Zoetis, Veterinary Medicine Research and Development, 333 Portage St., Kalamazoo, MI, 49007, USA.
Parasit Vectors. 2020 Mar 1;13(1):98. doi: 10.1186/s13071-020-3952-3.
One randomized, controlled clinical field study was conducted in 18 general veterinary practices throughout the USA to evaluate the safety and efficacy of a novel oral chewable combination tablet, Simparica Trio™, containing sarolaner, moxidectin and pyrantel for the treatment and prevention of fleas on dogs.
Client-owned dogs, from households of three or fewer dogs were eligible for enrollment. Four hundred and twenty-two dogs from 251 households were enrolled. Households were randomly assigned in a 2:1 ratio to treatment with either Simparica Trio™ at the minimum label dose of 1.2 mg/kg sarolaner, 24 µg/kg moxidectin and 5 mg/kg pyrantel (as pamoate salt) or afoxolaner (NexGard, Boehringer-Ingelheim) at the label dose. One dog per household was selected as the primary dog for efficacy evaluations. Treatments were dispensed and dogs were dosed in their home environment on Day 0 and on approximately Day 30. Flea counts and examination for clinical signs of flea allergy dermatitis (FAD) were performed at the initial visit the day before or on Day 0 prior to treatment and on Days 30 and 60. Additionally, all dogs were examined for general health at each visit and blood and urine were collected for clinical pathology at screening and Day 60.
Simparica Trio™ reduced geometric mean live flea counts by 99.0% by Day 30 and by 99.7% by Day 60. As a result of the rapid reduction in flea infestations, clinical signs associated with FAD substantially improved following treatment. Simparica Trio™ was well-tolerated and a diverse range of concomitant medications were administered to dogs during the course of the study. Simparica Trio™ chewable tablets were well-accepted by dogs, with the majority of flavored chewable tablets (91.9%) voluntarily consumed by free choice without, or when offered in food.
Simparica Trio™ administered orally once monthly for two consecutive treatments was safe and effective against natural flea infestations and substantially improved clinical signs associated with FAD in client-owned dogs in a field study conducted in the USA.
在美国 18 家普通兽医诊所进行了一项随机、对照的临床实地研究,以评估一种新型口服咀嚼片 Simparica Trio™的安全性和疗效,该咀嚼片含有 Sarolaner、莫昔克丁和吡喹酮,用于治疗和预防犬跳蚤。
符合条件的犬只来自家庭饲养 3 只或 3 只以下犬只的家庭。共有 251 户家庭的 422 只犬参与了研究。家庭以 2:1 的比例随机分配接受 Simparica Trio™治疗,剂量为 1.2mg/kg Sarolaner、24μg/kg 莫昔克丁和 5mg/kg 吡喹酮(作为帕莫酸盐)或 Afoxolaner(NexGard,Boehringer-Ingelheim)的标签剂量。每个家庭选择一只犬作为主要犬进行疗效评估。在第 0 天和大约第 30 天,在家庭环境中分发治疗药物并给犬只用药。在初次就诊前一天或第 0 天治疗前、第 30 天和第 60 天,进行跳蚤计数和临床跳蚤过敏皮炎(FAD)体征检查。此外,每次就诊时还检查所有犬只的一般健康状况,并在筛查和第 60 天采集血液和尿液进行临床病理学检查。
Simparica Trio™在第 30 天和第 60 天使活跳蚤的几何平均计数减少了 99.0%和 99.7%。由于跳蚤感染迅速减少,FAD 的临床症状在治疗后有了显著改善。Simparica Trio™耐受性良好,在研究过程中,给犬只使用了各种伴随药物。Simparica Trio™咀嚼片犬只接受度高,大多数口味咀嚼片(91.9%)经自由选择,无需或与食物一起提供时可自愿食用。
Simparica Trio™每月口服一次,连续治疗两次,对美国实地研究中犬自然跳蚤感染安全有效,并显著改善了与 FAD 相关的临床症状。