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Reviewed by MyPeptideMatch Editorial TeamLast reviewed February 2026Updated February 2026

Retatrutide Dosing Protocol: 5 mg Vial — Week-by-Week Titration & Supplies

Complete dosing protocol for retatrutide (LY3437943) using the 5 mg compounded vial, based on Phase 2 trial titration schedules.

Quickstart highlights

Retatrutide (LY3437943, Eli Lilly) is a once-weekly GLP-1/GIP/glucagon receptor triagonist with 24.2% mean body weight reduction at 48 weeks in Phase 2 (NCT04881760, 12 mg arm) — the highest weight loss reported for any anti-obesity drug to date.

  • Concentration: 5 mg/mL (5 mg vial + 1 mL bacteriostatic water).
  • At 5 mg/mL: 1 mg = 20 units, 2 mg = 40 units, 4 mg = 80 units, 5 mg = 100 units.
  • Phase 2 trial: 12 mg dose produced 24.2% mean body weight reduction at 48 weeks — highest for any anti-obesity drug studied to date.
  • One 5 mg vial provides 5 starting doses at 1 mg, or 1 dose at 4 mg maintenance.
  • Doses above 5 mg require two vials per injection; consider higher-mg vials for maintenance.

Dosing table

For educational reference only. Your prescribing provider may adjust doses based on your clinical profile and response.

WeekDose (µg)UnitsFrequencyNotes
1-4100020Once weekly1 mg starting dose — 20 units on U-100 syringe; one 5 mg vial provides 5 doses
5-8200040Once weekly2 mg dose — 40 units; vial provides 2–3 doses at this level
9-12400080Once weekly4 mg dose — 80 units; assess tolerability before advancing
13+8000160Once weekly8 mg maintenance — requires 2 vials (160 units at 5 mg/mL = 1.6 mL; use two separate draws or reconstitute higher concentration)

Gradual approach

WeekDose (µg)UnitsNotes
1-8100020Slow ramp — hold 1 mg x 8 weeks to minimize GI side effects
9-122000402 mg for 4 weeks before advancing

Reconstitution steps

  1. Draw 1 mL bacteriostatic water; inject slowly down the vial wall to prevent foaming.
  2. Swirl gently until lyophilized powder fully dissolves (1–3 minutes); avoid shaking.
  3. Final concentration: 5 mg/mL. At this concentration, doses above 5 mg require combining two vials.
  4. Label with date and concentration; refrigerate at 2–8 °C immediately.

Supplies needed

8-week plan

  • 2 vials
  • 8 syringes
  • 2 mL bac water
  • 8 alcohol swabs

12-week plan

  • 3 vials
  • 12 syringes
  • 3 mL bac water
  • 12 alcohol swabs

16-week plan

  • 5 vials
  • 16 syringes
  • 5 mL bac water
  • 16 alcohol swabs
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Protocol overview & cycle notes

Initiate the retatrutide triple agonist protocol at 1 mg weekly, titrating to 4–8 mg maintenance over 12 weeks to capture the superior weight loss potential of GLP-1/GIP/glucagon co-agonism while minimizing GI adverse effects.

Cycle length: 16 weeks on.

Off-cycle: 8–12 weeks off; monitor weight, appetite, and metabolic labs during off-cycle.

Storage & handling

Lyophilized: store below 25 °C. Reconstituted: refrigerate 2–8 °C; use within 28 days. Do not freeze. For doses above 5 mg, reconstitute a second vial for the same injection day.

Injection & tracking tips

  • Rotate injection sites (abdomen, thigh, upper arm) every week to minimize local reactions.
  • For the 8 mg dose (160 units at 5 mg/mL = 1.6 mL), draw into a 3 mL syringe combining volume from two fresh vials on injection day.
  • Retatrutide's glucagon agonism increases thirst and urination — ensure adequate hydration (2.5+ L/day) at doses ≥4 mg.

Tracking

Logging helps you and your provider spot patterns and adjust dose or timing.

  • Log body weight every Monday fasted; expect 1–3% loss per month at therapeutic doses.
  • Record nausea and GI symptom severity (0–10) weekly for the first 12 weeks.
  • Track fasting glucose weekly; glucagon agonism can transiently affect blood sugar regulation.
Log your cycle in the calculator →

How this works & references

Retatrutide (LY3437943, Eli Lilly) is a once-weekly GLP-1/GIP/glucagon receptor triagonist with 24.2% mean body weight reduction at 48 weeks in Phase 2 (NCT04881760, 12 mg arm) — the highest weight loss reported for any anti-obesity drug to date. The glucagon receptor component drives hepatic fat oxidation and thermogenesis, while GLP-1/GIP components manage appetite and insulin secretion. Phase 3 trials (NCT05668520, TRIUMPH-1/2) are ongoing.

Frequently asked questions

How does retatrutide compare to tirzepatide for weight loss?
Retatrutide's 24.2% weight loss at 12 mg (Phase 2) exceeds tirzepatide's 20.9% at 15 mg (Phase 3), though direct head-to-head trials are not yet published. The additional glucagon receptor agonism in retatrutide drives hepatic fat oxidation and thermogenesis beyond what dual GIP/GLP-1 agonism alone provides.
What GI side effects should I expect with retatrutide?
Nausea (45–60%), vomiting (25–30%), diarrhea (20–30%), and decreased appetite are most common in weeks 1–8. Incidence decreases significantly after 8 weeks. Starting at 1 mg weekly minimizes early GI burden.
Is retatrutide FDA-approved?
No — retatrutide is currently in Phase 3 clinical trials (TRIUMPH program, NCT05668520) as of 2026. It is available as a compounded research peptide only. FDA approval is not expected before 2027 at earliest.
Why does my 8 mg dose require two vials?
At 5 mg/mL, an 8 mg dose requires 1.6 mL — more than a single 5 mg vial (1 mL maximum). For doses above 5 mg, either use a 10 mg or 20 mg vial reconstituted to 10 mg/mL, or draw from two 5 mg vials on the same injection day.
Does retatrutide affect liver health?
Positively — the glucagon receptor component increases hepatic fat oxidation, and Phase 2 data showed significant improvement in liver fat percentage (MRI-PDFF). It is also being studied for metabolic-associated steatohepatitis (MASH).

Related protocols

This content is for informational purposes only and does not constitute medical advice. Consult a licensed healthcare provider before starting any peptide therapy. Dosing and protocols may vary by formulation and prescriber.