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Ebola vaccine trial 100 per cent effective
Ebola
Results published in The Lancet show that the vaccine had a 100 per cent success rate when it was given immediately.

Experts say results are 'remarkable'

Early results of a trial investigating the effects of an ebola vaccine have shown a 100 per cent success rate, according to the World Health Organisation.

The trial vaccine was given to thousands of people living in affected communities in Guinea who had been in close proximity of individuals with the infection - a method called 'ring vaccination'. Half were given the vaccine immediately, while the other half were given the vaccine after a wait of three weeks.

Results published in The Lancet show that the vaccine had a 100 per cent success rate when it was given immediately. None of the participants showed any symptoms of ebola up to 10 days after being the vaccine immediately after exposure. In  those in the delayed vaccination group, 16 participants developed symptoms.

The World Health Organisation say that while the vaccine up to now shows 100 per cent efficacy in individuals, more conclusive evidence is needed on its ability to protect populations through what is called 'herd immunity'. For this reason the Guinean national regulatory authority and ethics review committee have approved continuation of the trial.

Commenting on the results, Dr Margaret Chan, director-general of the World Health Organisation said: "This is an extremely promising development.  The credit goes to the Guinean Government, the people living in the communities and our partners in this project.  An effective vaccine will be another very important tool for both current and future Ebola outbreaks."

Dr Jeremy Farrar, director of the Wellcome Trust, one of the funders of the trial, added that it was 'a remarkable result' and was the product of international collaboration.

The trial is now set to include 12-17-year-olds and possibly 6-12-year-old children on the basis of new evidence of the vaccine's safety.  A trial of the same vaccine will also be conducted on frontline workers.

Image (C) CDC Global

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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. 

Click here for more...
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.