VIVA-ELISA: Advanced Laboratory Test for Rapid Detection of NLRP3 Inflammasome Activation in Critical Septic Patientsbroad
VIVA-ELISA · Horizon Europe grant · 2025-04-01–2028-03-31
EC contribution
Total cost
Beneficiaries
About the data
Source: CORDIS (official EU open data), Horizon Europe. Framework HORIZON · call HORIZON-EIC-2024-TRANSITION-01 · scheme HORIZON-EIC · topic HORIZON-EIC-2024-TRANSITIONOPEN-01. CORDIS record →
Objective
Sepsis causes almost 20% of global annual deaths. It involves a dysregulated systemic inflammatory response driven by proinflammatory cytokines. If untreated, it progresses to organ dysfunction, low blood pressure, and septic shock. Current diagnosis methods have low predictability, delays in diagnosis, lack of sensitivity, and an inability to predict the course of the patients deterioration: there is thus a need for a rapid, accurate, affordable and early identification of the mortality risk.VIVA-ELISA is a follow-up to the ERC project SPEDI-TEST conducted at the Biomedical Research Institute of Murcia (IMIB), of which Viva in Vitro is a spin-off. Studies show that 100% of deaths of septic patients are correlated to early impairment of the NLRP3 inflammasome activation in monocytes, in the initial 24 h. A novel in vitro diagnostic method was developed for the fast detection of early impairment of the NLRP3 inflammasome activation. This method can stratify patients at a higher risk of developing life-threatening complications, resulting in an early and more accurate prognosis. VIVA-ELISA will advance this concept by developing an easy-to-use, highly sensitive immunoassay that can be seamlessly implemented into hospitals and clinics, reducing time-to-treatment, variability in data interpretation, and hospitalization costs, currently averaging $32,000 per patient. Our solution, designed as a classic quantitative sandwich ELISA, requires only a small blood sample to measure ex vivo NLRP3 activation. We aim to reduce sepsis mortality rates by 25 to 40%, reduce morbidity and recovery time, reduce chronic sequelae for patients and enable the possibility of personalized treatments and immunotherapy, while also contributing to the sustainability of healthcare systems.VIVA-ELISA will also validate this technology in initial clinical studies and will carry out the necessary work to comply with current EU/US regulations before its introduction into the market.
Beneficiaries (1)
| Organisation | Country | Role | EC contribution | SME |
|---|---|---|---|---|
| VIVA IN VITRO DIAGNOSTICS SL | ES | coordinator | €2,493,004 | Yes |
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