AOD-9604

Growth-hormone fragment

AOD-9604

A modified fragment of human growth hormone developed to preserve proposed fat-metabolism effects without the growth-promoting and diabetogenic activity of full-length HGH.

hGH 177–191 analogObesity programWADA prohibited
Quick facts

AOD-9604 at a glance

Structure16 amino acidshGH 177–191 plus N-terminal tyrosine
Original goalObesity drugOral and injected development
GH / IGF-1Not intended to raiseUnlike full HGH
Largest trial536 adultsOPTIONS obesity study
ResultNo significant loss12- and 24-week endpoints
StatusNot FDA approvedProhibited in tested sport
Design and mechanism

A fragment built around a metabolic hypothesis

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C-terminal fragment

AOD-9604 is based on residues 177–191 of HGH with an added tyrosine. It is not the same as HGH and is not a GH secretagogue.

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Lipolysis research

Animal and cell work suggested increased fat breakdown and reduced fat formation without the broad anabolic signaling of intact GH.

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No IGF-1 goal

The development strategy aimed to avoid raising IGF-1. That may reduce some GH-class concerns but does not prove efficacy or long-term safety.

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Oral ambition

Developers explored oral dosing—unusual for a peptide. Human pharmacokinetic information remains limited and route-specific claims are uncertain.

Important distinction: evidence that a compound does not act like full HGH is not evidence that it causes meaningful human fat loss.
AOD-9604 design map showing the HGH 177 to 191 fragment and intended fat metabolism effects

Suggested graphic: full HGH versus the AOD-9604 fragment and intended pathway · 1500 × 900

Human evidence

The obesity program reached the decisive test—and missed

What looked encouraging

  • Obese-animal studies reported increased lipolysis
  • Early human studies explored oral and intravenous routes
  • Some dose-finding signals encouraged larger development
  • It was intended to avoid IGF-1 and glucose liabilities of HGH

What the larger trial found

  • 536 adults with obesity entered the OPTIONS study
  • Diet and exercise were incorporated
  • Weight loss versus placebo was not statistically significant
  • Primary and secondary 12- and 24-week endpoints failed
  • Obesity development was terminated
ClaimEvidenceBest interpretation
Promotes lipolysisPrimarily preclinicalMechanistically interesting
Causes human weight lossLarge obesity study negativeNot demonstrated
Works without dietNo reliable evidenceUnsupported
Does not raise IGF-1Development characteristicDoes not guarantee safety
Targets injection-site fatNo credible human evidenceLocal-fat claim unsupported
AOD-9604 evidence timeline from animal research to the failed 536-person obesity trial

Suggested graphic: promising preclinical work → early studies → failed OPTIONS trial · 1500 × 900

How biohackers use it

Community protocols persist despite the trial result

Commonly discussed

  • Range: 250–500 mcg subcutaneously daily
  • Timing: fasted morning or before cardio
  • Cycles: commonly 8–12 weeks
  • Higher use: 500 mcg twice daily in some discussions
  • Stacks: GLP-1 drugs, carnitine, or other fat-loss agents

What users believe

  • Mobilizes stubborn fat without HGH effects
  • Supports fasted training
  • Preserves glucose control
  • Targets abdominal or local fat
  • Works gradually without appetite suppression
Community anecdotes sometimes report waist or composition changes, but diet changes, stacks, training, water balance, and measurement noise make those observations unable to overturn a negative randomized development program.
Reconstitution reference

A practical 5 mg example

2 mg vial

Liquid2 mL

Per unit10 mcg

250 mcg25 units

5 mg vial

Liquid2 mL

Per unit25 mcg

500 mcg20 units

10 mg vial

Liquid4 mL

Per unit25 mcg

250 mcg10 units

5 mg ÷ 2 mL = 2.5 mg/mL = 25 mcg per U-100 unit
Verify concentration every time. See What Is Reconstitution?, the U-100 Syringe Guide, and the Reconstitution Calculator.
Safety and sport

“No HGH effects” is not a safety certificate

FDA concerns

There is no FDA-approved AOD-9604 drug. FDA identifies compounded AOD-9604 as potentially presenting significant immunogenicity, impurity, and characterization risks, with limited safety information and serious adverse-event reports whose causality is unclear.

Practical considerations

  • Injection-site irritation, headache, nausea, fatigue, or flushing are discussed
  • Product identity, purity, sterility, endotoxin, and storage are major variables
  • Long-term injected-use safety is not established
  • WADA’s 2026 Prohibited List includes AOD-9604 as a GH fragment
  • Tested athletes should treat it as prohibited at all times
Frequently asked questions

Common questions about AOD-9604

Is AOD-9604 HGH?
No. It is a modified C-terminal HGH fragment intended to isolate proposed metabolic effects without functioning like full-length growth hormone.
Did it work in human obesity trials?
The largest 536-person study did not show statistically significant weight loss versus placebo at its main 12- or 24-week endpoints, and obesity development was terminated.
Does it target belly fat?
There is no strong human evidence for selective abdominal or injection-site fat loss.
Is AOD-9604 FDA approved?
No. No AOD-9604 drug has FDA approval.
Is it banned in sport?
Yes. WADA lists AOD-9604 among prohibited growth-hormone fragments.

A clever mechanism still has to survive a real trial.

AOD-9604 remains biologically interesting, but its reputation as a proven fat-loss peptide conflicts with the human development record.

Educational research reference only · Community protocols are not medical advice · Last evidence review: July 2026