Research use only.  Educational reference. Not medical advice. Not for human consumption.
⚖️ Triple GLP-1 / GIP / Glucagon Agonist

Retatrutide GLP-3 RT (5 mg Vial) Dosage Protocol

Retatrutide is a triple-receptor agonist (GLP-1 / GIP / glucagon) studied in Phase 2 trials for body-weight reduction up to 24% at 48 weeks. It is among the most potent incretin compounds in clinical investigation. This page covers the 5 mg vial.

⚡ Quickstart Highlights

Vial contents
5 mg Retatrutide
Final volume
1 mL
Concentration
5 mg/mL
One U-100 unit
50 mcg in 0.01 mL

Dosing & Reconstitution Guide

The same phase 2 and phase 3 schedules converted for a 5 mg vial

Phase 2 Trial Schedule (1 mL = 5 mg/mL)

Study PhaseWeekly DoseU-100 UnitsVolume
Weeks 1 to 42 mg40 units0.4 mL
Weeks 5 to 84 mg80 units0.8 mL
Weeks 9 to 128 mg160 units1.6 mL
Weeks 13+12 mg240 units2.4 mL

Frequency: Once weekly by subcutaneous administration. This table shows the lower-start 12 mg arm from the 48-week phase 2 obesity trial. The study also evaluated separate 1 mg, 4 mg, and 8 mg target arms. Rows above 100 units exceed the capacity of one 1 mL syringe, so the supply calculation counts the required number of syringes.

Phase 3 Trial Schedule (1 mL = 5 mg/mL)

Study PhaseWeekly DoseU-100 UnitsVolume
Weeks 1 to 42 mg40 units0.4 mL
Weeks 5 to 84 mg80 units0.8 mL
Weeks 9 to 126 mg120 units1.2 mL
Weeks 13 to 169 mg180 units1.8 mL
Weeks 17+12 mg240 units2.4 mL

Frequency: Once weekly by subcutaneous administration. The phase 3 program began at 2 mg and increased every four weeks until the assigned 4 mg, 9 mg, or 12 mg target was reached. Rows above 100 units exceed the capacity of one 1 mL syringe, so the supply calculation counts the required number of syringes.

Reconstitution Steps

  1. Clean the vial stopper and gather the sterile supplies required by the research procedure.
  2. Add 1 mL bacteriostatic water slowly down the vial wall.
  3. Gently swirl or roll until dissolved. Do not shake.
  4. Label the vial 5 mg/mL with the preparation date and follow the documented refrigerated storage period.

The weekly amounts remain identical across the Retatrutide family. The 5 mg vial changes only the concentration, U-100 units, volume, and supply calculations.

Supplies Needed

Straightforward 12-week and 24-week planning for a 5 mg vial at 5 mg/mL.

ItemPhase 2, 12 weeksPhase 2, 24 weeksPhase 3, 12 weeksPhase 3, 24 weeks
Retatrutide vials (5 mg each)Minimum 12 vials (56 mg required).Minimum 40 vials (200 mg required).Minimum 10 vials (48 mg required).Minimum 36 vials (180 mg required).
U-100 insulin syringes (1 mL capacity)16 new syringes.52 new syringes.16 new syringes.48 new syringes.
Bacteriostatic water (10 mL bottles)2 bottles by volume (12 mL required).4 bottles by volume (40 mL required).1 bottle by volume (10 mL required).4 bottles by volume (36 mL required).
Alcohol swabs32 swabs minimum; 1 box of 100 covers the calculation.104 swabs minimum; 2 boxes of 100 covers the calculation.32 swabs minimum; 1 box of 100 covers the calculation.96 swabs minimum; 1 box of 100 covers the calculation.

Sharps disposal: One appropriately sized container for used syringes.

Stability planning: Vial and diluent totals are minimum arithmetic quantities. Follow the exact product documentation for sterility, storage, handling loss, and discard timing.

Protocol Overview

Retatrutide is positioned at the high end of the incretin landscape. The compound has no validated "aggressive" or accelerated path — every clinical trial uses the same paced ramp. After cessation, weight regain is the norm without lifestyle anchoring (protein, resistance training, sustainable caloric intake).

Storage Instructions

StateTemperatureDuration
Lyophilized−20°C (−4°F)Up to 24 months, dry & dark
Reconstituted2–8°C (35–46°F)Up to 28 days, protect from light

Important Notes

⚠ Research Use Only: Retatrutide is investigational and currently in Phase 3 trials. There is no "aggressive" or accelerated protocol — the slow 4-week-per-step titration is the only validated approach.

How This Works

Retatrutide simultaneously activates GLP-1, GIP, and glucagon receptors — the only triple-agonist in clinical trials. GLP-1 activation slows gastric emptying and enhances satiety. GIP augments insulin secretion in response to glucose and modulates lipid metabolism. The glucagon-receptor component drives an increase in energy expenditure absent from dual or single agonists.

The molecule is fatty-acid acylated to bind albumin in serum, slowing renal clearance and enabling once-weekly dosing. The combined three-receptor profile produces greater body-weight reduction in trials than any prior incretin compound.

Potential Benefits & Side Effects

Potential Benefits

Side Effect Profile

Lifestyle Factors

Injection Technique

References

1
Jastreboff AM et al. 'Triple-Hormone-Receptor Agonist Retatrutide for Obesity — A Phase 2 Trial' — NEJM, 2023 View source ↗
2
Rosenstock J et al. 'Retatrutide for type 2 diabetes — Phase 2' — Lancet, 2023 View source ↗
3
Sanyal AJ et al. 'Triple Hormone Receptor Agonist Retatrutide for MASLD' — Nat Med, 2024 View source ↗