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Trialmetrics home
  • Features
  • About
  • Pricing

About Trialmetrics

Clinical trial data, made usable for everyone

The information about who is running trials, where and how well is public. The tools to make sense of it usually aren't. We built Trialmetrics to change that.

Who we are

Trialmetrics is run by an independent team. We're not backed by a large corporation or investors, and we bring together experience from both sides of the problem.

Our clinical research experience spans nine years on the sites, sponsors and CROs side of trials. That experience shapes which questions the tool answers and how the metrics are defined. Our analytics experience builds the data pipeline, cleans the records and makes sure the numbers hold up.

Between us, we kept seeing the same thing: large organisations can pay for expensive trial intelligence, while smaller sites, CROs, biotechs, patients and rare disease groups are left to dig through raw registry data. Trialmetrics is our way of giving them the same view.

The Trialmetrics team

Clinical trials tracked
606k+
Research sites with 2+ trials
146k+
New trials in the last 7 days
595

From ClinicalTrials.gov, refreshed every week. Includes registry updates up to 9 October 2026.

Who it's for

Trialmetrics is simpler than enterprise trial platforms, and built for the people they tend to leave out.

Research sites

Add your site and make it public so sponsors and CROs can find you. Then use Sponsor Search to see who is running trials in your therapeutic areas and countries, and who is about to start recruiting.

Smaller CROs and biotechs

Compare sites on completion rates, investigator depth and experience without an enterprise contract. See which sponsors are active in your space and where.

Patients and caregivers

Search trials by condition and location, with plain-language summaries of what a study involves and who can take part.

The rare disease community

Trials are matched against the Orphanet list of rare diseases, so smaller studies that are easy to miss are easier to find.

How we're different

Free to start, no demo calls

Search, site profiles and sponsor search are open to use. You don't need a sales call to see if the data is useful to you.

Real registry data, not guesswork

Every number comes from public ClinicalTrials.gov records. We use AI only to summarise trial descriptions in plain language, never to calculate scores or metrics.

We show our working

How we clean the data and how each metric and score is calculated is published in plain language, including what the numbers can't tell you.

A real person replies

We're a small team. If you email us, one of us will read it and reply.

Where our data comes from

All trial data comes from ClinicalTrials.gov, the largest public registry of clinical studies. Every week we load the latest records, group the different spellings of the same research site into one profile, standardise country names and map conditions to therapeutic areas. Rare disease trials are identified using the Orphanet nomenclature of rare diseases.

Site metrics and the site score are calculated from those records using published rules, so you can see exactly what goes into every number.

Read our methodology

Questions, feedback or a data issue?

Email us and one of us will reply. If you spot something wrong in the data, tell us and we'll look into it.

support@trialmetrics.com