Liraglutide
Saxenda / Victoza
Liraglutide is an acylated analog of human GLP-1, modified with a C16 fatty acid chain that enables reversible albumin binding and extends the half-life to approximately 13 hours — sufficient for once-daily subcutaneous dosing. It was first approved by the FDA as Victoza for type-2 diabetes in 2010, and as Saxenda (at a higher 3 mg dose) for chronic weight management in 2014, becoming the first GLP-1 agonist with an obesity indication. Clinical trial data (SCALE) demonstrated approximately 6–8% mean weight reduction at 56 weeks, substantially less than the 15% produced by once-weekly semaglutide (Wegovy) that displaced it in 2021. Liraglutide remains in widespread use because of generic-entry timing (biosimilars available in some jurisdictions), prescriber familiarity, and its longer post-market safety record. Cardiovascular outcome data (LEADER trial, 2016) showed a 13% reduction in major adverse cardiovascular events in type-2 diabetes patients at high CV risk — an important first-in-class finding for GLP-1 agonism.
Specifications
| Dose Range | 0.6–3 mg daily (escalating) |
| Origin / Manufacturer | Recombinant / synthetic |
| Regulatory Status | FDA-approved (Victoza, Saxenda) |
| Form Factor | Prefilled daily pen |
Frequently Asked Questions
Sources & References
Every clinical claim on this page traces to a primary peer-reviewed source.
- 1Pi-Sunyer X, Astrup A, Fujioka K, et al.. A Randomized, Controlled Trial of 3.0 mg of Liraglutide in Weight Management (SCALE). NEJM. 2015;373:11-22. doi:10.1056/NEJMoa1411892 PMID:26132939
- 2Marso SP, Daniels GH, Brown-Frandsen K, et al.. Liraglutide and Cardiovascular Outcomes in Type 2 Diabetes (LEADER). NEJM. 2016;375:311-322. doi:10.1056/NEJMoa1603827 PMID:27295427
Reviewed by
Clinical Research Review Board
Pharmacology & Endocrinology Review
All clinical claims cross-checked against primary sources. Read our editorial policy →