Zoetis Inc. has announced that the Committee for Veterinary Medicinal Products (CVMP) of the European Medicines Agency $(EMA)$ has issued a positive opinion recommending the granting of marketing authorization for Portela® (relfovetmab). This new monoclonal antibody therapy is designed to alleviate pain associated with osteoarthritis in cats. If approved, Portela will be the first long-acting anti-NGF monoclonal antibody therapy for cats, offering a solution that requires injections only once every three months. The European Commission is expected to make a decision during the fourth quarter of 2025, with commercial availability anticipated in the European Union in 2026. This development marks another milestone in Zoetis' commitment to advancing feline medicine and enhancing the quality of life for cats with osteoarthritis.