The Trial Navigator connects everyday care with clinical research. Matching trials find their way into your practice, not the other way round.
Matching trials are hard to find. The search costs time the day does not have, and patients miss out on new treatments.
Identifying trials that fit a specific patient is slow, manual work.
Time that the day in an office-based practice simply does not have.
Practices remain outside clinical research, although they could contribute a great deal.
In the background the Trial Navigator screens your patient base continuously and matches trial criteria against routine care data.
Your patient base is checked against open trials again and again, not once.
Inclusion and exclusion criteria are compared against the routine data you already hold.
You receive prepared, plausible candidates rather than a long list to work through.
Candidates are identified without personal identifiers leaving your practice.
The patient base is matched against open trials in the background.
Eligible candidates are recognised against the trial criteria.
You decide whom to approach, and participation is prepared with you.
Matching runs on de-identified data. There is no automatic enrolment: consent is obtained separately, and the decision to approach a patient stays with the treating physician.
You can open access to therapies your patients would otherwise never hear about.
Your practice contributes to clinical research without building a study team.
Relevant studies find their way into the practice, instead of you searching for them.
Participation in research can bring additional income into the practice.
Proximity to research matters to junior staff, referring colleagues and patients alike.
Every eligible patient you surface moves a therapy closer to the people who need it.
Bundles lab values, diagnoses and longitudinal data, the same structured basis trial criteria are matched against.
Finds patient groups for prevention, follow-up and coding, using the criteria logic trial matching is built on.
Candidates reach you as proposals. Consent is obtained separately and stays a clinical decision.
More time for your patients. And a contribution to research, if you choose.