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UPA MAGTIDELIRA 33 (Maglutide 33mg) Pre-Filled Pen | Research Peptide

R 2,150.00 R 1,990.00

UPA Magtidelira 33 mg — Pre-Filled Pen

Metabolic Research | GLP-1 & GIP Signalling | Appetite Regulation

Product Overview

UPA Magtidelira 33 mg is a pre-filled pen-format product marketed as a hybrid formulation containing tirzepatide and semaglutide, with a labelled total strength of 33 mg.

Tirzepatide acts on two metabolic hormone receptors, GIP and GLP-1, while semaglutide selectively activates the GLP-1 receptor. These pathways are involved in appetite signalling, blood-glucose regulation and energy balance.

Both compounds have been extensively studied in clinical research, particularly in relation to type 2 diabetes and weight management. However, their combination in a single product is a separate formulation that requires its own evidence of safety, quality and efficacy.

Key Clinical Research Findings

1. Body-Weight Reduction

In the 72-week SURMOUNT-1 trial, average body-weight reductions with tirzepatide were 15.0%, 19.5% and 20.9% across the three studied dose groups.

In the 68-week STEP 1 trial, semaglutide 2.4 mg produced an average body-weight reduction of approximately 14.9%, compared with 2.4% with placebo.

These results demonstrate the potential of the individual medicines in their studied populations. They are not predictions of weight loss from Magtidelira.

2. Appetite Regulation

Tirzepatide and semaglutide influence incretin pathways involved in appetite and food intake. Clinical studies of their respective authorised formulations have demonstrated meaningful effects on body weight.

However, there is insufficient clinical evidence to conclude that combining both compounds produces greater appetite control or superior weight-loss outcomes.

3. Blood-Glucose Regulation

Both medicines have demonstrated improvements in blood-glucose control in clinical trials involving people with type 2 diabetes. Tirzepatide's dual GIP/GLP-1 receptor activity and semaglutide's GLP-1 receptor activity have been studied in their respective authorised formulations.

These findings cannot establish the efficacy or safety of an unverified combination product.

4. Metabolic Health Research

Clinical trials of tirzepatide and semaglutide have examined changes in body weight and several cardiometabolic markers. The findings have contributed to significant scientific interest in incretin-based treatments for metabolic health.

The extent to which these outcomes apply to Magtidelira is unknown without appropriate product-specific clinical evidence.

Key Features

33 mg labelled total quantity: Identified as MAGTIDELIRA 33 (Maglutide 33 mg). The labelled quantity is not a verified breakdown of individual ingredients.

Pre-filled pen presentation: Supplied in a pen-format presentation for laboratory and scientific research purposes.

Incretin research context: Marketed as a tirzepatide–semaglutide formulation. Research on these compounds individually does not establish the safety or efficacy of this combined product.

Batch-specific verification: Consult verified manufacturer documentation and the applicable Certificate of Analysis, where available, to assess identity, composition, purity and quality.

Dosage & Usage

Magtidelira 33 — Product Information Printed on the Box

  • Product strength: 33 mg
  • Format: Solution for injection in a pre-filled pen
  • Volume: 5 × 3 mL
  • Dose per injection: 0.3 mL per dose
  • Labelled doses: 33 doses × 1 mg

Click / Dial / Inject

0.3 mL per dose

1 mg per dose

FAQ's & Tips


What is MAGTIDELIRA 33? MAGTIDELIRA 33 is a research product labelled as Maglutide 33mg and supplied in a pre-filled pen format. What is it supplied for? It is supplied for laboratory and scientific research purposes only. Does it come with a COA? Batch-specific COA documentation should be provided where available.

Research

Research context

The following peer-reviewed studies investigate tirzepatide and semaglutide as separate medicines. They did not evaluate MAGTIDELIRA 33, its labelled 33 mg formulation, or a combined tirzepatide–semaglutide product. These findings therefore do not establish this product’s composition, quality, safety or efficacy.

1. Tirzepatide and body weight: SURMOUNT-1 (2022)

In a randomised, placebo-controlled trial involving 2,539 adults with obesity or overweight and a weight-related complication, excluding diabetes, average body-weight reductions at 72 weeks were 15.0%, 19.5% and 20.9% across the tirzepatide groups, compared with 3.1% with placebo. Gastrointestinal adverse events were the most common. These are results for the studied medicine, not expected outcomes for MAGTIDELIRA 33.

Read: Tirzepatide Once Weekly for the Treatment of Obesity, New England Journal of Medicine

2. Semaglutide and body weight: STEP 1 (2021)

In a randomised trial of 1,961 adults with overweight or obesity without diabetes, semaglutide plus lifestyle intervention produced an average body-weight reduction of 14.9% at 68 weeks, compared with 2.4% with placebo plus lifestyle intervention. Nausea and diarrhoea were common, and gastrointestinal events led to treatment discontinuation in some participants.

Read: Once-Weekly Semaglutide in Adults with Overweight or Obesity, New England Journal of Medicine

3. Blood-glucose research: SURPASS-2 (2021)

This 40-week, randomised, open-label trial involving 1,879 people with type 2 diabetes compared tirzepatide against semaglutide. Tirzepatide produced greater average reductions in glycated haemoglobin (HbA1c) at the studied doses. The trial compared the two medicines; it did not combine them and does not support claims of added benefit from using both together. Gastrointestinal adverse events were common in both groups.

Read: Tirzepatide versus Semaglutide Once Weekly in Patients with Type 2 Diabetes, New England Journal of Medicin

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