Current partner codePEPTIDESDE
Research onlyWeight lossSubcutaneousEvidence 2/5

HGH Fragment 176-191

Also known as: HGH Frag 176-191

A synthetic C-terminal fragment of human growth hormone claimed to stimulate adipocyte lipolysis without binding the GH receptor or raising IGF-1, though human fat-loss evidence is weak.

This page is a structured profile. Narrative evidence, dosing context and FAQs live on the research guide — not duplicated here as a second full article.

Illustrative subcutaneous database profile for HGH Fragment 176-191
Illustrative profileSubcutaneous
Database profileResearch only
HGH Fragment 176-191Weight loss
Drug class
Growth hormone C-terminal lipolytic fragment
Primary targets
Adipocyte lipid metabolism
Dose reference
No established human dose; research-only
Half-life
Very short (minutes); poorly characterized
Developer / origin
Ng et al. (Monash University)
Reference year
1994
Evidence score
2/5 - Weak
Evidence 2/5

Weak

Animal and isolated-tissue studies show the hGH 176-191 domain stimulates lipolysis without GH's IGF-1 effects, but there is no convincing controlled human fat-loss evidence; its optimized analog AOD-9604 failed a human obesity trial.

Mostly animal, ex vivo, cell, or indirect evidence.

Evidence basis

  • Synthetic hGH 177-191 reduced adipose mass and lipogenesis in obese mice
  • Stimulated hormone-sensitive lipase without binding the GH receptor
  • No controlled human fat-loss trial for the unmodified fragment
  • Optimized analog AOD-9604 failed human obesity development

How to read this entry

Dose references and half-life values are pulled from trial protocols, labels, reviews, or published summaries where available. They are context for research and comparison, not a personal dosing recommendation.

Status matters: approved drugs have regulated indications; investigational compounds are still being studied; research-only peptides do not have established human dosing, safety, or efficacy for consumer use.

HGH Fragment 176-191 guides

Read the matching guide or adjacent research pages for more context.

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