August 12, 2026Blog9 min read
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Written by PX1 Research Team

PX1 chemists and research educators with hands-on experience in US-based peptide manufacturing, HPLC / mass-spectrometry lot testing, and endotoxin QC. All content is citation-backed and peer-reviewed for accuracy.

Retatrutide Dosage Chart (2026): Titration Schedule and Volume Table

Research Guide
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PX1 QC — Analytical Chemistry Team

Every article is reviewed by PX1's in-house analytical team for accuracy on mechanism, dosing ranges reported in the literature, and lab-handling guidance. We do not publish clinical or medical advice.


Quick answer

A complete retatrutide dosage chart built from published Phase 2 titration data, with reconstitution volumes in mL and insulin-syringe units for 5 mg/mL and 10 mg/mL preparations.

Reviewed by PX1 Research scientific team

Key takeaways

  • Lot-specific HPLC purity ≥99.0% with the chromatogram attached
  • LC-MS mass confirmation against the expected 4731.6 Da
  • LAL endotoxin reported in EU/mg
  • Karl Fischer moisture within spec

How this chart was built

Retatrutide (LY-3437943) is a GLP-1 / GIP / glucagon triple agonist still in clinical development. Every number below is derived from the published Phase 2 obesity protocol (Jastreboff et al., NEJM 2023), which evaluated once-weekly doses of 1, 4, 8 and 12 mg over 48 weeks with a stepped titration. This is a laboratory reference, not a dosing recommendation.

The dosage chart

Phase (weeks)Weekly doseVolume at 5 mg/mLVolume at 10 mg/mL
1–41 mg0.20 mL (20 units)0.10 mL (10 units)
5–82 mg0.40 mL (40 units)0.20 mL (20 units)
9–124 mg0.80 mL (80 units)0.40 mL (40 units)
13–166 mg1.20 mL0.60 mL (60 units)
17–208 mg1.60 mL0.80 mL (80 units)
21–2410 mg2.00 mL1.00 mL
25+12 mg1.20 mL

Units refer to an insulin syringe graduated in 100 units per 1 mL.

Two things researchers get wrong most often when reading a chart like this:

  1. The chart is not the protocol. Trials held each step for roughly four weeks before escalating. Compressing the schedule is what generated the GI adverse-event signal in the fast-titration arms.
  2. The volume column depends entirely on your reconstitution. A 10 mg vial reconstituted with 2 mL is 5 mg/mL; the same vial with 1 mL is 10 mg/mL. Recalculate every time the fill or diluent changes.

The only formula you need

`volume (mL) = target dose (mg) ÷ concentration (mg/mL)`

And to get concentration:

`concentration (mg/mL) = vial fill (mg) ÷ diluent volume (mL)`

Worked example: a 15 mg vial reconstituted with 1.5 mL of bacteriostatic water gives 10 mg/mL. A 6 mg step is 6 ÷ 10 = 0.60 mL, which is 60 units on a U-100 insulin syringe.

Run your own numbers with the reconstitution calculator.

Why titration is structured the way it is

The glucagon-receptor arm of retatrutide's activity increases energy expenditure but also amplifies the gastrointestinal profile shared by the incretin class. Published data show adverse events cluster around escalation weeks, not steady-state weeks — which is why every trial arm used a hold period rather than continuous ramping.

Half-life and interval

A fatty-acid side chain binds serum albumin and extends retatrutide's half-life to approximately six days, which is what makes once-weekly administration the standard interval across all published protocols. Splitting a weekly dose into smaller more frequent fractions has no published pharmacokinetic basis.

Documentation to verify before any dosing work

  • Lot-specific HPLC purity ≥99.0% with the chromatogram attached
  • LC-MS mass confirmation against the expected 4731.6 Da
  • LAL endotoxin reported in EU/mg
  • Karl Fischer moisture within spec

PX1 publishes all four per lot at /purity-reports. Current retatrutide lots are listed in the catalog.

Research use only. Not for human consumption. Not intended to diagnose, treat, cure, or prevent any disease.

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