Forster Sophie, Boegel Annette, Despa Simona, Trout Candace, King Stephen
Elanco Animal Health Ltd, Hook, UK.
Elanco Animal Health GmbH, Leverkusen, Germany.
Vet Dermatol. 2025 Apr;36(2):165-176. doi: 10.1111/vde.13319. Epub 2025 Jan 6.
Janus kinase inhibitors (JAKi) have been shown to reduce pruritus and improve associated inflammatory skin lesions in canine atopic dermatitis (cAD).
To evaluate the efficacy and safety of ilunocitinib, in comparison to oclacitinib, for the control of cAD in a randomised, blinded trial.
Three-hundred-and-thirty-eight dogs with cAD.
Dogs were randomised to receive oclacitinib (0.4-0.6 mg/kg twice daily for 14 days; then once daily) or ilunocitinib (0.6-0.8 mg/kg once daily), for up to 112 days. Owners assessed pruritus using an enhanced Visual Analog Scale (PVAS). Investigators assessed skin lesions using the Canine Atopic Dermatitis Extent and Severity Index, 4th interaction (CADESI-04).
Reduction in pruritus and CADESI-04 scores was similar for both treatment groups from Day (D)0-D14. PVAS scores increased between D14 and D28 for oclacitinib and decreased for ilunocitinib. On D28 to D112, mean PVAS and CADESI-04 scores were significantly lower for ilunocitinib compared to oclacitinib (p ≤ 0.003 and p ≤ 0.023, respectively). On D28 to D112, a greater number of ilunocitinib-treated dogs achieved clinical remission of pruritus (i.e. PVAS score <2). Subjective assessment of overall response was significantly better for ilunocitinib on D28 to D112 (p ≤ 0.002). Both drugs demonstrated similar safety throughout the study.
Ilunocitinib rapidly and safely controlled signs of cAD. Ilunocitinib demonstrated significantly better control of pruritus and skin lesions compared to oclacitinib, with more dogs achieving clinical remission of pruritus.
已证明Janus激酶抑制剂(JAKi)可减轻犬特应性皮炎(cAD)的瘙痒,并改善相关的炎症性皮肤病变。
在一项随机、盲法试验中,与奥克拉替尼相比,评估伊鲁替尼对控制cAD的疗效和安全性。
338只患有cAD的犬。
将犬随机分为接受奥克拉替尼(0.4 - 0.6mg/kg,每日两次,共14天;然后每日一次)或伊鲁替尼(0.6 - 0.8mg/kg,每日一次)治疗,最长治疗112天。主人使用改良视觉模拟评分量表(PVAS)评估瘙痒情况。研究者使用犬特应性皮炎范围和严重程度指数第4版(CADESI - 04)评估皮肤病变。
从第0天到第14天,两个治疗组的瘙痒减轻情况和CADESI - 04评分相似。奥克拉替尼组在第14天到第28天PVAS评分增加,而伊鲁替尼组则降低。在第28天到第112天,与奥克拉替尼相比,伊鲁替尼的平均PVAS和CADESI - 04评分显著更低(分别为p≤0.003和p≤0.023)。在第28天到第112天,接受伊鲁替尼治疗的犬中有更多达到瘙痒的临床缓解(即PVAS评分<2)。在第28天到第112天,对伊鲁替尼的总体反应主观评估明显更好(p≤0.002)。在整个研究中,两种药物显示出相似的安全性。
伊鲁替尼能快速、安全地控制cAD的症状。与奥克拉替尼相比,伊鲁替尼在控制瘙痒和皮肤病变方面表现明显更好,更多犬达到瘙痒的临床缓解。