GLP-1 & incretin
Retatrutide
Triple GIP/GLP-1/glucagon receptor agonist.
Also known as LY3437943 · Reta · Triple-G
At a glance
Dose summary
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.
Same dose, other vial sizes
| Vial | Water | Concentration | Draw | Units | Doses |
|---|---|---|---|---|---|
| 5 mg | 2 mL | 2.50 mg/mL | 1.600 mL | 160 units | 1 |
| 10 mg | 2 mL | 5.00 mg/mL | 0.800 mL | 80 units | 2 |
| 12 mg | 2 mL | 6.00 mg/mL | 0.667 mL | 66.7 units | 3 |
| 20 mg | 2 mL | 10.00 mg/mL | 0.400 mL | 40 units | 5 |
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.
| Step | Weeks | Dose | Note |
|---|---|---|---|
| 1 | 1–2 | 500 mcg | starting dose |
| 2 | 3–4 | 1 mg | — |
| 3 | 5–8 | 2 mg | — |
| 4 | 9–12 | 4 mg | — |
| 5 | 13–16 | 8 mg | — |
| 6 | 17–20 | 12 mg | trial 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
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.