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Drug library

Oclacitinib

Janus kinase inhibitor

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Oclacitinib

Oclacitinib is a Janus kinase inhibitor used principally to control allergic pruritus and atopic dermatitis in dogs. Its relatively rapid effect reflects interruption of cytokine signaling involved in itch and inflammation. Veterinary products are directed toward canine allergic skin disease, while experience in other species is more limited.

Group

Janus kinase inhibitor

Mechanism of Action

Oclacitinib preferentially inhibits JAK1-dependent intracellular signaling downstream of several cytokine receptors. Reduced JAK–STAT activation limits responses to cytokines involved in allergy and inflammation, including IL-31-associated itch signaling. Interference with these pathways reduces pruritic stimulation and inflammatory activity in affected skin. Selectivity is relative and depends on drug concentration.

Dose Rates

Dogs

Use / stageDoseRouteScheduleInstructions
Allergic pruritus and atopic dermatitis — Initial0.4–0.6 mg/kgPOEvery 12 hUp to 14 days; Do not use in: Dogs younger than 12 months, Serious infections
Allergic pruritus and atopic dermatitis — Maintenance0.4–0.6 mg/kgPOEvery 24 hDo not use in: Dogs younger than 12 months, Serious infections

Indications

Contraindications

Interactions

Adverse effects

Preparations

PreparationFormStrengthRoute
Apoquel 3.6 mgTablet3.6 mg / tabletPO
Apoquel 5.4 mgTablet5.4 mg / tabletPO
Apoquel 16 mgTablet16 mg / tabletPO

Monitoring and Administration

After the first 14 days, reduce canine administration to once daily. Check CBC when warranted and assess for infection, demodicosis and new masses.

Store tablets at 20-25 C. Compounded formulations lack established potency and stability.

Cats: Small observational reports describe 0.4-0.6 mg/kg twice daily for 14 days followed by once daily; the clinical guidance states that an established feline dose is lacking and does not explicitly specify the route in the reported regimen.

Veterinary use

For veterinary reference. Confirm the indication, dose, route, interval, product strength and any applicable withdrawal period before administration.