Boehringer Ingelheim Vetmedica GmbH, Kathrinenhof Research Center, Walchenseestr. 8-12, 83101, Rohrdorf, Germany.
Boehringer Ingelheim Animal Health USA Inc., Missouri Research Center, 6498 Jade Road, Fulton, MO, 65251, USA.
Parasitol Res. 2022 Jul;121(7):2173-2178. doi: 10.1007/s00436-022-07529-0. Epub 2022 May 3.
In an effort to generate data for regulatory purposes on the therapeutic efficacy of eprinomectin 5% w/v extended-release injection (Eprinomectin ERI) (LongRange®, Boehringer Ingelheim) against infections of immature and adult stages of some nematode species (or stages) which are generally less common or predominantly seen in younger cattle, nine studies (minimum two per parasite and stage) were conducted in the USA and Germany. A total of 218 young cattle were included in seven experimentally induced infection studies (180 animals) and two studies with naturally acquired nematode infections (38 animals), which were compliant with WAAVP and VICH guidelines. In each study, cattle were randomly assigned into groups which received 1 mL per 50 kg body weight of either saline (controls) or Eprinomectin ERI (equivalent to 1 mg eprinomectin per kg body weight) via subcutaneous injection when the parasites were developing fourth-stage larval (L4) or adult nematodes. Following necropsy and parasite recovery, percentage efficacy was calculated based on the comparison of geometric mean nematode counts of the Eprinomectin ERI- vs. the saline-treated animals. Eprinomectin ERI-treated cattle had significantly (p < 0.05) lower counts of each species and stage of nematodes than the controls. Eprinomectin ERI treatment was demonstrated to be efficacious (> 90%) against L4 and adult Bunostomum phlebotomum and Nematodirus helvetianus; against L4 Haemonchus placei, Oesophagostomum radiatum, and Trichostrongylus colubriformis; and against adult H. contortus. Percentage efficacy against L4 H. contortus was variable (69.6 to 100%). All treatments were well accepted, and no treatment-related health problems were observed in any study.
为了生成有关依普菌素 5% w/v 长效注射液(依普菌素 ERI)(LongRange®,勃林格殷格翰)治疗某些线虫幼虫和成虫阶段(或阶段)感染的治疗效果的监管数据,在美国和德国进行了九项研究(每个寄生虫和阶段至少两项)。共有 218 头小牛参加了七项实验性感染研究(180 头动物)和两项自然获得性线虫感染研究(38 头动物),这些研究符合 WAAVP 和 VICH 指南。在每项研究中,牛被随机分配到接受每 50 公斤体重 1 毫升生理盐水(对照)或依普菌素 ERI(相当于每公斤体重 1 毫克依普菌素)皮下注射的组中,当寄生虫发育为第四期幼虫(L4)或成年线虫时。剖检和寄生虫回收后,根据依普菌素 ERI 与生理盐水处理动物的几何平均线虫计数比较计算功效百分比。与对照组相比,依普菌素 ERI 处理的牛的每种线虫种类和阶段的计数明显(p<0.05)较低。依普菌素 ERI 治疗对 L4 和成年 Bunostomum phlebotomum 和 Nematodirus helvetianus ;对 L4 Haemonchus placei、Oesophagostomum radiatum 和 Trichostrongylus colubriformis ;以及对成年 H. contortus 均有效(>90%)。针对 L4 H. contortus 的功效百分比各不相同(69.6%至 100%)。所有治疗均被很好地接受,任何研究中均未观察到与治疗相关的健康问题。