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Layer 16 of 21 · Action and continuity

TrialGraph Clinical trial matching and prioritisation.

Clinical trials can offer access to treatments under investigation, but finding relevant ones is difficult. TrialGraph is intended to identify trials that may be relevant to the case for the treating team to review, with the reasons for each match.

Why it's needed

Which clinical trials may be relevant for further review based on the case and available trial criteria?

A prioritised list of trials to review, with match rationale and known gaps.

What it draws on

4 of 8 evidence domains.

Molecular & genomicClinical contextTreatment exposureEvidence ecosystemDiagnosis, biomarkers, prior therapy and location, compared against trial criteria.

What it produces

Potential trial matches and a rationale for review, if the product supports that output.

Explain how disease, biomarker, location and eligibility information are compared where supported.

Why it's essential

Layer 16 of 21.

Produces the clinical-trial-matches section of the report. Trial intelligence is a Twin capability, not a separate product.

1 · What it does

What TrialGraph does

Clinical trials can offer access to treatments under investigation, but finding relevant ones is difficult. TrialGraph is intended to identify trials that may be relevant to the case for the treating team to review, with the reasons for each match.

2 · Scientific question

The question it addresses

Which clinical trials may be relevant for further review based on the case and available trial criteria?

Intended function

Explain how disease, biomarker, location and eligibility information are compared where supported.

3 · Data inputs and required context

What it draws on

  • 01 Molecular & genomic
  • 03 Clinical context
  • 06 Treatment exposure
  • 08 Evidence ecosystem

Diagnosis, biomarkers, prior therapy and location, compared against trial criteria.

4 · Scientific basis

The science behind it

Scientific basis

Trial matching compares structured case features with eligibility criteria published in trial registries. Criteria are often free text, incomplete or subject to change, and final eligibility is always determined by the trial team after screening.

5 · Output and evidence sources

What it produces

Main output

Potential trial matches and a rationale for review, if the product supports that output.

Output type

  • Evidence-linked interpretation. Connects a finding to published or curated evidence, which has a source and a date.

6 · Why it\u2019s essential

How it powers the Twin

Produces the clinical-trial-matches section of the report. Trial intelligence is a Twin capability, not a separate product.

Capability

Explore

Review treatment-relevant evidence, resistance-related findings and potential trial matches.

7 · Why it\u2019s needed

What it changes — for doctors, patients and researchers

Clinicians

A prioritised list of trials to review, with match rationale and known gaps.

Doctor & Clinical Team

Patients & caregivers

A potential match is a starting point for a conversation, not an offer of a place.

Patient & Caregiver

Researchers

Biomarker-defined trial landscapes.

Industry & Research

8 · Dependencies and limitations

Limitations

  • A potential match is not confirmed eligibility, enrolment, slot availability or a guarantee of sponsor acceptance.
  • Registry information can be out of date, and recruitment status changes.

9 · Review and uncertainty

How the output is handled

Output status

An AI-assisted analytical output presented as structured findings for clinician review. It becomes part of a report only after the treating oncologist has reviewed and signed it.

How uncertainty is communicated

Each match shows the criteria met, the criteria unknown and the criteria that need checking.

10 · Claim boundary

What this layer does not establish

It does not confirm that a patient is eligible for, or will be accepted into, any trial.

The treating oncologist owns every decision. Every Twin report is reviewed and signed by the treating oncologist, then taken to KPCIRC's Molecular Tumour Board.

KPCIRC sign-off process

Continue the journey

Longitudinal monitoring

Every change goes in.

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