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Peptide

Liraglutide

Injectable analog of the gut hormone GLP-1. Used in type 2 diabetes (Victoza) and, at a higher dose, for weight loss in obesity (Saxenda).
Regulatory status
Approved (FDA / EMA)
Family
GLP-1 receptor agonist
Scientific evidence
Very high
Number of findings
2
Where it acts
Hormones and metabolism · Digestive and weight · Heart and blood
Also known as
liraglutide, Victoza, Saxenda, Xultophy (with insulin degludec)

Regulatory status

FDA (US): Approved (2010, Victoza) for type 2 diabetes and, since 2017, to reduce cardiovascular events in people with diabetes and cardiovascular disease; Saxenda (2014) for weight management in adults and, since 2020, adolescents aged 12 years and older.

EMA (EU): Approved (2009, Victoza) for type 2 diabetes; Saxenda (2015) for weight management in adults and adolescents aged 12 years and older.

Dose

Diabetes (Victoza): start with 0.6 mg/day subcutaneously and increase to 1.2–1.8 mg/day. Obesity (Saxenda): increase by 0.6 mg each week up to 3.0 mg/day (FDA/EMA labels).

Safety

Nausea, vomiting, diarrhea or constipation, especially at the start. Risk of pancreatitis and gallstones. Contraindicated with a personal or family history of medullary thyroid carcinoma or MEN 2 (boxed warning in the US because of tumors in rodents). Requires a prescription and medical follow-up.

Interactions

Greater risk of hypoglycemia with insulin or sulfonylureas (adjust doses). By slowing gastric emptying, it may change the absorption of oral drugs.

Differences between women and men

Should not be used in pregnancy: Saxenda is contraindicated during pregnancy and should be stopped if the woman becomes pregnant. In the main obesity trial (SCALE), 78.5% of participants were women, so the data in men are more limited. View the study →

Effect by goal · level of evidence

Weight loss in obesity (SCALE)

improves Very high RCT (AA) in people
−8.4 kg vs −2.8 kg

3,731 adults without diabetes with obesity or overweight and comorbidity, 56 weeks, alongside diet and exercise. They lost 8.4 kg with liraglutide 3.0 mg vs 2.8 kg with placebo; 63% lost at least 5% of their weight (27% with placebo).

View the study (RCT) →

Cardiovascular events in type 2 diabetes (LEADER)

reduces High RCT (AA) in people
−13% CV events

9,340 patients with type 2 diabetes and high cardiovascular risk, median follow-up of 3.8 years. Liraglutide reduced the composite of cardiovascular death, nonfatal heart attack, or stroke (13.0% vs 14.9%; HR 0.87) and cardiovascular death (4.7% vs 6.0%).

View the study (RCT) →

In depth

Where it acts

Hormones and metabolism, Digestion and weight, Heart and blood

How it works

It mimics GLP-1: it stimulates insulin only when glucose is high, suppresses glucagon, slows stomach emptying, and acts in the brain to reduce appetite. It lasts about 13 hours, which is why it is injected once a day.

What the evidence says

In people

  • Weight loss in obesity (SCALE). 3,731 adults without diabetes who had obesity or overweight with a comorbidity, 56 weeks, alongside diet and exercise. They lost 8.4 kg with liraglutide 3.0 mg versus 2.8 kg with placebo; 63% lost at least 5% of their weight (27% with placebo). PubMed 26132939
  • Cardiovascular events in type 2 diabetes (LEADER). 9,340 patients with type 2 diabetes and high cardiovascular risk, median follow-up of 3.8 years. Liraglutide reduced the composite of cardiovascular death, nonfatal heart attack, or nonfatal stroke (13.0% versus 14.9%; HR 0.87) and cardiovascular death (4.7% versus 6.0%). PubMed 27295427

References

  1. PubMed 26132939
  2. PubMed 27295427

Information, not medical advice. Prescription or unapproved peptides should only be used under medical supervision.

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