SciTransfer
Organization

ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI

Milan-based pharmacological research institute specializing in kidney disease, toxicology, clinical trials, and epidemiology across 30 H2020 projects.

Research institutehealthIT
H2020 projects
30
As coordinator
1
Total EC funding
€11.5M
Unique partners
381
What they do

Their core work

Mario Negri Institute is a leading Italian pharmacological research centre based in Milan, specializing in kidney disease, cardiovascular disease, toxicology, and epidemiology. They run and contribute to large-scale clinical trials (e.g., the SECURE polypill trial for cardiovascular prevention), develop animal-free toxicity testing methods using computational modelling and adverse outcome pathways, and investigate biomarkers for diseases like Alzheimer's and diabetes. Their work bridges fundamental molecular research with regulatory science and public health policy, including tobacco control and environmental risk assessment of pharmaceuticals.

Core expertise

What they specialise in

Kidney disease and nephrologyprimary
4 projects

Core expertise across NEPHSTROM (diabetic kidney disease therapy), CKD AKI (their only coordinated project, on kidney epidemiology), BEAt-DKD (kidney biomarkers), and TrainCKDis (CKD drug discovery).

Toxicology and chemical safety assessmentprimary
5 projects

Major contributor to EU-ToxRisk, OBERON, in3, ONTOX, and ALTERNATIVE — all focused on mechanism-based, animal-free toxicity testing and risk assessment.

Cardiovascular and neurological diseaseprimary
5 projects

Spans the SECURE cardiovascular prevention trial, ESCAPE-NET (sudden cardiac arrest), ENTRAIN (neuroinflammation), BBDiag (Alzheimer's blood biomarkers), and NECTAR (Alzheimer's treatment).

Epidemiology and public health policysecondary
4 projects

Evident in TackSHS and EUREST-RISE (tobacco control and regulation), CKD AKI (kidney epidemiology), and ESCAPE-NET (genetic epidemiology of cardiac arrest).

Personalised medicine and clinical trialssecondary
4 projects

PERMIT (personalised medicine trial design), UNITI (personalised tinnitus treatment), BEAt-DKD (omics-based patient stratification), and CCE_DART (data-rich clinical trials).

4 projects

Growing presence through NanoCarb (glyco-nanoparticles), LASER OPTIMAL (gold nanoparticle tumour ablation), MIMIC-KeY (extracellular vesicle-mimicking nanoparticles), and nPETS (nanoparticle health impacts).

Evolution & trajectory

How they've shifted over time

Early focus
Kidney disease and clinical trials
Recent focus
Computational toxicology and omics

In their early H2020 period (2015–2018), Mario Negri focused heavily on kidney disease clinical trials, cardiovascular prevention, and foundational toxicology work — projects like NEPHSTROM, SECURE, and EU-ToxRisk dominated. From 2019 onward, their portfolio shifted toward computational and systems-based approaches: animal-free toxicity testing with AI/ontology methods (ONTOX, OBERON), multi-omics integration (metabolomics, transcriptomics, proteomics), and nanomedicine applications. There is a clear move from traditional clinical research toward data-driven, regulatory-science-oriented work that combines molecular biology with computational modelling.

Mario Negri is increasingly investing in animal-free safety assessment, AI-driven toxicology, and multi-omics data integration — positioning them as a go-to partner for next-generation chemical and pharmaceutical risk evaluation.

Collaboration profile

How they like to work

Role: specialist_contributorReach: European30 countries collaborated

Mario Negri operates almost exclusively as a consortium partner (27 of 30 projects), with only one coordination role (CKD AKI, a small Marie Curie fellowship). They are a reliable specialist contributor who brings deep pharmacological and epidemiological expertise to large research consortia. With 381 unique partners across 30 countries, they are exceptionally well-networked and comfortable working in large, multi-national teams — a strong indicator that they integrate smoothly into complex EU project structures.

Extensively connected across Europe with 381 unique consortium partners spanning 30 countries, reflecting deep integration into the EU biomedical and toxicology research landscape. Their network is pan-European with no narrow geographic concentration.

Why partner with them

What sets them apart

Mario Negri is one of Italy's most established independent pharmacological research institutes (founded 1963, non-profit), which gives them scientific credibility without commercial bias — a trait valued by regulators and public health bodies. Their rare combination of clinical trial experience, regulatory toxicology expertise, and epidemiological capacity makes them uniquely able to bridge the gap between laboratory findings and health policy. For consortium builders, they offer a partner who can handle both the molecular science and the population-level evidence needed to translate research into real-world impact.

Notable projects

Highlights from their portfolio

  • SECURE
    Largest single EC contribution (EUR 1.03M) — a major cardiovascular prevention trial testing a polypill strategy in elderly patients across multiple countries.
  • ONTOX
    EUR 828K for an ambitious project combining ontology and AI to replace animal testing in toxicology — represents their strategic direction toward computational safety science.
  • CKD AKI
    Their only coordinated H2020 project, a Marie Curie fellowship evaluating global kidney disease epidemiology — signals their core institutional strength in nephrology.
Cross-sector capabilities
Environment (pharmaceutical ecotoxicology, chemical safety assessment)Transport (brake system emissions, nanoparticle health impacts)Manufacturing (nanotechnology safety, polymer nanoparticle testing)Digital (computational modelling, AI-driven toxicity prediction)
Analysis note: Rich dataset with 30 projects, clear keyword data, and well-defined expertise clusters. The institute's non-profit, independent status is well-known publicly and relevant to understanding their positioning. Project descriptions are detailed enough to draw confident conclusions about expertise evolution.