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Novel cancer treatment shows promise for cats and humans
Thirty-five per cent of cats in the study had their disease controlled with minimal side effects.

The drug targets the transcription factor STAT 3. 

Researchers at the University of California have conducted the first-ever clinical trial of a new class of targeted therapy for pet cats with head and neck squamous cell carcinoma (HNSCC).

The drug, which is the first to target the transcription factor STAT3, showed promising results, and is likely to be effective for humans with the disease. 

Writing in the journal Cell Press, researchers describe how 35 per cent of cats in the study had their disease controlled with minimal side effects. Among them was a nine-year-old black domestic shorthair named Jak, who lived eight months after his diagnosis, and much longer than expected.

Jak’s owner, Tina Thomas, said: “It was meaningful to us because he was here in our lives. During that time, my son finished college and my daughter finished her master’s program. Jak got to spend one more Christmas with us, and he loved our Christmas tree. He was worth every bit of the effort.” 

Interestingly, researchers believe conducting clinical trials in pets could be a better model of how drugs work in humans, compared with lab mice. The team is currently working with a small biotech firm to advance the treatment in clinical trials for pets and humans. 

First author Jennifer Grandis, said: “This study is a great example of how we can think more carefully about spending our very limited resources on studies in lab mice that are not even the best models of human cancers.

“By partnering with veterinary oncologists and doing clinical trials in companion animals, we can learn an enormous amount about how these drugs work while also helping people’s pets. None of the cats in these trials were harmed, and many of them benefited.” 

Image (C) Shutterstock.

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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.