Survodutide — reference
Investigational dual GLP-1/glucagon receptor agonist studied for weight management and MASH.
Regulatory status
Investigational. Investigational (Boehringer Ingelheim/Zealand) and not FDA-approved. Verify current status directly with the FDA.
Reported cautions
Pharmacokinetics
Published figures give an elimination half-life of ~6 days. Boehringer Ingelheim/Zealand Phase 2/3 data; not FDA-approved.
This figure is tagged Clinical trial in our evidence system. This figure comes from published human trial data rather than an approved label. It is real data, but it has not been through regulatory review, and the compound may not be approved for any use. You can see the shape this implies between doses in the Half-Life Visualizer, and compare it against every other compound in the Half-Life Data Table. Our sourcing page explains what each tier means.
Remember that an estimated curve is a model built from a population figure, not a measurement of your blood. Individual clearance varies, and for depot injections the figure describes release from the injection site rather than the compound clearing. Half-life explained →
What Peptide Plug does and does not publish
This page carries regulatory status, general context and published pharmacokinetics. It carries no dose, frequency or cycle information — that is a deliberate editorial line, because dosing is a clinical decision rather than reference data. We also do not sell, supply, source or link to vendors for any compound.
Frequently asked
Is Survodutide FDA-approved?
What is the half-life of Survodutide?
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