
- dvm360 March 2021
- Volume 53
NRC guidelines open door for durable canine OA pain relief
With a single intra-articular injection of Synovetin OA, dogs with elbow arthritis may remain pain-free for up to a year.
The Nuclear Regulatory Commission (NRC) recently issued licensing guidelines for the use of Synovetin OA (Exubrion Therapeutics), a new veterinary device administered via intra-articular injection that is intended to reduce synovitis and associated pain in dogs with elbow osteoarthritis (OA). The NRC guidelines, issued to all relevant regulatory agencies, establish a protocol for veterinary practices that want to offer this treatment for their patients.
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The active agent in Synovetin OA is the conversion electron radiotherapeutic Tin-117m. According to the product
Safety and efficacy of Synovetin OA were demonstrated in 3 multicenter studies, showing a 92% treatment success rate in dogs with grade 1 and 2 elbow OA and a 71.4% success rate in dogs with grade 3 elbow OA. Pet owners and veterinarians reported up to 12 months of sustained effectiveness following a single injection, with no clinically significant systemic or local side effects observed.
“This procedure is commonly and safely performed in people,” explains Exubrion CEO Peter Selover in the release. “With the recent NRC guidelines, we expect to have at least 50 veterinary hospitals around the country licensed to use Synovetin in the first half of 2021, offering relief to pets whose pain may not be adequately managed by current therapies, and pet owners who think surgery may be their only option to relieve their dog’s pain.”
For more information, including the Synovetin OA package insert with instructions for use, visit
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