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GLP-1 & metabolic · Treatment of obesity and type 2 diabetes

Mazdutide

1.5 → 6 mg weekly, titrated

Dual GLP-1/glucagon receptor agonist (LY3305677/IBI362) discovered in 2018, combining GLP-1 and glucagon signaling for stronger metabolic effects than single-receptor drugs. In Phase 3 trials for obesity and type 2 diabetes, showing notable weight loss and glycemic improvement.

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Reconstitution

Concentration by vial size and water volume
Vial1 mL water2 mL water
10 mg10 mg/mL5 mg/mL
  1. Use bacteriostatic water as the diluent.
  2. Add the water slowly, letting it run down the inside wall of the vial rather than onto the powder.
  3. Swirl gently to mix, then leave it to dissolve. Do not shake.
  4. Give it a few minutes. The finished solution should be clear and colourless.

Protocol

Route: Subcutaneous

Standard titration (once weekly, subcutaneous)

  • Weeks 1 to 4: 1.5 mg
  • Weeks 5 to 8: 3 mg
  • Weeks 9 to 12: 4.5 mg
  • Week 13 onward: 6 mg as the maintenance dose
  • (A simpler 2 mg, then 4 mg, then 6 mg version on the same 4-week steps is also used.)

Watch fasting glucose early

  • Because of the glucagon side of this drug, a small temporary rise in fasting blood sugar in the first 1 to 2 weeks is normal and usually settles by week 3 to 4
  • A persistent rise means slow the titration down

Dosing detail

  • Start at 1.5 mg and step up every 4 weeks. Going too fast is the top reason people quit, almost always from nausea.
  • Maintenance is commonly 6 mg weekly. China approved it at 4 mg and 6 mg in 2025 (brand name Xinermei), and a higher 9 mg dose (titrated 3, 6, 9) is under review there for severe obesity.
  • Some step down to 4.5 mg or 3 mg once at goal to hold results with fewer side effects.
  • One consistent day per week. Half-life is about 6.5 days.

Duration

  • Titrate over 12 to 16 weeks, then maintain. Like the other GLP-1 class drugs, stopping tends to bring weight back.

Notes

  • A GLP-1 / glucagon dual agonist, so appetite suppression plus a metabolic bump are the headline effects.
  • Inject subcutaneously and rotate sites.
  • GI effects are dose-related and ease with slow titration.

Storage and handling

  • Keep the powdered (lyophilized) vial in a cool, dark place. Refrigerate it for longer-term storage before mixing.
  • Once reconstituted and refrigerated at 2–8 °C away from light, use the vial within 90 days.
  • Do not freeze a reconstituted vial, and keep it away from heat and sunlight.
  • If the solution turns cloudy, develops floating particles, or shows any other sign of degradation, stop using that vial.