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Approved Profile FDA Approved Liraglutide

Liraglutide

The GLP-1 pioneer that proved peptides could transform metabolic disease.

Metabolic Health / Weight Loss/178+ studies cited/Subcutaneous
Educational Use Only

This content is for informational purposes and does not constitute medical advice. Clinical supervision is still required, but the evidence and regulatory context are materially stronger than research-only peptides.

Decision Summary

Start with the research signal and risk posture before you read the full protocol discussion.

What It Is

Liraglutide

Evidence Signal

2 indexed studies support the article, but the strength of evidence should be read from the cited data and context below.

Primary Caution

Use this page to separate approved use from broader mechanism and protocol discussion.

Half-Life

~13 hours

Routes

Subcutaneous

Aliases

Victoza, Saxenda

Regulatory Posture

Backed by approved use and stronger late-stage evidence.

On this page

Overview

Liraglutide was Novo Nordisk’s first long-acting GLP-1 receptor agonist and the commercial predecessor to semaglutide. Approved as Victoza for type 2 diabetes in 2010, it became Saxenda (at higher dose) for obesity management in 2014 β€” marking the first time a GLP-1 agonist received approval specifically for weight management.

Though largely supplanted by semaglutide in prescribing practice (due to less frequent dosing and greater efficacy), liraglutide represented a landmark in metabolic medicine and established the clinical proof-of-concept for the GLP-1 class in cardiovascular risk reduction (LEADER trial, 2016).

Mechanism of Action

Liraglutide has 97% amino acid sequence homology with human GLP-1, modified with a C16 fatty acid chain (via a linker) enabling albumin binding and extending half-life from minutes (native GLP-1) to ~13 hours. This allows once-daily dosing.

Actions mirror the GLP-1 class:

  • Glucose-dependent insulin secretion
  • Glucagon suppression
  • Gastric emptying delay (satiety prolongation)
  • Hypothalamic appetite suppression
  • Direct cardiovascular effects (GLP-1R on cardiomyocytes)

Clinical Research & Evidence

Evidence Level: 🟒 EL1 β€” Multiple Phase III RCTs, FDA approved

TrialNKey Finding
LEADER9,34013% reduction in MACE (CV death, MI, stroke) vs. placebo in T2DM
SCALE Obesity3,7318.4% mean weight loss at 3.0 mg vs. 2.8% placebo (56 weeks)
SCALE Maintenance422Maintained weight loss vs. placebo after diet-induced weight loss

FDA-Approved Indications

  • Victoza (1.2–1.8 mg/day): Type 2 diabetes + CV risk reduction in T2DM with CVD
  • Saxenda (3.0 mg/day): Chronic weight management β€” adults BMI β‰₯30, or β‰₯27 with comorbidity; adolescents 12+ years, BMI β‰₯30 kg/mΒ²

Side Effects & Contraindications

Same class profile as semaglutide: nausea (most common), vomiting, constipation, pancreatitis (rare), thyroid C-cell tumor warning.

Contraindications:

  • Personal/family history of MTC or MEN2
  • Pregnancy

FDA approved (Victoza 2010, Saxenda 2014). EMA approved. Available globally.

Research Citations

  1. Marso SP, et al. Liraglutide and Cardiovascular Outcomes in Type 2 Diabetes. N Engl J Med. 2016 (LEADER).
  2. Pi-Sunyer X, et al. A Randomized, Controlled Trial of 3.0 mg of Liraglutide in Weight Management. N Engl J Med. 2015 (SCALE).
  3. Davies MJ, et al. Liraglutide in Pediatric Obesity. N Engl J Med. 2021.

Clinical Research

2 studies
EL1LEADER2016·New England Journal of Medicine
N=9,340

Liraglutide and Cardiovascular Outcomes in Type 2 Diabetes (LEADER)

Marso SP, Daniels GH, Brown-Frandsen K, et al.

Liraglutide 1.8 mg daily reduced MACE by 13% versus placebo in type 2 diabetes patients at high cardiovascular risk.

EL1SCALE Obesity2015·New England Journal of Medicine
N=3,731

A Randomized, Controlled Trial of 3.0 mg of Liraglutide in Weight Management (SCALE Obe...

Pi-Sunyer X, Astrup A, Fujioka K, et al.

Liraglutide 3.0 mg daily produced a mean weight loss of 8.4% versus 2.8% with placebo in adults with obesity, leading to FDA approval of ...

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