We start from a question someone already has and could not answer, build the smallest system that tests it, and publish what we find.

In a five-year national cohort study, cancer risk after a diagnosis of immune-mediated inflammatory disease was highest in the first year and fell steadily after it. The shape of that decline points at inflammation rather than at treatment.
Cancers 2026;18(6):1027 ↗In every programme below, the answer already existed in data somebody already held. What was missing was the time and the method to get it out.
A national cohort sat in hospital discharge records for five years before anyone joined it up. A hospital sees a medicine it should have switched a year after the window closed. A tumour board's evidence is in a guideline nobody had the evening to read.
The moonshot
That the distance between a question somebody has and an answer they can defend collapses from years to days.
Can we say, years ahead of a diagnosis, which subgroups carry which risk, and why?
Can a model stand in for an experiment that is too slow, too small or too expensive to run?
Can a group of patients too small for the statistics still be learned from?
Can an organisation act on what it already knows, inside the year it matters?
Where is the line between software that informs a clinical decision and software that makes one?
Six programmes, each listed at the stage it has actually reached. Two are complete, one is waiting on a regional approval, and three are live.
356,022 patients across five years of Italian hospital discharge records. Which cancers, how much more often, and when in the disease course.
Genotype, lifestyle and socioeconomic data read together at population level. One of the algorithms delivered under CODIGE. Population associations, never an individual risk score.
A clinician enters a case, the agent searches published AIOM and ESMO guidance and returns one page the panel can read in the room. Built with an Italian local health authority. The pilot is waiting on regional approval and the agent is not in use in care.
Months pass between outpatient visits, and every visit begins from a reconstruction by memory. What is worth capturing in between, and does capturing it change the next one.
A hospital already holds every figure it needs to see where value is leaking. It is not organised in a way that points anywhere. This reads the flows an authority already produces and points at the molecule, the channel and the ward where the money is going.
When a disease affects a handful of people in a country, the statistics built for thousands stop working. We are testing what can still be learned from a cohort that small, starting with propionic acidemia in Saudi Arabia.
The same three steps every time, whatever the field.
A clinician, a discovery scientist or a pharmacy lead who has the problem and could not solve it. Not a technology looking for an application.
Documented, versioned and evaluated. What was not evaluated is written down next to what was, because a reader cannot tell the difference otherwise.
A programme is completed when its question has been answered. Where the answer is useful beyond us, the route out is a publication, a tool other groups can run, or a company.
Peer reviewed, and checkable without asking us. Every entry resolves from its DOI.
Castro-Aldrete L, Einsiedler M, ... Putignano G, ... Santuccione Chadha A
doi:10.1038/s44222-025-00355-w ↗Giordani B, Pirtoli L, Putignano G, Giordano A, Marotto D, Baglio G
doi:10.3390/cancers18061027 ↗Putignano G, Ruiperez-Campillo S, Yuan Z, Millet J, Guerrero-Aspizua S
doi:10.3389/fimmu.2025.1581210 ↗The problems come first: everything else exists to get them solved. The badges indicate what the Foundation provides directly and what the community makes available.
Real problems brought by clinicians and research centres, with the institution that posed them named.
Shared equipment you can apply to use, with a short statement of what you intend to do with it.
Capacity for model training and biomedical data analysis.
Hands-on support on NIDI, Mini-PIA, PIA, ZES and European calls.
Guidance across regulatory strategy, clinical development, IP and commercialisation.
Offices, meeting rooms and operational space opened up by members.
One operational home today, and two locations in development. Taranto is where the work happens now.
Our founding home, with a physical Startup Hub and the Distributed Lab. A Special Economic Zone with real tax benefits.
A strategic hub for European and international partnerships, embedded in one of the world's leading life-sciences ecosystems.
A strategic presence aligned with Vision 2030, opening access to a fast-growing Saudi healthcare market.
A selection of recent milestones from across the ecosystem.
Our launch, research pillars, first members and upcoming events.
Read more →
The Apulian leader in in-vivo diagnostics and imaging joins the ecosystem.
Read more →
An Italian portfolio startup scaling toward clinical genomics.
Read more →The first members of the Foundation, already building alongside us. More to come soon.
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Active memberA free 10-week programme for high school students. Go from understanding what AI agents are to building and demonstrating a working prototype. No prior coding experience required.
Build real AI agents that solve genuine problems. Choose your track: no-code, low-code, or full-code. Earn a verified certificate on completion.
Start learning →Due giornate con scienziati, medici e campioni dello sport. Iscrizione gratuita, posti limitati.
We are looking for co-investigators, cohorts to replicate on, and clinical partners who have a problem they own. If one of the programmes above is close to something you work on, write to us.