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Mazdutide

$69.99

Mazdutide — a dual GLP-1/glucagon receptor agonist (IBI362) developed by Innovent Biologics. Studied in Phase II/III trials in China for obesity and T2DM, showing significant weight reduction and glycemic benefits with strong hepatic activity. Supplied lyophilized at ≥98% purity (HPLC-verified) with batch-specific COA. For research use only.

SKU: RPS-MAZDU-001 Category: Tags: ,

Mazdutide Research Peptide — Scientific Overview

Mazdutide (IBI362) is a dual GLP-1 and glucagon receptor agonist developed by Innovent Biologics (China). It belongs to the same mechanistic class as Survodutide — simultaneously engaging GLP-1R for satiety, insulin secretion, and glucose regulation, and GCGR for hepatic fat mobilization and energy expenditure. Mazdutide is distinguished by its acylated design enabling once-weekly subcutaneous dosing and by its clinical development program largely conducted in Chinese populations.

Mazdutide (IBI362) is a dual GLP-1 and glucagon receptor agonist developed by Innovent Biologics (China). It belongs to the same mechanistic class as Survodutide — simultaneously engaging GLP-1R for satiety, insulin secretion, and glucose regulation, and GCGR for hepatic fat mobilization and energy expenditure. Mazdutide is distinguished by its acylated design enabling once-weekly subcutaneous dosing and by its clinical development program largely conducted in Chinese populations. Phase II data for Mazdutide showed significant body weight reductions (approximately 11% at 24 weeks) and robust glycemic improvements in Type 2 diabetes patients. Phase III trials (GLORY series) are ongoing for obesity and Type 2 diabetes in China, with submission for approval expected. Mazdutide’s clinical data contribute to the body of evidence supporting dual GLP-1/glucagon agonism as a therapeutic approach in metabolic disease, and provide a comparator for researchers studying this class.

Research Background

Phase II data for Mazdutide showed significant body weight reductions (approximately 11% at 24 weeks) and robust glycemic improvements in Type 2 diabetes patients. Phase III trials (GLORY series) are ongoing for obesity and Type 2 diabetes in China, with submission for approval expected. Mazdutide’s clinical data contribute to the body of evidence supporting dual GLP-1/glucagon agonism as a therapeutic approach in metabolic disease, and provide a comparator for researchers studying this class.

Key Research Areas

  • GLP-1/Glucagon Dual Agonism Research: GCGR and GLP-1R co-activation studies in metabolic models
  • Obesity Research: Weight reduction, adipose biology, and energy metabolism studies
  • Type 2 Diabetes Research: Glycemic control, insulin secretion, and β-cell biology
  • NAFLD/MASH Research: Hepatic fat content reduction and liver biology studies
  • Comparative Pharmacology: Mazdutide vs. other dual/triple agonists — mechanism comparison
  • Metabolic Syndrome Research: Multi-faceted cardiometabolic risk factor modulation studies

Technical Specifications

Parameter Value
Classification Dual GLP-1/Glucagon receptor agonist (IBI362)
Developer Innovent Biologics
Purity ≥98% (HPLC-verified)
Form Lyophilized powder, sealed under argon
Storage −20°C (long-term)
Documentation Batch-specific COA (HPLC + Mass Spec)

Storage & Handling (Research Laboratories)

Lyophilized Mazdutide should be stored at −20°C for long-term preservation, protected from light and moisture. For short-term active research use, 4°C storage is acceptable for up to approximately 4 weeks. Minimize repeated freeze-thaw cycles. Follow standard laboratory peptide reconstitution and handling protocols for all experimental use.

Frequently Asked Questions — Mazdutide Research

How does Mazdutide compare to other GLP-1/Glucagon dual agonists?
The GLP-1/glucagon dual agonist class includes Survodutide (BI 456906, Boehringer Ingelheim) and Pemvidutide (ALT-801, Altimmune) alongside Mazdutide. All three share the core mechanism — combining GLP-1R agonism for appetite suppression with GCGR agonism for hepatic fat mobilization. Differences exist in their molecular structure, GLP-1R:GCGR potency ratio, and clinical development context. Mazdutide’s development is primarily in China, making it particularly relevant for research into Asian metabolic disease populations. All are investigational compounds not approved for human therapeutic use.
What weight loss data has been reported for Mazdutide in Phase II trials?
Phase II results for Mazdutide in patients with overweight or obesity showed approximately 11-12% body weight reduction at 24 weeks in the highest dose groups — comparable to or exceeding GLP-1R-only agonists and reflecting the additional metabolic contributions of GCGR activation. Glycemic improvements (HbA1c reduction) were also observed in diabetic subgroups. Phase III data from the GLORY trials is forthcoming.
Why is the GLP-1R:GCGR potency ratio important in dual agonist research?
Different dual GLP-1/glucagon agonists have different potency ratios at their two target receptors. A higher GLP-1R:GCGR ratio (more GLP-1 activity) produces more insulin secretion, stronger appetite suppression, and better glycemic control but less hepatic fat reduction. A higher GCGR ratio drives more hepatic fat mobilization, thermogenesis, and potentially greater weight loss but carries greater hyperglycemia risk without adequate GLP-1R offsetting. Researchers use these compounds with different ratios to probe the contribution of each receptor axis to metabolic outcomes.
Is Mazdutide approved for human use?
Mazdutide has not received regulatory approval. Phase III trials are ongoing. Research Peptides Supplies supplies Mazdutide for qualified laboratory research use only.
What documentation comes with Mazdutide?
Mazdutide from Research Peptides Supplies is verified at ≥98% purity by HPLC, with identity confirmed by Mass Spectrometry. A batch-specific COA is provided with every order.
⚗️ Research Use Only: This product is strictly intended for qualified laboratory and scientific research use by trained professionals in appropriate laboratory settings. It is not intended for human or veterinary administration, therapeutic use, food supplement applications, or any use outside controlled research environments. Not for human consumption.
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