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Lixisenatide (Adlyxin)_Dosage, benefits & legal status

Also known as Adlyxin, Lyxumia, AVE0010

Published August 24, 2026 · Updated October 5, 2026

An approved GLP-1 that lost the race and left the US market.

Blood sugarGLP-1 receptor agonistFDA-approved
DoseSet by the label
FrequencyOnce daily
RouteUnder the skin (subcutaneous)
StatusFDA-approved (US marketing ended)
CycledSet by the prescription

Common vial size is what vendors typically sell, not a recommendation. Enter your own vial in the calculator.

See how this dose compares across the library →

01

What is Lixisenatide (Adlyxin)?

Plain language first. The technical label stays, but it never stands alone.

Overview

A real approved GLP-1 that got beaten by the weekly ones and pulled from the market. It still exists inside a combination pen with insulin.

The technical version

Lixisenatide, a short-acting GLP-1 receptor agonist, FDA-approved 27 July 2016 as Adlyxin for glycaemic control in adults with type 2 diabetes. Sanofi discontinued the standalone product globally for commercial reasons. The molecule remains available in the US inside Soliqua, a fixed-ratio combination with insulin glargine. The label carries warnings for anaphylaxis and acute pancreatitis and states it is not recommended in end stage renal disease.

What it's used for

A daily injected GLP-1 for type 2 diabetes. No longer marketed in the US on its own.

02

How does Lixisenatide (Adlyxin) work?

What it does in the body, and where.

Lixisenatide is a useful reference point for how quickly this drug class moved.

  1. 01
    It is a short-acting, meal-time GLP-1
    Given once daily, it acts mainly on the glucose rise after eating. Semaglutide and dulaglutide are weekly and act more on fasting glucose, which is part of why they displaced it.
  2. 02
    Approved in 2016, and largely gone by 2023
    The FDA approved it in July 2016. Sanofi discontinued it globally for commercial reasons, not safety ones, and it is no longer marketed as a standalone product in the US.
  3. 03
    It survives inside a combination product
    Soliqua pairs lixisenatide with insulin glargine in one pen, and that product remains available.
Receptors
HITSGLP-11

Acts on one receptor.

03

What else is it used for?

Each use below carries its own evidence level. Approved means regulators have cleared it for that purpose. Investigational means it is in trials. Early research means it is being studied and is not established.

  • Type 2 diabetes, alongside diet and exerciseFDA-approved
  • As part of Soliqua, a fixed combination with insulin glargineFDA-approved
  • Weight loss on its own, which is not its approved indicationnone

The published record

Research index

778

Papers and trials about Lixisenatide (Adlyxin)

376 papers tagged human · 184 not reviews or lab · 90 clinical trial publications

75 registered trials · 27 with posted results

Furthest stage reached: Approved in the US, no longer sold

Compare this against the whole library →

In animals69
In the lab1
Reviews155
Senior author shareSpread across many groups

Evidence summary

Counted from Europe PMC indexing, not read by a person; a human tag can land on reviews, commentary or lab papers; clinical trial publications is the narrower count. 461 papers and 75 trials indexed in detail.

Lixisenatide (Adlyxin) vial rendering
Compound field notes

At a glance

Four things to know about Lixisenatide (Adlyxin)

01

Evidence

FDA-approved

02

Category

Weight loss and metabolic

03

Common vial

Varies

04

Half-life

About 3 hours

04

How much, and do you cycle it?

The range, and whether you take breaks.

Set by the label, once daily. Set by the prescription FDA label

This is a prescription drug. Duration and schedule are set by the label and the prescriber, not by a cycling convention.

Compare this against the whole library →

05

How long does it stay in the body?

The half-life, and where the figure comes from.

About 3 hoursFDA label

Terminal half-life after repeated dosing in people with type 2 diabetes. This is the short-acting end of the GLP-1 family, which is why it is given once daily rather than weekly.

Source: Adlyxin label section 12.3

You can compare this against the whole library to see where it sits.

06

How do I dose and price it?

Enter your vial and your dose. Pick a mix. We show the draw and the cost.

The vial holds a fixed amount of drug. Adding more water does not make more drug, it just spreads it thinner, so you draw a bigger number on the syringe for the same dose.

Your vial size (mg)
Printed on the vial.
What you paid per vial
$
Used for cost per dose only.
Your dose (mcg)
Commonly referenced range: 10 up to 20 mcgFDA label

Choose your mix

This amount is too small to measure with any of these mixes. Check whether you meant mg or mcg.

your own mL
units · —
Enter your own volume

Measuring the water1 mL = one full 100-unit syringe.

YOUR DRAW0.2 / 100 units
0.2 units is a very small line to read, so a small slip is a large error. A larger water volume above spreads the same dose across more units.
07

How do you store it?

Before mixing, and after.

Dry powder in the freezer or fridge. Once mixed, fridge, and use within about a month.

Unmixed lyophilized Lixisenatide (Adlyxin) keeps for a long time cold. Once you add water the clock starts: most reconstituted vials hold up for roughly 28 to 30 days at fridge temperature. Keep it out of light, and do not freeze it after mixing.

08

What are the side effects and cautions?

Known cautions and warnings for this compound.

Solubility, computed: 39% charged residues, 32% hydrophobic. Water usually sufficient.

A first-pass rule from peptide manufacturers' guidance. It does not account for disulfide bridges, salt form or how the powder was dried, and it predicts what should be easy rather than what will happen in your vial.

Who should avoid it

Check these before anything else.
  • Severe hypersensitivity to lixisenatide or any component of the product
  • Pregnancy or breastfeeding, without medical advice
  • End stage renal disease, where the label says it is not recommended
  • A history of pancreatitis

Stop and get help

These are emergencies. Seek care.
  • Severe or persistent abdominal pain, which can signal pancreatitis
  • Signs of an allergic reaction, including facial or throat swelling or trouble breathing
  • Symptoms of very low blood sugar

Common effects

Expected, and usually mild.
  • Nausea
  • Vomiting
  • Headache
  • Low blood sugar when combined with other diabetes drugs
  • Injection site reactions

Where this page says nothing is established, that means nobody has studied it, not that a compound is safe.

09

Is Lixisenatide (Adlyxin) approved?

And where the numbers on this page come from.

Approved, but no longer sold in the United States. Lixisenatide (Adlyxin) was approved by the FDA, and the US product has since been discontinued.

  • Approval status
    FDA-approved
  • Route
    Under the skin (subcutaneous)
  • Checked
    24 August 2026
  • Dose
    From the drug label. The manufacturer tested this range and a regulator reviewed it.
  • Vial size
    From what vendors typically list; not a recommendation.
  • Sources
    None traced yet.

What has happened recently

FDA-approved 27 July 2016 as Adlyxin for type 2 diabetes. The standalone product was discontinued globally by Sanofi for commercial reasons, not safety. Lixisenatide remains available in the US within Soliqua, a fixed-ratio combination with insulin glargine.

Guides for this compound

Sources

No primary source has been traced for this compound yet. Treat everything on this page as unverified until one is. How we grade evidence

Beyond these, 536 records are indexed. Browse the records