What the survodutide phase 2 actually administered, and why the design matters
The regimen, as recorded on the guide from the paper's own abstract: Dose: 2.4, 4.8 or 6.0 m…
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For Research & Educational Discussion Only. Not Medical Advice
Dual glucagon and GLP-1 receptor agonist
Also known as BI 456906, BI456906
A dual glucagon/GLP-1 agonist in phase 3 for obesity and for MASH. Real trials, real sponsor, no approval anywhere yet, and the phase 3 readouts that matter are not published.
In shortA drug that acts on two receptors, one of them glucagon, in late-stage testing for weight and liver disease. Mid-stage results were positive. Nothing from late-stage testing has been published yet, which is the fact that should lead any discussion of it.
Survodutide is an investigational peptide that activates both the GLP-1 receptor and the glucagon receptor. The rationale for hitting glucagon as well as GLP-1 is that glucagon agonism raises energy expenditure, where GLP-1 mostly suppresses intake, so the two are expected to add rather than overlap.
It is developed by Boehringer Ingelheim and is in phase 3 for obesity and for metabolic dysfunction-associated steatohepatitis. That places it in a different category from most of this compendium: the trials are registered, sponsored and running, and the open question is what they report, not whether they exist.
In shortIt combines the familiar gut-hormone effects with glucagon receptor activity, the same pairing as mazdutide but on a different backbone. The glucagon side is proposed to raise energy expenditure and cut liver fat, with its blood sugar downside offset by the other half.
Co-agonism at the GLP-1 and glucagon receptors. GLP-1 agonism slows gastric emptying, increases satiety and improves glucose-dependent insulin secretion. Glucagon receptor agonism increases hepatic fat oxidation and resting energy expenditure, and is the reason this class is of interest in liver disease specifically rather than only in weight.
The same glucagon arm is why the class needs watching. Glucagon raises hepatic glucose output, and balancing that against the GLP-1 arm is a dose-finding problem rather than a solved one.
In shortMid-stage results in obesity and in liver disease have been published and hit their main targets. Late-stage trials are running and none has reported. Treat anything describing its effectiveness in confident terms as describing mid-stage work. The gap between a mid-stage signal and a late-stage result is where a large share of metabolic drugs have historically failed.
Phase 2 results in obesity and in MASH have been published and were positive on their primary endpoints. Phase 3 is running. As of writing, no phase 3 result is published, and the registry is the honest place to look rather than any summary of it, including this one.
Treat anything describing survodutide's efficacy in confident terms as describing phase 2. The gap between a phase 2 signal and a phase 3 result is where a large fraction of metabolic drugs have historically failed.
In shortMid-stage side effects were dominated by stomach problems, as across this class, mostly while the dose was going up, and enough people stopped for it to matter. Longer-term safety is not characterised because the trials that would characterise it have not reported. Anything sold as survodutide outside a trial is not survodutide: it is unverified material sold under a name.
Adverse events reported in phase 2 were dominated by gastrointestinal effects, consistent with the GLP-1 class: nausea, vomiting, diarrhoea, mostly during escalation. Discontinuation for tolerability was not trivial.
Longer-term safety is not characterised, because the trials that would characterise it have not reported. The glucagon arm raises questions about hepatic glucose handling and heart rate that phase 3 is designed to answer and phase 2 is not powered to.
Anything sold as survodutide outside a trial is not survodutide from the sponsor. It is material of unverified identity sold under a name.
In shortNot approved anywhere. Investigational, in registered late-stage trials. Any supply outside a clinical trial is outside the regulatory system entirely, and it is banned in sport.
Not approved anywhere. Investigational, in registered phase 3 trials. Any supply outside a clinical trial is outside the regulatory system entirely.
Prohibited in sport under WADA's S0 category, which covers substances with no current approval for human therapeutic use.
3 studies indexed. Findings and limitations get equal weight, on purpose.
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Everything above is free to read. What an account opens is the evidence underneath it: 3 studies with their limitations, and the regimen each trial actually reported.
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Reading is free, an account is not the same as paying. 43 compound guides, every study with its limitations written underneath, and the regimens those trials actually used. A free account opens all of it. A membership is a separate decision, and it opens the forum. What membership costs.
The wider literature
17 indexed papers and 24 registered trials mentioning Survodutide, straight from PubMed and ClinicalTrials.gov. 23 of 24 administer it; the rest measure it. These have not been read by us. Unlike the studies above, they carry no findings and no limitations written by anyone here, because writing either would mean claiming a reading nobody has done. They are a starting point for yours.
Boehringer Ingelheim2026NCT07407348
interventionalphase1recruitingn=80
Boehringer Ingelheim2026NCT07754461
interventionalphase3recruitingn=600
Boehringer Ingelheim2026NCT07768813
interventionalphase1not yet recruitingn=44
Boehringer Ingelheim2026NCT07413913
interventionalphase1completedn=56
University Medical Center Groningen2026NCT07206290
interventionalphase2not yet recruitingn=120
Boehringer Ingelheim2025NCT07221591
interventionalphase1completedn=100
Boehringer Ingelheim2025NCT07071974
interventionalphase1completedn=16
Boehringer Ingelheim2025NCT06745284
interventionalphase1active not recruitingn=64
Boehringer Ingelheim2025NCT06772532
interventionalphase1completedn=30
Boehringer Ingelheim2024NCT06200467
interventionalphase1completedn=110
Boehringer Ingelheim2024NCT06214741
interventionalphase3completedn=307
Boehringer Ingelheim2024NCT06176365
interventionalphase3completedn=274
Boehringer Ingelheim2024NCT05202353
interventionalphase1active not recruitingn=29
Boehringer Ingelheim2024NCT06632444
interventionalphase3recruitingn=1800
Boehringer Ingelheim2024NCT06309992
interventionalphase3completedn=218
Boehringer Ingelheim2024NCT06564441
interventionalphase1completedn=34
Boehringer Ingelheim2024NCT06632457
interventionalphase3recruitingn=1590
Boehringer Ingelheim2024NCT06492135
interventionalphase1completedn=30
Boehringer Ingelheim2023NCT05896384
interventionalphase1completedn=32
Boehringer Ingelheim2023NCT06077864
interventionalphase3completedn=5531
Boehringer Ingelheim2023NCT06066528
interventionalphase3completedn=755
Boehringer Ingelheim2022NCT05296733
interventionalphase1completedn=82
Boehringer Ingelheim2021NCT04667377
interventionalphase2completedn=387
Boehringer Ingelheim2021NCT04771273
interventionalphase2completedn=295
Kaplan LM, et al.Nature medicine2026PMID 42252333
journal articlerandomized controlled trialclinical trial, phase iii
le Roux CW, et al.The New England journal of medicine2026PMID 42253238
journal articlerandomized controlled trialmulticenter studyclinical trial, phase iii
Son JW, et al.Endocrine reviews2026PMID 41054801
journal articlereview
Rubio-Herrera MA, et al.Medicina clinica2025PMID 40865172
journal articlereview
Sinha B, et al.Obesity (Silver Spring, Md.)2025PMID 40685589
journal articlenetwork meta-analysissystematic review
Newsome PN, et al.The Journal of clinical investigation2025PMID 40590228
journal articlereviewresearch support, n.i.h., extramuralresearch support, non-u.s. gov't
Kokkorakis M, et al.Pharmacological reviews2025PMID 39952695
journal articlesystematic review
Souza M, et al.Hepatology (Baltimore, Md.)2025PMID 39903735
journal articlesystematic reviewcomparative studynetwork meta-analysis
Stefanakis K, et al.Metabolism: clinical and experimental2024PMID 39481534
journal articlereview
le Roux CW, et al.The lancet. Diabetes & endocrinology2024PMID 38330987
clinical trial, phase iijournal articlemulticenter studyrandomized controlled trialresearch support, non-u.s. gov't
Singh A, et al.World journal of gastroenterology2024PMID 39735270
reviewjournal article
Blüher M, et al.Diabetologia2024PMID 38095657
randomized controlled trialmulticenter studyclinical trial, phase iijournal articleresearch support, non-u.s. gov't
Drucker DJDiabetes care2024PMID 38843460
journal articlereviewresearch support, non-u.s. gov't
Sanyal AJ, et al.The New England journal of medicine2024PMID 38847460
journal articleclinical trial, phase iirandomized controlled trialmulticenter study
Dissanayake HA, et al.Current diabetes reports2024PMID 38150106
journal articlereview
Kosiborod MN, et al.JACC. Heart failure2024PMID 39453356
clinical trial protocoljournal articleresearch support, n.i.h., extramural
Zimmermann T, et al.Molecular metabolism2022PMID 36356832
journal articleresearch support, non-u.s. gov't
Survodutide has its own forum, split by the same six categories as the rest of the site.
The regimen, as recorded on the guide from the paper's own abstract: Dose: 2.4, 4.8 or 6.0 m…
Members only. Join to read the rest
Survodutide is a Dual glucagon and GLP 1 receptor agonist. The guide is up and this is its f…
Members only. Join to read the rest
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For Research & Educational Discussion Only. Not Medical Advice
This guide is educational reference material compiled from published literature. It is not medical advice, not a recommendation, and not a substitute for a clinician who knows your history. Nothing here should be used to make a decision about your own health without one.
Talk to a licensed healthcare professional.