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New foot-and-mouth vaccine marks a significant milestone
Scientists hope the vaccine will address the current shortfall in availability.

Vaccine less reliant on cold-chain transport and storage

A new affordable vaccine to protect livestock against several serotypes of foot-and-mouth-disease (FMD) has been granted for development by The Pirbright Institute.

Researchers say the new vaccine is more stable than existing FMD vaccines and less reliant on a cold-chain during vaccine distribution - characteristics that give the vaccine greater potential to relieve the burden placed on regions where the disease is endemic.

The vaccine is the result of a long-standing collaboration between Pirbright, the University of Oxford, Diamond Light Source, the University of Reading and MSD Animal Health, who will now be taking the technology into development.


It also marks a significant milestone in years of research to develop a new synthetic vaccine.

“We are proud and excited that our research has resulted in a vaccine that is undergoing commercial development and will have a major impact on the health and wellbeing of those people whose livelihoods have been most severely affected by this devastating disease,” said Professor Bryan Charleston, director of The Pirbright Institute. 


“The vaccine’s properties allow for a greater degree of flexibility during production, storage and transportation, which will result in a more affordable solution and therefore better access to those living in areas such as Asia and Africa.”


The vaccine is comprised of small, synthetic protein shells called ‘virus-like particles’ (VLPs). These VLPs mimic the outer shell of FMDV, stimulating an immune response.

Unlike inactivated FMD vaccines, the VLPs do not require high containment facilities for production and have been designed to remain stable up to temperatures of 56 degrees celsius, therefore reducing reliance on cold-chain transport and storage.

It is hoped that these factors combined will revolutionise vaccination in areas of Africa and Asia, where the disease continues to circulate.

Defra chief veterinary officer Christine Middlemiss said: “This is a major milestone in tackling the foot-and-mouth disease in the developing countries where it is endemic.

“The increased robustness of this new vaccine has the potential to not only protect livestock but to transform the lives of people whose livelihoods have previously been threatened by this disease. Many people have worked for years to get to this point, and I am delighted to see the vaccine receive its commercial licence.”

 

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FIVP launches CMA remedies survey

News Story 1
 FIVP has shared a survey, inviting those working in independent practice to share their views on the CMA's proposed remedies.

The Impact Assessment will help inform the group's response to the CMA, as it prepares to submit further evidence to the Inquiry Group. FIVP will also be attending a hearing in November.

Data will be anonymised and used solely for FIVP's response to the CMA. The survey will close on Friday, 31 October 2025. 

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News Shorts
CMA to host webinar exploring provisional decisions

The Competition and Markets Authority (CMA) is to host a webinar for veterinary professionals to explain the details of its provisional decisions, released on 15 October 2025.

The webinar will take place on Wednesday, 29 October 2025 from 1.00pm to 2.00pm.

Officials will discuss the changes which those in practice may need to make if the provisional remedies go ahead. They will also share what happens next with the investigation.

The CMA will be answering questions from the main parties of the investigation, as well as other questions submitted ahead of the webinar.

Attendees can register here before Wednesday, 29 October at 11am. Questions must be submitted before 10am on 27 October.

A recording of the webinar will be accessible after the event.