Boehringer-Ingelheim Animal Health, 3239 Satellite Blvd, Duluth, 30096 GA, USA (until 2020).
Boehringer-Ingelheim Animal Health, 1730 Olympic Drive, Athens, 30601 GA, USA.
Parasite. 2021;28:18. doi: 10.1051/parasite/2021015. Epub 2021 Apr 2.
The safety profile of NexGard Combo, a novel topical product for cats combining esafoxolaner, eprinomectin and praziquantel, for the treatment and prevention of internal and external parasites, was evaluated in kittens, in two margin-of-safety studies (Studies #1 and #2), and in an oral tolerance study (Study #3). In the margin of safety studies, kittens were dosed several times topically with multiples of the maximum exposure dose (1×): in Study #1, 3× and 5× doses four times at 2-week intervals; in Study #2, 1×, 3× and 5× doses six times at 4-week intervals. In Study #3, kittens were dosed orally once with a 1× dose. Furthermore, in Study #1, another group of kittens was dosed topically twice at a 4-week interval with a formulation of esafoxolaner as the sole active ingredient dosed at 23×. Physical examinations and clinical pathology analyses were performed throughout the studies, followed by necropsy and detailed histopathological evaluation in Studies #1 and #2. No significant treatment related effects were observed in the three studies, except for one occurrence of reversible neurological signs attributed to eprinomectin in one cat after the third 5× dose in Study #2, with clinical signs observed nine hours after dosing, pronounced for a few hours, significantly improved the next day, and absent 2 days after dosing. In conclusion, NexGard Combo was demonstrated safe in kittens following repeated topical administrations and following oral ingestion, and very high topical doses of esafoxolaner were well tolerated.
NexGard Combo 是一种新型猫用局部用产品,含有埃索昔拉菌素、依普菌素和吡喹酮,用于治疗和预防内外寄生虫感染。在两项安全性边际研究(研究 #1 和 #2)和一项口服耐受性研究(研究 #3)中评估了 NexGard Combo 在小猫中的安全性。在安全性边际研究中,小猫多次接受局部多点给药,剂量是最大暴露剂量的倍数(1×):在研究 #1 中,在 2 周间隔内进行 3×和 5×剂量的 4 次给药;在研究 #2 中,在 4 周间隔内进行 1×、3×和 5×剂量的 6 次给药。在研究 #3 中,小猫口服给予 1×剂量。此外,在研究 #1 中,另一组小猫在 4 周间隔内两次接受局部用埃索昔拉菌素制剂作为唯一活性成分的给药,剂量为 23×。在整个研究过程中进行了体格检查和临床病理学分析,随后在研究 #1 和 #2 中进行了尸检和详细的组织病理学评估。除了在研究 #2 中,一只猫在第三次 5×剂量后出现可逆性神经症状,被归因于依普菌素,临床症状在给药后 9 小时出现,持续数小时,第二天明显改善,给药后 2 天消失外,在这三项研究中均未观察到与治疗相关的显著影响。结论是,在多次局部给药和口服摄入后,NexGard Combo 在小猫中表现出安全性,并且非常高的局部用埃索昔拉菌素剂量耐受性良好。