Oxyntomodulin

Fat LossEndogenous dual GLP-1/glucagon receptor agonistExperimental

Oxyntomodulin is a glucagon receptor agonist in the GLP-1 Agonist class. Oxyntomodulin is produced from proglucagon in intestinal L cells and comprises the glucagon sequence plus an eight-residue C-terminal extension.

Calculate Dose

For research use only.

Key Facts

CAS
62340-29-8
Molecular Weight (MW)
4422 g/mol
Half-life
—
FDA status
Not Approved
Evidence level
Limited Human Evidence
Human dose established
No
Administration Route
Not established in humans
Frequency
Not established in humans
Last updated
Nov 7, 2026
Reviewed
Nov 7, 2026

Research summary

Naturally occurring 37-amino-acid gut hormone that activates both GLP-1 and glucagon receptors. It is the endogenous template for the dual-agonist drug class and is studied rather than marketed. Not FDA-approved.

Research evidence

  • Regulatory review (FDA label)None in reviewed sources
  • Controlled human trials4 reviewed sources
  • Early or uncontrolled human studiesNone in reviewed sources
  • Lab & animal studiesNone in reviewed sources
How it works

Each step shows whether the sources Peptide Library has reviewed include that kind of research. Counts are reviewed sources, not every study ever published. Reviews and programme summaries that describe human use are shown as "reported", not as trials, and registered trials without published results are listed but not counted. A higher step means research has progressed further; it does not mean a compound works better or is safer. Compounds whose evidence has not been reviewed yet show "Not reviewed" instead of a guess.

Peptide Library's Oxyntomodulin profile summarises 5 cited studies listed in the Science section, the compound's regulatory status, and research-protocol parameters reported for it. It is a research reference, not medical advice.

Oxyntomodulin dosage: no established human dose

Oxyntomodulin has no established human dosage. It is a natural gut hormone, and the human evidence is a handful of small experimental studies: intravenous infusions of 3.0 pmol/kg per minute in healthy volunteers, and self-injected doses under the skin three times a day before meals for 4 days or 4 weeks in people with overweight or obesity. The indexed abstracts of the injection studies do not give the amount injected.

Limited Human Evidence

No established human dosage.

Human clinical evidence: None identified.

Preclinical research: Oxyntomodulin is a peptide hormone made from proglucagon in the gut that acts on both the GLP-1 and glucagon receptors. People have received it only in small experimental studies: brief intravenous infusions in volunteers, and self-injections under the skin before meals for up to 4 weeks. These studies measured appetite, food intake, energy expenditure and short-term weight change; none tested a dose for treatment, and no oxyntomodulin product has been approved.

Animal dosing is not converted into a human dose anywhere on this page. Where research figures appear below, they are reported as studied, not recommended.

Dosage evidence summary for Oxyntomodulin
Human dosing establishedNo
RouteNot established; studied as an intravenous infusion and as subcutaneous injections
Evidence levelLimited Human Evidence
Last reviewed2026-11-07

Human research reported

Doses as studied, one row per regimen. Different trials used different regimens; they are listed separately rather than averaged.

Research-reported dosing for Oxyntomodulin, one row per studied regimen
Study / contextPopulationDoseRouteFrequencyDurationOutcome studiedSource
Intravenous infusion study (Cohen et al., 2003)Clinical trial · Randomized, double-blind, placebo-controlled crossover studyHealthy volunteers (n=13)3.0 pmol/kg per minuteIntravenous infusionSingle infusion per study visitAcute (crossover visits)Food intake at a buffet meal 19.3% lower than with saline; less hunger; no nauseaOxyntomodulin suppresses appetite and reduces food intake in humans. J Clin Endocrinol Metab. 2003.
Subcutaneous injection, 4 weeks (Wynne et al., 2005)Clinical trial · Randomized, double-blind, parallel-group controlled trialHealthy overweight and obese volunteers (n not stated in the indexed abstract)Not stated in the indexed abstractSubcutaneousThree times daily, 30 minutes before each meal4 weeksBody weight fell 2.3 kg against 0.5 kg with salineSubcutaneous oxyntomodulin reduces body weight in overweight and obese subjects: a double-blind, randomized, controlled trial. Diabetes. 2005.
Subcutaneous injection, 4 days (Wynne et al., 2006)Clinical trial · Randomized, double-blind, controlled crossover trialOverweight and obese men and women (n=15)Not stated in the indexed abstractSubcutaneousThree times daily before meals4 daysEnergy intake at a study meal 17.3% lower; activity-related energy expenditure 26.2% higherOxyntomodulin increases energy expenditure in addition to decreasing energy intake in overweight and obese humans: a randomised controlled trial. Int J Obes (Lond). 2006.
Infusion comparison with GLP-1 and glucagon (2015)Clinical trial · Double-blind, randomized crossover studyHealthy young men (n=15)3 pmol/kg per minuteIntravenous infusionSingle infusion per study visit4-hour meal testsFood intake fell by a similar amount with oxyntomodulin, GLP-1, glucagon and glucagon plus GLP-1; resting energy expenditure did not changeEffect of Oxyntomodulin, Glucagon, GLP-1, and Combined Glucagon+GLP-1 Infusion on Food Intake, Appetite, and Resting Energy Expenditure. J Clin Endocrinol Metab. 2015.

Where sources disagree

  • The infusion dose of 3 pmol/kg per minute is a research rate for a few hours in a clinic. It is not an injectable dose and does not convert into one.
  • Engineered dual GLP-1 and glucagon agonists such as cotadutide, survodutide and pemvidutide are different molecules. Their trial doses are not evidence for oxyntomodulin, and oxyntomodulin's studies are not evidence for them.

Sequence & molecular data

Sequence and molecular data for Oxyntomodulin
Molecular formulaC192H295N59O60S
Molecular weight4422 g/mol
CAS number62340-29-8
PubChem CID16144019
ChEMBLCHEMBL2401865

Identifiers link to the public PubChem, FDA Substance Registration (UNII), ChEMBL and DrugBank records for the same entity.

Science

Mechanism of Action

Oxyntomodulin is produced from proglucagon in intestinal L cells and comprises the glucagon sequence plus an eight-residue C-terminal extension. It is a relatively weak agonist at both the GLP-1 and glucagon receptors compared with the native ligand of each, but engaging both simultaneously combines GLP-1-mediated appetite suppression and insulin secretion with glucagon-mediated increases in energy expenditure. This combination is the pharmacological rationale behind engineered dual agonists such as cotadutide and survodutide.

Research statistics

301 PubMed publications · 19.1% human clinical research · 4 registered trials

Counts of published research through 2026-11-01, not evidence that it works. Publications by year, study types and trials · How publications are counted

Regulatory & research status

Oxyntomodulin is not an FDA-approved product. It is sold for laboratory research and has no approved medical use.

Regulatory and research status for Oxyntomodulin
FDA statusNot Approved
Research statusResearch-only compound; no approval pathway listed
AvailabilityResearch-Only
WADA (sport)Unknown / Not Listed
Library classificationResearch-Only

How FDA approval, compounding and research-only status differ

Benefits

—

Oxyntomodulin side effects

No side effects listed yet for this entry.

Storage & stability

This compound is not supplied as a powder to be mixed, so the freeze-dried powder and reconstitution handling described for research peptides does not apply. Storage conditions are product-specific: follow the label or packaging of the product itself.

Oxyntomodulin: frequently asked questions

What is Oxyntomodulin?

Naturally occurring 37-amino-acid gut hormone that activates both GLP-1 and glucagon receptors. It is the endogenous template for the dual-agonist drug class and is studied rather than marketed. Not FDA-approved.

How does Oxyntomodulin work?

Oxyntomodulin is produced from proglucagon in intestinal L cells and comprises the glucagon sequence plus an eight-residue C-terminal extension. It is a relatively weak agonist at both the GLP-1 and glucagon receptors compared with the native ligand of each, but engaging both simultaneously combines GLP-1-mediated appetite suppression and insulin secretion with glucagon-mediated increases in energy expenditure.

Is Oxyntomodulin FDA approved?

No. Oxyntomodulin is not approved by the FDA for any indication and is categorised as research-only. It has not been reviewed for safety or efficacy as a medicine, and published research should be read as investigation rather than established use.

What peptides are similar to Oxyntomodulin?

Compounds most often compared with Oxyntomodulin include Retatrutide, Survodutide, Pemvidutide and Cotadutide. They are grouped by shared mechanism or research area rather than by equivalence, and their regulatory status and evidence base differ.

References

Related research, comparisons & guides

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Compiled by Peptide Library Editorial · Reviewed Aug 30, 2026 · Updated Nov 7, 2026 · Version 2

This Oxyntomodulin profile is compiled from published literature (5 cited studies linked above), public regulatory records and chemical registries. It describes what research reports; it is not medical advice, and nothing here is a dosing recommendation for humans. Peptide Library does not sell peptides. Editorial policy · How profiles are compiled · Report an error

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