The right phenotype for your trial: sourced, matched and alerted.

Faster to market, with less friction for the practitioners and admin staff behind every trial.

Drug developers use Weva's deidentified real-world data to define the ideal patient phenotype for a trial and locate exactly where it exists. Weva then alerts both the treating practitioners and the phenotype-matched patients to encourage uptake, cutting the time and cost of recruitment dramatically.

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The Problem

Recruitment is where trials stall and budgets blow out. Many trials miss their enrolment timelines because the ideal phenotype is a guess,  and even when it's known, reaching the right patients at scale is slow and expensive. Weva fixes both.

How Weva works

Define the phenotype

Sponsors interrogate Weva's de-identified real-world data to build the ideal patient phenotype,  the precise clinical profile most likely to be eligible, respond and complete.

Locate the phenotype

Weva maps where that phenotype concentrates: the practitioners, sites and populations already caring for the patients your trial needs.

Alert and encourage
uptake

Weva sends targeted alerts to both practitioners and their phenotype-matched patients, putting the trial in front of exactly the right people and driving enrolment,  saving months of recruitment time and significant cost.

Deliver better trials,
faster

With the right patients identified and engaged from the start, sponsors close higher-quality trials in less time and more patients reach the therapies they're entitled to, sooner.

Why It Saves Time and Money

Recruit faster by starting with the ideal phenotype instead of finding it the hard way. Screen-fail less because phenotype-matched patients mean fewer wrong-fit candidates through the door. Spend less with fewer sites, less broad advertising, and shorter timelines.

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Who It's For

Weva serves the entire clinical trials ecosystem

01

Sponsors

Design smarter protocols using phenotypes to improve recruitment quality with potential for real-time global digital trial registries.

02

CROs

Bring phenotype-led recruitment intelligence that wins studies and delivers them on time.

02

Facilities

Can engage in Clinical Trials when they previously couldn't with improved uptake and less administrative burden.

02

Patients

Have greater health literacy and streamlined access to therapies that they are entitled to.

84 patients recruited within a short period of time

Result: #1 global recruiter in the cohort

Result: #1 global recruiter in the cohort. Nightingale Research Adelaide used Weva digital phenotypes to recruit 84 patients within a short period of time for a clinical trial in early 2026, becoming the number one global recruiter in that cohort.

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With digital phenotyping we are able to identify the participants much earlier and more easily than we have ever been able to do before

Catherine - Trial Manager Nightingale Research
Private by design
Every phenotype is built from deidentified, compliant real-world data, and every patient alert runs through consented, appropriate channels. Sponsors get real-world precision with no identifiable patient data and no privacy risk. [Reference the standards you meet - e.g. the Privacy Act 1988, HIPAA, GDPR.]
Full HIPAA Compliance
Meeting US healthcare privacy and security requirements

Full GDPR Compliance
Protecting patient data rights under European law
SOC 2 Type II Certified
Independently audited security controls
ISO 27001 Certified
International information security management standards
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Your next trial deserves the ideal phenotype from the start.

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