Zoetis Inc. has received marketing authorization from the European Commission for Lenivia® (izenivetmab), a new monoclonal antibody therapy designed to reduce pain associated with osteoarthritis (OA) in dogs. Lenivia provides pain relief for three months with a single injection by targeting nerve growth factor (NGF) and offers a novel binding mechanism compared to existing therapies. This regulatory approval marks a significant advancement in veterinary pain management, expanding Zoetis' portfolio of OA pain products for dogs. No other organizations were mentioned as recipients of this regulatory approval.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Zoetis Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20251126421523) on November 26, 2025, and is solely responsible for the information contained therein.
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