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TL;DR — Evidence Boundary

Mounjaro is the brand name for tirzepatide, a dual GIP/GLP-1 receptor agonist. UAE records place tirzepatide inside the regulated medicine framework. This page summarizes public regulatory and trial evidence only; it does not report current price, stock, seller or clinic information and does not provide individual medical guidance.

UAE regulatory context

The UAE national essential medicines list published in 2025 includes tirzepatide dose strengths.[1] Abu Dhabi's standard for non-surgical management of obesity also places tirzepatide within clinician-managed care.[2] These documents establish regulatory and clinical context; they do not establish real-time inventory, price, insurance coverage or suitability for a particular person.

Medicine registration, prescribing, reimbursement and stock are separate questions. This article addresses the first and the evidence base. Readers needing medical decisions should use a licensed UAE healthcare professional and current official medicine information.

How tirzepatide works

Tirzepatide activates the glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptors. In clinical studies, these pathways affect glucose-dependent insulin secretion, glucagon signaling, gastric emptying, appetite-related signaling and body weight. Mechanism does not, by itself, establish benefit or risk for an individual.

For a receptor-level comparison that includes investigational compounds, see the GLP-1, GIP and glucagon mechanism guide.

SURMOUNT-1 obesity trial

In SURMOUNT-1, adults with obesity or overweight without diabetes were randomized to tirzepatide 5 mg, 10 mg or 15 mg or placebo. At 72 weeks, mean body-weight changes were -15.0%, -19.5% and -20.9% for the three tirzepatide groups and -3.1% for placebo.[3]

Those are group means from a controlled trial. They are not a personal outcome prediction, dosing recommendation or comparison of UAE care programs.

SURPASS-2 type 2 diabetes trial

SURPASS-2 compared once-weekly tirzepatide 5 mg, 10 mg and 15 mg with semaglutide 1 mg in adults with type 2 diabetes. All three tirzepatide doses were noninferior and superior to semaglutide for mean A1C change at 40 weeks, and mean body-weight reductions were greater in the tirzepatide groups.[4]

The trial compared specified regimens in a defined population. It does not determine which medicine is appropriate for a particular person or jurisdiction.

Mounjaro is not retatrutide

FeatureMounjaroRetatrutide
CompoundTirzepatideRetatrutide / LY3437943
Receptors studiedGIP + GLP-1GIP + GLP-1 + glucagon
StatusRegulated prescription medicine; label varies by jurisdictionInvestigational; no approved prescribing label
Remy COA archiveNo Mounjaro recordsFour named historical batch records

For the current investigational timeline, use the retatrutide approval tracker. The retatrutide batch-documentation guide explains what those historical COAs can and cannot establish.

What this page intentionally does not provide

Further reading

Mounjaro is the brand name for tirzepatide, a dual GIP and GLP-1 receptor agonist. It is a regulated prescription medicine; its approved indications and label depend on the jurisdiction.
The 2025 UAE national essential medicines list includes tirzepatide strengths, and Abu Dhabi clinical standards treat tirzepatide as a clinician-managed medicine. Those records establish regulatory and clinical context, not real-time stock, price or suitability for an individual.
In adults with obesity or overweight without diabetes, SURMOUNT-1 reported mean body-weight changes at 72 weeks of -15.0%, -19.5% and -20.9% with tirzepatide 5 mg, 10 mg and 15 mg, respectively, versus -3.1% with placebo. These are trial results, not individual-use guidance.
In adults with type 2 diabetes, all three tirzepatide doses were noninferior and superior to semaglutide 1 mg for mean A1C change at 40 weeks, and mean body-weight reductions were greater with tirzepatide. The study does not determine which medicine is appropriate for an individual.
No. Mounjaro contains tirzepatide, a dual GIP and GLP-1 receptor agonist. Retatrutide is an investigational GIP, GLP-1 and glucagon receptor agonist and is not an approved substitute.
No. This page is an informational regulatory and evidence reference. It does not report current prices, stock, seller links, clinic packages or referral routes.
No. The published archive identifies four historical retatrutide batch records. It must not be read as evidence about Mounjaro or tirzepatide medicine quality.

How We Built This Reference

This update uses the UAE national essential medicines list, the Abu Dhabi non-surgical obesity standard, and the peer-reviewed SURMOUNT-1 and SURPASS-2 publications. Retail listings and clinic pages were removed because they do not belong in the site's informational model. Read our editorial policy →

RP
Editorial Review

Editorial Board, Remy Peptides

The Remy Peptides Editorial Board reviews research articles covering GLP-1 receptor agonists, triple agonists, and the obesity drug pipeline. Its review spans peptide analytical chemistry, HPLC purity validation, and clinical trial data interpretation.

About the editorial team →
References & Citations
  1. Emirates Drug Establishment. National essential medicines list, 2025 decision including tirzepatide strengths. Official PDF.
  2. Department of Health — Abu Dhabi. Standard for non-surgical management of obesity, February 17, 2025. Official PDF.
  3. Jastreboff AM, et al. Tirzepatide once weekly for the treatment of obesity. N Engl J Med. 2022;387:205–216. PubMed.
  4. Frias JP, et al. Tirzepatide versus semaglutide once weekly in patients with type 2 diabetes. N Engl J Med. 2021;385:503–515. PubMed.