Naturally occurring disease
Spontaneous onset and progression, not engineered or induced, with the variation that trials meet in practice.
Translational evidence platform
Armidus collects consented clinical records, follow-up outcomes and biological samples from animals treated in partner veterinary clinics, then links them to molecular profiles. Pharma, biotech, CROs and academic groups can license the data or commission new cohorts.
Subject A-0142
Canine · [BREED] · [AGE]
Why animal data
Companion animals develop many of the same diseases as people, in the same homes, with intact immune systems. Their care records capture what induced models cannot.
Spontaneous onset and progression, not engineered or induced, with the variation that trials meet in practice.
Immunocompetent patients, relevant wherever host immunity shapes response, from oncology to inflammation.
Animals live alongside people and share many of the same exposures, diets and microbes.
Shorter lifespans mean disease course and outcomes can be observed in a fraction of the human timeframe.
How it works
Partner clinics use Armidus to guide owners through post-visit care.
The clinic signs a data-sharing agreement. Each owner gives written consent.
Structured clinical records, owner-reported follow-up and biological samples.
Samples are profiled and linked to each patient's longitudinal outcomes.
De-identified datasets licensed to partners, or new cohorts built to spec.
What partners get
Every sample is tied to the same patient's clinical history and what happened after the visit, so molecular findings can be read against real outcomes.
Diagnoses, treatments, medications and clinician notes, structured at the point of care.
Adherence, symptoms, recovery and escalations, reported by owners between visits.
Germline and tissue samples, collected with consent during routine care.
[ASSAY TYPES, e.g. genomic, transcriptomic] linked to each patient record.
Applications
Find and test candidate mechanisms against naturally occurring disease and its outcomes.
Add real-world efficacy and response data to support go or no-go decisions.
Outcome-linked tissue and reference data for developers of new approach methodologies (NAMs).
Multimodal, longitudinal data with documented consent and provenance.
Consent & governance
Armidus uses clinic and patient data for research only with explicit written consent: a signed data-sharing agreement from the clinic and written consent from the owner. Clinics that do not sign an agreement keep full use of Armidus, and their data is never shared.
Read how Armidus handles dataArmidus helps clinics support owners after the visit. Learn more about the clinic product.
Contact us
Share the indication, species or question you are working on. We will tell you what existing data covers it, or how a new cohort could.