- |||||||||| Ozempic (semaglutide SC once-weekly) / Novo Nordisk, semaglutide SC once-daily (NN9536) / Novo Nordisk
Journal: Switching from other GLP-1 receptor agonists to semaglutide - impact on HbA1c and body weight: A model-based approach. (Pubmed Central) - Aug 21, 2019 Exposure-response modelling suggests that switching to semaglutide from liraglutide, dulaglutide or exenatide extended-release results in further reductions in HbA1c and body weight. Initial slight deterioration in outcome values when switching to semaglutide 0.25 mg could be avoided by initiating semaglutide treatment at a higher dose.
- |||||||||| Ozempic (semaglutide SC once-weekly) / Novo Nordisk
Enrollment closed, Enrollment change, Real-world evidence, Real-world: SURE CANADA: A Research Study Looking at How Semaglutide Works in People With Type 2 Diabetes in Canada, as Part of Local Clinical Practice (clinicaltrials.gov) - Jul 23, 2019 P=N/A, N=460, Active, not recruiting, Not yet recruiting --> Recruiting Enrolling by invitation --> Active, not recruiting | N=217 --> 460
- |||||||||| semaglutide SC once-daily (NN9536) / Novo Nordisk
Review, Journal: Glucagon-like peptide-1 receptor agonists in type 2 diabetes treatment: are they all the same? (Pubmed Central) - May 30, 2019 The primary pharmacodynamic difference between short-acting (i.e. exenatide twice daily, lixisenatide) and long-acting (i.e. albiglutide, dulaglutide, exenatide once weekly, liraglutide, semaglutide) GLP-1 RAs is that short-acting agents primarily delay gastric emptying (lowering postprandial glucose) and long-acting agents affect both fasting glucose (via enhanced glucose-dependent insulin secretion and reduced glucagon secretion in the fasting state) and postprandial glucose (via enhanced postprandial insulin secretion and inhibition of glucagon secretion). Other advantages of long-acting GLP-1 RAs include smaller fluctuations in plasma drug concentrations, improved gastrointestinal tolerability profiles, and simpler, more convenient administration schedules (once daily for liraglutide and once weekly for albiglutide, dulaglutide, the long-acting exenatide formulation and semaglutide), which might improve treatment adherence and persistence.
- |||||||||| Clinical, Journal, HEOR: Management of Patients with Type 2 Diabetes with Once-Weekly Semaglutide Versus Dulaglutide, Exenatide ER, Liraglutide and Lixisenatide: A Cost-Effectiveness Analysis in the Danish Setting. (Pubmed Central) - May 18, 2019
Other advantages of long-acting GLP-1 RAs include smaller fluctuations in plasma drug concentrations, improved gastrointestinal tolerability profiles, and simpler, more convenient administration schedules (once daily for liraglutide and once weekly for albiglutide, dulaglutide, the long-acting exenatide formulation and semaglutide), which might improve treatment adherence and persistence. Semaglutide represents a cost-effective alternative to other GLP-1 receptor agonist therapies available in Denmark, demonstrating clinical benefits versus dulaglutide, exenatide ER, liraglutide and lixisenatide for the treatment of patients with T2D.
- |||||||||| LAI287/semaglutide (NN1535) / Novo Nordisk, Ozempic (semaglutide SC once-weekly) / Novo Nordisk, Awiqli (insulin icodec) / Novo Nordisk
Enrollment closed, Enrollment change: A Research Study to Look at How Insulin 287 and Semaglutide Work in the Body of People With Type 2 Diabetes When Taken Alone or Together (clinicaltrials.gov) - May 9, 2019 P1, N=30, Active, not recruiting, Active, not recruiting --> Completed Recruiting --> Active, not recruiting | N=60 --> 30
- |||||||||| Victoza (liraglutide) / Novo Nordisk, Ozempic (semaglutide SC once-weekly) / Novo Nordisk, semaglutide SC once-daily (NN9536) / Novo Nordisk
Review, Journal: The Discovery and Development of Liraglutide and Semaglutide. (Pubmed Central) - Apr 30, 2019 Furthermore, the development of an oral formulation for semaglutide may provide individuals with additional benefits in relation to treatment adherence. In addition to T2D, liraglutide is used in the treatment of obesity, while semaglutide is currently under investigation for use in obesity and NASH.
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