Survodutide: separating the mechanism from the marketing
Purity across our Survodutide samples ranged from 98.2% to 99.4%. Here is the context.
ResearchAlso known as: LY2189265
A weekly GLP-1 agonist fused to an antibody fragment to extend its half-life, studied primarily for glycaemic control and cardiovascular risk.
Dulaglutide is classified as a glp-1 receptor agonist (fc fusion). Its current development status is: fda-approved (branded forms). Multiple randomised controlled trials in humans support the primary claims made for this compound.
The Peptide Institute tracks Dulaglutide because it is actively sold through research-compound and telehealth channels. Our interest is narrow and specific: what is actually in the vial, whether the label is accurate, and whether the sellers of it can document what they claim. We take no position on whether anyone should use it.
Independent Testing
Every company below was evaluated with product the Institute purchased anonymously and sent for third-party laboratory analysis. Ranked by Index Score™.
97.3% average purity across 1 sample
Purity & Testing 81 Transparency 90 Samples 1 84 View companyImmunogenicity and stability profile of Dulaglutide
Adds to the Dulaglutide evidence base without resolving the central question of human efficacy.
Dulaglutide in preclinical models: efficacy and translational limits
Characterises Dulaglutide activity in a controlled setting. Endpoints are surrogate measures rather than clinical outcomes.
Laboratory verification of Dulaglutide products across the companies we index.
Purity across our Survodutide samples ranged from 98.2% to 99.4%. Here is the context.
Research7 independently tested samples across 4 companies, and what the results say about Cagrilintide.
Study SummaryA close reading of the Cagrilintide evidence, without the marketing layer.
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