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First stem cell-based veterinary medicine approved
“A quarter of the entire equine population develops osteoarthritis at some point in their life."
Arti-Cell Forte for equine lameness available from May 2019 

The first stem cell-based veterinary medicine, used for treating equine lameness, will be available from May and June 2019.

Boehringer Ingelheim has launched Arti-Cell Forte in Europe for the ‘reduction of mild to moderate recurrent lameness associated with non-septic joint inflammation in horses’.

Described as a ‘groundbreaking first-ever approved treatment’, the drug targets lameness by utilising specifically primed, chondrogenic induced stem cells. It comes in an ultra-low frozen and ready-to-use format.

Boehringer said current treatments for lameness are not satisfactory for all cases and ‘there is a clear need for innovation and new treatment options’, looking at the underlying cause rather than just treating symptoms.

The company formed a partnership with Global Stem Cell Technology (GST) last year to develop new treatments and solutions to improve animal health.

Jan Spaas, CEO of GST, said: “A quarter of the entire equine population develops osteoarthritis at some point in their life. Priming the cells towards cartilage aids them to deliver the right activities in the affected joint.

“We are absolutely delighted with our first marketing authorisation from the European Commission and the first stem cell-based product in animal health. We are sure that with our partner Boehringer Ingelheim this product will become a game changer in equine health.”

Dr Erich Schoett, of Boehringer, added: “We are proud to continue to set new standards of care for horses to optimise their health and well-being in partnership with veterinarians. Early disease detection and early treatment are key to ensure that horses are healthy and live longer, happier lives.”

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Annual submission deadline small pet animal exemptions

News Story 1
 Companies marketing medicines for small pets exempt from authorisation must submit their annual return to the Veterinary Medicines Directorate (VMD) by 30 November 2026.

Submitting this annual return ensures continued compliance with regulatory requirements for products marketed without a full Marketing Authorisation. The exemption specifically applies to products intended for animals, cage birds, terrarium animals, small rodents, ferrets and rabbits.

For further details and submission guidelines, visit the gov.uk website.  

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BVA urges 'continued vigilance' over bluetongue

The British Veterinary Association (BVA) has urged vigilance following a concerning rise in Bluetongue (BTV) cases in sheep and cattle.

In a recent statement, the BVA noted that members are reporting more severe clinical signs and higher mortality rates than in previous years.

'We know that farm vets are working hard to support farmers and animals affected by this outbreak, during what is an extremely difficult time for all involved,' they stated. 'Continued vigilance to identify disease early is vital and vaccination remains the best way of protecting animals from this disease.'