH effects.

2 min read 8 sources

Vial with white powder, a blue cap and a black TPD label for AOD-9604 on a white podium, next to it a large, branched molecule model of blue and white glass spheres in a bright lab
As LAT8881 up to phase 2 (pain) · not approved

Summary

At a glance

Sources checked on 26 Oct 2026

Length
16 amino acids

piece 177 to 191 of growth hormone plus a tyrosine at the start4

Less weight gain (rats)
>50 %

obese Zucker rats, 19 days, daily by mouth3

Registered weight-loss trials
0 trials

AOD9604 without results on ClinicalTrials.gov, as of 26 Oct 20265

Under the name LAT8881
3 trials

phase 1 and 2 on nerve pain, migraine and back pain6

  • AOD-9604 is a piece of growth hormone: building blocks 177 to 191 with an extra tyrosine at the start. It is meant to use the fat-burning part of the hormone.48
  • Obese Zucker rats given AOD9604 by mouth gained more than 50 percent less weight in 19 days. Their fat tissue broke down more fat.3
  • In obese mice fat burning and fat breakdown rose. Unlike growth hormone, AOD9604 did not raise blood sugar and did not bind to the growth hormone receptor.2
  • Under the name LAT8881 AOD-9604 reached phase 2 in three trials on pain and migraine. There is no registered trial on weight loss.765
  • AOD9604 is on the WADA prohibited list. Everything here is research, not a recommendation.4
Profile

Updated May 2026

Class
Modified GH fragment

lipolytic

Use
Subcutaneous

in mcg

Half-life
short
Status
Limited efficacy in human weight studies
Sizes
2 to 10 mg

3 sizes in the shop

Contents 15 sections
  1. At a glance
  2. What is AOD-9604?
  3. How it works
  4. What you need
  5. Reconstitution
  6. Dosing
  7. Injection
  8. What the research shows
  9. Research status
  10. Side effects
  11. Storage
  12. Related compounds
  13. FAQ
  14. Glossary
  15. Sources

What is AOD-9604?

AOD-9604 is a modified variant of the lipolytic GH fragment 176-191, which you also find individually in the lexicon. An extra chemical group makes it more stable. The idea is the same: use the fat-mobilizing part of growth hormone without its growth and blood-sugar effects.

Up front: in human weight-loss studies the effect was limited.

Comparison

Growth hormone and its pieces

Compounds from the TPD lexicon around growth hormone, as described there. Tap a card to open its entry.

Simplified: whole growth hormone acts through its receptor. AOD9604 did not bind to it in cell assays. There is no comparison in humans. 2

How it works

AOD-9604 stimulates fat burning in fat cells and inhibits the formation of new fat, without notably affecting IGF-1, insulin sensitivity or blood sugar. That is the selling point: the fat-loss part of GH without the typical GH side effects.

Where it acts

Where AOD9604 acted in experiments

Tap a point or a card. Colour = target, grey = observed. All from animal studies.

  1. Fat tissue

    More fat breakdown and more beta-3 receptor in fat, but the effect did not run directly through it (mice)1

    β3 receptor
  2. Blood sugar

    No raised blood sugar and no lower insulin release, unlike growth hormone (mice)2

    Observed in trials

Targets in the ChEMBL database7

Compound CHEMBL6068615 (LAT-8881): two recorded mechanisms, type of action on each card.

Beta-3 adrenergic receptor
Gene
ADRB3
UniProt
P13945
ChEMBL
CHEMBL246
Action
More expression in fat, but the effect not directly through it (mice)
Growth hormone receptor
Gene
GHR
UniProt
P10912
ChEMBL
CHEMBL1976
Action
No binding and no cell division via the receptor (cell assay)
Pale glass spheres as fat cells, large blue molecule chains docking onto their outer layer, glowing droplets coming out of the cells
Fat breakdown in the fat cell, shown in rats and mice. Symbolic image.

What you need

Supplies

2 things, numbered as in the picture

Tick off what you already have. Vial and BAC water are our real shop photos at the same size.

AOD-9604 vial and bacteriostatic water at the same size with the black TPD label, next to two U-100 insulin syringes, two alcohol swabs and a sharps container with a blue lid
  1. AOD-9604 vial

    The AOD-9604 vial (lyophilized powder).

    In the shop
  2. Water and supplies

    Bacteriostatic water, U-100 insulin syringes, alcohol swabs.

    In the shop

Reconstitution

Use the peptide calculator. A 5mg vial with 2ml water gives 2500mcg per ml, 300mcg is then 12 units on the U-100 syringe. Just add the water to the vial and let it dissolve.

Step by step

Dissolving the powder

Four steps, the same for every vial size.

  1. 1Wipe the cap

    Clean the rubber stopper with an alcohol swab.

  2. 2Add BAC water

    Just add it, it does not matter if it hits the powder directly.

  3. 3Swirl or shake

    Until everything has dissolved, both are fine.

  4. 4Draw up

    With the U-100 insulin syringe.

Less water higher concentration fewer units on the syringe Example: 5 mg + 2 ml = 2.5 mg/ml

Dosing

Dosing

Dosing, titration and syringe

Loading the dosing information …

  • Getting started and stepping up, drawn as a staircase
  • Units on the U-100 syringe for every step
  • How long one vial lasts

Injection

The injection is subcutaneous, into the fat layer under the skin. Common spots are the abdomen (keep about two finger-widths clear of the navel), the front and the inner side of the thigh, or the back of the upper arm.

The short version:

Injection

Where and at what angle

Pick a spot or switch the angle. Subcutaneous means: into the fat layer, not the muscle.

Rotate the spot each time, never the same one twice in a row.

90°More fat under the skin

Rule of thumb: where there is more fat under the skin, insert straight at 90 degrees. In lean people with little fat, 45 degrees, so the needle stays in the fat layer. Simplified diagram.

  1. Clean the spot with an alcohol swab and let it dry

  2. Pinch up a small fold of skin

  3. Insert the needle: at 90 degrees where there is more fat under the skin, at 45 degrees in lean people with little fat

  4. Inject slowly, wait a moment, then withdraw

  5. Put the needle straight into the sharps container

Rotate the site each time so the tissue does not get irritated. Never the same spot twice in a row.

AOD-9604 is ideally injected fasted before cardio.

What the research shows

The basis comes from the GH fragment (Heffernan, 2001): in obese mice GH and the fragment triggered weight loss and increased fat burning. Important: in later human weight-loss studies AOD-9604 showed only limited effects. Stay realistic, it does not replace a calorie deficit.

Study results

What the trials measured

Interactive: switch tabs, tap points, show or hide arms. Arms are named relative to each other, no dosing advice.

Weight gain of obese Zucker rats3

Gain over 19 days in grams, AOD9604 daily by mouth

Weight gain3
Control 35.6 g
AOD9604 15.8 g

Means from the abstract, error ranges omitted. Unlike with growth hormone, insulin sensitivity stayed unchanged. Rats, not humans.

Metal tray with a cluster of yellow fat cells under a glass dome and a glass knee joint, racks of test tubes behind them
Animal data on fat, in humans only trials on pain. Symbolic image.

Research status

Where the research stands

No trial is registered under the name AOD9604. ChEMBL also lists the compound as LAT8881, under this name there are three completed trials on pain and migraine. Weight-loss trials are not registered. As of 26 Oct 2026. 5

  1. Preclinical Rats and mice, fat metabolism
  2. Phase 1 1 trial, 1 completed
  3. Phase 2 2 trials, 2 completed
  4. Phase 3 no registered trial
  5. Approval not yet
Not approved. Under the name LAT8881 up to phase 2 for pain, there is no registered weight-loss trial.7
Show all 2 phase 2 trials on a timelineHide timeline 2 completed 0 running 0 with results
Phase 2

Bar: start to primary endpoint (planned for running trials). Green = completed, blue = progress until 26 Oct 2026. Phase 1: 1 trial on safety and pharmacokinetics, not shown as bars.

Side effects

  • Generally well tolerated, mainly local reactions at the injection site.
  • Since little effect on blood sugar and IGF-1, the typical GH side effects are largely absent.
  • The effect itself is less established in humans than hoped.

Storage

Before mixing the powder is robust, normal room temperature (around 20 to 25 degrees) is fine, ideally kept in the dark. After mixing, keep in the fridge (2 to 8 degrees), do not freeze. It stays good there for at least 4 to 6 months with barely any loss of potency, in practice considerably longer. Swirl or shake to mix, both are fine.

Shelf life

How long it keeps

Undissolved (powder) Room temperature, around 20 to 25 degrees, dark

Robust, no fridge needed. Best kept in the dark.

Dissolved (mixed) Fridge, 2 to 8 degrees, do not freeze

At least 4 to 6 months with barely any loss of potency. The bacteriostatic water brings a preservative.

  • Keep it dark
  • Dissolved: 2 to 8 degrees
  • Note the mixing date on the vial
Nine vials with white powder and blue caps in the door shelf of a bright fridge
Powder dark at room temperature, once dissolved into the fridge (2 to 8 degrees), stable there for at least 4 to 6 months. Symbolic image.

Related

Related compounds

A different path: all in the TPD lexicon.

FAQ

Common questions about AOD-9604

Short answers, each backed by the sources below.

What exactly is AOD-9604?

A piece of human growth hormone: building blocks 177 to 191 with an extra tyrosine at the start, 16 amino acids in total. In serum and urine fragments form, one of them is much more stable than the compound itself.48

Has AOD-9604 been studied in humans?

There is no registered trial and no publication listed in PubMed on weight loss. ChEMBL also lists the compound as LAT8881. Under this name three trials ran on nerve pain, migraine and back pain, two with capsules and one with an infusion.567

What do the animal studies show?

Obese Zucker rats given AOD9604 by mouth gained 15.8 instead of 35.6 grams in 19 days. In obese mice fat burning and fat breakdown rose over 14 days and weight gain fell. In mice without the beta-3 receptor the effect on weight did not occur.321

Does AOD-9604 act like growth hormone?

Only with regard to fat. In cell assays AOD9604 did not bind to the growth hormone receptor and did not stimulate cell division. Unlike growth hormone it did not raise blood sugar in mice and insulin sensitivity stayed unchanged in rats.23

Which side effects are known?

There are no solid human data listed in PubMed. The trials under the name LAT8881 have posted results in the registry but not published them.6

Is AOD-9604 allowed in sport?

No. AOD9604 is on the WADA prohibited list. Doping labs have developed a urine test. A stable breakdown product could extend the time window for detection.4

Glossary

Terms explained briefly

Dotted words in the text open these explanations directly.

Beta-3 receptor
An adrenaline receptor that triggers fat breakdown in fat cells.
Fat oxidation
Burning fatty acids to produce energy.
Growth hormone (GH)
A hormone of 191 amino acids from the pituitary gland. It controls growth and affects fat and sugar metabolism.
LAT8881
Development name under which AOD-9604 ran in trials on pain and migraine according to ChEMBL.
Lipolysis
The breakdown of stored fat in the fat cell into fatty acids and glycerol.
Lyophilisate
Freeze-dried powder. Without water a peptide keeps much longer.
Subcutaneous
Into the fat layer just under the skin.
WADA
World Anti-Doping Agency. It keeps the list of substances banned in sport.
Zucker rat
A rat strain that becomes obese because of a gene defect. The name has nothing to do with sugar.

Evidence

Sources

Show all 8 sourcesHide sources 4 Studies2 Trial registry2 Database checked 26 Oct 2026

Studies

  1. Growth hormone and AOD9604 in obese mice and mice without the beta-3 receptor

    Heffernan et al., Endocrinology, 2001

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  2. More fat burning in obese mice, no binding to the GH receptor

    Heffernan et al., International Journal of Obesity, 2001

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  3. Oral AOD9604 in obese Zucker rats

    Ng et al., Hormone Research, 2000

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  4. Structure, breakdown and doping detection of AOD9604

    Cox et al., Drug Testing and Analysis, 2015

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed

Trial registry

  1. Search on ClinicalTrials.gov (no trial under the name AOD9604)

    ClinicalTrials.gov, U.S. National Library of Medicine

    Checked 26 Oct 2026 via ClinicalTrials.gov API v2
  2. Trials with LAT8881 on ClinicalTrials.gov

    ClinicalTrials.gov, U.S. National Library of Medicine

    Checked 26 Oct 2026 via ClinicalTrials.gov API v2

Database

  1. AOD-9604 as LAT-8881 in ChEMBL (synonyms, highest phase)

    ChEMBL, EMBL-EBI (CHEMBL6068615)

    Checked 26 Oct 2026 via ChEMBL
  2. Structure of AOD-9604 in PubChem

    PubChem, U.S. National Library of Medicine (CID 71300630)

    Checked 26 Oct 2026 via PubChem

In the shop

AOD-9604 in the catalog

Sizes, prices and shipping times are on the product page.

To the product