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在美国作为兽医患者就诊的犬只身上,沙罗拉纳(Simparica™)对跳蚤的有效性和安全性。

Efficacy and safety of sarolaner (Simparica™) against fleas on dogs presented as veterinary patients in the United States.

作者信息

Cherni Judith A, Mahabir Sean P, Six Robert H

机构信息

Zoetis, Veterinary Medicine Research and Development, 333 Portage St., Kalamazoo, MI 49007, USA.

Zoetis, Veterinary Medicine Research and Development, 333 Portage St., Kalamazoo, MI 49007, USA.

出版信息

Vet Parasitol. 2016 May 30;222:43-8. doi: 10.1016/j.vetpar.2015.12.022. Epub 2015 Dec 28.

Abstract

The efficacy and safety of a novel isoxazoline parasiticide, sarolaner (Simparica™), for the control of fleas on dogs was evaluated in a randomized, controlled clinical study conducted in 19 general veterinary practices throughout the United States. Four hundred and seventy nine (479) dogs from 293 households were enrolled. Each household was randomly assigned to treatment with either sarolaner oral tablets (Simparica™, Zoetis) at the proposed label dose or an approved comparator product at the label dose (spinosad, Comfortis(®), Elanco). Dogs were dosed by their owners at home on Day 0 and on approximately Days 30 and 60. Dogs were examined at the clinics for general health, flea and tick infestation, and clinical signs of flea allergy dermatitis (FAD) at the initial visit and Days 14, 30, 60 and 90. Blood was collected for clinical pathology at screening and Day 90. Sarolaner was well-accepted by dogs with the majority of flavored chewable tablets (91.5%) accepted free choice, by hand or in food. Geometric mean live flea counts were reduced by >99% at the first time measured (14 days) after initiation of treatment and continued to reduce through the study. Treatment success (proportion of dogs with ≥90% reduction in fleas) for the sarolaner-treated dogs was superior to that for spinosad-treated dogs at Days 14 and 30 and non-inferior on Days 60 and 90 (P≤0.025) The rapid reduction in flea infestations resulted in a similar rapid resolution of the clinical signs associated with FAD. Sarolaner chewable tablets were well tolerated with no treatment related adverse reactions. Most of the clinical signs reported were consistent with allergies and dermatitis or sporadic occurrences of conditions commonly observed in the general dog population. A wide variety of concomitant medications, including many commercially available heartworm preventatives and other anthelmintic drugs, were administered to study dogs and all were well tolerated. Sarolaner administered orally to provide a minimum dosage of 2.0mg/kg (range 2-4mg/kg) once monthly for three consecutive treatments was safe and effective in the treatment and prevention of natural infestations of fleas and resulted in a substantial improvement of clinical signs associated with FAD.

摘要

一种新型异恶唑啉类杀寄生虫剂沙罗拉纳(Simparica™)用于控制犬只跳蚤的有效性和安全性,在一项在美国19家普通兽医诊所开展的随机对照临床研究中进行了评估。来自293个家庭的479只犬只参与了研究。每个家庭被随机分配接受按建议标签剂量使用的沙罗拉纳口服片剂(Simparica™,硕腾公司)治疗,或按标签剂量使用已获批的对照产品(多杀菌素,Comfortis(®),礼蓝公司)治疗。犬只由其主人于第0天以及大约第30天和第60天在家中给药。在诊所对犬只进行检查,在初次就诊时以及第14、30、60和90天检查其总体健康状况、跳蚤和蜱虫感染情况以及跳蚤过敏性皮炎(FAD)的临床体征。在筛查时和第90天采集血液进行临床病理学检测。沙罗拉纳很受犬只接受,大多数调味咀嚼片(91.5%)可自由选择,通过手工或与食物一起给予。在开始治疗后的首次测量时间(14天),几何平均活跳蚤数量减少了>99%,并且在整个研究过程中持续减少。在第14天和第30天,接受沙罗拉纳治疗的犬只的治疗成功率(跳蚤数量减少≥90%的犬只比例)高于接受多杀菌素治疗的犬只,在第60天和第90天不劣于后者(P≤0.025)。跳蚤感染的快速减少导致与FAD相关的临床体征迅速缓解。沙罗拉纳咀嚼片耐受性良好,未出现与治疗相关的不良反应。报告的大多数临床体征与过敏和皮炎或普通犬类群体中常见病症的偶发情况一致。给参与研究的犬只使用了多种伴随药物,包括许多市售的心丝虫预防药物和其他驱虫药物,所有这些药物耐受性均良好。每月口服一次沙罗拉纳,连续三次治疗,提供最低剂量为2.0mg/kg(范围为2 - 4mg/kg),在治疗和预防自然跳蚤感染方面是安全有效的,并使与FAD相关的临床体征有了显著改善。

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