Mazdutide
A weekly dual-hormone injection approved in China, with phase 3 weight-loss results.
Also called: IBI362, IBI-362, LY3305677, LY-3305677, Xinermei.
GLP-1 / glucagon dual agonists · GLP-1 and glucagon receptor dual agonist · Evidence: Approved drug.
What Mazdutide does
Mazdutide activates GLP-1 and glucagon receptors. China approved it for adult weight management and type 2 diabetes in 2025. It has phase 3 results, but no FDA or EMA label. Stomach symptoms are common, and long-term outcomes remain uncertain.
- In phase 3 trials, adults lost weight; China approved it for adult weight management in June 2025, but the US has not. (Studied in a trial)
- In type 2 diabetes trials, blood sugar improved, and early conference results favored it over semaglutide 1 mg. (Studied in a trial)
- Some people report more energy or better appetite control when pairing it with tirzepatide. (Reported by users)
Uses in the sources
Mazdutide dosage
Typical reported dose: 2 mg once a week to start, up to 6 mg
- Early single 5 mg: 5 mg single dose single dose, under the skin. Studied in a trial. Studied in: Healthy adults. (source)
- Early obesity trial: 3 mg: 1 mg once weekly, then 2 mg once weekly, then 3 mg once weekly once weekly, under the skin. Studied in a trial. Studied in: Chinese adults with overweight plus a complication, or obesity. (source)
- Early obesity trial: 4.5 mg: 1.5 mg once weekly, then 3 mg once weekly, then 4.5 mg once weekly once weekly, under the skin. Studied in a trial. Studied in: Chinese adults with overweight plus a complication, or obesity. (source)
- Early obesity trial: 6 mg: 2 mg once weekly, then 4 mg once weekly, then 6 mg once weekly once weekly, under the skin. Studied in a trial. Studied in: Chinese adults with overweight plus a complication, or obesity. (source)
- Early diabetes trial: 3 mg: 1 mg once weekly, then 2 mg once weekly, then 3 mg once weekly once weekly, under the skin. Studied in a trial. Studied in: Chinese adults with type 2 diabetes, with/without metformin. (source)
- Early diabetes trial: 4.5 mg: 1.5 mg once weekly, then 3 mg once weekly, then 4.5 mg once weekly once weekly, under the skin. Studied in a trial. Studied in: Chinese adults with type 2 diabetes, with/without metformin. (source)
Highest studied: Highest published weekly SC target found: 16 mg..
These are doses reported in labels, trials or user reports, not a personal plan. Check the source behind each one.
How to mix Mazdutide
Comes as: Community-reported powder vials.
Mixed with: No dependable user-log diluent and compatibility data were verified..
Common vial sizes: 10 mg. Common water amounts: mL.
- 10 mg vials occur in a forum log. Frequency and true contents are unknown.
- Approved Chinese product instructions were not available; do not borrow storage or mixing rules from another GLP-1.
Before mixing: Unknown for unregulated vials; no verified storage instructions were recovered.
After mixing: No validated home-mixed stability or beyond-use time was found.
Mazdutide side effects and risks
Reported side effects
- Vomiting: GLORY 2 9 mg: 53.1% vs 1.3% placebo., moderate (source)
- Nausea: GLORY 2 9 mg: 46.9% vs 3.2% placebo., moderate (source)
- Diarrhea: GLORY 2 9 mg: 39.4% vs 6.5% placebo., moderate (source)
- Constipation: Early 16 mg cohorts: 16.7% and 33.3%; placebo: 12.5%., moderate (source)
- Fatigue: Early 16 mg cohorts: 25.0% and 75.0%; placebo: 0%., moderate (source)
- Low blood sugar: Phase 2 diabetes: 10% pooled mazdutide vs 8% placebo., moderate (source)
- Injection site reaction: Phase 2 obesity: 4.8%/1.6%/3.3% at 3/4.5/6 mg; placebo: 6.5%., mild (source)
- Heart rate increase: Observed in early trials; incidence depends on how the event was defined., moderate (source)
- Pancreatitis, severe allergy or dehydration-related kidney injury: Class concerns; available trials cannot establish reliable rare event rates., serious (source)
Stop and get help if
- Severe or persistent belly pain, especially into the back: Stop dosing and get urgent medical assessment.
- Trouble breathing; swelling of lips, tongue or throat: Call emergency services now.
- Chest pain, fainting or a sustained racing heart: Seek emergency care.
- Sudden vision loss or a major vision change: Seek urgent eye/emergency assessment.
- Confusion, seizure or low blood sugar that does not resolve: Call emergency services; do not take another dose.
- Repeated vomiting, inability to keep fluids down or very little urine: Get urgent care for dehydration or kidney injury.
- Belly swelling with vomiting and inability to pass stool or gas: Seek urgent medical assessment.
- Fever or spreading redness, heat or swelling after an injection: Get urgent medical care for possible infection.
Who should avoid it
- pregnant: Excluded from trials; no established pregnancy safety.
- breastfeeding: No established infant safety; avoid exposure while breastfeeding.
- tryingToConceive: Plan stopping and contraception with a clinician; no verified compound-specific washout is given here.
- under18: Pediatric safety and dosing remain limited.
- mtcOrMen2: Personal/family medullary thyroid cancer or MEN2 was excluded. Human thyroid-cancer risk is not established.
- eatingDisorderHistory: Appetite suppression may worsen restrictive eating; this is a precautionary screen.
- pancreatitisHistory: Review prior pancreatitis before exposure; this is also a GLP-1 class precaution.
- gallbladderDisease: Gallbladder symptoms need review during substantial weight loss.
- gastroparesis: Delayed stomach emptying can worsen severe stomach-motility problems.
- diabeticRetinopathy: Rapid glucose improvement can worsen existing eye disease; direct long-term risk is uncertain.
- kidneyDisease: Vomiting and diarrhea can cause dehydration and kidney injury. Special-population data are incomplete.
- liverDisease: Advanced liver disease needs specialist review; trial findings do not establish self-dosing.
- heartCondition: Heart rate rose in early trials; review rhythm problems and symptoms.
- uncontrolledBloodPressure: Review uncontrolled pressure before use; blood pressure changes and dehydration need monitoring.
- surgeryPlanned: Tell the anesthesia team about use; delayed stomach emptying can raise aspiration risk.
- other: Prior severe reaction to this compound or its ingredients should stop re-exposure.
- testedAthlete: No named 2026 prohibition found. China approval changes the S0 analysis; confirm with the anti-doping authority.
Interactions
- Insulin: Additive low-glucose risk; insulin doses may need clinician adjustment.
- Sulfonylureas: Additive low-glucose risk; review dose and glucose checks.
- Other GLP-1 or related appetite injections: Overlapping actions may worsen stomach symptoms and dehydration. No verified home stack has a tested dose.
- Narrow-window oral medicines: Slower stomach emptying or vomiting may alter exposure. Monitoring needs are medicine-specific.
- Oral contraception: Vomiting may reduce pill reliability. A tirzepatide-specific backup rule cannot be assumed for this drug.
- Oral anticoagulants: Illness and poor intake may change anticoagulation. No direct interaction magnitude is established here.
Product quality risks
- No independent published assay series of online mazdutide products was found.
- Indirect evidence: online semaglutide samples had 7%–14% purity and 29%–39% excess content; one had elevated endotoxin.
- FDA names this compound in warnings about unapproved research-labeled GLP-1 products of unknown quality.
- Wrong identity, wrong amount, contamination and counterfeit packaging are separate risks.
What to expect
China-approved. 45 distinct registered human protocols plus one case report found. Planned studies are included; a master-protocol duplicate and nonspecific registry are excluded.
Key studies
- First doses (ADA 2021): A small single-dose study supported weekly development. (source)
- Early repeat dosing: Conference-only results leave important dose and safety details missing. (source)
- Early diabetes dosing: Conference-only results leave important dose and safety details missing. (source)
- Early obesity trial: Weight or glucose improved; stomach symptoms limited tolerability. (source)
- Early diabetes trial: Weight or glucose improved; stomach symptoms limited tolerability. (source)
- Early 9 mg cohort: Weight or glucose improved; stomach symptoms limited tolerability. (source)
Mazdutide FAQ
- Is Mazdutide FDA-approved? No FDA approval or dosing label found. China approved adult weight management in June 2025 and diabetes in September 2025; these are not US approvals.
- How do people take it? Under the skin, once weekly. 48 weeks. Source: studied in a trial.
- What's the difference between Mazdutide and Tirzepatide? Mazdutide: a weekly dual-hormone injection approved in China, with phase 3 weight-loss results. Tirzepatide: a weekly GIP/GLP-1 injection with strong diabetes and weight-loss evidence and common stomach side effects. Why people pair them: people seek a glucagon effect alongside appetite control.
- Can I take it with Tirzepatide? People seek a glucagon effect alongside appetite control. Overlapping GLP-1 effects; no trial validates the home combination. Source: reported by users. Ask a doctor before combining anything.
- Is it banned in sport? It is unclear (WADA 2026). China approval means S0 is not automatic. No named listing found; obtain an authoritative sport-specific ruling.
- How long does a mixed vial last? No validated home-mixed stability or beyond-use time was found.
Related to Mazdutide
- Survodutide: A weekly dual-hormone injection with phase 3 weight-loss data and frequent stomach side effects.
- Tirzepatide: A weekly GIP/GLP-1 injection with strong diabetes and weight-loss evidence and common stomach side effects.
Sources
- 21 CFR 216.23 — Bulk drug substances that can be used to compound drug products in accordance with section 503A of the Federal Food, Drug, and Cosmetic Act., Office of the Federal Register · eCFR · 2026
- 503B Bulk Drug Substances List, FDA · FDA · 2026
- Bulk Drug Substances Nominated for Use in Compounding Under Section 503A of the Federal Food, Drug, and Cosmetic Act, FDA · FDA · 2026
- Bulk Drug Substances Used in Compounding Under Section 503A of the FD&C Act, FDA · FDA · 2026
- FDA’s Concerns with Unapproved GLP-1 Drugs Used for Weight Loss, FDA · FDA · 2026
- Find product information about medicines, Medicines and Healthcare products Regulatory Agency · MHRA · 2026
- Medicines, European Medicines Agency · European Medicines Agency · 2026
- The 2026 Prohibited List, World Anti-Doping Agency · WADA · 2026
- The Prohibited List, World Anti-Doping Agency · World Anti-Doping Agency · 2026
- Understanding your responsibilities when importing, compounding and supplying unapproved peptide products, Therapeutic Goods Administration · Therapeutic Goods Administration · 2026
- WEGOVY- semaglutide injection, solution WEGOVY- semaglutide tablet, DailyMed · DailyMed · 2026
- Bulk Drug Substances Nominated for Use in Compounding Under Section 503B of the Federal Food, Drug, and Cosmetic Act, FDA · FDA · 2025
- Nutritional priorities to support GLP-1 therapy for obesity: a joint Advisory from the American College of Lifestyle Medicine, the American Society for Nutrition, the Obesity Medicine Association, and The Obesity Society., Mozaffarian D et al. · The American journal of clinical nutrition · 2025
- Weight loss medicine Mazdutide approved for commercialization in China, Shanghai Municipal Government · Shanghai Municipal Government · 2025
- Australian Register of Therapeutic Goods (ARTG), Therapeutic Goods Administration · TGA
Sources checked: 2026-10-18.
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