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Unfortunately, veterinary application, trials, and research in dogs are still 510 years behind human medicine, but interest in the field is rapidly accelerating

The approval is based on data from the randomized, open-label Phase III PAPILLON trial that showed the Rybrevant-based regimen cut the risk of disease progression or death by 60% versus chemotherapy alone

Human evidence, regulatory authorisation and online product identity are separate questions

The newly approved formulation offers more flexibility with the most once-daily doses of any vesicular monoamine transporter 2 (VMAT2) inhibitor, for these conditions, according to Tevas press release