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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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Defra shares new Sanitary and Phytosanitary guidance

News Story 1
 Defra has published guidance for the vet sector ahead of a proposed UK-EU Sanitary and Phytosanitary agreement.

The agreement, which will change the movement and trade of animals and related products, could see reductions in checks, paperwork and certification. As well as describing regulatory developments, the advice highlights the importance of animal ID, registration and traceability in disease control and other compliance arrangements.

The guidance can be found here. More detail is expected as negotiations progress. 

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News Shorts
Lords Committee opens Pet Parasite Medication inquiry

The House of Lords Environment and Climate Change Committee will launch its inquiry into Pet Parasite Medication (PPM) on Wednesday (3 June).

Focusing on treatments containing fipronil and imidacloprid, the inquiry will seek to understand distribution pathways and the impacts of PPM use and non-use on biodiversity and human health. It will also cover current regulation, monitoring, and the potential implications for pets and their owners.

The committee will hear evidence from environmental non-governmental organisations and research institutes. The public can follow the proceedings live on Parliament TV or in person in the Palace of Westminster.