Neither of these drugs is available anywhere yet — but they're not racing on equal footing. CagriSema has already been filed with the FDA. Retatrutide is still completing its phase 3 programme.
| CagriSema | Retatrutide | |
|---|---|---|
| Maker | Novo Nordisk | Eli Lilly |
| Mechanism | Semaglutide (GLP-1) + cagrilintide (amylin analogue) combination | Single molecule, triple receptor agonist (GLP-1 + GIP + glucagon) |
| Best reported weight loss | 22.7% (REDEFINE-1), 23% (REDEFINE-4) — both below Novo's own 25% target | Up to 30.3% (TRIUMPH-1) |
| Vs tirzepatide (Mounjaro) head-to-head | Failed to show non-inferiority to tirzepatide in REDEFINE-4 | No direct head-to-head trial run yet |
| Regulatory status | FDA application submitted December 2025 | FDA submission planned Q1 2027 |
These aren't competing versions of the same idea — they're different bets on which biology drives the best result.
Combine an established GLP-1 (semaglutide) with an amylin analogue (cagrilintide), targeting appetite regulation through two separate hormone systems rather than one molecule doing more jobs.
One molecule, three receptors, including glucagon — adding a metabolic (energy-burning) mechanism on top of the appetite-suppressing GLP-1/GIP pathways.