Liraglutide
The first once-daily GLP-1 analog to be FDA-approved for both type 2 diabetes (Victoza) and chronic weight management (Saxenda).
A 31-amino-acid synthetic GLP-1 analog with 97% sequence homology to native GLP-1, modified with a palmitoyl (C16) fatty acid at Lys26 to extend half-life to roughly 13 hours.
Mechanism of action
Agonist at the GLP-1 receptor. Enhances glucose-dependent insulin secretion, suppresses glucagon, slows gastric emptying, and acts on hypothalamic appetite centers. The daily dosing requirement reflects its shorter half-life compared with semaglutide — which also means faster onset and offset of both therapeutic and adverse effects.
Primary uses
- Type 2 diabetes mellitus (Victoza)
- Chronic weight management (Saxenda, BMI ≥30 or ≥27 with comorbidity)
- Pediatric obesity (Saxenda, ≥12 years)
- Cardiovascular risk reduction in T2DM with established CVD (LEADER trial)
Typical dosing
Victoza titrated 0.6 → 1.2 → 1.8 mg daily over 2 weeks. Saxenda titrated 0.6 → 3.0 mg daily over 5 weeks to minimize GI side effects.
Regulatory status
FDA-approved as Victoza (T2DM, 2010) and Saxenda (chronic weight management, 2014). Manufactured by Novo Nordisk. Generic liraglutide approved in 2024.
References
- [fda-pi] Victoza (liraglutide) Prescribing Information. Novo Nordisk.
- [fda-pi] Saxenda (liraglutide) Prescribing Information. Novo Nordisk.
- [clinical-trial] Pi-Sunyer X, et al. "A Randomized, Controlled Trial of 3.0 mg of Liraglutide in Weight Management (SCALE)." N Engl J Med, 2015;373:11-22.
- [clinical-trial] Marso SP, et al. "Liraglutide and Cardiovascular Outcomes in Type 2 Diabetes (LEADER)." N Engl J Med, 2016;375:311-322.
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This entry is for educational purposes only and does not constitute medical advice. Dosing information reflects published regulatory or research data and is not a recommendation. Many compounds described here are not approved for human use in the United States. Consult a licensed medical professional before considering any peptide therapy.