If you are a drug discovery firm dealing with the high risk of single-target drug failure — this project developed a library of over 300,000 molecules that provides a diversified starting point for broad-spectrum antivirals. This reduces the time needed to find hits against multiple viral families.
Rapid Response Platform for Developing Broad-Spectrum Antiviral Drugs Against Pandemic Viruses
Imagine having a master key that can unlock many different doors; this project is building a 'master key' medicine that works against several different families of dangerous viruses. Instead of waiting for a new virus to appear and then starting from scratch, they are finding molecules that already work against a wide range of threats. It's like having a fire extinguisher ready for any type of fire before the spark even happens.
What needed solving
Current antiviral treatments are too specific, meaning new medicines must be developed from scratch during every new pandemic. This delay increases mortality and overwhelms healthcare systems.
What was built
A high-throughput screening platform and a library of 300,000 molecules, alongside validated ex vivo lung models and nano-conjugation delivery systems.
Who needs this
Who can put this to work
If you are a research lab dealing with the difficulty of testing dangerous pathogens — this project developed human precision-cut lung slices and BSL-4 validation protocols. This allows for safer and more accurate testing of 17 confirmed compounds against Ebola virus.
If you are a developer dealing with poor drug delivery efficiency — this project developed innovative delivery systems using nano conjugation. This improves how antivirals reach their target in the body during a public health crisis.
Quick answers
What is the cost or price of the developed antivirals?
Based on available project data, there is no information regarding the pricing or cost of the resulting antiviral candidates.
Can these antivirals be produced at an industrial scale?
The project focuses on discovery, preclinical validation, and early clinical evaluation. Based on available project data, industrial scale-up details are not yet specified.
How is the IP and licensing handled for the 160+ hits?
Based on available project data, the specific IP and licensing terms for the identified molecules are not provided.
What is the timeline for clinical availability?
The project runs from 2024-01-01 to 2028-12-31, with a roadmap including an adaptive platform trial for early clinical evaluation of 3 antivirals.
How will these drugs be integrated into public health systems?
The project aims to facilitate long-term implementation of broad-spectrum antivirals in public health preparedness to reduce the burden on healthcare systems.
Who built it
The consortium is a diverse 12-partner group across 9 countries, blending high-level research with commercial interests. With a 17% industry ratio (including 2 industry partners and 1 SME), the project maintains a strong academic and research core (9 partners) while ensuring a path toward commercialization and clinical application.
Contact the European Research Infrastructure on Highly Pathogenic Agents in Belgium
Talk to the team behind this work.
Contact us to explore licensing opportunities for the 160+ identified antiviral hits.