Mazdutide for Health & Longevity - Quick Reference Sheet

Mazdutide for Health & Longevity

Created on 10/06/2026 – Quick Reference based on Evidence Review created using AI4L / Opus 5.5 – Audit

Mazdutide, a once-weekly injectable medication imitating a fullness-signaling gut hormone and an energy-releasing hormone, is approved only in China for weight management and type 2 diabetes. Evidence for weight and waist loss, lower blood sugar and cholesterol is strong. Main costs are frequent stomach and bowel side effects and a higher resting heart rate. Weight partly returns after stopping. Trials are short and nearly all company-funded; long-term safety is unknown. (Full Review)

Protocol

Trial-tested weight-management regimen (China)
4 mg or 6 mg once weekly
Reached by 2 mg steps every 4 weeks
Higher-dose regimen for BMI of 30 or more
9 mg once weekly
Escalated 3 mg, 6 mg, then 9 mg at 4-week intervals
Time of day
Any time, same weekday each week
Single weekly subcutaneous injection, with or without food
Time to effect
Weight loss
Clear by 12 weeks
Appetite drops within the first weeks; loss continued to 48–60 weeks
Blood sugar
Tracks weight loss
HbA1c lower than placebo at 24 weeks
Liver fat
Tracks weight loss
Marked fall at 48 weeks in an imaging subset

Benefits

Contraindications
  • Personal or family history of medullary thyroid carcinoma or MEN2
  • History of pancreatitis
  • Type 1 diabetes
  • Proliferative diabetic retinopathy, diabetic macular edema, or retinopathy requiring acute treatment
  • Two or more episodes of ketoacidosis, hyperosmolar state or lactic acidosis within 6 months
  • History of moderate to severe depression, severe mental illness, or any lifetime suicide attempt
  • Pregnancy and breastfeeding
  • Children and adolescents outside trials
Key Interactions
  • Insulin and sulfonylureas (insulin glargine, glimepiride, gliclazide): Caution (theoretical)
  • Other GLP-1 receptor agonists and DPP-4 inhibitors (semaglutide, tirzepatide, sitagliptin): Avoid (theoretical)
  • Oral drugs with narrow dosing margins (warfarin, levothyroxine): Monitor (theoretical)
  • Oral contraceptives (ethinyl estradiol with levonorgestrel): Monitor (theoretical)
  • Blood-pressure drugs (amlodipine, lisinopril, hydrochlorothiazide): Monitor (theoretical)
  • Diuretics and SGLT2 inhibitors (furosemide, empagliflozin): Caution (theoretical)
  • Heart-rate-raising drugs (stimulants such as methylphenidate, pseudoephedrine): Caution (theoretical)
  • Over-the-counter pain relievers, NSAIDs (ibuprofen, naproxen): Caution (theoretical)
  • Glucose-lowering supplements (berberine, chromium, cinnamon extract): Monitor (theoretical)
  • Blood-pressure-lowering supplements (aged garlic extract, beetroot nitrate, magnesium): Monitor (theoretical)
  • Stimulant weight-loss supplements (high-dose caffeine, synephrine, yohimbine): Avoid (theoretical)
  • Bulk fiber supplements (psyllium, glucomannan): Monitor (theoretical)
  • Alcohol: Caution (theoretical)
  • Very-low-calorie diets or prolonged fasting: Caution (theoretical)

Risk & Side Effects

  • High: Gastrointestinal adverse events
  • Medium: Increased resting heart rate
  • Low: Gallbladder and bile duct disease; loss of lean mass; lipase elevation and pancreatitis; hypoglycemia with insulin or sulfonylureas; delayed stomach emptying and anesthesia aspiration; worsening diabetic retinopathy
  • Speculative: Thyroid C-cell tumors; anti-drug antibodies

Monitoring

Marker Target Why
Body weight and waist circumference No established target; track percent change from own baseline Expected to change
Lean mass (DEXA) No established target; track lean-mass change from own baseline Expected to change (safety-relevant)
HbA1c 4.0–5.6% (standard reference range) Expected to change
LDL cholesterol No established target; track percent change from own baseline Expected to change
Triglycerides No established target; track percent change from own baseline Expected to change
ALT 7–55 U/L (standard reference range) Safety check and expected to change
Lipase Within the laboratory's upper limit of normal (standard reference range) Safety check
Serum uric acid 3.5–7.2 mg/dL (standard reference range) Expected to change
Resting heart rate 60–100 beats per minute (standard reference range) Safety check
Blood pressure No established target; track change from own baseline Expected to change
eGFR No established target; track change from own baseline Safety check

Cadence: Weekly weight and resting heart rate during escalation; blood tests 4 weeks after reaching maintenance dose, then every 3–6 months in the first year and every 6–12 months thereafter; DEXA scan at 6–12 months.

Qualitative Assessment

  • Appetite control and reduced food cravings
  • Gastrointestinal tolerance (nausea, bowel habits)
  • Energy levels and exercise performance
  • Strength in key lifts or grip strength
  • Sleep quality and daytime alertness
  • Mood and relationship with food