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Safety evaluation of orally administered afoxolaner and milbemycin oxime in eight-week-old dogs

机译:在八周老狗口服给药的安全性评价及南莫尔塞米霉素肟

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摘要

The safety profile of afoxolaner (an isoxazoline molecule) when combined with milbemycin oxime (a macrocyclic lactone) was evaluated according to the regulatory requirements when administered six times orally in a soft chewable formulation at a dose of at least 1x, 3x, or 5x the maximum exposure dose in 8-week-old Beagle dogs. Thirty-two healthy puppies (16 males and 16 females) were enrolled and allocated randomly to one of four treatment groups. Three doses were administered at 28-day intervals (Days 0, 28, and 56), followed by three additional doses administered with 14-day intervals (Days 84, 98, and 112). The study ended on Day 126. Treatment groups were as follows: Group 1: untreated, sham-dosed control; Group 2: afoxolaner/milbemycin oxime chews administered at a dose of at least 5 and 1mg/kg, respectively (1x); Group 3: afoxolaner/milbemycin oxime chews administered at a dose of at least 15 and 3mg/kg, respectively (3); and Group 4: afoxolaner/milbemycin oxime chews administered at a dose of at least 25 and 5mg/kg, respectively (5x). All dogs were examined for general health twice a day beginning on Day -14. Physical examinations, and blood collections for clinical pathology analysis and afoxolaner and milbemycin oxime plasma concentrations, were performed throughout the study. No afoxolaner/milbemycin oxime treatment-related changes were observed in growth, physical variables, clinical pathology variables, or tissues examined histologically. No clinically relevant or statistically significant health abnormalities related to the administration of afoxolaner/milbemycin oxime were observed. No signs of macrocyclic lactone sensitivity were observed at any time during the study. Vomiting and diarrhea were observed sporadically across all groups including the controls. Based upon the results of this study, afoxolaner/milbemycin oxime soft chewables were shown to be safe when administered repeatedly at up to 5x the maximum exposure dose in dogs as young as 8weeks of age.
机译:当在剂量至少1倍,3x或5倍的剂量时,根据调节要求,根据调节要求评价AFOXOLANER(异恶唑啉分子)的安全谱根据调节要求。 8周老比格犬的最大曝光剂量。将三十两只健康的小狗(16名男性和16名女性)进行注册并随机分配给四个治疗组中的一个。以28天的间隔(第0,28和56天)施用三个剂量,然后用14天间隔(第84,98和112天)施用三个另外的剂量。该研究于126天结束。治疗组如下:第1组:未经处理的假手术控制;第2组:以至少5和1mg / kg的剂量(1x)施用的AFOXOLANER / MILBIMYCIN肟咀嚼物;第3组:AFOXOLANER / MILBIMYCIN肟咀嚼剂,分别以至少15和3mg / kg的剂量施用(3);第4组:AFOXOLANER / MILBIMYCIN肟咀嚼剂分别以至少25和5mg / kg的剂量施用(5倍)。在第14天开始每天两次检查所有狗的一般健康两次。在整个研究中,在整个研究中进行身体检查和临床病理分析和血液溶剂和米拉米霉素血浆血浆浓度的血液收集。在生长,物理变量,临床病理变量或组织上检查的组织中,观察到AFOXOLANER / MILBIMYCIN肟治疗相关的变化。没有观察到与AFOXOLANER / MILBIMYCIN肟相关的临床相关或统计学上的健康异常。在研究期间,任何时候都没有观察到大环内酯敏感性的迹象。在包括对照的所有群体中均偶发呕吐和腹泻。基于本研究的结果,当反复施用时,AFOXOLANER / MILBIMYCIN肟软咀嚼物被证明是安全的,在狗的最大暴露剂量为8周的狗的最大曝光剂量时,可以安全。

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  • 来源
    《Cereal Research Communications》 |2017年第1期|共7页
  • 作者单位

    Merial Inc 3239 Satellite Blvd Duluth GA 30096 USA;

    Merial Inc 3239 Satellite Blvd Duluth GA 30096 USA;

    Merial Inc 3239 Satellite Blvd Duluth GA 30096 USA;

    Merial Inc 3239 Satellite Blvd Duluth GA 30096 USA;

    Merial Inc 3239 Satellite Blvd Duluth GA 30096 USA;

    Merial Inc 3239 Satellite Blvd Duluth GA 30096 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 农作物;
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