★ Metabolic

Survodutide

Metabolic · 10mg × 10 vials

GLP-1 + glucagon dual agonist. Mechanism comparable to mazdutide; studied in metabolic and hepatic trials.

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Pricing
$400from · 10-vial kit
Shipping: $40 US · $60 international (10-vial kits only) · single vials $20, US only · free over $1,000
10mg × 10 vials$400
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0 days
Half-life
Metabolic / Weight Loss
Class
Overview

What Is Survodutide?

Survodutide is a synthetic dual agonist of the GLP-1 receptor and the glucagon receptor, developed by Boehringer Ingelheim in partnership with Zealand Pharma. Structurally derived from oxyntomodulin and engineered with fatty-acid acylation for a long-acting half-life, it shares its core pharmacology with mazdutide, the other major GLP-1/glucagon dual agonist, with different receptor-binding ratios and pharmacokinetic tuning.

The dual-agonism rationale is the same: GLP-1 agonism drives appetite suppression, delayed gastric emptying, and glucose-dependent insulin release, while glucagon agonism adds hepatic lipid oxidation, elevation of basal metabolic rate, and improved hepatic insulin sensitivity. Survodutide's clinical programme has emphasised metabolic dysfunction-associated steatohepatitis (MASH, formerly NASH) as a primary indication alongside obesity, with Phase 2 histology showing resolution of MASH without worsening fibrosis in more than 60% of participants at 48 weeks at the higher doses. The obesity Phase 3 programme is ongoing, and the compound is not approved in any market.

Published Safety Data

What the published studies measured.

What the studies show
Measured in clinical trials
  • Nausea: 51-65% across active arms (Phase 2 obesity, 46 wk) - mild to moderate, peaks during dose escalation, the highest nausea rate of any published dual or triple agonist
  • Diarrhea: 27-35% - mild to moderate
  • Vomiting: 27-38% - mild to moderate, mostly at titration steps, also class-leading rate
  • Constipation: 15-22% - generally mild
  • Injection-site reactions: 8-15% - redness, small welt at site; more common than on sema/tirz, mechanism likely the glucagon component
  • Decreased appetite: 35-44% - this is the intended effect, flagged as an AE in trials
  • Heart rate increase: mean +5-8 bpm at top doses - generally not symptomatic, larger signal than mazda's +3-5 bpm but smaller than reta's +6-10 bpm at 12 mg
  • Hypoglycemia: rare in non-diabetic subjects, low single digits. Same balance logic as mazda, the GLP-1 arm's insulin amplification dynamically counterbalances the glucagon arm's gluconeogenesis push.
The Research

Peer-reviewed studies and clinical guidelines - tap any to read the source.

PubMed / LancetLe Roux et al, Survodutide Phase 2 Obesity Trial, Lancet 2024

00027-3/fulltext) - pivotal Phase 2, 387 pts, 46 weeks, 18.7% loss at 4.8 mg, 19.0% loss at 6 mg

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PubMed / NEJMSanyal et al, Survodutide in MASH Phase 2, NEJM 2024

83% MASH resolution at 6 mg, 48 weeks, no fibrosis worsening

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PubMedBoehringer/Zealand dual agonist preclinical pharmacology, Cell Metabolism 2022

receptor balance, glucagon-leaning vs balanced

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PubMedSurvodutide cardiovascular and hepatic outcomes review, J Hepatol 2025

class comparison, MASH positioning

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Clinical guidelinesBoehringer Ingelheim SYNCHRONIZE Phase 3 program announcement

Phase 3 program in obesity and MASH, breakthrough therapy designation

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Clinical guidelinesFDA Breakthrough Therapy Designation for Survodutide in MASH, 2024

regulatory positioning

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+ 5 more studies & references

Reconstitution & Storage

Storage: refrigerated 2-8°C, ~28 days after reconstitution. Lyophilized vials stored at -20°C long-term, room-temp shipping is fine short-term. Avoid freeze-thaw cycles.

All products sold for research purposes only. Not for human or animal consumption. Must be 21 or older to purchase. By placing an order you confirm compliance with all applicable local laws and regulations.