Compound library / GLP-1s & weight loss / Fat Loss / GLP-1

Survodutide

Boehringer Ingelheim's dual GLP-1/glucagon receptor agonist in late-stage trials for obesity and MASH (fatty liver disease).

CategoryFat Loss / GLP-1
Regulatory standingNo approved product cited
Typical routeSubcutaneous
Half-life~5-6 days
Common dose rangeTrial dosing varies, not yet commercially approved
Typical cycle lengthNot yet established outside trials

BioHack Track models Survodutide at a half-life of 132 hours, so every dose you log is decayed against that curve and the app shows estimated active levels — not just what you typed.

No approved product cited

No FDA-approved product for this compound is cited on this page, and no approved human dose is quoted. Treat the range below as research and community practice rather than a prescribed dose.

Reconstitution

Not commercially available outside clinical trials.

Storage

N/A — investigational.

Cautions

Still investigational, not FDA-approved. Any access outside trials is grey-market with unverifiable sourcing/purity.

Track Survodutide in BioHack Track. Half-life, dose range and route come pre-filled from this library — log a dose and the app counts your vial down, models what is in your system, and puts it on the same chart as your labs and body composition.

Others in Fat Loss / GLP-1

What the evidence says

Evidence Check asks 10 questions about every compound. For Survodutide it can answer 1 of them, from the papers we hold — graded by how strong the study design is, not by whether the findings are flattering. These are the same verdicts the app gives.

Some Clinical EvidenceWeight loss

Clinical trials in humans have looked at this.

  • Survodutide Once Weekly for the Treatment of Adults with ObesityRandomized Controlled Trial · N Engl J Med · 2026 · PMID 42253238
  • Dual Glucagon and GLP-1 Receptor Agonist Survodutide Improves Biomarkers of Beta-Cell Function and Insulin Sensitivity in People With Type 2 Diabetes or Living With Overweight/ObesityRandomized Controlled Trial · Diabetes Obes Metab · 2026 · PMID 42331726
  • Baseline characteristics in the SYNCHRONIZE™-2 randomized phase 3 trial of survodutide, a glucagon receptor/GLP-1 receptor dual agonist, for obesity in people with type 2 diabetesRandomized Controlled Trial · Diabetes Obes Metab · 2026 · PMID 41216778

Look up the research

These open a search of each database for Survodutide — they are not citations, and nothing here is evidence for any particular dose. The same links are in the app.

Work it out

Selected published studies

6 papers naming Survodutide in the title, drawn from PubMed and limited to reviews, meta-analyses and trials. Each was checked against PubMed’s own record for its title, journal and year. This is a starting point, not an evidence review — nothing here is offered as support for the dose range above, and the list is not exhaustive. See the editorial policy.

Where these figures come from

The half-life, route and dose range on this page are compiled from published pharmacokinetic literature, manufacturer and product monographs where one exists, and the ranges commonly reported in clinical and research use. They are kept as a range rather than a single figure because that is what the sources actually support — a half-life varies with route, formulation and the person.

These are not citations, and this page is not a review of the evidence. Where a number matters to you, follow the database links above and read the source. We say so plainly rather than dressing a compiled reference up as one.

Nothing on this page has been reviewed by a named clinician. It is a reference for people already tracking a protocol, not a recommendation to start one.

Published by Creative Images LLC · Last updated · Corrections: support