Tirzepatide

Tirzepatide

Research peptide

Dual GLP-1 + GIP agonist · weight, glucose, sleep apnea and heart · the molecule in Mounjaro and Zepbound

Strong evidence
Molecule approved in United States, European Union, United Kingdom and 5 more · 2022What this means ›
🇺🇸 United States · Approved🇪🇺 European Union · Approved🇬🇧 United Kingdom · Approved🇯🇵 Japan · Approved🇨🇳 China · Approved🇨🇦 Canada · Approved🇦🇺 Australia · Approved🇧🇷 Brazil · Approved

The molecule is approved as a medicine in United States, European Union, United Kingdom and 5 more, under the brand Mounjaro · Zepbound. In the US it holds five indications: Mounjaro for type 2 diabetes in adults (May 2022) and from age 10 (SURPASS-PEDS, 19 December 2025), Zepbound for weight management (November 2023), Zepbound for obstructive sleep apnoea (December 2024) and Mounjaro to reduce cardiovascular risk in type 2 diabetes (August 2026, SURPASS-CVOT). The European Union, the UK, Japan, China, Canada, Australia and Brazil have approved it for type 2 diabetes and, in most, for weight management; in Europe the EMA added the heart-failure data to the label (January 2026) without a separate indication. It is the dual GLP-1 + GIP agonist with the most human data on the market.

What is approved is the molecule under that pharmaceutical brand. Our vial is research material (RUO).

Source: FDA · Mounjaro (2022; desde 10 años, 19 dic 2025; riesgo cardiovascular ago 2026), Zepbound (2023; apnea del sueño dic 2024) · EMA (IC en ficha, ene 2026), MHRA, MHLW, NMPA, Health Canada, TGA y Anvisa

Overview

What has it been researched for?

  • Controls appetite and satiety Main focusStrong evidence
  • Lowers body weightStrong evidence
  • Reduces liver fatStrong evidence
  • Improves glucose controlStrong evidence
  • Improves lipids and blood pressureStrong evidence
  • Protects the heartStrong evidence
  • Protects the kidneyStrong evidence
  • Reduces sleep apneaStrong evidence
  • Slower pace of agingEarly evidence

Research protocols

The SBL research protocol and what the literature reports. Not medical advice.

SBL research protocol · no established clinical regimen in people

Dose
1.5 → 3 mg
Frequency
1×/semana
Duration
16 weeks
Route
Subcutaneous
Evidence level
Human study

Tools

Evidence and studies

See studies →

Protocols

Research protocols

SBL research protocol · no established clinical regimen in people

Research use, with no established clinical regimen in people.

Dose
1.5 → 3 mg
Frequency
1×/semana
Timing
cualquier hora
Duration
16 weeks
Break
No break
Route
Subcutaneous
Evidence level
Human study

Example dose

05010015
15 u= 1.5 mg

100-unit U-100 insulin syringe · Starting dose of its protocol, with 1 ml of water in the 10 mg vial.

What it pairs with

Preparation and dosing

Quick reference

Vial10 mg
Diluent1 ml
Concentration10 mg/ml
1 unit =0.1 mg

Preparation

Diluent
Bacteriostatic water

Open calculator →See the guide →

Evidence

Each effect with its evidence level and, where available, its source.

Strong evidence(8)Moderate evidence(0)Early evidence(1)
  • Controls appetite and satietyHuman studySee study · 2023
  • Lowers body weightApprovedSee study · 2022
  • Reduces liver fatHuman studySee study · 2022
  • Improves glucose controlApprovedSee study · 2021
  • Improves lipids and blood pressureHuman studySee study · 2022
  • Protects the heartHuman studySee study · 2025
  • Protects the kidneyHuman studySee study · 2022
  • Reduces sleep apneaApprovedSee study · 2024
  • Slower pace of agingExtrapolatedSee study · 2026

The science

Mechanisms, studies and references

Dual GLP-1/GIP

Safety

It makes sense if you want

  • Lose weight & curb appetite
  • Lose weight — most potent
  • Longevity & deep anti-aging

It does not make sense if

  • Personal or family history of medullary thyroid cancer or MEN2
  • Active cancer or oncology treatment in the last 5 years
  • Pregnancy or breastfeeding
  • Gastroparesis or slow gastric emptying
  • Active eating disorder

Talk to your doctor first if this applies (17)

  • Oral contraceptive (the pill)
  • Severe heart disease or recent cardiac event
  • Major surgery in the last 3 months
  • Type 1 diabetes
  • Type 2 diabetes / prediabetes
  • Gallbladder disease or gallstones
  • GLP-1 (Ozempic, Wegovy, Mounjaro, Saxenda)
  • Severe liver impairment
  • Severe kidney impairment
  • Insulin
  • Blood pressure meds
  • Thyroid meds
  • History of pancreatitis
  • Planning a pregnancy in the next 3 months
  • Diabetic retinopathy
  • Sulfonylureas / metformin
  • Thyroid disorder

The certificate of analysis (CoA) certifies the identity and purity of the batch. It does not certify safety of use.

Verify your batch →

For research use only (RUO). This consult is educational and does not replace your doctor.

Questions

Frequently asked questions

What is it reconstituted with, and how much?

With bacteriostatic water: 1 ml into the 10 mg vial, giving 10 mg/ml.

What is the starting dose of the research protocol?

1.5 → 3 mg, 1×/semana. This is the SBL research protocol, with no established clinical regimen in people.

How long is the cycle, and how long does a vial last?

16 weeks. At the starting dose, the 10 mg vial lasts ~3 sem.

Which route is used in research?

Subcutaneous.

When does it make no sense?

It makes no sense with: Personal or family history of medullary thyroid cancer or MEN2, Active cancer or oncology treatment in the last 5 years, Pregnancy or breastfeeding, Gastroparesis or slow gastric emptying, Active eating disorder. Details in the Safety tab.

What is it combined with?

It goes well with MOTS-c, Tesamorelin. The reasons are in the Protocols tab.

How do I check my batch?

With the code on the vial, in the verifier. The CoA certifies the identity and purity of the batch, not safety of use.

Verify your batch →

See kit

For research use only (RUO). This consult is educational and does not replace your doctor.