Childhood Cancer Intelligence

Finding the Right Trial for Every Child

Compass uses AI to search the world's clinical trials, research programmes, and specialist centres — producing comprehensive, personalised reports for children with rare cancers.

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Request a ReportSee How It Works

The Challenge Families Face

When your child has a rare cancer, the information you need exists — but it's scattered across the world.

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Fragmented Data

Clinical trials are spread across ClinicalTrials.gov, EudraCT, ISRCTN, WHO ICTRP, and dozens of institutional registries. No single search covers them all.

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Siloed Knowledge

The researcher who published on your child’s exact gene mutation is in Lyon. The trial that fits is in Houston. The surveillance guidelines are in a journal you’ve never heard of. None of them know about each other.

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Months of Searching

Families spend weeks or months navigating complex medical databases, contacting institutions one by one, and hoping they haven’t missed something critical. Time their child may not have.

What Compass Does

Three layers of intelligence working together to find answers faster.

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Knowledge Graph

A living map of the entire paediatric cancer landscape.

  • •Every cancer type, subtype, fusion status, and molecular marker
  • •Cancer predisposition syndromes and causal gene mappings
  • •Active clinical trials ingested nightly from global registries
  • •Specialist researchers and institutions with published expertise
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Matching Engine

AI that connects your child’s profile to the world’s knowledge.

  • •Input a clinical profile — diagnosis, genetics, treatment history, complications
  • •AI searches globally across trials, researchers, and institutions
  • •Eligibility pre-screening against known trial criteria
  • •Draft outreach messages ready to send to specialists
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Dual Interface

The right information for the right audience.

  • •Families receive plain-language guidance they can act on
  • •Oncologists receive clinical-grade reports with molecular rationale
  • •Both perspectives from the same underlying intelligence
  • •Contact routes and next steps for every lead

How It Works

From submission to actionable report in three simple steps.

1

Submit a Profile

Share your child’s diagnosis, genetic findings, treatment history, and current situation. We only ask for what’s needed.

2

AI Searches Globally

Compass searches hundreds of trial registries, research databases, specialist centres, and expert networks worldwide.

3

Receive Your Report

A comprehensive, personalised report with ranked leads, eligibility assessments, contact details, and ready-to-send outreach letters.

What Makes Compass Different

Not another database. A system that thinks like an oncologist and communicates like a friend.

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Predisposition-Aware

Understands that MVA causes rhabdomyosarcoma via BUB1B — not just that they co-occur. Genetic context changes everything.

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Actionable, Not Encyclopaedic

Outputs are “contact this person, at this email, about this trial” — not a Wikipedia article.

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Cross-Network Search

Searches COG, EpSSG, ITCC, SIOPE, ERN PaedCan simultaneously. No more navigating each network separately.

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Complication-Aware

Knows that ifosfamide in a young child risks nephrotoxicity, and factors that into trial suitability assessments.

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Living Data

Updated nightly from global trial registries. When a new trial opens that matches your child’s profile, we know.

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Dual Audience

Families get plain language they can understand. Oncologists get clinical detail they can act on. Same data, two views.

A Real Story

One Family's Search

A young child was diagnosed with a rare form of cancer at just two years old. He also has Mosaic Variegated Aneuploidy — an ultra-rare chromosomal disorder that affects fewer than 100 known families worldwide.

His family needed answers. Which clinical trials might he qualify for? Which researchers study his exact genetic condition? Which specialist centres could help with his complex mix of cancer, kidney disease, and recurrent infections?

We ran Compass for this family. In under 10 minutes, the system found:

90+Actionable Leads
36Clinical Trials
50+Specialist Institutions
10Countries

The report identified the two most relevant clinical trials — both at his own hospital. It found the researchers who discovered the genetic link to his cancer. It drafted outreach letters ready to send. It mapped every specialist centre in Europe and the US that could help.

No family should have to get lucky to find the right trial or the right specialist.

Who It's For

Different perspectives, same mission — better outcomes for children with rare cancers.

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Families

Plain-language reports with pre-written outreach letters. Know what questions to ask and who to ask them to.

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Oncologists

Clinical-grade reports with trial eligibility assessments, molecular rationale, and direct contact routes for specialists.

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Researchers

Discover cohorts, connect with collaborators, and identify unmet needs across rare paediatric cancers.

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Networks

ERN, COG, EpSSG — see which of your trials match unmet cases and where the gaps are in coverage.

Request a Report

Tell us about your child's situation. We'll review your request and generate a comprehensive, personalised report searching the world's clinical trials and specialist centres.

Your information is encrypted and never shared with third parties. We only use it to generate your report.

GDPR compliant. We ask for your child's first name only — never full identifying details.

We aim to respond within 48 hours with your personalised report.