Database / CagriSema
CagriSema
No brand yet · Novo Nordisk. Semaglutide plus cagrilintide, a long-acting amylin. Would be the first amylin-based obesity medicine. FDA decision expected in Q4 2026.
Average weight loss
22.7%
Stopped for side effects
6%
Trial length
68 wk
Ranking score
5.2
REDEFINE 1 results
Phase 3 · 68 weeks · 2.4 mg cagrilintide + 2.4 mg semaglutide
Adults with obesity, no diabetes (n=3,417)
Weight loss
22.7%
Nausea
55.0%
Vomiting
26.1%
Diarrhean/r
Constipation
30.7%
Quit due to side effects
6.0%
n/r = not reported. Counting everyone who started, weight loss was 20.4%. Placebo group: 2.3%.
Worth knowing
- Missed its goal against tirzepatide in the head-to-head REDEFINE 4 trial.
- Diarrhea rate not published in sources we could verify; scored on 3 of 4 stomach measures.
Next catalysts
Q4 2026 FDA decision on CagriSema for obesity (Company guidance)
5.2
GLP-1 Performance Index
Rank 3 of 6 ranked drugs
Stomach = (55.0 + 26.1 + 30.7) ÷ 3
= 37.3
Burden = 37.3 + 1 × 6.0 = 43.3
Index = 22.7 ÷ 43.3 × 10 = 5.25
Scored on 3 of 4 stomach measures; one rate is not published.
At a glance
- Company
- Novo Nordisk
- Targets
- Amylin, GLP-1
- Molecule
- Peptide
- Dosing
- Injection, weekly
- Status
- Under FDA review
Sources
History
- CagriSema: new EASD data on food cravings and liver fat; FDA decision still expected Q4 2026.