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Repeated oral dose tolerance in dogs treated concomitantly with ciclosporin and oclacitinib for three weeks

BACKGROUND: Ciclosporin and oclacitinib are immunomodulators approved for the treatment of canine atopic dermatitis. The administration of a short course of prednisolone at the beginning of ciclosporin therapy hastens the efficacy of this drug; oclacitinib has a rapid antipruritic effect similar to...

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Autores principales: Panteri, Alessandro, Strehlau, Günther, Helbig, Rainer, Prost, Christine, Doucette, Kelly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737300/
https://www.ncbi.nlm.nih.gov/pubmed/26660461
http://dx.doi.org/10.1111/vde.12278
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author Panteri, Alessandro
Strehlau, Günther
Helbig, Rainer
Prost, Christine
Doucette, Kelly
author_facet Panteri, Alessandro
Strehlau, Günther
Helbig, Rainer
Prost, Christine
Doucette, Kelly
author_sort Panteri, Alessandro
collection PubMed
description BACKGROUND: Ciclosporin and oclacitinib are immunomodulators approved for the treatment of canine atopic dermatitis. The administration of a short course of prednisolone at the beginning of ciclosporin therapy hastens the efficacy of this drug; oclacitinib has a rapid antipruritic effect similar to that of prednisolone. OBJECTIVES: To evaluate the oral tolerance of oclacitinib and ciclosporin given concurrently for three weeks. ANIMALS: Two groups of eight beagles. METHODS: Dogs were randomized to receive oclacitinib alone (0.4–0.6 mg/kg twice daily for 14 days then once daily for seven days) or in combination with ciclosporin (5 mg/kg once daily) for three weeks. They were examined every day and adverse events were recorded. Blood samples were collected during the acclimatization phase, weekly during treatment and at the end of the study for haematology, clinical chemistry and coagulation evaluation. RESULTS: There were no abnormal clinical observations following treatment with oclacitinib given alone or concomitantly with ciclosporin, with the exception of diarrhoea in two dogs receiving both drugs. Three dogs from each group experienced transient inappetence; three dogs treated with oclacitinib had mild weight loss. Clinical pathology parameters remained within the reference range for beagle dogs at that facility. CONCLUSIONS AND CLINICAL IMPORTANCE: The concomitant administration of ciclosporin and oclacitinib for three weeks to beagles was well tolerated and was not associated with an increase in the number of adverse events or laboratory abnormalities beyond those associated with oclacitinib given alone.
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spelling pubmed-47373002016-02-12 Repeated oral dose tolerance in dogs treated concomitantly with ciclosporin and oclacitinib for three weeks Panteri, Alessandro Strehlau, Günther Helbig, Rainer Prost, Christine Doucette, Kelly Vet Dermatol Scientific Papers BACKGROUND: Ciclosporin and oclacitinib are immunomodulators approved for the treatment of canine atopic dermatitis. The administration of a short course of prednisolone at the beginning of ciclosporin therapy hastens the efficacy of this drug; oclacitinib has a rapid antipruritic effect similar to that of prednisolone. OBJECTIVES: To evaluate the oral tolerance of oclacitinib and ciclosporin given concurrently for three weeks. ANIMALS: Two groups of eight beagles. METHODS: Dogs were randomized to receive oclacitinib alone (0.4–0.6 mg/kg twice daily for 14 days then once daily for seven days) or in combination with ciclosporin (5 mg/kg once daily) for three weeks. They were examined every day and adverse events were recorded. Blood samples were collected during the acclimatization phase, weekly during treatment and at the end of the study for haematology, clinical chemistry and coagulation evaluation. RESULTS: There were no abnormal clinical observations following treatment with oclacitinib given alone or concomitantly with ciclosporin, with the exception of diarrhoea in two dogs receiving both drugs. Three dogs from each group experienced transient inappetence; three dogs treated with oclacitinib had mild weight loss. Clinical pathology parameters remained within the reference range for beagle dogs at that facility. CONCLUSIONS AND CLINICAL IMPORTANCE: The concomitant administration of ciclosporin and oclacitinib for three weeks to beagles was well tolerated and was not associated with an increase in the number of adverse events or laboratory abnormalities beyond those associated with oclacitinib given alone. John Wiley and Sons Inc. 2015-12-11 2016-02 /pmc/articles/PMC4737300/ /pubmed/26660461 http://dx.doi.org/10.1111/vde.12278 Text en © 2015 Elanco Animal Health. Veterinary Dermatology published by JohnWiley & Sons Ltd on behalf of ESVD and ACVD This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Scientific Papers
Panteri, Alessandro
Strehlau, Günther
Helbig, Rainer
Prost, Christine
Doucette, Kelly
Repeated oral dose tolerance in dogs treated concomitantly with ciclosporin and oclacitinib for three weeks
title Repeated oral dose tolerance in dogs treated concomitantly with ciclosporin and oclacitinib for three weeks
title_full Repeated oral dose tolerance in dogs treated concomitantly with ciclosporin and oclacitinib for three weeks
title_fullStr Repeated oral dose tolerance in dogs treated concomitantly with ciclosporin and oclacitinib for three weeks
title_full_unstemmed Repeated oral dose tolerance in dogs treated concomitantly with ciclosporin and oclacitinib for three weeks
title_short Repeated oral dose tolerance in dogs treated concomitantly with ciclosporin and oclacitinib for three weeks
title_sort repeated oral dose tolerance in dogs treated concomitantly with ciclosporin and oclacitinib for three weeks
topic Scientific Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737300/
https://www.ncbi.nlm.nih.gov/pubmed/26660461
http://dx.doi.org/10.1111/vde.12278
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