UBT251
Also known as: UBT-251, triple-G agonist, United Biotechnology UBT251, triple-G
Status
In trials. Investigational. Developed by United Biotechnology and licensed exclusively to Novo Nordisk in March 2025. Phase 3 trials in obesity and type 2 diabetes were registered in 2026; it is not FDA-approved, and no approval elsewhere is listed in this entry's sources.
What it is
A triple agonist — one peptide engaging the GLP-1, GIP and glucagon receptors, the same three-receptor design as retatrutide, arriving from a different developer through Novo Nordisk's licensing deal.
What published research measured
A Chinese phase 2 trial in overweight or obesity reported mean weight loss of up to 19.7% after 24 weeks (company announcement, February 2026). A second phase 2 in type 2 diabetes reported HbA1c reductions of up to 2.16% (March 2026). Both were topline announcements, not peer-reviewed publications, and the trials were conducted in China. Cross-trial comparisons with retatrutide and the other triple agonists are unreliable.
Source
Novo Nordisk / The United Laboratories announcements, Feb–Mar 2026; ClinicalTrials.gov NCT07648225, NCT07653477
Sources
Educational use only, never medical advice. No doses.