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Cagrisema produces greater weight loss than semaglutide in obesity meta-analysis

Cagrisema produces greater weight loss than semaglutide in obesity meta-analysis
Photo by DIANA HAUAN / Unsplash
Key Takeaway
Consider cagrisema for greater weight loss in obesity, but note increased adverse events with combination therapy.

This is a systematic review and meta-analysis with meta-regression focusing on obesity treatments. The authors synthesized evidence from trials comparing cagrisema or cagrilintide monotherapy versus semaglutide. The main finding was that cagrisema produced significantly greater weight loss than semaglutide, with a mean difference of -7.47% (95% CI: -10.58, -4.36; p < 0.001) for percentage change and -7.60 kg (95% CI: -10.33, -4.86; p < 0.001) for absolute change. Cagrilintide monotherapy weight loss was comparable to semaglutide. For secondary outcomes, LDL-C was modestly higher with combination therapy (MD 0.29 mmol/L; 95% CI: 0.02, 0.55; p = 0.03). Safety data showed overall and serious adverse events were comparable between cagrisema and semaglutide, but combination therapy increased administration-site conditions (RR 3.27; 95% CI: 1.27, 8.46) and nausea (RR 1.64; 95% CI: 1.01, 2.66). Cagrilintide monotherapy had a higher risk of serious adverse events compared to semaglutide (RR 1.83; 95% CI: 1.03, 3.24). The authors did not report limitations or funding conflicts. Practice relevance should consider these mixed efficacy and safety signals.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedJun 2026
View Original Abstract ↓
BACKGROUND: Obesity is a complex chronic disease requiring effective long-term management. We performed a systematic review and meta-analysis to evaluate the efficacy and safety of cagrisema and cagrilintide monotherapy compared with semaglutide in individuals with obesity. METHODS: We searched MEDLINE, Embase, Scopus, Cochrane, and ClinicalTrials.gov for randomized controlled trials accessing cagrisema or cagrilintide versus semaglutide for weight loss. Efficacy outcomes were percentage change in body weight, absolute change in body weight, fasting plasma glucose, HbA1c, and BMI. Lipid parameters included total cholesterol, LDL-C, HDL-C, VLDL-C, and triglycerides. A random-effects model was used to estimate mean differences (MD) or risk ratios (RR) with 95% CIs. RESULTS: Three RCTs (n = 3545) were included. Cagrisema produced significantly greater percentage [MD -7.47% (95% CI: -10.58, -4.36); p < 0.001] and absolute [MD -7.60 kg (95% CI: -10.33, -4.86); p < 0.001] weight loss than semaglutide. Cagrilintide monotherapy weight loss was comparable to semaglutide. Lipids parameters were mostly similar between groups, though LDL-C was modestly higher with combination therapy versus semaglutide [MD 0.29 mmol/L (95% CI: 0.02, 0.55); p = 0.03]. Overall and serious adverse events were comparable between cagrisema and semaglutide, but combination therapy increased administration-site conditions [RR 3.27 (95% CI: 1.27, 8.46)] and nausea [RR 1.64 (95% CI: 1.01, 2.66)]. Cagrilintide monotherapy had a higher risk of serious adverse events [RR 1.83 (95% CI: 1.03, 3.24)] compared to semaglutide. CONCLUSION: Cagrisema is more effective than semaglutide in reducing weight and increasing glycemic control. Cagrisema is safe and has a comparable side effect profile to currently accepted treatments. This regimen has enormous potential in dual-agonist therapy for obese patients.
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