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Zoetis Receives European Commission Marketing Authorization for Solensia® (frunevetmab), a New Therapy for Feline Osteoarthritis Pain

Share: Solensia is the first injectable monoclonal antibody (mAb) licensed for alleviation of pain associated with osteoarthritis (OA) in cats Solensia works as a monthly treatment targeting Nerve Growth Factor (NGF), a key player in OA pain European Commission Marketing Authorization for a similar product in dogs, Librela ®, was received in November 2020 Zoetis Inc. (NYSE:ZTS) today announced that the European Commission has granted the marketing authorization for Solensia ® (frunevetmab), a new feline osteoarthritis treatment to alleviate pain. Osteoarthritis in cats is a very prevalent condition 1, existing in 40% of cats, and may generate pain and limit a cat s comfort and quality of life if not treated.

Zoetis Inc : Zoetis Receives European Commission Marketing Authorization for Solensia (frunevetmab), a New Therapy for Feline Osteoarthritis Pain

Zoetis Inc.: Zoetis Receives European Commission Marketing Authorization for Solensia (frunevetmab), a New Therapy for Feline Osteoarthritis Pain Solensia works as a monthly treatment targeting Nerve Growth Factor (NGF), a key player in OA pain European Commission Marketing Authorization for a similar product in dogs, Librela , was received in November 2020 Zoetis Inc. (NYSE:ZTS) today announced that the European Commission has granted the marketing authorization for Solensia (frunevetmab), a new feline osteoarthritis treatment to alleviate pain. Osteoarthritis in cats is a very prevalent condition 1, existing in 40% of cats, and may generate pain and limit a cat s comfort and quality of life if not treated.

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