Abstract | BACKGROUND: HYPOTHESIS/OBJECTIVES: ANIMALS: Dogs that were at least moderately pruritic with a presumptive diagnosis of allergic dermatitis were enrolled in Portugal, Hungary, France and Germany by 12 primary care practitioners and two veterinary dermatology referral specialists. METHODS AND MATERIALS: Dogs were randomised to receive either placebo (saline) or lokivetmab (1.0-3.3 mg/kg) by subcutaneous injection on Day (D)0. Owners evaluated pruritus using a validated Visual Analog Scale ( pVAS) daily until D7 and then weekly until D28. The severity of dermatitis was assessed by the investigators using a modified VAS on D0, D7, D14 and D28. RESULTS: Beginning at D1, owner-assessed pVAS least square means were significantly reduced in the treatment group versus the placebo group (57.7% versus 21.8% reduction on D28). For all time points, investigator-assessed VAS means were significantly reduced in the lokivetmab group versus the placebo group (57.1% versus 20.5% reduction on D28). Overall, the occurrence of adverse health events during the evaluation period was comparable between the two groups. CONCLUSIONS AND CLINICAL IMPORTANCE:
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Authors | Leen Van Brussel, Hilde Moyaert, Monica Escalada, Sean P Mahabir, Michael R Stegemann |
Journal | Veterinary dermatology
(Vet Dermatol)
Vol. 32
Issue 5
Pg. 477-e131
(Oct 2021)
ISSN: 1365-3164 [Electronic] England |
PMID | 34180084
(Publication Type: Journal Article, Randomized Controlled Trial, Veterinary)
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Copyright | © 2021 Zoetis. Veterinary Dermatology published by John Wiley & Sons Ltd on behalf of the European Society of Veterinary Dermatology and The American College of Veterinary Dermatology. |
Chemical References |
- Antibodies, Monoclonal
- lokivetmab
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Topics |
- Animals
- Antibodies, Monoclonal
- Dermatitis, Atopic
(drug therapy, veterinary)
- Dog Diseases
(drug therapy)
- Dogs
- Pruritus
(veterinary)
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