Fat Loss + GLP-1sFDA-approvedApprovedUpdated 2026-04-24

Peptide reference file

Lixisenatide

Trending #17 in Fat8.4k searches/moProven

Lixisenatide is a GLP-1 receptor agonist used in approved metabolic-disease contexts.

Current readout: approved evidence, fda-approved status, approved approval state, human evidence appears in the current trail, registered trials are linked, and 3 linked sources in the seed trail.

PubChem CID 90472060 | 724 PubMed results | 75 trial records | 1 DailyMed label | 2 Drugs@FDA applications

Lixisenatide is mostly discussed because it rounds out the GLP-1 map and shows how much broader the incretin category is than the newest blockbuster names.

The public claim is straightforward: It rounds out the GLP-1 map and shows how much broader the incretin category is than the newest blockbuster names. Regulated GLP-1 therapy with source-backed human evidence.

In plain language, lixisenatide is a GLP-1 receptor agonist used in approved metabolic-disease contexts.

ApprovedFDA-approved
GLP-1 receptorGlucose controlAppetite signaling

Aliases: Adlyxin, Lyxumia

SpecimenLixisenatide specimen
CCCCHHHHHHHNOS
Formula
C215H347N61O65S
Mass
4858
Evidence
Approved
Elements
5

Most commonly discussed in relation to GLP-1 receptor, Glucose control, Appetite signaling.

What Lixisenatide is

Lixisenatide is a GLP-1 receptor agonist used in approved metabolic-disease contexts.

Lixisenatide is grouped under Fat Loss + GLP-1s / Approved / Clinical on PeptideFactCheck because it rounds out the GLP-1 map and shows how much broader the incretin category is than the newest blockbuster names.

The useful starting point is to separate the molecule itself from the internet story around it. It rounds out the GLP-1 map and shows how much broader the incretin category is than the newest blockbuster names.

Why people keep looking it up

It rounds out the GLP-1 map and shows how much broader the incretin category is than the newest blockbuster names.

Lixisenatide is a GLP-1 receptor agonist used in approved metabolic-disease contexts.

Lixisenatide tends to stay in the conversation because it touches a familiar public theme: glp-1 receptor, glucose control, and appetite signaling. That makes it easy for the claim to travel faster than the evidence.

What the evidence can support right now

Regulated GLP-1 therapy with source-backed human evidence.

Human trials and labeling support specific approved use cases.

Mechanistic support follows established GLP-1 receptor biology.

Why this page carries the current tier: Regulated GLP-1 therapy with source-backed human evidence.

The current seed trail for Lixisenatide is pulling from 1 labels source, 1 regulatory source, and 1 literature source.

Safety, limits, and regulatory context

Approved does not erase the need to read route, contraindication, and warning sections directly from labels.

FDA-approved lixisenatide products exist or have existed for specific indications depending on market timing.

Editorial boundary: PeptideFactCheck does not publish dosing, cycling, sourcing, injection, or administration instructions for Lixisenatide. The job here is to explain the public claim, the mechanism story, the evidence strength, and the current limits.

Molecular and identifier data

The current PubChem match for Lixisenatide is CID 90472060. That gives the page a source-backed chemistry record rather than a placeholder identifier block.

PubChem CID
90472060
Formula
C215H347N61O65S
Molecular weight
4858
InChIKey
XVVOERDUTLJJHN-IAEQDCLQSA-N

Matched synonyms include Lixisenatide, Adlyxin, Lyxumia, ZP10A peptide, 320367-13-3, ZP 10, AVE0010, AQVE-10010.

Open PubChem record

Clinical trial snapshot

The current ClinicalTrials.gov intervention query for Lixisenatide returns 75 study records. This does not prove efficacy by itself, but it does show whether the peptide is showing up in a formal trial registry rather than only in forums or vendor copy.

Literature snapshot

The current PubMed query for Lixisenatide returns 724 results. The articles below are a quick literature surface so the page shows actual papers instead of only generic evidence labels.

Label and regulatory records

For approved or clinically developed peptides, the page now pulls in official labeling and FDA-facing records where they exist. That makes the regulatory section materially more useful than a generic approved or not-approved tag.

Brand names
Soliqua 100/33
Generic names
INSULIN GLARGINE AND LIXISENATIDE
Routes
SUBCUTANEOUS
Application numbers
BLA208673

Indications and usage. 1 INDICATIONS AND USAGE SOLIQUA 100/33 is a combination of insulin glargine and lixisenatide and is indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. SOLIQUA 100/33 is a combination of insulin glargine, an insulin analog, and lixisenatide, a glucagon-like peptide-1 (GLP-1) receptor agonist, indicated as an adjunct to diet and exercise to improve glycemi...

Warnings and cautions. 5 WARNINGS AND PRECAUTIONS Anaphylaxis and Serious Hypersensitivity Reactions : Severe, life-threatening, and generalized allergic reactions can occur. Instruct patients to discontinue use if a reaction occurs and promptly seek medical attention. ( 5.1 ) Acute Pancreatitis : Has been observed in patients treated with GLP-1 receptor agonists, including SOLIQUA 100/33. Discontinue if pancreatitis is suspected. ( 5.2 )...

Contraindications. 4 CONTRAINDICATIONS SOLIQUA 100/33 is contraindicated: During episodes of hypoglycemia [see Warnings and Precautions (5.6) ] . In patients with serious hypersensitivity to insulin glargine, lixisenatide, or any of the excipients in SOLIQUA 100/33. Hypersensitivity reactions including anaphylaxis have occurred with both lixisenatide and insulin glargine [see Warnings and Precautions (5.1) and Adverse Reactions (6.1)...

Source trail

Each linked source is shown directly so the page can be audited. The page now combines its editorial seed trail with automated official-source enrichment generated on 2026-04-24 from PubChem, ClinicalTrials.gov, PubMed, DailyMed, openFDA label, and Drugs@FDA.

Safety noteThis content is educational only and does not replace medical advice. Peptide use may carry risks and should be discussed with a qualified medical professional.