{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,21]],"date-time":"2026-09-21T00:03:17Z","timestamp":1789948997518,"version":"4.0.1"},"reference-count":15,"publisher":"Wiley","license":[{"start":{"date-parts":[[2026,9,20]],"date-time":"2026-09-20T00:00:00Z","timestamp":1789862400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,9,20]],"date-time":"2026-09-20T00:00:00Z","timestamp":1789862400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Veterinary Dermatology"],"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Oclacitinib is approved for the treatment of canine atopic dermatitis (AD) and pruritus. The conventional administration protocol includes twice\u2010daily oral dosing for 14\u2009days with a subsequent reduction to once\u2010daily administration. This reduction sometimes leads to an increase in pruritus.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Hypothesis\/Objectives<\/jats:title>\n                    <jats:p>The aim of this study was to compare the changes in skin lesions and pruritus following a shortened induction versus the conventional protocol for oclacitinib.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Animals<\/jats:title>\n                    <jats:p>Forty\u2010five client\u2010owned dogs with AD were randomised into two groups.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Material and Methods<\/jats:title>\n                    <jats:p>The conventional protocol group (CP) received oclacitinib tablets at 0.4\u20130.6\u2009mg\/kg twice\u2010daily for 14\u2009days, then once\u2010daily for 7\u2009days. In the shortened induction protocol group (SIP), oclacitinib was administered twice\u2010daily for 6\u2009days, then once\u2010daily for 15\u2009days. Pruritus was assessed daily by the owners using a pruritus Visual Analog Scale (PVAS). Lesions were scored with the Canine Atopic Dermatitis Lesion Index (CADLI) at Day (D) 0 and D21.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Data from 40 dogs were available. Mean CADLI scores decreased from 13.4 to 8 in the CP group (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.12) and from 12.9 to 6.9 in the SIP group (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.01), respectively. Mean pruritus scores decreased from 6.4 to 2.1 and from 5.7 to 1.9, respectively (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u20090.0001 each). No between\u2010group differences were observed. An increase in pruritus following dose reduction was seen in two dogs (CP) and one dog (SIP).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions and Clinical Relevance<\/jats:title>\n                    <jats:p>The SIP was not significantly different to the CP with respect to improvement in lesion severity or pruritus.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/vde.70127","type":"journal-article","created":{"date-parts":[[2026,9,20]],"date-time":"2026-09-20T23:44:33Z","timestamp":1789947873000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Evaluation of Two Induction Protocols for Oclacitinib in Dogs"],"prefix":"10.1111","author":[{"ORCID":"https:\/\/orcid.org\/0009-0005-7601-6409","authenticated-orcid":false,"given":"Paulina J. C.","family":"Popp","sequence":"first","affiliation":[{"name":"Small Animal Clinic LMU Munich  Munich Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5835-5910","authenticated-orcid":false,"given":"Ralf S.","family":"Mueller","sequence":"additional","affiliation":[{"name":"Small Animal Clinic LMU Munich  Munich Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Laura","family":"Widorn","sequence":"additional","affiliation":[{"name":"Small Animal Clinic LMU Munich  Munich Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Laura","family":"Udraite\u2010Vovk","sequence":"additional","affiliation":[{"name":"Small Animal Clinic LMU Munich  Munich Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0001-4935-1042","authenticated-orcid":false,"given":"Ulrike","family":"Mueller","sequence":"additional","affiliation":[{"name":"Small Animal Clinic LMU Munich  Munich Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-8068-2288","authenticated-orcid":false,"given":"Tamara","family":"Weitzer","sequence":"additional","affiliation":[{"name":"Small Animal Clinic LMU Munich  Munich Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2026,9,20]]},"reference":[{"key":"e_1_2_11_2_1","doi-asserted-by":"crossref","first-page":"587","DOI":"10.1111\/vde.12088","article-title":"A Blinded, Randomized, Placebo\u2010Controlled Trial of the Efficacy and Safety of the Janus Kinase Inhibitor Oclacitinib (Apoquel) in Client\u2010Owned Dogs With Atopic Dermatitis","volume":"24","author":"Cosgrove S. 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