If you are a pharma company developing cancer drugs for children — this project built virtual patient models that can simulate treatment responses in silico. With a consortium of 23 partners across 11 countries generating harmonized clinical and molecular data, these models could dramatically reduce the cost and time of paediatric clinical trials by pre-screening drug candidates computationally before testing them on real patients.
Virtual Patient Models That Help Doctors Pick the Best Cancer Treatment for Each Child
Imagine a doctor could create a digital twin of a sick child — a computer copy that lets them test different cancer treatments before giving real medicine. That's what this project built: cloud-based virtual patient models for children with cancer. Instead of trial-and-error with harsh treatments, doctors can simulate which drug combinations would work best for that specific child. The team pulled together data from hospitals, labs, and clinical trials across 11 countries to make these simulations as accurate as possible.
What needed solving
Children with cancer often receive treatments based on protocols designed for adults or broad patient groups, not tailored to their individual biology. Doctors lack computational tools to simulate how a specific child's tumour will respond to different drug combinations before starting treatment. This means precious time and health can be lost on ineffective therapies, especially for rare paediatric cancers where clinical experience is limited.
What was built
The project built a cloud-based platform with virtual patient models for paediatric oncology, including a functioning in silico prototype of hepatocyte metabolism, a Data Access Committee portal for managing clinical data credentials, standardized metadata and analytical workflows for harmonizing multi-omics cancer data, and an initial cloud infrastructure demonstrator for running computational simulations at scale.
Who needs this
Who can put this to work
If you run a paediatric oncology department struggling with treatment decisions for rare childhood cancers — this project developed a cloud-based platform where caregivers can query virtual patient models and compare benefits and drawbacks of specific treatment combinations for each child. The platform was built to integrate with clinical workflows and tested against prospective clinical trial data.
If you are a health IT company looking to add precision oncology capabilities to your platform — iPC built cloud infrastructure with standardized metadata, a data access credential portal, and analytical workflows for multi-omics paediatric cancer data. The platform was designed for integration with the European Open Science Cloud, giving you a head start on interoperable clinical data infrastructure.
Quick answers
What would it cost to license or adopt this platform?
Based on available project data, no specific licensing fees or pricing models are mentioned. The project received EUR 14,748,400 in EU funding and was designed to make models and data available through a cloud-based platform linked to the European Open Science Cloud. Commercial licensing terms would need to be negotiated with the consortium coordinator.
Can this scale to handle real hospital workloads?
The platform was built on cloud computing and high-performance computing infrastructure specifically to handle large-scale data processing. The consortium harmonized data across 23 partner institutions in 11 countries, suggesting the architecture was designed for multi-site, multi-country deployment. The initial infrastructure demonstrator was delivered for further optimization.
Who owns the intellectual property?
The project is a Research and Innovation Action (RIA) funded under Horizon 2020, meaning IP typically stays with the partners who generated it. With 23 consortium partners including 3 SMEs and 4 industry organizations, IP rights are likely distributed. The coordinator TECHNIKON (Austria, SME) would be the first point of contact for licensing discussions.
Has this been tested with real patient data?
The project objective states they planned to test predictions prospectively on data from clinical trials and test therapies in pre-clinical settings. Deliverables confirm a functioning in silico prototype of hepatocyte metabolism was generated, along with validated analytical workflows. The platform was designed to work with real molecular, clinical, and pre-clinical study data.
What types of cancer does this cover?
Based on the project objective, iPC focused on a select panel of paediatric tumours including both high-incidence and high-risk tumour types. The project combined data from molecular assays, clinical studies, and pre-clinical studies, working with European Centres of Excellence and clinical trials for personalized medicine.
How does this comply with health data regulations?
The project built a dedicated Data Access Committee (DAC) portal for managing access credentials, based on strategies from the EGA archive. This deliverable describes procedures for dissemination of access policies and presents a structured process to apply for data access, suggesting GDPR-aware design for sensitive paediatric health data.
Can this integrate with existing hospital IT systems?
The project objective explicitly mentions contributing to the digitalization of clinical workflows and enabling the EU Digital Single Market data infrastructure. The platform was designed for cloud-based deployment with standardized metadata across datasets and data types, which supports integration with existing systems.
Who built it
The iPC consortium is large and research-heavy: 23 partners from 11 countries, with 8 universities and 9 research organizations forming the backbone. The industry presence is modest at 17% (4 partners, 3 of which are SMEs), which is typical for health research at this stage — the science needs to be proven before larger industry players commit. The coordinator is TECHNIKON, an Austrian SME specializing in research management, which means commercialization decisions may be distributed across the technical partners rather than centralized. For a business looking to adopt this technology, the key contacts would be the clinical partners running the trials and the IT partners who built the cloud infrastructure. The international spread (Austria, Germany, France, Italy, Netherlands, Belgium, Spain, Slovenia, Switzerland, Australia, and the US) signals broad applicability but also complex IP arrangements.
- TECHNIKON FORSCHUNGS- UND PLANUNGSGESELLSCHAFT MBHCoordinator · AT
- LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHENparticipant · DE
- UNIVERSITEIT GENTparticipant · BE
- XLAB RAZVOJ PROGRAMSKE OPREME IN SVETOVANJE DOOparticipant · SI
- IBM RESEARCH GMBHparticipant · CH
- BAYLOR COLLEGE OF MEDICINEparticipant · US
- UNIVERSITA DEGLI STUDI DI NAPOLI FEDERICO IIparticipant · IT
- DEUTSCHES KREBSFORSCHUNGSZENTRUM HEIDELBERGparticipant · DE
- ALACRIS THERANOSTICS GMBHparticipant · DE
- INSTITUT DE INVESTIGACIO EN CIENCIES DE LA SALUT GERMANS TRIAS I PUJOLparticipant · ES
- CONSIGLIO NAZIONALE DELLE RICERCHEparticipant · IT
- INSTITUT CURIEparticipant · FR
- STICHTING AMSTERDAM UMCparticipant · NL
- CHARITE - UNIVERSITAETSMEDIZIN BERLINparticipant · DE
- PRINSES MAXIMA CENTRUM VOOR KINDERONCOLOGIE BVparticipant · NL
- UNIVERSITATSKLINIKUM HEIDELBERGparticipant · DE
- UNIVERSITAT ZURICHparticipant · CH
- THE CHILDREN'S HOSPITAL OF PHILADELPHIA NON PROFIT ORGparticipant · US
- TECHNISCHE UNIVERSITAT DARMSTADTparticipant · DE
- MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EVparticipant · DE
- FUNDACIO CENTRE DE REGULACIO GENOMICAthirdparty · ES
- BARCELONA SUPERCOMPUTING CENTER CENTRO NACIONAL DE SUPERCOMPUTACIONparticipant · ES
TECHNIKON Forschungs- und Planungsgesellschaft mbH, Austria (SME) — research and technology management company. Contact via project website or CORDIS contact form.
Talk to the team behind this work.
Want to explore how iPC's virtual patient models could support your paediatric oncology R&D or clinical decision-making? SciTransfer can arrange an introduction to the right consortium partner for your specific needs.