Victoza contains liraglutide, a synthetic analog of human glucagon-like peptide-1(GLP-1) and acts as a GLP-1 receptor agonist. Liraglutide is 97% similar to native human GLP-1, differing primarily by substituting arginine for lysine at position 34. Liraglutide is made by attaching a C-16 fatty acid (palmitic acid) with a glutamic acid spacer on the remaining lysine residue at position 26 of the peptide precursor. Liraglutide was granted FDA approval on January 25, 2010.
Saxenda, a formulation of liraglutide intended for weight loss, is indicated as an adjunct to diet and exercise for chronic weight management in adult patients who are obese (BMI≥30 kg/m), or who are overweight (BMI≥27 kg/m) and have at least one weight-related comorbidity. It is also indicated for chronic weight management in pediatric patients ≥12 years old who weigh ≥60 kg and have an initial BMI corresponding to obesity based on international cut-offs.
Victoza, a formulation of liraglutide used in diabetes, is indicated as an adjunct to diet and exercise to improve glycemic control in patients ≥10 years old with type 2 diabetes mellitus. It is also indicated to reduce the risk of major adverse cardiovascular events in adult patients with type 2 diabetes and established cardiovascular disease.
Liraglutide is also available in combination with insulin degludec as an adjunct to diet and exercise to improve glycemic control in adult patients with type 2 diabetes mellitus.
Novo Nordisk Investigational Site, Yokohama-shi, Japan
Novo Nordisk Investigational Site, Neuss, Germany
Novo Nordisk Investigational Site, Charleston, West Virginia, United States
Novo Nordisk Investigational Site, Yaxley. Peterborough, United Kingdom
Novo Nordisk Investigational Site, Ann Arbor, Michigan, United States
Novo Nordisk Investigational Site, Worksop, United Kingdom
Novo Nordisk Investigational Site, Bad Lauterberg, Germany
Novo Nordisk Investigational Site, Frederiksberg C, Denmark
Novo Nordisk Investigational Site, Århus C, Denmark
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