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Liraglutide
GLP-1 Analogs

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 Range0.6–3 mg daily (escalating)
Origin / ManufacturerRecombinant / synthetic
Regulatory Status
FDA-approved (Victoza, Saxenda)
Form FactorPrefilled daily pen

Frequently Asked Questions

Sources & References

Every clinical claim on this page traces to a primary peer-reviewed source.

  1. 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
  2. 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 →

Reviewed by Clinical Research Review BoardPharmacology & Endocrinology Review

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