A blinded, randomized, placebo-controlled trial of the safety of oclacitinib in cats.


Journal

BMC veterinary research
ISSN: 1746-6148
Titre abrégé: BMC Vet Res
Pays: England
ID NLM: 101249759

Informations de publication

Date de publication:
08 May 2019
Historique:
received: 12 12 2018
accepted: 29 04 2019
entrez: 10 5 2019
pubmed: 10 5 2019
medline: 24 5 2019
Statut: epublish

Résumé

Oclacitinib is a Janus kinase (JAK) 1 enzyme inhibitor and blocks JAK1-dependent cytokines and is used to control pruritus. Studies available in cats are very limited and as there is a potential role for oclacitinib in the control of pruritus in this specie, the aim of this study was to evaluate the safety and clinical effects of oral oclacitinib maleate in healthy cats. Thirty mixed-breed cats weighing from 2.1 to 5.3 kg each were randomly allocated to three treatment groups of 10 animals each. Cats in two groups received oclacitinib at 1 mg/kg or 2 mg/kg q 12 h orally for 28 days. Cats in the third group were given placebo tablets (cornstarch) q 12 h orally for 28 days. Oclacitinib maleate was well tolerated during the study and few adverse events were observed in treated cats. Clinical signs of toxicity were not observed in any animals treated at 1 mg/kg. Gastrointestinal clinical signs observed in the 2 mg/kg group included vomiting in two of the 10 cats and soft stools in two cats. One cat treated with placebo also exhibited soft stools. No significant differences were observed between the groups for hematologic analyses performed during the study. There was a slight increase in neutrophils and monocytes and a decrease in eosinophil mean counts in treated cats. Mean renal and liver enzymes remained normal throughout the entire study. A small, but significant increase in fructosamine levels was observed for both treated groups compared with placebo; however, values remained within the normal reference range. There were no significant difference between treated groups and the placebo group for urine specific gravity, pH, or urine protein to creatinine ratio mean values. Oclacitinib maleate was well tolerated by cats at 1 mg/kg and 2 mg/kg and appeared to be safe for this species when administered orally twice daily for 28 days. More studies would be needed to demonstrate if oclacitinib maleate may be a suitable alternative to treat pruritic cats.

Sections du résumé

BACKGROUND BACKGROUND
Oclacitinib is a Janus kinase (JAK) 1 enzyme inhibitor and blocks JAK1-dependent cytokines and is used to control pruritus. Studies available in cats are very limited and as there is a potential role for oclacitinib in the control of pruritus in this specie, the aim of this study was to evaluate the safety and clinical effects of oral oclacitinib maleate in healthy cats.
RESULTS RESULTS
Thirty mixed-breed cats weighing from 2.1 to 5.3 kg each were randomly allocated to three treatment groups of 10 animals each. Cats in two groups received oclacitinib at 1 mg/kg or 2 mg/kg q 12 h orally for 28 days. Cats in the third group were given placebo tablets (cornstarch) q 12 h orally for 28 days. Oclacitinib maleate was well tolerated during the study and few adverse events were observed in treated cats. Clinical signs of toxicity were not observed in any animals treated at 1 mg/kg. Gastrointestinal clinical signs observed in the 2 mg/kg group included vomiting in two of the 10 cats and soft stools in two cats. One cat treated with placebo also exhibited soft stools. No significant differences were observed between the groups for hematologic analyses performed during the study. There was a slight increase in neutrophils and monocytes and a decrease in eosinophil mean counts in treated cats. Mean renal and liver enzymes remained normal throughout the entire study. A small, but significant increase in fructosamine levels was observed for both treated groups compared with placebo; however, values remained within the normal reference range. There were no significant difference between treated groups and the placebo group for urine specific gravity, pH, or urine protein to creatinine ratio mean values.
CONCLUSIONS CONCLUSIONS
Oclacitinib maleate was well tolerated by cats at 1 mg/kg and 2 mg/kg and appeared to be safe for this species when administered orally twice daily for 28 days. More studies would be needed to demonstrate if oclacitinib maleate may be a suitable alternative to treat pruritic cats.

Identifiants

pubmed: 31068210
doi: 10.1186/s12917-019-1893-x
pii: 10.1186/s12917-019-1893-x
pmc: PMC6506962
doi:

Substances chimiques

Pyrimidines 0
Sulfonamides 0
oclacitinib 99GS5XTB51

Types de publication

Clinical Trial, Veterinary Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

137

Subventions

Organisme : Zoetis
ID : doanted oclacitinib tablets
Organisme : CAPES
ID : Finance code 001

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Auteurs

Natália Lôres Lopes (NL)

Veterinary Medicine, Universidade Federal Rural do Rio de Janeiro (UFRRJ), Seropédica, Brazil. natloresvet@gmail.com.

Diefrey Ribeiro Campos (DR)

Veterinary Science, UFRRJ, Seropédica, Brazil.

Marília Alves Machado (MA)

Veterinary Science, UFRRJ, Seropédica, Brazil.

Mariana Silva Revoredo Alves (MSR)

Veterinary Science, UFRRJ, Seropédica, Brazil.

Manuela Silva Gomes de Souza (MSG)

School of Veterinary Medicine, UFRRJ, Seropédica, Brazil.

Cristiano Chaves Pessoa da Veiga (CCP)

Veterinary Hospital, UFRRJ, Seropédica, Brazil.

Alexandre Merlo (A)

Zoetis Industry of Veterinary Products, São Paulo, Brazil.

Fábio Barbour Scott (FB)

Animal Parasitology Department, UFRRJ, Seropédica, Brazil.

Julio Israel Fernandes (JI)

Veterinary Medicine and Surgery Department, UFRRJ, Seropédica, Brazil.

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Classifications MeSH