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Weight ManagementModerate evidence#1 in Weight LossSubcutaneous · Into fat, under the skin

Retatrutide

Also known as LY3437943

Retatrutide is an investigational triple hormone receptor agonist that activates GLP-1, GIP, and glucagon receptors. In mid-stage clinical trials it produced some of the largest average body-weight reductions reported for an injectable weight-management agent to date. It is not yet approved by regulatory agencies and remains under study in late-stage clinical trials. Research to date is limited to controlled trial populations, and long-term safety and outcome data are still being gathered. It should not be considered an approved treatment, and any use outside of a clinical trial or licensed prescriber's supervision is not supported by current evidence.

Reported benefits

  • Associated with substantial reductions in body weight in clinical trial participants
  • May improve markers of glycemic control
  • Combined incretin/glucagon activity may support fat oxidation
  • Once-weekly dosing schedule in studies to date

How it works

Retatrutide binds and activates three separate incretin-related receptors: GLP-1, GIP, and the glucagon receptor. Combined GLP-1/GIP activity slows gastric emptying and increases satiety signaling, while added glucagon receptor activity is believed to raise energy expenditure and support hepatic fat metabolism. This triple-receptor approach is proposed to produce greater metabolic effect than single- or dual-receptor agonists, though the relative contribution of each receptor pathway in humans is still being characterized.

Dosing ranges

TierDoseFrequency
Low2 mgonce weekly
Moderate4 mgonce weekly
High12 mgonce weekly

Estimate your dose

Dose estimator

Educational estimate for Retatrutide, scaled to body size. Not medical advice.

Read before using

This tool produces a rough, educational estimate by scaling commonly-published research ranges to lean body mass. It is not a prescription, medical advice, or a substitute for a licensed clinician. Most peptides use fixed dosing, not weight-based dosing. Individual needs vary. You are solely responsible for how you use this information.

Mixing & syringe units

Target dose follows the estimate above. Change it there, or edit it directly below.

Reconstitution calculator

How much water to add and how many insulin-syringe units to draw for Retatrutide. Educational only.

mL

Draw to this mark

80units

= 0.8 mL for a 4 mg dose

0100 u (1 mL)

Concentration

5 mg/mL

Doses per vial

2

A U-100 syringe reads 100 units per mL. This is a reconstitution math helper only, not a prescription or dosing advice. Verify every calculation and consult a qualified healthcare provider.

Possible side effects

Nausea, vomiting, and diarrhea, especially during dose escalationDecreased appetitePotential for gallbladder-related eventsInjection-site reactionsTheoretical thyroid C-cell risk based on the GLP-1 drug class

Stacking notes

Not established; combining with other incretin-based agents is not supported by published research and may increase gastrointestinal side effects.

Common protocols

Trial-based titration schedules starting at low doses and increasing every 4 weeksWeekly subcutaneous injection with rotation of injection sites

Common questions

What is Retatrutide used for?

Retatrutide is an investigational triple hormone receptor agonist that activates GLP-1, GIP, and glucagon receptors. In mid-stage clinical trials it produced some of the largest average body-weight reductions reported for an injectable weight-management agent to date. It is not yet approved by regulatory agencies and remains under study in late-stage clinical trials. Research to date is limited to controlled trial populations, and long-term safety and outcome data are still being gathered. It should not be considered an approved treatment, and any use outside of a clinical trial or licensed prescriber's supervision is not supported by current evidence. Reported benefits include associated with substantial reductions in body weight in clinical trial participants, may improve markers of glycemic control, combined incretin/glucagon activity may support fat oxidation.

What is a typical Retatrutide dose?

Reported ranges run 2-12 mg. A low protocol is 2 mg once weekly, and a high protocol is 12 mg once weekly. This is reference information, not a dosing recommendation.

What is the half life of Retatrutide?

Approximately 17 days in trial pharmacokinetic reports, consistent with once-weekly dosing. That is what sets the dosing frequency, and it is why the timing guidance is weekly · same day, any time.

How is Retatrutide administered?

Subcutaneous: into fat, under the skin.

How long is a Retatrutide cycle?

Continuous use with gradual up-titration over several months in trial protocols on, followed by Not established outside of trial discontinuation; no standard off-cycle described in published research off. Dose increases are typically spaced several weeks apart to reduce gastrointestinal side effects.

What are the side effects of Retatrutide?

Reported side effects include nausea, vomiting, and diarrhea, especially during dose escalation, decreased appetite, potential for gallbladder-related events, injection-site reactions, theoretical thyroid c-cell risk based on the glp-1 drug class. Evidence level for this compound is moderate evidence.

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Educational use only, not medical advice. This profile is provided for research and educational purposes. Retatrutide may be a research compound or a prescription medication; nothing here is intended to diagnose, treat, cure, or prevent any disease. Dosing figures reflect commonly-published research ranges, not a prescription. Consult a qualified healthcare provider before making any health decision. Read the full disclaimer →

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Educational use only. The information and calculators on this site are provided for research and educational purposes and are not medical advice, a diagnosis, a prescription, or a substitute for a licensed healthcare provider. Many compounds described are research compounds or prescription medicines not approved for general use. You must be 21 or older. Always consult a qualified clinician before making any health decision. Read the full disclaimer · Privacy Policy

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