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Compound Evidence InstituteEvidence synthesis · established 2023Graded assessments of compounds, trials, methods and supply
Document set current to 30 July 2026
Compound monograph · §2

Survodutide — pharmacology

Molecular targets, mechanism of action, pharmacokinetics and interactions as characterised in humans.

Document identifier
CEI-MN-013/2
Series
Compound monograph
Version
3.1
Published
19 Nov 2025
Last reviewed
19 Nov 2025
Next review
19 Nov 2027
Identifier
10.71829/cei.mono.13
Certainty
Moderate
Cycle
2025 Q4

§2Pharmacology

§2.1Molecular targets

Table 2. Molecular targets recorded for Survodutide, with the character of the interaction and the potency where the Institute holds it.

TargetInteractionNote
Glucagon receptor (GCGR)AgonistHigher relative potency than in retatrutide
GLP-1 receptor (GLP1R)AgonistBalanced against the glucagon arm

§2.2Mechanism of action

Glucagon receptor agonism increases hepatic fatty-acid oxidation, resting energy expenditure and hepatic lipid clearance; GLP-1 receptor agonism supplies appetite suppression and offsets the glycaemic consequences of glucagon signalling. The combination is of particular interest in steatohepatitis, where a direct hepatic mechanism is mechanistically attractive rather than purely weight-mediated.[1,2]

§2.3Pharmacokinetics

Terminal half-life
≈6 days
Time to maximum concentration
approximately 24–48 h
Volume of distribution
not published
Plasma protein binding
high
Clearance
not published
Bioavailability
not published

Assumed proteolytic with beta-oxidation of the diacid.

Reconstructed plasma concentration–time profilePlasma concentration plotted against time after dosing, reconstructed from published pharmacokinetic parameters.0.00.51.01.50200400600800Time after first dose (hours)Relative concentrationt max ≈ 551 ht½ ≈ 144 h
Modelled profileSimulated observationsDose administration
Figure 2. Illustrative. Plasma concentration–time profile reconstructed by the Institute from the published half-life and time-to-maximum-concentration parameters using a one-compartment model with first-order absorption. The curve is not digitised from a published figure and its vertical scale is relative. It is published to convey the shape of the profile and the approach to steady state, not to supply a concentration at any time point.

§2.4Interactions

  • Not characterised

References cited on this page

References are numbered in order of first citation in this document. Each superscript in the text links to its entry below.

  1. le Roux CW, Steen O, Lucas KJ, Startseva E, Unseld A, Hennige AM. Glucagon and GLP-1 receptor dual agonist survodutide for obesity: a randomised, double-blind, placebo-controlled, dose-finding phase 2 trial. The Lancet Diabetes & Endocrinology 2024;12(3):162–173. doi:10.1016/S2213-8587(23)00356-X · PMID 38330977
  2. Sanyal AJ, Bedossa P, Fraessdorf M, Neff GW, Lawitz E, Bugianesi E, Anstee QM, Hussain SA, Newsome PN, Ratziu V, Hosseini-Tabatabaei A, Schattenberg JM. A phase 2 randomized trial of survodutide in MASH and fibrosis. New England Journal of Medicine 2024;391(4):311–319. doi:10.1056/NEJMoa2401755 · PMID 38847460

Identifiers are reproduced only where the Institute holds them. Where a digital object identifier or PubMed identifier is not shown, the Institute has recorded the journal and year and has not constructed an identifier.

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