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NexGard range approved for treatment of serious skin diseases
Nexgard was the first oral medication to treat both fleas and ticks in dogs.
Label claims expanded for two brands in the EU and Australia

NexGard and NexGard Spectra have been approved for the treatment of two serious skin diseases in dogs, demodicosis and sarcoptic mange.

Boehringer Ingelheim received approval to expand the label claims for the brands, both in the EU and Australia.

Nexgard was the first oral medication to treat both fleas and ticks in dogs, while NexGard Spectra also protects against parasites such as heartworm, lungworm and the most common gastrointestinal parasites.

Canine demodicosis, or demodectic mange, is considered to be one of the most severe skin diseases in dogs and can be life threatening. It is caused by the Demodex canis mite, which lives in the hair follicles and sebaceous glands. The majority of dogs are healthy carriers and are able to inhibit mite proliferation.

If, however, a dog develops generalised demodicosis, it usually means the immune system is compromised.

Sarcoptic mange is a generalised dermatitis and is often hard to diagnose. It is caused by the highly contagious skin parasite, Sarcoptes scabiei. Mites burrow into the skin and cause severe itching, which may result in scabs and hair loss.

Professor Fred Beugnet, head of global veterinary technical services at Boehringer, said: “Sarcoptes mites are not only easily transferred between dogs, but are zoonotic parasites which can be passed from animals to humans. This is why the treatment of this disease is crucial for animals’ as well as humans’ health.”

Approval to expand the label claim was granted on the basis of three experimental studies and two well-controlled field studies. According to Boehringer, the canine demodicosis study showed an overall efficacy of more than 98 per cent, while the studies on sarcoptic mange showed at almost 100 per cent efficacy after just one administration. 

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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.