Tirzepatide dosage in published studies and labels

These are the doses used for Tirzepatide in FDA labelling and published clinical studies, reported as each source states them, one row per regimen. They describe what was studied or approved for a specific population. They are not a recommendation, and none of them is a dose for any individual.

Research and educational reference only. This is not medical advice, and no figure on this page is a dosing recommendation.

Last checked against primary sources:

Studied regimens and sources

Tirzepatide has an FDA-approved human dosage. Both approved products start at 2.5 mg subcutaneously once weekly for 4 weeks and escalate in 2.5 mg steps at intervals of at least 4 weeks: Zepbound to a maintenance dose of 5, 10 or 15 mg once weekly, and Mounjaro to a maximum of 15 mg once weekly for type 2 diabetes.

FDA Approved
Dosage evidence summary for Tirzepatide
Human dosing establishedYes
Studied dose range2.5–15 mg once weekly
RouteSubcutaneous
FrequencyOnce weekly
Duration studiedContinuous; long-term for weight maintenance
Titration2.5 mg once weekly for 4 weeks, then 5 mg once weekly. Further increases in 2.5 mg increments after at least 4 weeks at the current dose.
Half-lifeApproximately 5 days
Evidence levelFDA Approved
Last reviewed2026-09-05

Research-reported dosing

Doses as studied, one row per regimen. Different trials used different regimens; they are listed separately rather than averaged.

Research-reported dosing for Tirzepatide, one row per studied regimen
Study / contextPopulationDoseRouteFrequencyDurationOutcome studiedSource
FDA label — Zepbound, weight reductionFDA-approved label · FDA prescribing informationAdults with obesity, or overweight with at least one weight-related comorbid condition5 mg, 10 mg or 15 mg maintenance; 2.5 mg starting doseSubcutaneousOnce weeklyLong termReduction and maintenance of body weightZEPBOUND (tirzepatide) injection — FDA prescribing information, DailyMed
FDA label — Zepbound, obstructive sleep apnoeaFDA-approved label · FDA prescribing informationAdults with obesity and moderate-to-severe obstructive sleep apnoea10 mg or 15 mgSubcutaneousOnce weeklyLong termModerate to severe obstructive sleep apnoeaZEPBOUND (tirzepatide) injection — FDA prescribing information, DailyMed
FDA label — Mounjaro, type 2 diabetesFDA-approved label · FDA prescribing informationAdults with type 2 diabetes mellitus2.5 mg starting dose, escalated in 2.5 mg steps to a maximum of 15 mgSubcutaneousOnce weeklyContinuousGlycaemic controlMOUNJARO (tirzepatide) injection — FDA prescribing information, DailyMed
SURPASS-2 — phase 3 head-to-head against semaglutideClinical trial · Phase 3 open-label randomised controlled trialAdults with type 2 diabetes on metformin (n=1879)5 mg, 10 mg or 15 mgSubcutaneousOnce weekly40 weeksChange in glycated haemoglobin versus semaglutide 1 mgFrías JP et al. Tirzepatide versus Semaglutide Once Weekly in Patients with Type 2 Diabetes. N Engl J Med. 2021.

Where sources disagree

  • The 2.5 mg dose is an escalation step in both labels and is explicitly not a maintenance dose. It is sometimes presented elsewhere as a standalone low-dose protocol, which the labelling does not support.
  • Maximum dose is 15 mg once weekly for both approved products. Higher weekly doses occasionally quoted in non-clinical sources exceed every approved regimen and every published phase 3 arm.