GLP-1 & incretin
Liraglutide
A once-daily GLP-1 receptor agonist approved for type 2 diabetes and weight management, and the first in its class shown to reduce cardiovascular events.
What it is
Liraglutide is a synthetic 31-amino-acid peptide that is 97% identical to human GLP-1, with a fatty-acid side chain that lets it bind albumin in the blood. That binding extends its half-life to roughly 13 hours, which allows once-daily dosing. It is a prescription medicine (Victoza for type 2 diabetes, Saxenda for weight management at a higher dose).
How it works
- 1
Binds and activates the GLP-1 receptor on pancreatic, gut and brain cells.
- 2
Increases insulin release and reduces glucagon release in a glucose-dependent manner, so hypoglycaemia is uncommon on its own.
- 3
Slows gastric emptying, so nutrients arrive in the small intestine more gradually.
- 4
Acts on hypothalamic appetite centres to reduce hunger and food intake.
- 5
Cardiovascular benefit seen in trials is thought to involve effects on inflammation, endothelial function and blood pressure in addition to weight loss.
What it's studied for
Reported and studied effects
- HbA1c reduction of roughly 1–1.5 percentage points in trials
- Mean weight loss of about 8% at 56 weeks with the 3.0 mg dose (SCALE Obesity and Prediabetes)
- 13% relative reduction in major cardiovascular events in adults with type 2 diabetes at high risk (LEADER)
- Reduced progression from prediabetes to diabetes over three years
- Lower blood pressure and modest improvements in lipids
Research protocol notes
Research context onlyResearch context only — liraglutide is a prescription medicine and its use is set by a doctor. Trials escalated weekly in steps: 0.6 mg to 1.8 mg daily for diabetes, or 0.6 mg to 3.0 mg daily for weight management, over 40–56 weeks. Nothing here is a dosing suggestion.
These figures are described so you can understand what researchers did. They are not a dose, a schedule, or a suggestion — and they are not a substitute for a doctor.
Possible side effects and contraindications
Safety profile
Possible side effects
- Nausea, vomiting and diarrhoea, mostly during dose escalation
- Constipation and abdominal discomfort
- Gallbladder disease, including gallstones
- Pancreatitis (rare)
- Injection-site reactions
- Hypoglycaemia when combined with insulin or a sulfonylurea
- Thyroid C-cell tumours in rodents — human relevance not established
Contraindications and cautions
- Personal or family history of medullary thyroid carcinoma
- Multiple endocrine neoplasia syndrome type 2
- Pregnancy — weight-management use is contraindicated
- Previous serious allergic reaction to liraglutide
- Suspected pancreatitis needs medical assessment before continuing
A side-effect list is never complete, and these are not the only situations that warrant caution. Anything unexpected, or anything you are unsure about, should be discussed with a doctor before use.
Evidence assessment
Large randomised controlled trials with pre-specified outcomes, including a 9,340-participant cardiovascular outcomes trial, plus regulatory approval in the EU and US.
References
- 01Marso et al., Liraglutide and Cardiovascular Outcomes in Type 2 Diabetes (LEADER), NEJM 2016
- 02Pi-Sunyer et al., A Randomized Controlled Trial of Liraglutide 3.0 mg in Weight Management (SCALE), NEJM 2015
- 03European Medicines Agency — Victoza product information
References link to published literature, regulator pages or literature indexes. Where a link points to a search, it collects the peer-reviewed work on that molecule rather than a single study.
Related
Related peptides
Other entries in GLP-1 & incretin.
GLP-1 & incretin
Cagrilintide
A long-acting amylin analogue that slows digestion and reduces appetite, studied alone and combined with semaglutide for obesity.
GLP-1 & incretin
Dulaglutide
A once-weekly GLP-1 receptor agonist approved for type 2 diabetes, with proven cardiovascular benefit in people at high risk.
GLP-1 & incretin
Exenatide
A GLP-1 receptor agonist derived from Gila monster saliva, approved for type 2 diabetes in twice-daily and once-weekly forms.