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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.Activates GLP-1 receptors on pancreatic beta cells, raising glucose-dependent insulin release.
- 2.Suppresses glucagon after meals.
- 3.Slows gastric emptying, which is the main driver of its effect on post-meal glucose.
- 4.Reduces appetite through central GLP-1 signalling.
- 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.