Tirzepatide GLP-2 Vial

Tirzepatide (CAS 2023788-19-2) is a synthetic, once-weekly dual glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptor agonist that has been the subject of multiple large-scale, peer-reviewed randomized controlled trials published in The New England Journal of Medicine, including investigations of body weight, glycemic control, and cardiovascular outcomes in adult human participants.

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Description


Tirzepatide (CAS 2023788-19-2) is a synthetic, once-weekly dual glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptor agonist that has been the subject of multiple large-scale, peer-reviewed randomized controlled trials published in The New England Journal of Medicine, including investigations of body weight, glycemic control, and cardiovascular outcomes in adult human participants.

In the 72-week SURMOUNT-1 trial, adults receiving once-weekly subcutaneous tirzepatide achieved mean body weight reductions ranging from 15.0% (5 mg amount) to 20.9% (15 mg amount), compared with 3.1% in the placebo group [1].

Published Research on Tirzepatide

The following peer-reviewed studies are summarized below. Full citations and direct links to each publication appear in the References section. All studies described in this section were conducted in adult human participants.

SURMOUNT-1 Trial — Jastreboff et al., New England Journal of Medicine (2022)

Jastreboff and colleagues conducted the SURMOUNT-1 trial: a 72-week, double-blind, randomized, placebo-controlled phase 3 trial. The trial enrolled 2,539 adults with a body mass index of 30 kg/m² or greater, or 27 kg/m² or greater with at least one weight-related complication, excluding individuals with type 2 diabetes. Participants were randomized to receive once-weekly subcutaneous tirzepatide at 5 mg, 10 mg, or 15 mg, or placebo, alongside lifestyle intervention.

The authors reported that tirzepatide produced substantial and sustained reductions in body weight at all three amounts [1]. Mean percentage changes in body weight at week 72 were −15.0%, −19.5%, and −20.9% for the 5 mg, 10 mg, and 15 mg amounts respectively, compared with −3.1% in the placebo arm. Approximately 91% of participants in the 15 mg arm achieved at least 5% weight reduction, and 57% achieved at least 20%.

Read the full study: Tirzepatide Once Weekly for the Treatment of Obesity (NEJM 2022).

SURPASS-2 Trial — Frías et al., New England Journal of Medicine (2021)

Frías and colleagues conducted the SURPASS-2 trial: a 40-week, open-label, randomized, parallel-group, phase 3 head-to-head comparison of tirzepatide and semaglutide in adults with type 2 diabetes. The trial randomized 1,879 patients (1:1:1:1) to once-weekly tirzepatide at 5 mg, 10 mg, or 15 mg, or once-weekly semaglutide at 1 mg, all as add-on therapy to metformin. Mean baseline HbA1c was 8.28% and mean baseline body weight was 93.7 kg.

The authors concluded that tirzepatide was noninferior and superior to semaglutide with respect to mean change in glycated hemoglobin from baseline at week 40 [2]. Mean reductions in body weight were 7.6 kg, 9.3 kg, and 11.2 kg for the 5 mg, 10 mg, and 15 mg tirzepatide amounts respectively, compared with 5.7 kg for semaglutide 1 mg.

Read the full study: Tirzepatide versus Semaglutide Once Weekly in Patients with Type 2 Diabetes (NEJM 2021).

SURPASS-CVOT Trial — Nicholls et al., New England Journal of Medicine (2025)

Nicholls and colleagues conducted the SURPASS-CVOT trial: a randomized, double-blind, active-comparator, noninferiority phase 3 trial conducted at 640 sites globally. The trial enrolled 13,299 adults with type 2 diabetes and established atherosclerotic cardiovascular disease, comparing once-weekly tirzepatide with once-weekly dulaglutide (a GLP-1 receptor agonist with prior cardiovascular benefit established in earlier outcomes trials) over a mean follow-up of approximately four years.

The authors reported that tirzepatide was noninferior to dulaglutide with respect to the primary composite outcome of cardiovascular death, non-fatal myocardial infarction, or non-fatal stroke (12.2% vs. 13.1%; HR 0.92; P = 0.003 for noninferiority) [3]. The investigators also observed greater reductions in HbA1c, body weight, and a 16% relative reduction in all-cause mortality compared with the dulaglutide group.

Read the full study: Cardiovascular Outcomes with Tirzepatide versus Dulaglutide in Type 2 Diabetes (NEJM 2025).

SURMOUNT-1 Three-Year Extension — Jastreboff et al., New England Journal of Medicine (2025)

In a longer-term analysis of the original SURMOUNT-1 cohort, Jastreboff and colleagues reported three-year safety and efficacy outcomes for tirzepatide in adults with both obesity and prediabetes. Participants continued once-weekly subcutaneous tirzepatide (5 mg, 10 mg, or 15 mg) or placebo, with body weight and progression to type 2 diabetes assessed over 176 weeks.

The authors concluded that three years of treatment resulted in sustained weight reduction and a markedly lower risk of progression to type 2 diabetes compared with placebo [4]. Among participants with obesity and prediabetes at baseline, the cumulative incidence of progression to type 2 diabetes was substantially lower in all tirzepatide arms than in the placebo arm.

Read the full study: Tirzepatide for Obesity Treatment and Diabetes Prevention (NEJM 2025).

About the Compound

Tirzepatide is a synthetic, 39-amino-acid linear peptide that functions as a dual agonist at two incretin receptors: the glucose-dependent insulinotropic polypeptide (GIP) receptor and the glucagon-like peptide-1 (GLP-1) receptor. The molecule is structurally based on the native GIP backbone, with substitutions and modifications that confer cross-reactivity with the GLP-1 receptor while resisting enzymatic degradation by dipeptidyl peptidase-4 (DPP-4). A C-20 fatty diacid moiety is attached via a γ-glutamic acid and 2x[2-(2-aminoethoxy)ethoxy]acetic acid (AEEA) linker, enabling reversible binding to serum albumin and producing a circulatory half-life of approximately five days. This pharmacokinetic profile supports once-weekly administration in research models.

  • CAS Number: 2023788-19-2
  • Molecular Formula: C225H348N48O68
  • Molecular Weight: 4813.45 g/mol
  • Synonyms: LY3298176, GIP/GLP-1 dual agonist
  • Receptor targets (in research literature): GIP receptor and GLP-1 receptor (dual agonist)

Product Specifications

Omnix Peptides supplies tirzepatide as a sterile, lyophilized (freeze-dried) powder in a sealed glass vial intended exclusively for in vitro laboratory research. Each production lot is independently characterized using high-performance liquid chromatography (HPLC) and liquid chromatography–mass spectrometry (LC–MS) protocols.

  • Regulatory status (as of publication): FDA-approved as Mounjaro® (May 2022) for type 2 diabetes and as Zepbound® (November 2023) for chronic weight management; EMA-approved in equivalent indications.
  • Format: Lyophilized powder
  • Available strengths: 5 mg · 10 mg per vial
  • Verified Purity: >99% (HPLC, LC–MS)
  • Container: Sterile, sealed glass vial
  • Documentation: Batch-specific Certificate of Analysis (COA) available

Storage, handling, intended-use, and regulatory information are provided in the corresponding tabs on this product page.

References

  1. Jastreboff AM, Aronne LJ, Ahmad NN, et al; SURMOUNT-1 Investigators. Tirzepatide once weekly for the treatment of obesity. N Engl J Med. 2022;387(3):205-216. doi:10.1056/NEJMoa2206038
  2. Frías JP, Davies MJ, Rosenstock J, et al; SURPASS-2 Investigators. Tirzepatide versus semaglutide once weekly in patients with type 2 diabetes. N Engl J Med. 2021;385(6):503-515. doi:10.1056/NEJMoa2107519
  3. Nicholls SJ, Pavo I, Bhatt DL, et al; SURPASS-CVOT Investigators. Cardiovascular outcomes with tirzepatide versus dulaglutide in type 2 diabetes. N Engl J Med. 2025;393(24):2409-2420. doi:10.1056/NEJMoa2505928
  4. Jastreboff AM, le Roux CW, Stefanski A, et al; SURMOUNT-1 Investigators. Tirzepatide for obesity treatment and diabetes prevention. N Engl J Med. 2025;392(10):958-971. doi:10.1056/NEJMoa2410819
For research use only. Not for human consumption.