Retatrutide Dosage Chart: Doses, Units & Titration (2026)

Full retatrutide dosage chart: community starting doses, week-by-week titration, and exact mg-to-units syringe conversions for common vial sizes.

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Compilado por Equipe PeptiScience · Atualizado em 26 de abril de 2026

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Full retatrutide dosage chart: community starting doses, week-by-week titration, and exact mg-to-units syringe conversions for common vial sizes.

Community-reported protocols start at 0.25–0.5 mg/week and titrate to 1.5–4 mg/week over 8–12 weeks as GI tolerance is assessed. Phase 2 trials used up to 12 mg/week and produced 24.2% body weight loss at 48 weeks — community protocols are deliberately more conservative.

Research-context information only. Retatrutide is an investigational drug not approved by the FDA. Protocols, doses, and reactions reported below come from published clinical trials and self-reported community sources. This article reports what has been documented, not what should be done. Possession or use of investigational drugs outside an authorized clinical trial may be illegal in your jurisdiction. Consult a licensed physician for personal medical decisions.

Retatrutide is a triple-agonist peptide targeting GLP-1 + GIP + glucagon receptors simultaneously — the most pronounced weight-loss data from any metabolic peptide studied to date. Below: the standard 8-on/8-off protocol, week-by-week titration math, side-effect-driven adjustments, and how community doses compare to the trial-published 12 mg/week ceiling.

Retatrutide Dosing Table

Match your vial size below — reconstitution and dose math update automatically.

Math assumes U-100 insulin syringes (1 mL = 100 units). Verify your syringe matches before injecting. Round half-units to the nearest visible mark.

Math assumes U-100 insulin syringes (1 mL = 100 units). Verify your syringe matches before injecting. Round half-units to the nearest visible mark.

Math assumes U-100 insulin syringes (1 mL = 100 units). Verify your syringe matches before injecting. Round half-units to the nearest visible mark.

Math assumes U-100 insulin syringes (1 mL = 100 units). Verify your syringe matches before injecting. Round half-units to the nearest visible mark.

Math assumes U-100 insulin syringes (1 mL = 100 units). Verify your syringe matches before injecting. Round half-units to the nearest visible mark.

Math assumes U-100 insulin syringes (1 mL = 100 units). Verify your syringe matches before injecting. Round half-units to the nearest visible mark.

Quick Reference: Standard Protocol

Community-reported standard protocol (self-reported; compiled from community dosing logs and reconstitution guides — documentation of what sources describe, not a recommendation):

Self-reported starting doses are typically 0.25 mg for the first week to assess GI tolerance, before increasing to 0.5 mg.

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Cycling Details

The standard cycle is 0.5 mg 3x/week (1.5 mg/week total) for 8 weeks, then 8 weeks off. Some users run goal-oriented cycles — continuing until target weight loss, then cycling off. Maintenance phases may drop to 2x/week (1 mg/week total).

The 3x/week split (vs. single weekly injection used in clinical trials) may provide more stable receptor activation throughout the week.

Routes of Administration

Subcutaneous injection is the only route. Retatrutide cannot be taken orally.

  • Sites: Abdomen, thigh, or anywhere with subcutaneous fat
  • Volume: 0.1 mL with insulin syringe (29-31 gauge)
  • Rotation: Trial protocols describe rotating injection sites to minimize lipodystrophy risk

Reconstitution Quick Reference

Math: 10 mg / 2 mL = 5 mg/mL. For 0.5 mg: 0.5 / 5 = 0.1 mL = 10 units.

Community protocols describe gentle swirling — not shaking — to avoid degradation, with storage at 2–8°C and use within 28 days of reconstitution. For step-by-step instructions and vial size comparisons, see the full Retatrutide Reconstitution Guide .

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Where These Numbers Come From

Community doses represent a conservative approach compared to clinical trials.

Phase 2 obesity trial: Escalating weekly doses from 1 mg to 12 mg over 48 weeks. Maximum weight loss: 24.2% at 12 mg/week ( Jastreboff et al., 2023 ).

Phase 2 diabetes trial: Dose-dependent HbA1c reductions — minimum effective dose for meaningful glucose control was 4 mg/week ( Rosenstock et al., 2023 ). Community protocols at 1.5 mg/week fall below this threshold.

Why community doses are lower: No FDA approval means conservative self-titration. Lower doses reduce GI side effects. The clinical trial starting dose (1 mg/week) is already close to the community protocol (1.5 mg/week split 3x). Many see significant effects at these lower levels.

Research Vial Sizing

Larger vials offer better per-mg pricing. Compare current vial options and verified vendors at Best Retatrutide Vendors .

Stacking Protocols

Retatrutide already hits three major metabolic pathways, leaving few complementary targets. Adding other GLP-1 agonists ( semaglutide , tirzepatide ) is redundant and increases side effects. Stacking with other weight loss peptides is generally unnecessary.

Side Effects & Safety

  • Nausea — most common (~33% at high doses), dose-dependent, typically improves over time
  • GI effects — vomiting, diarrhea, constipation, slowed gastric emptying (GLP-1 class effects)
  • Heart rate changes — transient increases observed in trials, peaked at 24 weeks then declined
  • Injection site reactions — mild redness or irritation
  • Gallbladder risk — rapid weight loss increases gallstone risk (common with any rapid weight loss method)
  • No major safety signals in 48-week trial up to 12 mg weekly
  • At community doses (1.5 mg/week), side effects are notably milder than high-dose trial groups

Dosage Chart

This dosage chart consolidates the doses reported in published Phase 2 trials and self-reported community protocols, expressed in milligrams (mg) and converted to units on a standard 100-unit / 1mL insulin syringe.

Self-reported titration described in community sources: 0.25 mg 3x/week for week 1, then 0.5 mg 3x/week thereafter, with optional 8-week-on / 8-week-off cycling.

mg to Units Conversion

On a standard 100-unit insulin syringe, each "unit" equals 0.01 mL (so 100 units = 1 mL). Once retatrutide is reconstituted, the conversion from a target mg dose to syringe units depends entirely on the chosen dilution.

The two reconstitution ratios most often described in community protocols are below.

Reconstitution A: 10 mg vial + 2 mL BAC water (5 mg/mL) — the standard "20 units = 1 mg" dilution that keeps draws in the practical 5-80 unit range.

Reconstitution B: 10 mg vial + 1 mL BAC water (10 mg/mL) — half the volume per dose, useful when storing small total volumes; mid-range doses still fit on one syringe.

These conversions reflect the dilutions documented in published reconstitution protocols and self-reported community sources. They are reporting how reconstitution math is described, not a recommended dosing schedule.

Frequently Asked Questions

Related Guides

  • Retatrutide Peptide Page — Vendor pricing, comparisons, and full profile
  • Retatrutide Reconstitution Guide — Step-by-step mixing and dilution charts
  • Retatrutide Bloodwork Guide — What labs to track and optimal ranges
  • Tirzepatide Dosing Guide — Dual agonist alternative
  • Semaglutide Dosing Guide — Single GLP-1 agonist reference
  • Retatrutide Phase 3 Results — Latest clinical trial updates
  • Best Retatrutide Vendors of 2026 — ranked by price, purity testing, and buyer trust
  • Calculate Your Retatrutide Cycle Cost — estimate vials needed and total cost for your protocol
  • Where to Buy Retatrutide — COA verification, vial sizes, and vendor comparison

Related Reading

  • How Much Bacteriostatic Water for Retatrutide — bacteriostatic water sizing reference (research use) on bacwatercatalog

References

This article is for educational and informational purposes only. It is not medical advice. Retatrutide is not FDA-approved for any indication. Consult a licensed healthcare provider before using any peptide.

Tabelas de referência

DoseSyringe unitsmL volumeSchedule
0.5 mg5 units0.05 mLWeekly (start dose) Weeks 1-2
1 mg10 units0.1 mLWeekly Weeks 3-4
2 mg20 units0.2 mLWeekly Weeks 5-8
4 mg40 units0.4 mLWeekly (target) Weeks 9+
8 mg80 units0.8 mLWeekly (advanced)
DoseSyringe unitsmL volumeSchedule
0.5 mg5 units0.05 mLWeekly (start dose) Weeks 1-2
1 mg10 units0.1 mLWeekly Weeks 3-4
2 mg20 units0.2 mLWeekly Weeks 5-8
4 mg40 units0.4 mLWeekly (target) Weeks 9+
8 mg80 units0.8 mLWeekly (advanced)
DoseSyringe unitsmL volumeSchedule
0.5 mg8 units0.08 mLWeekly (start dose)
1 mg17 units0.17 mLWeekly
2 mg33 units0.33 mLWeekly
4 mg67 units0.67 mLWeekly (target)
DoseSyringe unitsmL volumeSchedule
0.5 mg10 units0.1 mLWeekly (start dose)
1 mg20 units0.2 mLWeekly
2 mg40 units0.4 mLWeekly
4 mg80 units0.8 mLWeekly (target)
DoseSyringe unitsmL volumeSchedule
0.5 mg13 units0.13 mLWeekly (start dose)
1 mg25 units0.25 mLWeekly
2 mg50 units0.5 mLWeekly
DoseSyringe unitsmL volumeSchedule
1 mg8 units0.08 mLWeekly
2 mg17 units0.17 mLWeekly
4 mg33 units0.33 mLWeekly (target)
8 mg67 units0.67 mLWeekly (advanced)
ParameterDetail
Vial10 mg
BAC Water2 mL
Concentration5 mg/mL
Dose0.5 mg (10 units on insulin syringe)
RouteSubcutaneous
TimingAM, empty stomach (community-reported)
Frequency3x/week (Mon/Wed/Fri)
Cycle8 weeks on, 8 weeks off
StorageRefrigerate, use within 28 days
Vial SizeBAC WaterConcentration0.25 mg0.5 mg1 mg
10 mg2 mL5 mg/mL5 units10 units20 units
TimeframeClinical DoseWeekly Total
Weeks 0-41 mg weekly1 mg/week
Weeks 4-84 mg weekly4 mg/week
Weeks 8-128 mg weekly8 mg/week
Weeks 12-4812 mg weekly12 mg/week
Vial SizeNot a Single DoseProvides
12 mg12 mg is the vial total24 doses of 0.5 mg
24 mg24 mg is the vial total48 doses of 0.5 mg
60 mg60 mg is the vial total120 doses of 0.5 mg
StackPurposeProtocol
Retatrutide + BPC-157GI protection during GLP-1 useBPC-157 250-500 mcg/day alongside retatrutide
ProtocolDose (mg)FrequencyWeekly TotalSource
Community starter0.25 mg3x/week0.75 mgSelf-reported community
Community standard0.5 mg3x/week1.5 mgSelf-reported community
Phase 2 starting1 mgWeekly1 mgJastreboff 2023
Phase 2 mid-titration4 mgWeekly4 mgJastreboff 2023
Phase 2 high8 mgWeekly8 mgJastreboff 2023
Phase 2 maximum12 mgWeekly12 mgJastreboff 2023
Dose (mg)Volume (mL)Units (insulin syringe)
0.25 mg0.05 mL5 units
0.5 mg0.10 mL10 units
1.0 mg0.20 mL20 units
1.5 mg0.30 mL30 units
2.0 mg0.40 mL40 units
4.0 mg0.80 mL80 units
Dose (mg)Volume (mL)Units (insulin syringe)
0.25 mg0.025 mL2.5 units
0.5 mg0.05 mL5 units
1.0 mg0.10 mL10 units
1.5 mg0.15 mL15 units
2.0 mg0.20 mL20 units
4.0 mg0.40 mL40 units
CitationTopicPMID
Jastreboff AM, et al., N Engl J Med (2023)Phase 2 trial: Triple-hormone agonist for obesity37366315
Rosenstock J, et al., Lancet (2023)Phase 2 trial: Retatrutide for type 2 diabetes37385280

Perguntas frequentes

What dosing protocols are reported for retatrutide weight loss research?

Community protocols self-report 0.5 mg subcutaneous 3 times per week (1.5 mg/week total), morning timing, cycled 8 weeks on / 8 weeks off. Reconstitution is typically described as a 10 mg vial dissolved in 2 mL BAC water (5 mg/mL); community protocols document a 10-unit draw on a standard insulin syringe per dose.

Why are research vials sold as 12mg, 24mg, or 60mg?

These are total vial contents for multi-week research protocols, not single doses. A 24mg vial provides 48 doses of 0.5mg.

What starting doses do community sources report?

Self-reported starting doses are around 0.25mg for the first week to assess GI tolerance before increasing to 0.5mg. Phase 2 trials began at 1mg but reported better tolerability at lower starting doses.

Can retatrutide be taken orally?

No — retatrutide is a peptide destroyed by digestive enzymes. All published protocols describe subcutaneous injection.

Peptídeo referenciado

Fontes

  1. [1]Triple-Hormone-Receptor Agonist Retatrutide for Obesity - A Phase 2 Trial N Engl J Med, 2023
  2. [2]Retatrutide, a GIP, GLP-1 and glucagon receptor agonist, for people with type 2 diabetes: a randomised, double-blind, placebo and active-controlled, parallel-group, phase 2 trial conducted in the USA Lancet, 2023

Literatura citada. A inclusão de um estudo não implica endosso de uso.