VRX-0075: Findings from Animal Research
VRX-0075 is an experimental peptide that activates five receptors at once: GLP-1, GIP, glucagon, amylin and calcitonin. At the American Diabetes Association's 86th Scientific Sessions in 2026, researchers reported it produced more weight loss than retatrutide in obese rats at the same molar dose. That result got attention. It is also a late-breaking abstract from an animal study, with no human data behind it.
What the abstract reports
- Targets: one long-acting molecule activating GLP-1, GIP, glucagon, amylin and calcitonin receptors
- In vitro (lab tests on cells): potency comparable to retatrutide at GLP-1, GIP and glucagon, and comparable to cagrilintide at amylin and calcitonin
- Obese rats: significantly greater weight loss than retatrutide at the same molar dose
- Half-life: about 50% longer than semaglutide in obese rats, which the authors suggest could support weekly dosing in humans, a hypothesis, not a finding
- Safety: no observable toxicology findings, in what the authors describe as a non-regulatory setting, not a formal toxicology program
Source: Douros J, Mowery S, Kalwat M, Dodson S, Shrinivasan R, Knerr PJ. 2839-LB: A Long-Acting Quintuple Agonist for the GLP-1, GIP, Glucagon, Amylin, and Calcitonin Receptors Induces Greater Weight Loss than Retatrutide in Obese Rats. Diabetes. 2026;75(Supplement 1):2839-LB.
Where it sits on the receptor ladder
Semaglutide targets GLP-1. Tirzepatide adds GIP. Retatrutide adds glucagon and is in phase 3. VRX-0075 keeps those three and adds amylin and calcitonin signaling, the pathway cagrilintide is built around. See our comparison of semaglutide, tirzepatide and retatrutide for the first three steps.
Why add amylin and calcitonin to a triple agonist?
Does "beat retatrutide in rats" mean it will beat it in people?
Can you buy VRX-0075?
Research use only. Not for human or veterinary use. Not approved by the Thai FDA. Educational content, not medical advice. VRX-0075 is an experimental compound and the findings discussed are preclinical.