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Pick up to three peptides to see how their mechanisms, studied uses and evidence levels differ. Rows where the entries disagree are marked with a blue edge.

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Comparison
Lixisenatide

GLP-1 & incretin

Evidence level
Strong evidence
Approval status
Approved drug
Mechanism of action
  1. 1.Activates GLP-1 receptors on pancreatic beta cells, raising glucose-dependent insulin release.
  2. 2.Suppresses glucagon after meals.
  3. 3.Slows gastric emptying, which is the main driver of its effect on post-meal glucose.
  4. 4.Reduces appetite through central GLP-1 signalling.
  5. 5.The added tail stabilises the peptide against DPP-4, allowing once-daily dosing.
Studied for
  • Type 2 diabetes as add-on therapy (GetGoal programme)
  • Cardiovascular safety in high-risk type 2 diabetes (ELIXA)
  • Combination with basal insulin
  • Postprandial glucose control
  • Weight as a secondary endpoint
Reported effects
  • HbA1c reductions of roughly 0.5 to 0.9 percentage points
  • Marked reduction in post-meal glucose excursions
  • Modest weight loss
  • ELIXA found no cardiovascular harm and no clear benefit
  • More gastrointestinal effects than long-acting GLP-1 agonists
Side effects
  • Nausea and vomiting, more common with rapid dose escalation
  • Diarrhoea
  • Headache and dizziness
  • Hypoglycaemia when combined with insulin or a sulfonylurea
  • Pancreatitis (rare)
  • Injection-site reactions
Research protocol

Research context only - prescription medicine. Labelled dosing is 10 micrograms subcutaneously once daily for 14 days, then 20 micrograms once daily, injected within an hour before the first meal of the day; ELIXA followed participants for a median of 25 months.

Research context only

Evidence justification
The GetGoal randomised programme plus ELIXA, a cardiovascular outcome trial in over 6,000 people with recent acute coronary syndrome.