Research Reference

Retatrutide Pen Dosage Guide.

A reference for researchers working with retatrutide (LY-3437943) pre-mixed pens — titration schedule, pen-unit math, mechanism summary, and safety notes. Pairs with our semaglutide & tirzepatide guide.

For research use only. The values below are reference figures for in-vitro and laboratory workflows. Not medical advice and not for human or veterinary use.

What is retatrutide?

Retatrutide is an investigational triple agonist that simultaneously activates the GLP-1, GIP, and glucagon receptors. That third axis — glucagon — increases energy expenditure on top of the appetite and insulinotropic effects familiar from semaglutide and tirzepatide. Phase 2 trials have reported the largest weight-loss signal among incretin compounds to date.

  • Target

    GLP-1

    Satiety, insulin response

  • Target

    GIP

    Glucose-dependent insulin release

  • Target

    Glucagon

    Energy expenditure, lipolysis

Pen unit math

The standard retatrutide pen on this catalog is reconstituted to 10 mg/mL. The dial reads in units, where 100 units = 1 mL. To convert milligrams to units, divide dose by concentration and multiply by 100.

units = (dose_mg / concentration_mg_per_mL) × 100

# Example: 4 mg retatrutide on a 10 mg/mL pen
units = (4 / 10) × 100 = 40 units

Retatrutide titration schedule

Reference values based on a 10 mg/mL pen. Most published Phase 2 protocols escalate by 2 mg every 2–4 weeks based on tolerability, up to 8–12 mg weekly.

PhaseWeekly DosePen Units
Weeks 1–22 mg~20 units
Weeks 3–44 mg~40 units
Weeks 5–84–6 mg~40–60 units
Weeks 9–126–8 mg~60–80 units
Weeks 13+8–12 mg~80–120 units

Hold or step back one dose level if gastrointestinal side effects become limiting. Hold-then-resume is preferred over discontinuing.

Storage & handling

  • Store pens at 2–8°C; protect from light and freezing.
  • Allow the pen to reach room temperature before administration.
  • Prime the pen per manufacturer instructions before first use.
  • Rotate subcutaneous sites; use a new needle every dose.
  • Discard pens past their in-use period after first puncture.

Reported side effects

In published trials the most common adverse events were dose-dependent gastrointestinal: nausea, diarrhea, constipation, and vomiting — typically peaking during titration and tapering during maintenance. Slower titration (every 4 weeks rather than every 2) reduced incidence in Phase 2 data.

Frequently asked

How is retatrutide different from tirzepatide?+

Tirzepatide activates GLP-1 and GIP. Retatrutide adds a third axis — the glucagon receptor — which increases energy expenditure in addition to suppressing appetite.

How long does a 10 mg retatrutide pen last at a 4 mg weekly dose?+

A 10 mg / 1 mL pen contains roughly 2.5 weekly doses at 4 mg. Most research protocols allocate one pen per 2–3 weeks at this stage of titration.

Can retatrutide be combined with other peptides?+

In a research context retatrutide is studied as a monotherapy. Stacking with other incretins (semaglutide, tirzepatide) is not supported in the published literature and increases GI side-effect risk.

Get the retatrutide pen

Pre-mixed, batch-matched COA, cold-chain shipped. For in-vitro research only.

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