One harmonised trial database instead of a dozen registries with different formats, identifiers and spellings.
What's included
- Trial records with phase, status, conditions, interventions, design and target enrolment
- Cross-registry identifiers, so one trial registered in several places appears once
- Sponsors and collaborators normalised to parent organisations
- Site lists with facility, city and country, and a status history for each trial
- Flags for posted results and links back to each registry record
How buyers use it
- Competitive landscape analysis by indication, mechanism and phase
- Choosing countries and sites with experience in a therapeutic area
- Tracking competitor pipelines and expected readout dates
- Feeding investment research on biotech pipelines
Coverage and methodology
Willowbrook pulls registry updates daily from ClinicalTrials.gov, the EU Clinical Trials Information System and its predecessor EudraCT, and registries that feed the WHO International Clinical Trials Registry Platform. Records are de-duplicated across registries using registered secondary IDs, titles and sponsor matching, then conditions are mapped to MeSH terms. Sponsor names are normalised and linked to parent companies by analysts. Data covers trials registered since 2000. Trial records describe studies, not participants: no patient-level information is included.