At a glance

Targeted fat-loss intent (unproven in humans)
Appetite-neutral mechanism
Favourable short-term safety / tolerability
Unapproved / gray-market product-quality risk
Failed efficacy / not proven to work
Injection-site & GI nuisance effects
WADA-banned (anti-doping)
BenefitSide effectHealth risk· more & brighter bars = stronger

Effects

  • Targeted fat metabolism: Intended to promote fat breakdown in adipose tissue without affecting muscle, appetite or blood sugar — but human weight loss was modest at best and not clinically meaningful in the pivotal trial.[3][4]
  • Appetite-neutral: Acts peripherally on fat cells rather than centrally on hunger signals, so unlike GLP-1 drugs it does not suppress appetite.[4]
  • No IGF-1 / glucose effect: Did not raise IGF-1 or impair glucose tolerance in trials, distinguishing it from full-length growth hormone.[5][9]
  • Much weaker than GLP-1 drugs: Does not produce the level of weight loss seen with semaglutide or tirzepatide.[1]
Classification

hGH 176–191 peptide fragment; WADA-prohibited

Regulatory status

Not FDA-approved; FDA Category 2 / restricted compounding

Route

Subcutaneous injection (oral forms also studied)

Origin

Metabolic Pharmaceuticals, Australia (1990s)

Dosing frequency

Once daily (sometimes split AM/PM)