Select Therapeutic Agents for Atopic Dermatitis in Dogs

Select Therapeutic Agents for Atopic Dermatitis in Dogs

Agent

Dosagea

Key Points

Allergen-Specific Immunotherapy (ASIT)

Injectable ASIT: subcutaneous allergen-specific immunotherapy (SCIT)

Various protocols exist; patient-specific recommendations are typically provided by the serum manufacturer on the basis of testing results, patient history, allergen cross-reactivity, and geographical location.

Very specific targeted effect

Slow onset of action (up to 12 mo)

Not useful for acute flares

Most common adverse reaction: worsening of pruritus

Oral ASIT: sublingual allergen-specific immunotherapy (SLIT)

Pump dispenser directly onto oral mucosa, between lip and gum, q 12 h

Most common adverse reactions: face rubbing, transient worsening of pruritus, GI signs

Topical Glucocorticoids

Triamcinolone acetonide 0.015%

Topically q 12–24 hb

Indicated for acute flares and localized lesions

Apply to the affected area

Best suited for short-term use (7–14 d)

Potential adverse effects of note: cutaneous atrophy, calcinosis cutis

Hydrocortisone aceponate 0.0584%

Topically q 12–24 hc

Betamethasone valerate (various concentrations)

Topically q 12–24 hd

Mometasone furoate (various concentrations)

Topically q 12–24 hd

Oral Glucocorticoids

Prednisone or prednisolone

Induction or initial dose: 0.5–1.1 mg/kg, PO, q 24 he

Target dose after tapering: 0.25–0.5 mg/kg, PO, q 48 he

Indicated for acute flares

Fast acting

Broad, nonspecific anti-inflammatory response

Many potential adverse effects

Calcineurin Inhibitors

Cyclosporine

Initial dose: 5 mg/kg, PO, q 24 h; tapered to the lowest dose that controls the diseasee

Indicated for long-term management

Can take 4–6 wk to achieve clinical improvement

Not suitable for treatment of acute flares

Most common adverse effects: GI signs

Indicated for localized lesions

Appears safe for short-term use

Tacrolimus 0.1% ointment

Topically q 12–24 hb

Phosphodiesterase Inhibitors

Pentoxifylline

20 mg/kg, PO, q 8 hf

May be best suited as adjunctive therapy for chronic conditions

Slow onset of action (4–6 wk)

Not suited for acute flares

Good safety profile

Antihistamines

Fexofenadine

18 mg/kg, PO, q 24 hg

Helpful for mild pruritus

Best as part of combination therapy

Preventive role

Sparing agents for glucocorticoids

Not suitable for acute flares

Hydroxyzine

2 mg/kg, PO, q 12 hh

Hydroxyzine + chlorpheniramine

(20.9 mg + 0.7 mg)/10 kg (divided), PO, q 12 hi

Cetirizine

0.5–1 mg/kg, PO, q 12 hh

Essential Fatty Acids

High-quality fish oil (with EPA and DHA)

65–90 mg/kg, PO, q 24 h j,k,l

No evidence of superior efficacy of any particular combination, dosage, ratio, or formulation to improve skin and coat quality and decrease pruritus

Janus Kinase Inhibitors

Oclacitinib maleate (tablet or chewable tablet)

0.4–0.6 mg/kg, PO, q 12 h for 2 wk, then q 24 he

Indicated for acute flares and long-term management of pruritus in dogs 12 mo or older

Fast onset of action (within 24 h) for pruritus control

Most common adverse effects: GI signs

Contraindicated in dogs with serious infections or neoplasia

May increase susceptibility to infections, demodicosis, and neoplastic conditions

Acute kidney injury possible with toxic doses (eg, 27.3 mg/kg)m

Ilunocitinib 

0.6–0.8 mg/kg, PO, q 24 hn

Indicated for control of pruritus associated with allergic and atopic dermatitis in dogs 12 mo or older

  1. Contraindicated in dogs with serious infection

    1. Dogs should be current on vaccinations before starting this medication. Ilunocitinib should be discontinued for at least 28 d to 3 mo before vaccination and for at least 28 d after vaccination.

      1. Concurrent use with glucocorticoids, cyclosporine, or other immunosuppressive agents have not been tested.

Monoclonal Antibodies

Lokivetmab

2 mg/kg, SC, q 4–8 wko

Indicated for acute flares and long-term management

Fast onset of action (1–3 d) for pruritus control

Most common adverse effects: lethargy, vomiting

Adapted from Sandra Koch. What is new in the diagnosis and management of canine atopic dermatitis. Today’s Veterinary Practice. May/June 2015:95-102.

a For most antipruritic agents used to treat dogs with atopic dermatitis (glucocorticoids, calcineurin inhibitors, phosphodiesterase inhibitors, antihistamines, essential fatty acids, Janus kinase inhibitors, monoclonal antibodies), therapy typically continues until clinical signs have resolved. However, in many cases, long-term therapy is required to maintain control of clinical signs. When long-term therapy is required, medications should be tapered to the lowest dose and frequency that maintains remission of clinical signs.

b Olivry T, Foster AP, Mueller RS, McEwan NA, Chesney C, Williams HC. Interventions for atopic dermatitis in dogs: a systematic review of randomized controlled trials. Vet Dermatol. 2010;21(1):4-22. doi:10.1111/j.1365-3164.2009.00784.x

c Nuttall TJ, McEwan NA, Bensignor E, Cornegliani L, Löwenstein C, Rème CA. Comparable efficacy of a topical 0.0584% hydrocortisone aceponate spray and oral ciclosporin in treating canine atopic dermatitis. Vet Dermatol. 2012;23(1):4-10, e1-2. doi:10.1111/j.1365-3164.2011.00992.x

d Anecdotal evidence.

e Olivry T, DeBoer DJ, Favrot C, et al. Treatment of canine atopic dermatitis: 2015 updated guidelines from the International Committee on Allergic Diseases of Animals (ICADA). BMC Vet Res. 2015;11:210. doi:10.1186/s12917-015-0514-6

f Singh SK, Dimri U, Saxena SK, Jadhav RK. Therapeutic management of canine atopic dermatitis by combination of pentoxifylline and PUFAs. J Vet Pharmacol Ther. 2010;33(5):495-498. doi:10.1111/j.1365-2885.2009.01146.x

g Alja P, Silvestra K, Domanjko-Petric A, Kotnik T. The efficacy of antihistamine fexofenadine versus methylprednisolone in the treatment of atopic dermatitis in dogs. Slov Vet Res. 2009;46(1):5-12.

h Bizikova P, Papich MG, Olivry T. Hydroxyzine and cetirizine pharmacokinetics and pharmacodynamics after oral and intravenous administration of hydroxyzine to healthy dogs. Vet Dermatol. 2008;19(6):348-357. doi:10.1111/j.1365-3164.2008.00697.x

i Eichenseer M, Johansen C, Mueller RS. Efficacy of dimetinden and hydroxyzine/chlorpheniramine in atopic dogs: a randomised, controlled, double-blinded trial. Vet Rec. 2013;173(17):423. doi:10.1136/vr.101907

j Saevik BK, Bergvall K, Holm BR, et al. A randomized, controlled study to evaluate the steroid sparing effect of essential fatty acid supplementation in the treatment of canine atopic dermatitis. Vet Dermatol. 2004;15(3):137-145. doi:10.1111/j.1365-3164.2004.00378.x

k Schäfer L, Thom N. A placebo-controlled, double-blind study evaluating the effect of orally administered polyunsaturated fatty acids on the oclacitinib dose for atopic dogs. Vet Dermatol. 2024;35(4):408-417. doi:10.1111/vde.13246

l Müller MR, Linek M, Löwenstein C, et al. Evaluation of cyclosporine-sparing effects of polyunsaturated fatty acids in the treatment of canine atopic dermatitis. Vet J. 2016;210:77-81. doi:10.1016/j.tvjl.2015.11.012

m Damone JM, Lister S, Lyons BM. Oclacitinib (Apoquel) toxicosis resulting in acute kidney injury in a dog. J Am Vet Med Assoc. 2025;263(9):1-2. doi:10.2460/javma.25.04.0240

n Kuntz EA, Gabor L, Toutain CE. Safety of ilunocitinib tablets (Zenrelia™) after once daily oral administration in dogs. BMC Vet Res. 2025;21(1):144. doi:10.1186/s12917-025-04579-1

o Michels GM, Ramsey DS, Walsh KF, et al. A blinded, randomized, placebo-controlled, dose determination trial of lokivetmab (ZTS-00103289), a caninized, anti-canine IL-31 monoclonal antibody in client owned dogs with atopic dermatitis. Vet Dermatol. 2016;27(6):478-e129. doi:10.1111/vde.12376

Adapted from Sandra Koch. What is new in the diagnosis and management of canine atopic dermatitis. Today’s Veterinary Practice. May/June 2015:95-102.

a For most antipruritic agents used to treat dogs with atopic dermatitis (glucocorticoids, calcineurin inhibitors, phosphodiesterase inhibitors, antihistamines, essential fatty acids, Janus kinase inhibitors, monoclonal antibodies), therapy typically continues until clinical signs have resolved. However, in many cases, long-term therapy is required to maintain control of clinical signs. When long-term therapy is required, medications should be tapered to the lowest dose and frequency that maintains remission of clinical signs.

b Olivry T, Foster AP, Mueller RS, McEwan NA, Chesney C, Williams HC. Interventions for atopic dermatitis in dogs: a systematic review of randomized controlled trials. Vet Dermatol. 2010;21(1):4-22. doi:10.1111/j.1365-3164.2009.00784.x

c Nuttall TJ, McEwan NA, Bensignor E, Cornegliani L, Löwenstein C, Rème CA. Comparable efficacy of a topical 0.0584% hydrocortisone aceponate spray and oral ciclosporin in treating canine atopic dermatitis. Vet Dermatol. 2012;23(1):4-10, e1-2. doi:10.1111/j.1365-3164.2011.00992.x

d Anecdotal evidence.

e Olivry T, DeBoer DJ, Favrot C, et al. Treatment of canine atopic dermatitis: 2015 updated guidelines from the International Committee on Allergic Diseases of Animals (ICADA). BMC Vet Res. 2015;11:210. doi:10.1186/s12917-015-0514-6

f Singh SK, Dimri U, Saxena SK, Jadhav RK. Therapeutic management of canine atopic dermatitis by combination of pentoxifylline and PUFAs. J Vet Pharmacol Ther. 2010;33(5):495-498. doi:10.1111/j.1365-2885.2009.01146.x

g Alja P, Silvestra K, Domanjko-Petric A, Kotnik T. The efficacy of antihistamine fexofenadine versus methylprednisolone in the treatment of atopic dermatitis in dogs. Slov Vet Res. 2009;46(1):5-12.

h Bizikova P, Papich MG, Olivry T. Hydroxyzine and cetirizine pharmacokinetics and pharmacodynamics after oral and intravenous administration of hydroxyzine to healthy dogs. Vet Dermatol. 2008;19(6):348-357. doi:10.1111/j.1365-3164.2008.00697.x

i Eichenseer M, Johansen C, Mueller RS. Efficacy of dimetinden and hydroxyzine/chlorpheniramine in atopic dogs: a randomised, controlled, double-blinded trial. Vet Rec. 2013;173(17):423. doi:10.1136/vr.101907

j Saevik BK, Bergvall K, Holm BR, et al. A randomized, controlled study to evaluate the steroid sparing effect of essential fatty acid supplementation in the treatment of canine atopic dermatitis. Vet Dermatol. 2004;15(3):137-145. doi:10.1111/j.1365-3164.2004.00378.x

k Schäfer L, Thom N. A placebo-controlled, double-blind study evaluating the effect of orally administered polyunsaturated fatty acids on the oclacitinib dose for atopic dogs. Vet Dermatol. 2024;35(4):408-417. doi:10.1111/vde.13246

l Müller MR, Linek M, Löwenstein C, et al. Evaluation of cyclosporine-sparing effects of polyunsaturated fatty acids in the treatment of canine atopic dermatitis. Vet J. 2016;210:77-81. doi:10.1016/j.tvjl.2015.11.012

m Damone JM, Lister S, Lyons BM. Oclacitinib (Apoquel) toxicosis resulting in acute kidney injury in a dog. J Am Vet Med Assoc. 2025;263(9):1-2. doi:10.2460/javma.25.04.0240

n Kuntz EA, Gabor L, Toutain CE. Safety of ilunocitinib tablets (Zenrelia™) after once daily oral administration in dogs. BMC Vet Res. 2025;21(1):144. doi:10.1186/s12917-025-04579-1

o Michels GM, Ramsey DS, Walsh KF, et al. A blinded, randomized, placebo-controlled, dose determination trial of lokivetmab (ZTS-00103289), a caninized, anti-canine IL-31 monoclonal antibody in client owned dogs with atopic dermatitis. Vet Dermatol. 2016;27(6):478-e129. doi:10.1111/vde.12376