GLP-1 & incretin

Retatrutide

Controlled trials

Triple GIP/GLP-1/glucagon receptor agonist.

SubQIntermediateNot approved anywherefat lossappetite controlmetabolic health

Also known as LY3437943 · Reta · Triple-G

At a glance

Dose summary

Typical dose4 mg
Range500 mcg–12 mg
FrequencyWeekly
Half-life~6 days
ScheduleOnce a week
Cycle lengthNot cycled
RouteSubQ
Experience levelIntermediate
Evidence gradeControlled trials
ApprovalNot approved anywhere
Where the dose comes fromPublished trial dosing

Reconstitution

What to draw, at the usual vial

A 20 mg vial reconstituted with 2 mL of bacteriostatic water gives 10.00 mg/mL. A typical 4 mg dose is 0.400 mL — pull the plunger to 40 units on a U-100 syringe.

Concentration10.00 mg/mL
Draw volume0.400 mL
U-100 units40 units
Doses per vial5

Same dose, other vial sizes

VialWaterConcentrationDrawUnitsDoses
5 mg2 mL2.50 mg/mL1.600 mL160 units1
10 mg2 mL5.00 mg/mL0.800 mL80 units2
12 mg2 mL6.00 mg/mL0.667 mL66.7 units3
20 mg2 mL10.00 mg/mL0.400 mL40 units5

The highlighted row is the one quoted above: the smallest listed vial that holds at least four typical doses. Change any of it — a different vial, more or less water, a different dose — on the reconstitution calculator, which draws the syringe to true U-100 graduations.

Titration

Step-up ladder

This compound is escalated rather than held flat. Each step is a fixed number of weeks before the next increase — the side effects cluster in the days after a step, not at the top of the ladder.

StepWeeksDoseNote
11–2500 mcgstarting dose
23–41 mg
35–82 mg
49–124 mg
513–168 mg
617–2012 mgtrial maximum

Full ladder: 20 weeks from the starting dose to the top step.

Mechanism & evidence

What it is, and what is known

Triple GIP/GLP-1/glucagon receptor agonist. Phase 2 randomized human trials in obesity and type 2 diabetes used 1, 4, 8 and 12 mg once weekly with 4-week step-ups, and phase 3 is ongoing. It is investigational and NOT approved by any regulator, so there is no approved label, no long-term safety data, and no pharmacy-grade product. The glucagon arm adds a heart-rate signal that semaglutide and tirzepatide do not have to the same degree.

The caveat

Phase 2 complete and phase 3 ongoing. Investigational — no approved label, no long-term safety data, no pharmacy-grade product.

Tolerability

Reported side effects

  • Nausea and vomiting, worst in the weeks after a dose increase
  • Diarrhoea or constipation
  • Increased heart rate, seen dose-dependently in trials
  • Loss of appetite severe enough to under-eat protein
  • Fatigue and injection site reactions

Hard stops

Do not use this if

  • Pregnancy, possible pregnancy, or breastfeeding
  • Personal or family history of medullary thyroid carcinoma, or MEN2
  • History of pancreatitis
  • Existing thyroid disease

These are flags, not a screening. They do not replace a conversation with a clinician who knows your history.

Handling

Storage

Sealed powder, refrigerated24 months
After reconstitution, refrigerated56 days

Keep it cold, keep it dark, and label the vial with the date you mixed it. Discard anything cloudy or past the window above.

Where it shows up

Protocols using this compound

References

Sources

Educational information only, not medical advice. Talk to a licensed clinician before starting, changing, or stopping anything.