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Trial pre-screening

Antevion Research

Planned

Antevion Research is designed to place the sentences already written in signed reports next to the criteria of each open trial, so the research team can see them in time. People will decide eligibility; no verdict, no ranking.

Planned products are plans, not current operations. Each will be subject to its own regulatory review before any pilot.

The gap

What it addresses

The sentences that matter for a trial are already written in signed reports.

Antevion Research is designed to let a research centre see, in time, the patients its own teams are already reporting on. The sentences sit in imaging, pathology and clinic reports; Antevion Research will show them where the research coordinator works.

Workflow

How it is designed to work

  1. Will read signed reports

    It will read imaging and pathology reports and clinic letters, in Portuguese free text.

  2. Will show the source sentences

    It will show the sentences as written, next to each open trial's criteria, to the research coordinator.

  3. People will decide

    The investigator will decide eligibility and whether to approach the patient.

  4. Will keep the screening log

    It will record who was considered, when, and why not, for the sponsor and the ethics committee.

Example

A source sentence beside an open trial's criteria

Illustrative example

Quoted sentence

Carcinoma do pulmão de não pequenas células, sem tratamento sistémico prévio.

Quoted from the signed report, as written. Translation: “Non-small-cell lung carcinoma, with no prior systemic treatment.”

What is recorded

Open trial criterion

No prior systemic treatment

Screening log
Considered on 14/04

Eligibility Decided by the investigator

No verdict. No ranking.

Illustrative example with fictitious data. It does not represent a real patient, clinician or hospital. The sentence, criterion and date are fictional. The sentence will be shown, never scored.

Guardrails

Its guardrails

It will be built within these limits.

  • No eligible or not-eligible verdict.
  • No ranking of patients.
  • People will decide eligibility and whether a patient is approached.
  • Source sentences will be quoted as written, never paraphrased.
  • A separate regulatory review before any pilot.

Designed for

Clinical research centres, their coordinators and investigators, working with the hospital's own clinical teams.

Same core

Every Antevion product is designed on the same core: it quotes what a clinician wrote, gives it an owner and proves whether it happened. It never generates an interval or a verdict; a person decides.

See the product family

Talk to us about trial pre-screening

Antevion Research is planned on the same core as imaging follow-up. Tell us how your research centre finds patients for open trials today.