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Lixisenatide

Also known as: Adlyxin, Lyxumia, Soliqua (with glargine)

Once-daily GLP-1 receptor agonist approved in 2016 as Adlyxin for type 2 diabetes; US sales ended 2023, but it remains in Soliqua. Prescription.

Last updated

Mechanism of Action

Lixisenatide is a 44-amino-acid exendin-4 analog with a six-lysine C-terminal extension. It activates the GLP-1 receptor to increase glucose-dependent insulin secretion and suppress glucagon, and it slows gastric emptying more prominently than long-acting GLP-1 agonists. That makes its effect strongest on post-meal glucose after the meal it precedes.

Half-life
~3 hours
Administration Routes
Subcutaneous
Research Status
Clinical

Reported Benefits

  • Lowers post-meal and overall blood glucose in type 2 diabetes
  • Used with basal insulin as the fixed combination Soliqua 100/33
  • Cardiovascular safety shown in ELIXA after acute coronary syndrome
  • Studied for slowing motor progression in early Parkinson's disease

Potential Side Effects

  • Nausea, vomiting and diarrhea
  • Headache and dizziness
  • Hypoglycemia with insulin or sulfonylureas
  • Anaphylaxis and serious hypersensitivity (warning)
  • Pancreatitis (warning)

Common Dosing

Standalone Adlyxin was labeled at 10 mcg subcutaneously once daily for 14 days, then 20 mcg once daily, given within an hour before the first meal. Soliqua is dosed by its insulin glargine units. Dosing is set and supervised by the prescribing clinician.

The dosing information above is aggregated from research literature and anecdotal community reports for educational purposes only. It is not a recommendation, prescription, or medical advice. Peptides are sold as research chemicals only and are not intended for human use.

Contraindications

  • Serious hypersensitivity, including anaphylaxis, to lixisenatide
  • Not recommended with gastroparesis or severe kidney impairment
  • Lixisenatide in Patients with Type 2 Diabetes and Acute Coronary Syndrome

    2015

    View
  • Trial of Lixisenatide in Early Parkinson's Disease

    2024

    View

Yes. It was approved as Adlyxin in 2016, and as part of Soliqua 100/33 with insulin glargine in 2016. Sanofi stopped selling standalone Adlyxin in the US as of January 2023 for business reasons; Soliqua remains available.

A 2024 phase 2 trial found less progression of motor disability at 12 months versus placebo in early Parkinson's disease, with frequent gastrointestinal side effects. It is not approved for Parkinson's disease.

PeptideChat is for educational and research purposes only. Nothing on this site constitutes medical advice. Peptides are sold as research chemicals only and are not intended for human use. These statements have not been evaluated by the FDA and are not intended to diagnose, treat, cure, or prevent any disease. PeptideChat is an independent educational resource — not a pharmacy, compounding, or 503A/503B outsourcing facility — and does not sell products or provide medical advice.