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Peptide Profile

Liraglutide

Victoza · Saxenda

Liraglutide is a glucagon-like peptide-1 (GLP-1) receptor agonist approved for chronic weight management and type 2 diabetes, formulated as a daily subcutaneous injection that reduces appetite by activating GLP-1 receptors in the…

MetabolicFDA ApprovedPrescription
Used forfat loss
Half-life
13 hours
Routes
subcutaneous

Educational research information — not medical advice. Review primary sources and consult a qualified professional before any decision.

Educational research tools — not medical advice.

Overview

What Liraglutide is

About Liraglutide

GLP-1 receptor agonist; slows gastric emptying, increases satiety, reduces glucagon secretion

Liraglutide is a glucagon-like peptide-1 (GLP-1) receptor agonist approved for chronic weight management and type 2 diabetes, formulated as a daily subcutaneous injection that reduces appetite by activating GLP-1 receptors in the hypothalamus and brainstem. It mimics endogenous incretin hormone action — slowing gastric emptying, increasing satiety signaling, and reducing caloric intake through central and peripheral GLP-1 receptor pathways. The landmark SCALE Obesity trial, a large multicenter randomized controlled trial published in the New England Journal of Medicine, demonstrated significant weight loss of approximately 8% at 56 weeks with 3.0 mg liraglutide (Saxenda) compared to placebo. Liraglutide is an FDA-approved prescription medication available as Victoza (type 2 diabetes, 1.8 mg) and Saxenda (chronic weight management, 3.0 mg); it requires physician supervision and is contraindicated in patients with a personal or family history of medullary thyroid carcinoma. Liraglutide vs semaglutide: key distinctions Liraglutide is a daily subcutaneous injection; semaglutide is weekly. The dosing frequency difference reflects half-life: liraglutide's plasma half-life is approximately 13 hours, requiring daily administration to maintain therapeutic levels; semaglutide's albumin-binding modification extends its half-life to approximately 7 days. For weight management outcomes, semaglutide significantly outperforms liraglutide: STEP 1 reported ~15% mean weight reduction vs ~8% with liraglutide in SCALE. The practical implication is that liraglutide is generally appropriate for patients who have contraindications to once-weekly GLP-1 therapy, who are already established on liraglutide for T2D (Victoza), or who are in a jurisdiction where semaglutide is less accessible. Liraglutide has a longer post-approval safety record — it was approved in 2010 for T2D and 2014 for obesity management — while semaglutide's obesity indication was approved in 2021. The LEADER trial established cardiovascular risk reduction for liraglutide in T2D patients, adding an outcomes benefit beyond glucose control. Liraglutide cost and access: As a branded pharmaceutical (Victoza, Saxenda), liraglutide requires a prescription from a licensed provider. Saxenda (3.0mg/day for obesity) has an approximate monthly list price of $1,300–$1,500 USD; actual cost varies by insurance coverage and assistance programs. Generic liraglutide is now available in the US: the FDA approved a generic of Victoza (liraglutide for type 2 diabetes; Hikma) in December 2024, and a generic of Saxenda (liraglutide for weight management; Teva) was approved and launched in August 2025. Compounding pharmacies do not commonly produce liraglutide formulations given the availability of approved branded products. Providers offering GLP-1 agonist programs that include liraglutide are searchable in the PeptideBase provider directory.

Liraglutide Benefits & Research Areas

appetite suppressionweight lossblood sugar regulation

Research Signals

Commonly researched in the context of

Sedentary

Population research notes

30s40s50+

These signals reflect research interest areas, not treatment indications.

Pharmacokinetics

Liraglutide half-life calculator

Compound & timing

Half-lifefrom PeptideBase data
Source: "13 hours" · Liraglutide (PeptideBase)
to show amount remaining
13 h
0%25%50%75%100%01427415468time since dose (h)
Plasma decay curve for Liraglutide: 50% remaining at 13 h after the dose.
plasma level
50%remaining in plasmaat 13 h after the dose
Half-life
13 h
~97% cleared after
2.7 days

Model: single-dose, first-order (single-compartment) estimate. Real clearance is multi-compartment and varies by individual and route.

The Research

What the evidence says about Liraglutide

Research Evidence

based on 8 studies · 2 RCTs · most recent 2026

Regulatory Status

Availability Status
Prescription
FDA Status
FDA Approved
Effective Date
January 25, 2010

FDA-approved GLP-1 agonist. Victoza (NDA 022341, Jan 2010) for T2D; Saxenda (NDA 206321, Dec 2014) for weight management. Prescription only. Generic liraglutide available (generic Victoza, Dec 2024; generic Saxenda, Aug 2025).

Regulatory status reflects publicly available information and may change. This is not legal or medical advice.

Research Sources

8 sources cited · 3 strong · 5 weak

2 RCTs · 1 Meta-analysis · 3 Reviews · 2 Animals

  • Comparative Effects of Individual Glucagon-Like Peptide-1 Receptor Agonist-Based Medications on Direct Measurement of Body Composition Among Adults With Overweight or Obesity With or Without Type 2 Diabetes: A Systematic Review and Network Meta-Analysis of Randomised Controlled Trials.

    Diabetes Obes Metab · 2026

    # Summary Research found that among adults with overweight or obesity, subcutaneous GLP-1 receptor agonists—including liraglutide at higher doses—effectively reduced body fat and fat deposits while also producing reductions in lean mass that were most pronounced at higher treatment doses. This study demonstrated that while these medications substantially improve excess adiposity measures, their use is associated with unfavorable effects on lean tissue, particularly at elevated dosing levels.

    Meta-analysisStrongPMID 42209204
  • Semaglutide vs liraglutide for weight loss in adults with overweight or obesity

    JAMA · 2022

    The STEP 8 trial found that once-weekly subcutaneous semaglutide 2.4 mg reduced mean body weight by 15.8% compared with 6.4% for once-daily liraglutide 3.0 mg over 68 weeks in adults with overweight or obesity, providing direct comparative evidence for GLP-1 receptor agonist weight loss efficacy.

    RCTn=338StrongPMID 35015037
  • A randomized, controlled trial of 3.0 mg of liraglutide in weight management

    New England Journal of Medicine · 2015

    The SCALE Obesity and Prediabetes trial found that once-daily liraglutide 3.0 mg reduced mean body weight by 8.4 kg compared with 2.8 kg for placebo over 56 weeks in adults with overweight or obesity, with 63.2% of participants achieving at least 5% weight loss.

    RCTn=3,731StrongPMID 26132939
Show 5 more sources
  • Effects of the GLP-1 receptor agonist liraglutide on bupivacaine-induced sciatic nerve block in a rat model.

    J Anesth · 2026

    AnimalWeakPMID 42377486
  • Effects of the glucagon-like peptide-1 receptor agonist liraglutide on retinal endothelial function and oxidative stress during sepsis.

    Front Pharmacol · 2026

    AnimalWeakPMID 42375616
  • Beyond weight loss: multisystem benefits of obesity medications.

    Lancet Diabetes Endocrinol · 2026

    This systematic review of RCT and meta-analysis data found that liraglutide and other GLP-1 receptor agonists produce clinically meaningful multisystem benefits beyond weight loss, including improvements in type 2 diabetes, cardiovascular disease, metabolic liver disease, sleep apnoea, and depression, with growing evidence for direct weight-independent receptor-mediated effects.

    ReviewTheoreticalPMID 42208956
  • GLP-1 receptor agonists in pediatric obesity and diabetes: a systematic review of efficacy, metabolic effects, and safety.

    Diabetes Res Clin Pract · 2026

    ReviewTheoreticalPMID 42365860
  • GLP-1 Receptor Agonists and the Ocular Surface: A Narrative Review of Restoration, Remodeling, and Clinical Implications.

    Ophthalmol Ther · 2026

    ReviewTheoreticalPMID 42366332

Liraglutide Side Effects & Safety Considerations

Contraindications below are derived from the compound’s FDA label. Educational only — not medical advice.

Boxed warning — most serious warning class

Risk of thyroid C-cell tumors (dose- and duration-dependent in rodents; human relevance undetermined).

Absolute contraindications

Situations where this compound should not be used. Educational only — not medical advice.

Personal or family history of medullary thyroid carcinoma (MTC)Multiple Endocrine Neoplasia syndrome type 2 (MEN 2)Known hypersensitivity to the drug or excipients

Warnings & cautions

Acute pancreatitisPregnancy (discontinue; not for use in pregnancy)Gallbladder disease / cholelithiasisDiabetic retinopathy complications (reported with GLP-1 receptor agonist use)Severe GI disease / gastroparesis / ileus riskHypoglycemia when combined with insulin or sulfonylureasAcute kidney injury secondary to volume depletion

Source: FDA label

Common monitoring markers in research protocols

Under clinical review

Being verified by our medical team before we display monitoring guidance for this peptide.

Consult a qualified healthcare professional before making any health decisions. This information is educational only and does not constitute medical advice.

Frequently Asked Questions — Liraglutide

Liraglutide is a glucagon-like peptide-1 (GLP-1) receptor agonist approved for chronic weight management and type 2 diabetes, formulated as a daily subcutaneous injection that reduces appetite by activating GLP-1 receptors in the hypothalamus and brainstem. It mimics endogenous incretin hormone action — slowing gastric emptying, increasing satiety signaling, and reducing caloric intake through central and peripheral GLP-1 receptor pathways.

appetite suppression, weight loss, blood sugar regulation.

Research on Liraglutide primarily documents effects related to appetite suppression and weight loss and blood sugar regulation. These are areas covered in preclinical and clinical literature — individual response varies and effects depend on context of use.

Reported contraindications and considerations for Liraglutide include Personal or family history of medullary thyroid carcinoma (MTC), Multiple Endocrine Neoplasia syndrome type 2 (MEN 2), Known hypersensitivity to the drug or excipients. 7 additional considerations are noted in the safety profile above. This is educational information only — consult a qualified healthcare professional before use.

For Liraglutide, its FDA status is FDA-approved, and it is available by prescription. Regulatory status reflects publicly available information and may change. This is not legal or medical advice.

48 providers in the directory currently offer Liraglutide.

# Summary Research found that among adults with overweight or obesity, subcutaneous GLP-1 receptor agonists—including liraglutide at higher doses—effectively reduced body fat and fat deposits while also producing reductions in lean mass that were most pronounced at higher treatment doses. This study demonstrated that while these medications substantially improve excess adiposity measures, their use is associated with unfavorable effects on lean tissue, particularly at elevated dosing levels.

Access

How to get Liraglutide

Where to buy Liraglutide

48 providers
39 Clinics5 Telehealth2 Pharmacies2 Online Vendors52 in stock

Questions to ask your provider

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