Glucagon

AApproved (Rx)Established peptide medicines →GvokeBaqsimiGlucaGen
In one paragraphGlucagon is the 29-amino-acid pancreatic hormone that mobilises stored glucose from the liver, and the emergency treatment for severe hypoglycaemia in people with diabetes. Modern formulations removed the reconstitution step that made the old kits hard to use in a crisis: a ready-to-use injection and a nasal powder. In a 75-person crossover trial the nasal powder raised blood glucose successfully at all but one dosing visit, against all visits for intramuscular injection. It is prescription-only everywhere LYO covers.
Schematic 3D structure of Glucagon
29 residues · helical in solution at the C-terminus · schematic
Overall gradeA Established
Human trialsDecades of use; randomised crossover trials of newer formulations
Outcomes graded4
Last reviewed29 October 2026
EvidenceWhat it isHow it worksUnknownsMolecule & PKRegulationQuestionsReferences

What the human research shows

The counterpart to insulin, and on this site for the same reason: a peptide whose evidence is settled and whose dose–response is unambiguous. Grade A — and a useful reminder that the newer formulations were approved on pharmacodynamic equivalence, not on outcome trials.

MetabolicCardioMuscleHealingNeuroImmuneSexualSkinAgeing

Evidence profile0–5

  • Metabolic & weight—0.0
  • Cardiovascular—0.0
  • Muscle & growthD0.0
  • Healing & repair—0.0
  • Neuro & sleep—0.0
  • Immune & inflammation—0.0
  • Sexual & hormonal—0.0
  • Skin & appearance—0.0
  • Ageing & longevity—0.0
No benefit outcome for Glucagon has both human evidence and a measurable effect, so the profile is empty. That is the finding, not a gap in the chart.
OutcomeGradeEffect sizeHuman studiesWhere the evidence comes from
Reversal of severe hypoglycaemiaAEstablishedLargeDecades of use; approval programmeThe licensed indication: glucagon raises blood glucose within minutes by mobilising hepatic glycogen, and is the standard rescue treatment when someone with diabetes cannot take sugar by mouth. The effect is large, fast and uncontested.23
Nasal versus intramuscular deliveryAEstablishedModerate1 randomised crossover trial (n=75)Seventy-five adults with type 1 diabetes received insulin-induced hypoglycaemia and then either the 3 mg nasal powder or 1 mg intramuscular glucagon, each at separate visits. Treatment success was reached at all but one nasal visit and at every intramuscular visit — the basis for approving a formulation a bystander can actually use.1
Nausea and local discomfortadverseAEstablishedModerate1 randomised crossover trial (n=75); approval programmeNausea is intrinsic to glucagon and occurred at a third of visits by either route; the nasal route adds head and facial discomfort. Side effects that matter less than the hypoglycaemia being treated, and worth knowing before the emergency.1
Use for weight loss or body compositionDNo human evidenceNot measurableNoneGlucagon receptor agonism is part of several investigational obesity drugs (survodutide, mazdutide, pemvidutide, retatrutide) because it raises energy expenditure. Glucagon itself has no trial as a weight-loss treatment, is given by emergency routes, and raises blood glucose — the opposite of what a diabetes treatment is for.
AMultiple good human trials, consistentBSome human trials, mostly consistentCFew or weak human studiesDAnimal or anecdotal onlyeffect size · red = adverse

Literature searched to 29 October 2026. Human studies only; animal and cell work informs the mechanism section and nothing else.

Registered trials

ClinicalTrials.gov lists 12 interventional studies naming Glucagon as an intervention — 10 completed, 1 recruiting, and 9 with results posted to the registry.

A registration is not a result. Anyone can register a study, and many never report — so this list shows what has been attempted, not what has been shown. The graded evidence above is the answer to whether something works.

StudyPhaseStatusParticipantsSponsorResults
G-Pen Compared to Glucagen Hypokit for Severe Hypoglycemia Rescue in Adults With Type 1 DiabetesNCT03738865 · started Sept 2018Phase 3Completed132Xeris PharmaceuticalsPosted
Trial to Confirm the Efficacy and Safety of Dasiglucagon in the Treatment of Hypoglycemia in T1DM ChildrenNCT03667053 · started Sept 2018Phase 3Completed42Zealand PharmaPosted
Clinical Usability of Nasal Glucagon in Treatment of Hypoglycemia in Children and AdolescentsNCT02402933 · started Mar 2015Phase 3Completed26Eli Lilly and CompanyPosted
Glucagon Infusion in T1D Patients With Recurrent Severe Hypoglycemia: Effects on Counter-Regulatory ResponsesNCT03490942 · started Mar 2018Phase 2Terminated49Xeris PharmaceuticalsPosted
Safety, Tolerability, Pharmacokinetic (PK) and Pharmacodynamic (PD) Study of G-Pen(TM) (Glucagon Injection) to Treat Severe HypoglycemiaNCT01972152 · started Oct 2013Phase 2Completed30Xeris PharmaceuticalsPosted
Mini-Dose Glucagon to Treat Non-Severe HypoglycemiaNCT02411578 · started Sept 2015Phase 2Completed26Jaeb Center for Health ResearchPosted
Feasibility Trial Testing the Bionic Pancreas With ZP4207NCT02971228 · started Nov 2016Phase 2Completed13Zealand PharmaPosted
A Study Comparing User Experience of Different Delivery Devices for GlucagonNCT03765502 · started Nov 2018Phase 1Completed99Eli Lilly and CompanyPosted

4 further studies are registered. Participant counts marked * are the sponsor's estimate, not a final enrolment. Source: ClinicalTrials.gov, read directly from the registry and refreshed weekly.

What it is

Glucagon is a 29-amino-acid peptide released by pancreatic alpha-cells when blood glucose falls, and insulin's opposite number. As a medicine it has been in use since the 1960s, originally as a powder requiring reconstitution immediately before injection — a design that failed in practice, because severe hypoglycaemia leaves the patient unable to perform the steps and the bystander untrained. The current products are a ready-to-use subcutaneous injection (Gvoke) and a nasal powder (Baqsimi).

It is also used diagnostically — to relax the gut during imaging — and in hospital for beta-blocker overdose. On this site it sits alongside insulin as half of the glucose-regulation pair, and as the hormone whose receptor the newest obesity peptides deliberately activate.

How it is thought to work

Glucagon receptor activation in hepatocytes triggers glycogenolysis and gluconeogenesis, raising blood glucose within minutes, and increases lipolysis and energy expenditure in other tissues. The half-life is short — about half an hour by either route — which is why it is a rescue treatment rather than a maintenance one, and why food follows the injection.

What is still unknown

  • Nothing material about the emergency use; this is settled pharmacology.
  • Whether sustained glucagon receptor agonism is safe long-term — the question the dual and triple agonists will answer.

The molecule and how long it lasts

Identity
Formula
C153H225N43O49S
Molecular weight
3482.7 g/mol
CAS number
9007-92-5
PubChem
CID 16132283
Sequence
HSQGTFTSDYSKYLDSRRAQDFVQWLMNT

PubChem record, read 29 October 2026; the sequence was derived from that record's own structure and checked against the product label where one exists.

Pharmacokinetics
Route
Subcutaneous injection; also intranasal powder (Baqsimi), intramuscular and intravenous
Half-life
About 32 minutes subcutaneously; median about 35 minutes intranasally
Licensed regimen (Gvoke)
A single dose for severe hypoglycaemia, with a second dose if there is no response and emergency assistance called; the dose depends on the product and the person's age and weight

From the approved product's prescribing information: Gvoke prescribing information (DailyMed) The regimen is the label's own wording, reproduced as a regulatory fact.

Regulatory status

European Union
Approved, prescription-only

GlucaGen HypoKit and Baqsimi authorised for severe hypoglycaemia; also authorised for diagnostic use.

United States
Approved, prescription-only

Gvoke (ready-to-use injection, 2019) and Baqsimi (nasal powder, 2019), alongside older reconstituted kits.

United Kingdom
Licensed, prescription-only

GlucaGen HypoKit and Baqsimi licensed by the MHRA.

Australia
Registered, Schedule 4

GlucaGen HypoKit registered on the ARTG.

Canada
Authorised, prescription-only

Baqsimi and glucagon injection authorised with Drug Identification Numbers.

Sport (WADA)
Not prohibited

Not named on the Prohibited List.

Questions people actually ask

What is glucagon used for?
Emergency treatment of severe hypoglycaemia in people with diabetes, when they cannot safely take sugar by mouth. It is also used to relax the gut for imaging and in hospital for certain overdoses.
Does the nasal spray work as well as the injection?
In a 75-person crossover trial the nasal powder met the treatment-success criterion at all but one dosing visit, and injection at every visit. The point of the nasal product is that a frightened bystander can give it without assembling anything.
If glucagon burns fat, can it be used for weight loss?
No. Glucagon raises blood glucose and has a half-life of about half an hour; it has never been trialled for weight loss. Its receptor is one of the targets the investigational dual and triple agonists activate alongside GLP-1 — that is a different kind of molecule.

One page per claimed effect

References

  1. 1
  2. 2
    Gvoke (glucagon injection) prescribing information.DailyMed, read 29 Oct 2026Route, half-life and licensed use of the ready-to-use subcutaneous injection.
  3. 3
    Baqsimi (glucagon nasal powder) prescribing information.DailyMed, read 29 Oct 2026Nasal route; median half-life about 35 minutes.
  4. 4
    PubChem compound record: glucagon.PubChem, read 29 Oct 2026Formula, molecular weight, CAS and the 29-residue sequence used on this page.

Change log

  • 2026-10-29Initial publication. Grade A on the approval programme and the nasal-versus-intramuscular crossover trial.