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EMA committee recommends first stem cell-based veterinary medicine
Arti-cell Forte is recommended for use in horses with mild to moderate lameness related to joint inflammation.
Arti-cell Forte indicated for use in horses with lameness

The first stem cell-based veterinary medicine has been recommended for marketing authorisation in the European Union by The European Medicines Agency's (EMA) Committee for Medicinal Products (CVMP).

Arti-cell Forte is recommended for use in horses with mild to moderate lameness related to joint inflammation. It is available as a suspension for injection and is given as a single injection into the affected joint.

In a press release, the EMA said the stem cells in the medicine are treated so they develop towards cartilage cells. This can then help to repair damaged cartilage in the joint.

‘In a field study conducted in horses with lameness of the fetlock joint, Arti-Cell Forte showed a statistically significant improvement in the horses treated with the medicine compared with a placebo control group six weeks after treatment,’ the EMA writes. ‘The positive effect of treatment was sustained over one year.’

Common side effects of the medicine reported in the study were mild increase in lameness and injection site reactions in the week following treatment.

The CVMP’s recommendation will now be passed on to the European Commission for a decision on an EU-wide marketing authorisation. 

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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.