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New company launched to tackle canine osteoarthritis
The new company - Vetosine - will develop and commercialise new disease modifying osteoarthritis drugs (DMOAD) for dogs.

Human and animal health companies partner up to develop disease modifying drug.

Swiss animal health group Stonehaven Incubate has partnered with Regenosine – specialists in musculoskeletal regenerative therapies – to launch a new company focused on developing disease modifying osteoarthritis drugs for dogs.

The new company, named Vetosine, will produce adenosine-based treatments. Co-founder of Regenosine Dr Bruce Cronstein was one of the first researchers to highlight the role of adenosine in maintaining healthy joint cartilage.

Charlie Dawson, venture partner at Stonehaven Incubate, commented: “At the moment, veterinarians and pet owners have few therapy options for dogs with osteoarthritis beyond simple nonsteroidal anti-inflammatory drugs (NSAIDs), diet and exercise. Vetosine will provide a proven disease modifying drug that will strengthen clinical outcomes and improve the pet’s quality of life.”

Dr. Siddhesh Angle, co-founder and CEO of Regenosine, said: “We have now developed proprietary formulations for adenosine replacement which have demonstrated disease modifying outcomes in gold standard preclinical models for osteoarthritis.”

“While we endeavour to make this first-in-class therapy a success for human medicine, we are very excited to partner with Stonehaven Incubate to expand its horizon into the animal health space.”

According to Stonehaven Incubate, Vetosine will have an exclusive global license to develop the new technology in animal health, while Regenosine will maintain its focus on developing the same technology for the human health sector.

 

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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.