Home / News / Merck Animal Health Gets FDA approval for Numelvi (atinvicitinib tablets) for Canine Dermatitis 

Merck Animal Health Gets FDA approval for Numelvi (atinvicitinib tablets) for Canine Dermatitis 

Quick Takeaways  

  • Merck Animal Health has secured US FDA approval for Numelvi (atinvicitinib tablets), the first and only second-generation JAK inhibitor for controlling pruritus linked to allergic dermatitis in dogs aged 6 months and older. 
  • Numelvi is a once-daily, first-line therapy that delivers rapid itch relief from the first dose, with high JAK1 selectivity, helping reduce inflammation while maintaining a strong safety profile. It also offers convenient dosing, no vaccine schedule adjustments, and long shelf life. 
  • Expected to launch in spring 2026 across US veterinary clinics, the therapy addresses a major unmet need, as skin conditions account for up to 20% of vet visits, significantly impacting dogs’ quality of life and pet-owner well-being.  

Why It Matters? 

Merck Animal Health strengthens its dermatology franchise with a differentiated, second-generation JAK inhibitor positioned as a convenient, first-line option for allergic pruritus. 
Once-daily dosing and rapid onset are likely to shift prescribing from older therapies (including steroids and first-generation JAK inhibitors), increasing brand loyalty among dermatology-focused veterinarians. 
Given the high share of skin cases in small-animal practice, Numelvi can become a key driver of clinic revenue and deepen Merck’s integration into chronic care protocols for companion animals. 

Source: Businesswire  

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