Insulin

AApproved (Rx)Bone and endocrine peptide medicines →insulin humanHumulinNovolin
In one paragraphInsulin is the 51-amino-acid hormone that lets cells take up glucose; recombinant human insulin and its engineered analogues are the treatment for type 1 diabetes and a mainstay of type 2. The landmark trials are settled: intensive insulin therapy cut new diabetic eye disease by 76% over six and a half years in the DCCT, and intensive glucose control reduced microvascular complications by a quarter over ten years in UKPDS. The cost, quantified in the same trials, is severe hypoglycaemia. It is on this site as the reference peptide, and because it is on WADA's list.
Schematic 3D structure of Insulin
51 residues · two chains linked by three disulfide bonds · schematic
Overall gradeA Established
Human trialsDCCT (n=1,441), UKPDS (n=3,867) and a century of use
Outcomes graded4
Last reviewed7 October 2026
EvidenceWhat it isHow it worksUnknownsMolecule & PKRegulationQuestionsReferences

What the human research shows

The benchmark every other page is implicitly compared against: large randomised trials with hard endpoints, decades of follow-up, and a serious, well-measured harm. Grade A throughout.

MetabolicCardioMuscleHealingNeuroImmuneSexualSkinAgeing

Evidence profile0–5

  • Metabolic & weight—0.0
  • Cardiovascular—0.0
  • Muscle & growth—0.0
  • 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 Insulin 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
Diabetic retinopathy (type 1, intensive vs conventional)AEstablishedLarge1 large RCT (DCCT, n=1,441, 6.5 yr)Intensive insulin therapy — pump or three or more daily injections with frequent glucose monitoring — reduced new retinopathy by 76% and slowed existing retinopathy by 54%. Kidney and nerve complications fell too.1
Microvascular complications (type 2)AEstablishedModerate1 large RCT (UKPDS 33, n=3,867, 10 yr)Intensive glucose control with insulin or a sulphonylurea cut microvascular endpoints by 25% over ten years in newly diagnosed type 2 diabetes; the effect on heart attacks and deaths did not reach significance in the main trial, though it emerged in the ten-year follow-up.2
Severe hypoglycaemiaadverseAEstablishedLargeBoth landmark RCTsThe defining harm. Intensive therapy in the DCCT roughly tripled severe hypoglycaemia; in UKPDS the rate of major episodes on insulin was 1.8% a year against 0.7% on conventional treatment.12
Weight gainadverseAEstablishedSmallUKPDS and manyIntensive treatment added about 2.9 kg over ten years in UKPDS — the reason insulin is the wrong tool for anyone seeking to lose weight and one reason the GLP-1 drugs exist.2
AMultiple good human trials, consistentBSome human trials, mostly consistentCFew or weak human studiesDAnimal or anecdotal onlyeffect size · red = adverse

Literature searched to 7 October 2026. Human studies only; animal and cell work informs the mechanism section and nothing else.

Registered trials

ClinicalTrials.gov lists 66+ interventional studies naming Insulin as an intervention — 41 completed, 4 recruiting, and 12 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
A Clinical Trial Comparing Efficacy and Safety of Exubera® and Humalog®NCT00356421 · started Nov 2006Phase 4Terminated58PfizerPosted
Additional Insulin for Fat and Protein in Children With Diabetes StudyNCT02680054 · started Feb 2016Phase 4Terminated38Oxford University Hospitals NHS TrustPosted
Comparison of Insulins Aspart and Lispro in Insulin PumpsNCT00461331 · started Oct 2004Phase 4Completed20Tulane University Health Sciences CenterPosted
A Study of the Safety and Efficacy of MK-1293 Compared to Lantus™ in Participants With Type 1 Diabetes Mellitus (T1DM) (MK-1293-003)NCT02059161 · started Oct 2013Phase 3Completed508Merck Sharp & Dohme LLCPosted
Efficacy and Safety of Continuous Subcutaneous Insulin Infusion of Faster-acting Insulin Aspart Compared to NovoRapid® in Adults With Type 1 DiabetesNCT02825251 · started Jul 2016Phase 3Completed472Novo Nordisk A/SPosted
Exubera vs Lispro in a Lantus-based Regimen for Improved Glycemic Control in Type 2 DiabetesNCT00348374 · started Jun 2006Phase 3Completed191PfizerPosted
Feasibility Trial Testing the Bionic Pancreas With ZP4207NCT02971228 · started Nov 2016Phase 2Completed13Zealand PharmaPosted
Safety and Effectiveness Study of Intranasal Insulin Glulisine on Cognitive and Memory in Mild-Mod AD Patients.NCT01436045 · started Sept 2011Phase 2Completed12HealthPartners InstitutePosted

58 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

Insulin is a 51-amino-acid protein in two chains held by three disulfide bonds, made in the pancreas and, since 1922, given by injection to people who cannot make enough. Animal insulin gave way to recombinant human insulin in 1982 — the first recombinant medicine of any kind — and then to analogues with altered absorption: rapid (lispro, aspart, glulisine) and long-acting (glargine, detemir, degludec).

It sits on this site as the compound against which every grey-market claim should be read: a real peptide, with real trials, a real effect, and a real, dose-dependent, potentially fatal side effect. It is also bought outside prescription channels by bodybuilders, which is why it is on the WADA list and why insulin-related deaths occur outside diabetes.

How it is thought to work

Insulin binds its receptor on muscle, fat and liver cells and drives glucose out of the blood into cells; it also suppresses glucose production by the liver and promotes fat and protein storage. Too much, or a dose without enough food, drops blood glucose below the level the brain needs — hypoglycaemia — within minutes to hours.

What is still unknown

  • The best target and regimen for older adults, where the harm of hypoglycaemia can outweigh the benefit of tight control.
  • Whether weekly insulins (icodec, efsitora) change the balance of convenience and hypoglycaemia; both were approved in the US only in 2026.

The molecule and how long it lasts

Identity
Formula
C257H383N65O77S6
Molecular weight
5808 g/mol
CAS number
11061-68-0
PubChem
CID 118984375

Human insulin; the analogues differ by a few residues

PubChem record, read 23 September 2026.

Pharmacokinetics
Route
Subcutaneous injection; intravenous infusion in hospital
Half-life
About 1.5 hours after subcutaneous injection (range 40 minutes to 7 hours); about 20 minutes intravenous
Licensed regimen (Humulin R (insulin human))
Individualised to the person's metabolic needs, blood glucose monitoring and glycaemic goals; regular insulin is generally used with an intermediate- or long-acting insulin

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

Regulatory status

European Union
Approved, prescription-only

Human insulins and analogues centrally authorised; some countries allow pharmacy sale of human insulin without prescription.

United States
Approved; some human insulins available without prescription

Analogues are prescription-only. Human regular and NPH insulin (Humulin, Novolin) can be sold over the counter in most states. In 2026 the FDA approved two once-weekly basal insulins for adults with type 2 diabetes: Awiqli (insulin icodec) on 26 March and Onswik (insulin efsitora alfa) on 23 September.

United Kingdom
Licensed, prescription-only

All insulins are prescription-only medicines.

Australia
Registered, Schedule 4

Prescription-only; PBS-subsidised.

Canada
Authorised; human insulin available without prescription

Human insulins are Schedule II (behind the counter, no prescription); analogues vary.

Sport (WADA)
Prohibited at all times

Insulins are listed under S4 (hormone and metabolic modulators), in and out of competition; a therapeutic use exemption is required for athletes with diabetes.

Questions people actually ask

Why is insulin on a peptide reference site?
Because it is the original peptide medicine, the standard every other evidence page is measured against, and a compound misused outside medicine for muscle gain — which is why sport bans it.
Is insulin a peptide?
Yes — 51 amino acids in two chains, technically a small protein. It was the first protein sequenced (1951) and the first made by recombinant DNA (1982).
What is the main danger?
Hypoglycaemia: too much insulin for the food eaten drops blood sugar to levels that cause confusion, seizures and death. Every landmark trial that improved outcomes with tighter control also increased severe hypoglycaemia.

One page per claimed effect

References

  1. 1
  2. 2
  3. 3
    Humulin R (insulin human) prescribing information.DailyMedPharmacokinetics and description.
  4. 4
    FDA. Novel Drug Approvals for 2026 (Awiqli, insulin icodec-abae, 26 March 2026; Onswik, insulin efsitora alfa-gobe, 23 September 2026).FDA, read 7 Oct 2026Both approved to improve glycaemic control in adults with type 2 diabetes.

Change log

  • 2026-10-07US row: the two once-weekly basal insulins approved by the FDA in 2026 (Awiqli, 26 March; Onswik, 23 September) added. Grades unchanged.
  • 2026-09-23Initial publication as the reference peptide. Grade A on DCCT and UKPDS.