If you are a vaccine manufacturer dealing with the rise of tick-borne diseases due to climate change — this project developed mRNA vaccine candidates and a production roadmap that accelerates the path to Phase I clinical trials.
mRNA Vaccine and Antibody Therapy Development for Crimean-Congo Haemorrhagic Fever
Imagine a dangerous virus spread by ticks that causes severe bleeding. This work creates a high-tech 'instruction manual' (mRNA) to teach the body to fight it and develops custom-made antibodies that act like precision missiles to neutralize the virus. It's like building a double-layered security system for the body to prevent and treat a deadly infection.
What needed solving
There is a critical lack of effective vaccines and treatments for Crimean-Congo Haemorrhagic Fever, a severe zoonotic threat exacerbated by climate change.
What was built
An mRNA vaccine candidate, a pipeline for monoclonal antibodies from patient B cells, and a biobank of CCHF patient samples.
Who needs this
Who can put this to work
If you are a biotech firm dealing with a lack of therapeutic options for viral hemorrhagic fevers — this project developed a pipeline to produce monoclonal antibodies (mAbs) from patient B cells that can be used as immunotherapy.
If you are a health infrastructure provider dealing with fragmented sample data — this project developed a biobank from CCHF patients and harmonized pipelines for clinical sample collection and analysis.
Quick answers
What is the estimated cost or price of the developed vaccines?
Based on available project data, there is no information regarding the cost or pricing of the vaccine candidates.
Can these vaccines be produced at an industrial scale?
The project focuses on establishing a platform for mRNA-based vaccines and a roadmap for Phase I trials, but industrial scale-up data is not provided.
How is the intellectual property or licensing handled?
Based on available project data, specific IP or licensing terms are not mentioned.
What is the timeline for human application?
The project aims to develop a road map to bring the most efficacious candidates to clinical trial Phase I in humans by the end of the period in 2027.
How will the results be integrated into existing health systems?
Results will be shared with public health authorities, outbreak management teams, and hospitals to increase preparedness for new outbreaks.
Who built it
The consortium is heavily weighted toward research and academia, consisting of 15 partners across 10 countries. With 9 research organizations and 4 universities, and 0% industry participation, the project is currently in a high-science phase focused on discovery and pre-clinical validation rather than immediate commercialization.
Contact FOLKHALSOMYNDIGHETEN in Sweden
Talk to the team behind this work.
Contact us to identify potential licensing opportunities as the project moves toward Phase I trials.