CalcMyPeptide
GLP-1 AgonistAlso known as: Victoza, Saxenda

Liraglutide

First-generation once-daily GLP-1 receptor agonist FDA-approved for type 2 diabetes (Victoza) and weight management (Saxenda 3 mg). The predecessor to semaglutide with a shorter half-life requiring daily dosing.

Half-Life
~13 hours
Dose Range
0.6-3 mg/day
Frequency
1× daily
Vial Sizes
6 mg, 18 mg

🔬 Mechanism of Action

Liraglutide is a GLP-1 receptor agonist with 97% sequence homology to native human GLP-1. A C18 fatty acid chain attached to Lys26 enables reversible albumin binding, extending the half-life from ~2 minutes (native GLP-1) to approximately 13 hours — enabling once-daily dosing.

Liraglutide activates the GLP-1 receptor via multiple pathways: (1) Glucose-dependent insulin secretion from pancreatic beta cells — only active when blood glucose is elevated, reducing hypoglycemia risk. (2) Glucagon suppression from pancreatic alpha cells. (3) Gastric emptying delay — slowing nutrient absorption and extending satiety. (4) Central appetite suppression via hypothalamic GLP-1 receptors and the brainstem area postrema, reducing food intake by 15-30%.

The LEADER cardiovascular outcomes trial (2016) demonstrated a 13% reduction in major cardiovascular events in T2D patients, establishing GLP-1 agonists as cardioprotective — a class effect extended and amplified in subsequent semaglutide and tirzepatide trials.

Source: FDA Label (Saxenda), PMID: 24665709 (SCALE trial)

📜Background & History

Liraglutide was developed by Novo Nordisk and approved by the FDA in 2010 as Victoza for type 2 diabetes and in 2014 as Saxenda (3 mg/day) for obesity — making it the first GLP-1 agonist approved specifically for weight management. It has 97% sequence homology to human GLP-1 and a C18 fatty acid chain that enables albumin binding, extending the half-life from 2 minutes (native GLP-1) to 13 hours. Clinical trials (SCALE, 2015) demonstrated 8% body weight loss at the 3 mg dose. While now partially succeeded by semaglutide in the market, liraglutide remains widely prescribed globally due to its long safety record (13+ years), mature generics pipeline, and once-daily dosing flexibility.

🎯 Research Use Cases

  • Type 2 diabetes management (Victoza, 1.2-1.8 mg/day)
  • Chronic weight management (Saxenda, 3 mg/day)
  • Cardiovascular risk reduction in T2D (LEADER trial: 13% CV mortality reduction)
  • NASH (non-alcoholic steatohepatitis) — signal in Phase II trials
  • Bridging therapy before higher-potency GLP-1 agents

💉 Dosing Protocol

Typical Dose0.6-3 mg/day
Frequency1× daily
Half-Life~13 hours
Common Vial Sizes6 mg, 18 mg

🧪 Reconstitution Example

Vial
6 mg
Water
2 mL
Concentration
3 mg/mL
Per Unit (100u syringe)
30 mcg
Dose of 600 mcg = 20 units on a 100-unit insulin syringe

⚠️Safety & Considerations

FDA-approved for T2D (Victoza) and weight management (Saxenda). Well-established safety profile with 13+ years of real-world data. Common side effects: nausea, vomiting, diarrhea (usually transient). Boxed warning: thyroid C-cell tumor risk (rodent data) — contraindicated in personal/family history of medullary thyroid carcinoma or MEN 2. Monitor for pancreatitis. Not recommended in pregnancy.

Interactions & Contraindications

Same MTC/MEN2 contraindications as all GLP-1 agonists. Daily injections vs weekly for semaglutide — important adherence consideration. GI side effects (nausea, diarrhea) are more sustained than semaglutide due to shorter half-life creating less smooth exposure. Adjust timing of oral medications (slowed gastric emptying affects absorption). Pancreatitis risk — discontinue if persistent abdominal pain.

🔗Synergies & Common Stacks

BPC-157's GI-protective effects may help manage liraglutide-induced nausea and gastric side effects during dose escalation, improving tolerability.

Liraglutide drives appetite suppression and metabolic improvement; AOD-9604 adds targeted lipolysis. Complementary fat loss approaches without GLP-1 receptor overlap.

Liraglutide dosing guide infographic showing dose range 0.6-3 mg/day, half-life ~13 hours, and reconstitution example
Liraglutide dosing quick reference — 0.6-3 mg/day, 1× daily

Frequently Asked Questions

How does Saxenda (liraglutide) differ from Ozempic (semaglutide)?
Saxenda/liraglutide requires daily injections and has a 13-hour half-life; Ozempic/semaglutide requires weekly injections with a 7-day half-life. Semaglutide also achieves greater weight loss (~15-17% vs ~8% for liraglutide). However, liraglutide has a longer real-world safety record and is available as a generic in some markets.
What is the Saxenda dose escalation schedule?
Start at 0.6 mg/day for week 1, increase to 1.2 mg for week 2, then 1.8 mg for week 3, then 2.4 mg for week 4, then maintenance at 3.0 mg/day. Slow escalation minimizes GI side effects. Use our GLP-1 Dose Escalation Calculator for your schedule.
Can I inject liraglutide anywhere?
Yes — subcutaneous injection into the abdomen, thigh, or upper arm. Rotate injection sites. Unlike insulin, liraglutide does not need to be injected at the same time each day (consistent daily timing is still preferred).
Is compounded liraglutide available?
Yes — compounded liraglutide has been available from 503A pharmacies. Unlike semaglutide, liraglutide's compounding status is somewhat less regulated. Consult a licensed provider and verify pharmacy credentials before sourcing.

📖 References

  1. Armstrong MJ, et al. Liraglutide safety and efficacy in patients with non-alcoholic steatohepatitis (LEAN).” Lancet (2016). PMID: 26318520
  2. Pi-Sunyer X, et al. A randomized, controlled trial of 3.0 mg of liraglutide in weight management.” N Engl J Med (2015). PMID: 26132939

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