Weight Loss

HGH Fragment 176-191

Also known as: Frag 176-191, HGH Frag, AOD-9401

Clinical Trials
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Key Facts: HGH Fragment 176-191

Category
Weight Loss
FDA Status
Not FDA Approved
Clinical Status
Investigational - Research ongoing
Administration
Subcutaneous injection on empty stomach
Typical Dose
250-500 mcg daily
Frequency
1-2x daily, fasted
Duration
8-12 weeks
Also Known As
Frag 176-191, HGH Frag, AOD-9401

Mechanism of Action

This fragment is the C-terminal portion of growth hormone, the segment researchers identified as carrying its lipolytic (fat-breakdown) activity. In lab and animal work it stimulates fat cells to release and burn fat, increasing glycerol output and fat oxidation, apparently without binding the growth hormone receptor itself. That is the selling point: because it does not act on the GH receptor, it does not raise IGF-1, does not promote tissue growth, and does not impair glucose handling the way full growth hormone can. Some research points to involvement of beta-3 adrenergic signaling in fat tissue, though the exact human mechanism is not fully nailed down.

Research Summary

The animal data looked promising and the human data deflated it, which is the whole story here. In obese mice (International Journal of Obesity, 2001), both growth hormone and AOD-9604 reduced body-weight gain and increased fat oxidation, without the blood-sugar problems of full GH. A small 12-week phase 2 human study generated the famous early headline, with the 1 mg group losing about 2.8 kg versus 0.8 kg on placebo. But the larger, better-powered phase 2b trial of roughly 500 obese adults over 24 weeks failed to show a significant weight-loss advantage over placebo, and the developer abandoned obesity development. What survived is the safety record: across about six trials and roughly 900 people, AOD-9604 was as well tolerated as placebo, with no IGF-1 rise and no glucose effects (Journal of Endocrinology and Metabolism, 2013). So it is safe and it does not work as a meaningful fat-loss drug in humans.

Trial Progress:Preclinical
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FDA

Dosing Information

Human Trials·Human studies conducted, not FDA approved

Typical Dosing

Community experience

Common Dose

250-500 mcg daily

Range

200-600 mcg daily

Frequency

1-2x daily, fasted

Fat-burning fragment of HGH. Take on empty stomach. Often split into morning and pre-bed doses.

Research Dosing

Scientific studies

Doses from research protocols

Doses from Studies

Duration

8-12 weeks

Administration

Subcutaneous injection on empty stomach

Timing & Administration

Best Time to Take

Before bed or morning (fasted)

Follow specific peptide protocol

Food Recommendation

Take on empty stomach

Why This Timing?

GH-related peptides work best on an empty stomach to maximize growth hormone release.

Possible Side Effects

Not everyone experiences these effects. Individual responses vary based on dosage, duration, and personal factors.

  • Generally well-tolerated
  • Injection site reactions
  • Mild headache
  • Nausea
  • Does NOT cause typical HGH side effects
  • No effect on IGF-1 levels
  • GRAS status

References

Research This Peptide Further

Frequently Asked Questions

What does HGH Fragment 176-191 do?

HGH Fragment 176-191 is exactly what it sounds like: a short tail-end piece of the human growth hormone molecule, amino acids 176 through 191. The idea was to keep the fat-burning part of growth hormone while ditching the parts that raise blood sugar and IGF-1. The optimized drug version, AOD-9604, actually went through real human trials for obesity, and the blunt result is that it was very safe but did not produce meaningful weight loss.

How does HGH Fragment 176-191 work?

This fragment is the C-terminal portion of growth hormone, the segment researchers identified as carrying its lipolytic (fat-breakdown) activity. In lab and animal work it stimulates fat cells to release and burn fat, increasing glycerol output and fat oxidation, apparently without binding the growth hormone receptor itself. That is the selling point: because it does not act on the GH receptor, it does not raise IGF-1, does not promote tissue growth, and does not impair glucose handling the way full growth hormone can. Some research points to involvement of beta-3 adrenergic signaling in fat tissue, though the exact human mechanism is not fully nailed down.

Is HGH Fragment 176-191 FDA approved?

No, HGH Fragment 176-191 is not currently FDA approved. Current status: Investigational - Research ongoing

What are the side effects of HGH Fragment 176-191?

Reported side effects include: Generally well-tolerated, Injection site reactions, Mild headache, Nausea, Does NOT cause typical HGH side effects. Individual responses vary based on dosage, duration, and personal health factors.

What is the typical dose of HGH Fragment 176-191?

Community-reported common dose: 250-500 mcg daily (1-2x daily, fasted). Range: 200-600 mcg daily. Administration: Subcutaneous injection on empty stomach. Community-reported doses. Not medical advice. Consult healthcare provider.

Related Peptides

Peptides commonly compared with HGH Fragment 176-191 or used in similar applications.

AOD-9604

Clinical Trials

AOD-9604 is a synthetic fragment of human growth hormone, copying just the last 15 amino acids of the hormone (residues 176 to 191) plus a tyrosine cap. The idea was to keep the fat-burning end of growth hormone while leaving out the part that raises IGF-1 or messes with blood sugar. It was developed by Metabolic Pharmaceuticals in Australia and tested as an anti-obesity drug, but it is not approved by the FDA or any major regulator, and development stopped after it missed its weight-loss targets.

Weight Loss

Semaglutide

FDA

Semaglutide is a GLP-1 receptor agonist, a peptide engineered to mimic the natural gut hormone GLP-1 but with a roughly week-long half-life so it can be dosed once weekly. It is FDA-approved and sold as Ozempic and Rybelsus for type 2 diabetes and as Wegovy for chronic weight management, with cardiovascular benefit also on the label. This is one of the most rigorously tested peptides in existence, backed by large randomized trials, so the evidence here is in a completely different league from research-only peptides.

Weight Loss

Tirzepatide

FDA

Tirzepatide is a single peptide that activates two receptors at once: GIP and GLP-1, the two main incretin hormones your gut releases after eating. It is FDA-approved as Mounjaro for type 2 diabetes and as Zepbound for chronic weight management and obstructive sleep apnea, and it has produced the largest weight-loss numbers of any approved drug to date. Like semaglutide, this is a heavily trialed, fully approved medicine, not a gray-market research compound.

Weight Loss

Retatrutide

Clinical Trials

Retatrutide is the heavy hitter of the new weight-loss drugs: a once-weekly injectable peptide that hits three receptors at once - GIP, GLP-1, and glucagon - earning it the nickname triple-G agonist. In a phase 2 trial it produced some of the largest weight loss ever recorded for a drug, up to roughly 24 percent of body weight at the top dose. It is investigational, made by Eli Lilly, and not yet FDA approved as of 2026.

Weight Loss

Orforglipron

FDA

Orforglipron is Eli Lilly's oral, once-daily GLP-1 receptor agonist, and the headline is that it is a small molecule, not a peptide, so it survives the gut and can be taken as a plain pill with no food or water restrictions. It is being developed for type 2 diabetes and obesity and has completed multiple successful Phase 3 trials. As of mid-2026 it is filed for regulatory review but not yet approved.

Weight Loss

CagriSema

Clinical Trials

CagriSema is a once-weekly injectable that pairs two drugs in one shot: semaglutide (a GLP-1 receptor agonist, the molecule behind Ozempic and Wegovy) and cagrilintide (a long-acting amylin analog). It is being developed by Novo Nordisk for obesity and type 2 diabetes, and in 2025 it cleared its phase 3 REDEFINE trials. It is not yet approved by the FDA, though regulatory filings are underway.

Weight Loss

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