
10 mg · 20 mg
Tesamorelin
GHRH analog studied in GH/IGF-1 signaling and visceral fat, including trials in people with HIV and altered fat distribution.

For research use only
Investigational peptide targeting GIP, GLP-1 and glucagon receptors. Studied in clinical trials on body weight and glycemic control.
Clinical studies in adults with obesity or type 2 diabetes.
Retatrutide (LY3437943) is an investigational triple agonist that acts on the GIP, GLP-1 and glucagon receptors. It is one of the most closely followed incretin-based compounds in current metabolic research.
Its research spans metabolic signaling, appetite regulation and energy balance. A phase 2 trial published in The New England Journal of Medicine evaluated retatrutide in adults with obesity, with change in body weight as the primary outcome, and ongoing studies examine glycemic control in type 2 diabetes.
Available in 10, 20, 30 and 50 mg vials, supplied for laboratory research.
Triple-Hormone-Receptor Agonist Retatrutide for Obesity — A Phase 2 Trial
N Engl J Med, 2023 · PMID 37366315
View on PubMed
10 mg · 20 mg
GHRH analog studied in GH/IGF-1 signaling and visceral fat, including trials in people with HIV and altered fat distribution.

100 mg
Blend of GHK-Cu, BPC-157, TB-500 and KPV. Studies on the individual components do not evaluate the blend.
Out of stock40 mg
Mitochondrial-derived peptide studied in preclinical models of insulin sensitivity, metabolic adaptation and physical capacity.
$65
per vialIn stock

10 mg · 20 mg
GHRH analog studied in GH/IGF-1 signaling and visceral fat, including trials in people with HIV and altered fat distribution.

100 mg
Blend of GHK-Cu, BPC-157, TB-500 and KPV. Studies on the individual components do not evaluate the blend.
Out of stock40 mg
Mitochondrial-derived peptide studied in preclinical models of insulin sensitivity, metabolic adaptation and physical capacity.