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.

Strong evidenceApproved drugAdd to compare
01

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).

02

How it works

  1. 1

    Binds and activates the GLP-1 receptor on pancreatic, gut and brain cells.

  2. 2

    Increases insulin release and reduces glucagon release in a glucose-dependent manner, so hypoglycaemia is uncommon on its own.

  3. 3

    Slows gastric emptying, so nutrients arrive in the small intestine more gradually.

  4. 4

    Acts on hypothalamic appetite centres to reduce hunger and food intake.

  5. 5

    Cardiovascular benefit seen in trials is thought to involve effects on inflammation, endothelial function and blood pressure in addition to weight loss.

03

What it's studied for

Type 2 diabetes (LEADER and the phase 3 programme)
Chronic weight management in obesity (SCALE programme)
Major cardiovascular events in type 2 diabetes (LEADER)
Prediabetes and delay of type 2 diabetes onset
Adolescent obesity (SCALE Kids)
Obstructive sleep apnoea in obesity (secondary outcomes)
04

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 only

Research 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.

05

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.

06

Evidence assessment

Strong evidenceReplicated, large human trials
Replicated, large human trials

Large randomised controlled trials with pre-specified outcomes, including a 9,340-participant cardiovascular outcomes trial, plus regulatory approval in the EU and US.

07

References

  1. 01Marso et al., Liraglutide and Cardiovascular Outcomes in Type 2 Diabetes (LEADER), NEJM 2016
  2. 02Pi-Sunyer et al., A Randomized Controlled Trial of Liraglutide 3.0 mg in Weight Management (SCALE), NEJM 2015
  3. 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.