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SURVODUTIDE

A dual GLP-1 + glucagon receptor agonist. The GLP-1 side curbs appetite like semaglutide; the glucagon side raises energy expenditure and targets liver fat, it’s being developed primarily for fatty-liver disease (MASH).

Research referenceCommunity compiled

Molecular profile

The molecule itself: sequence, composition, mass, target, and registry identifiers.

Molecular formula
C₁₉₂H₂₈₉N₄₇O₆₁
Average mass
4232 Da
CAS number
2805997-46-8
Registry
PubChem CID 171378821
Receptor / pathway
GLP-1 receptorGlucagon receptor
Formula, mass and identifiers from PubChem CID 171378821.
Research & reference information

This profile compiles research and community-sourced reference information for educational purposes. Information may evolve as research and community knowledge develop. It is not individualized medical advice.

Overview

Survodutide is a breakthrough dual GLP-1 and Glucagon receptor agonist engineered for powerful metabolic weight loss and liver disease reversal.

What problem it targets: It targets severe obesity, metabolic dysfunction-associated steatohepatitis (MASH / NASH), advanced liver fibrosis, and stalled fat loss.

What It Does

• Dual-action metabolic synergy: GLP-1 activation suppresses appetite and reduces caloric intake, while glucagon activation fires up energy expenditure and liver fat oxidation.

• Reverses metabolic liver fibrosis: Directly targets hepatic cells to resolve liver inflammation, clear accumulated triglycerides, and reverse early fibrotic scarring.

• Keeps metabolic burn elevated during dieting: Prevents the natural dip in basal metabolic rate that usually occurs during substantial weight loss.

• Realistic expectations: Administered as a once-weekly subcutaneous injection. Clinical trials show exceptional liver clearance alongside ~19% body weight reduction in obese adults over 48 weeks.

Reconstitution

Vial sizeBAC water / SolventConcentration
10 mg+ 2 mL5 mg/mL

Protocol

Phase (4FrequencyDoseUnits (2.5 mg/mL)Notes
Weeks 1–4Once0.6 mg24uIntro phase, adapt to dual GLP-1 + glucagon stimulation. weekly
Weeks 5–8Once1.2–2.448–96uStep up only if well tolerated.
weeklymg
Weeks 9–16Once3.6–4.8(switch to 5 mg/mL:Target range. 4.8 mg/week is the trial target.
weeklymg72–96u)
MaintenanceOnce4.8–6–4.8 mg = Phase 2 target (NCT04667377); 6 mg = Phase 3 SYNCHRONIZE max. Do not exceed 6 mg,
weeklymghigher figures are unverified community claims. Cycle: titrate over 14–20 weeks; the glucagon component makes nausea more likely than pure GLP-1, so go slowly. Timing: same day each week, any time. Note: generally harsher on GI than mazdutide, don’t rush the ladder. Women: Women lose more than men at the same dose but report more GI (start lower). In PCOS they improve cycles, lower free testosterone and raise ovulation; a real unplanned-pregnancy risk. Stop before conceiving. Men: In men, excess fat lowers testosterone; GLP-1 raises total testosterone, SHBG and gonadotropins as weight drops, and improves sperm and erectile function; and preserves fertility, unlike TRT (which suppresses sperm).

Handling & Stacking

Injection site
SubQ, abdomen/thigh. Rotate.
Storage
  • Freeze-dried: -4°F.
  • Reconstituted: 36–46°F.
  • Best used within ~3–4 weeks, kept cold (structure-based estimate, no published data); that is close to the 28- day sterility limit, so use whichever comes first.
Side effects
Nausea, vomiting, diarrhea, decreased appetite, elevated heart rate (glucagon effect). GI effects dose-dependent.
What to expect
Appetite suppression + a metabolic-rate bump; weight and liver-fat drop over months. Investigational. Supply math 10mg → 5 vials (16-wk titration toward 4.8 mg/wk)
Pairs well with
Lipo-C / L-Carnitine (metabolic support)
Avoid
Personal/family history of medullary thyroid carcinoma or MEN2. Prior pancreatitis. Pregnancy. Stacking with other incretins

Safety & Patient Education

Contraindications
Personal/family history of medullary thyroid carcinoma or MEN2 (GLP-1 class warning) Prior pancreatitis Pregnancy and lactation Severe gastroparesis
Warnings
Thyroid C-cell tumor signal in rodents (GLP-1 class) Gallbladder disease with rapid weight loss Elevated heart rate from glucagon agonism Possible small glucose elevation from glucagon, monitor in diabetics Investigational compound, no long-term human safety outside trials
Drug interactions
Insulin / sulfonylureas: hypoglycemia risk, adjust and monitor Delayed gastric emptying alters oral drug absorption Other GLP-1 agents: do not combine
Labs
  • Fasting glucose / HbA1c (baseline + periodic) Liver enzymes (often the point of therapy, track ALT/AST) Lipase if pancreatitis suspected; renal function with GI losses Resting heart rate / blood pressure Out of range?
  • Rising glucose/HbA1c = sugar creeping up; rising ALT/AST = liver stress (often the point of therapy, track the trend).
Stop criteria
Severe persistent abdominal pain (pancreatitis) Persistent vomiting / dehydration Sustained tachycardia or palpitations Pregnancy
Patient education
The glucagon component adds GI harshness and can raise heart rate, titrate slowly
References
researchdosing · peptidedosages · PubMed · clinicaltrials.gov · GLP-1 sex differences · Jensterle 2020