Your data on MRCVSonline
The nature of the services provided by Vision Media means that we might obtain certain information about you.
Please read our Data Protection and Privacy Policy for details.

In addition, (with your consent) some parts of our website may store a 'cookie' in your browser for the purposes of
functionality or performance monitoring.
Click here to manage your settings.
If you would like to forward this story on to a friend, simply fill in the form below and click send.

Your friend's email:
Your email:
Your name:
 
 
Send Cancel

Treatment approved for allergic skin diseases

First JAK inhibitor to become available for veterinary use

A new treatment for the itch and inflammation associated with allergic skin disease in dogs has been approved by the European Commission.

Developed by Zoetis (formerly Pfizer), new drug APOQUEL (oclacitinib tablet) is for the treatment of the clinical manifestations of atopic dermatitis, and pruritis associated with allergic dermatitis in dogs of at least 12 months of age.

This treatment is aimed at stopping the cycle of itch and inflammation occurring in skin allergies by inhibiting the function of a range of allergic, itch and inflammatory cytokines which depend on Janus kinase (JAK) enzymes.

According to the animal health company, pruritis, or itch, is the most common symptom of allergic skin disease in dogs. The new drug is the first JAK inhibitor to be approved for veterinary use.

During clinical trials, pet owners reported a decrease in itch scores in their dog as quickly as 24-hours after the treatment was administered.

Veterinary surgeons who assessed skin lesion scores found they were significantly improved after one week and continued to improve for the next four months of the study.

The company says an estimated 5 million dogs in Europe suffer from both short and long-term allergic skin conditions, yet current treatments are limited.

The most common side effects to be reported in clinical trials for the product were vomiting and diarrhoea. Other side effects included lethargy, decreased appetite and skin irritation and infection.

The new treatment is to be available on prescription by a veterinary surgeon only, and dosed at 0.4 to 0.6mg/kg. Tablets are administered orally twice a day for 14 days, then once daily if medium or long-term treatment is needed.

The company plans to make the treatment available to veterinary surgeons in the European Union in 2014.

All trademarks are acknowledged

 

Become a member or log in to add this story to your CPD history

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.