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Retatrutide dosage

Review Retatrutide weekly injection dose levels and escalation patterns, with their respective starting schedules and course lengths. Calculate volume and syringe units using your own vial inputs.

Full Retatrutide library reference

Retatrutide dosage chart

This summary table compares available dose amounts and schedules by administration route.

RouteDoseFrequency & duration
Injectable1–12 mgOnce weekly · 48 weeks (phase 2)

Retatrutide dosage by administration route

Retatrutide injectable dosage

Documented investigational weekly doses are 1, 4, 8 and 12 mg, with lower starting amounts for the higher-dose schedules and a 48-week treatment period. These are distinct assigned dose levels, rather than instructions to increase automatically from 1 to 12 mg. Another reported weekly pattern starts at 2 mg for four weeks, uses 4 mg for the next four weeks, then 4–8 mg from week 9, for 24 weeks or longer. This is a separate reported progression, not a replacement for a specific investigational protocol.[1][17]

Retatrutide acts at GIP, GLP-1 and glucagon receptors. Its intended metabolic effects concern appetite, energy expenditure and body weight; it has no approved prescribing regimen.[1][2][3][4][5][6][7]

Frequency and timing

Use the same injection day each week.[1][3][4]

Cycle length and breaks

Injectable: 48 weeks (phase 2). A standard break interval between courses is not established.[1]

Retatrutide dosage calculator

Convert your chosen Retatrutide amount into volume and U-100 syringe units. Adjust the inputs to match your vial and preparation.

Retatrutide dosage calculator

Editable calculation example. Enter your chosen amount and the details of your vial; these starting values are not a recommended dose.

mcg
mg
mL
Concentration
10mg/mL
Draw units
—units
Total doses
—
Volume per dose
—mL
Average daily amount
—mcg
Estimated days per vial
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Retatrutide safety and side effects

Approval and product quality

Retatrutide is not an FDA-approved drug.[5][8]

Side effects and long-term safety

Nausea, vomiting, diarrhea and other gastrointestinal effects are relevant. Rare adverse effects, long-term safety, effects after discontinuation and safety in special populations remain uncertain. Retatrutide remains investigational.[1][12][16][7][8][9]

Route-specific dosing limits

The main cautions are unapproved-product toxicity alerts, import or supply risk, and unreviewed combinations with other incretin or weight-loss drugs. Additional schedules attributed to Everything Peptide are reported patterns; citing research does not make these schedules clinically established or approved product instructions.[9][15][1][7][17]

Common Retatrutide dosage questions

What weekly Retatrutide dose levels are listed?

Investigational dose levels are 1, 4, 8 or 12 mg once weekly over 48 weeks. Higher-dose schedules use lower starting amounts; the listed levels are not an automatic escalation sequence.[1][17]

When is Retatrutide administered?

Use the same injection day each week.[1][3][4]

Does Retatrutide have a standard cycle or break interval?

Injectable: 48 weeks (phase 2). A standard break interval between courses is not established.[1]

Sources

Show citationsHide citations
[1]Triple-Hormone-Receptor Agonist Retatrutide for ObesityNew England Journal of Medicine. human clinical.[2]Retatrutide phase 2 obesity trial registry recordClinicalTrials.gov. clinical trial registry.[3]TRIUMPH-1 retatrutide obesity and overweight trial registry recordClinicalTrials.gov. clinical trial registry.[4]TRANSCEND-T2D-1 retatrutide type 2 diabetes trial registry recordClinicalTrials.gov. clinical trial registry.[5]Search Drugs@FDA for retatrutideopenFDA / U.S. Food and Drug Administration. database query.[6]Retatrutide for type 2 diabetes: a randomised, double-blind, placebo and active-controlled phase 2 trialThe Lancet. human clinical.[7]Retatrutide: a triple agonist for obesity and metabolic diseasePeer-reviewed review. review.[8]FDA's concerns with unapproved GLP-1 drugs used for weight lossU.S. Food and Drug Administration. official guidance.[9]Toxicity linked to unapproved peptide product labelled RetatrutideVictoria Department of Health, 2026-06-19. official guidance.[10]TRIUMPH-2 retatrutide obesity or overweight with type 2 diabetes trial registry recordClinicalTrials.gov. clinical trial registry.[11]Retatrutide for the treatment of obesity, obstructive sleep apnea and knee osteoarthritis: Rationale and design of the TRIUMPH registrational clinical trialsDiabetes, obesity & metabolism, 2026. review.[12]Lilly's triple agonist, retatrutide, delivered powerful weight loss in pivotal Phase 3 obesity trialEli Lilly and Company, 2026-05-21. human clinical.[13]TRIUMPH-Outcomes retatrutide cardiovascular and kidney outcomes trial registry recordClinicalTrials.gov. clinical trial registry.[14]Lilly's triple agonist, retatrutide, delivered weight loss of up to an average of 71.2 lbs along with substantial relief from osteoarthritis pain in first successful Phase 3 trialEli Lilly and Company, 2025-12-11. human clinical.[15]Understanding responsibilities for unapproved peptide productsTherapeutic Goods Administration. official guidance.[16]TRIUMPH-3 retatrutide obesity with cardiovascular disease trial registry recordClinicalTrials.gov. clinical trial registry.[17]Retatrutide — Everything Peptide reported protocol (educational reference, not clinical evidence)Everything Peptide. reference catalog.

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