Becskei Csilla, De Bock Filip, Illambas Joanna, Cherni Judith A, Fourie Josephus J, Lane Melanie, Mahabir Sean P, Six Robert H
Zoetis, Veterinary Medicine Research and Development, Mercuriusstraat 20, Zaventem 1930, Belgium.
Zoetis, Veterinary Medicine Research and Development, Mercuriusstraat 20, Zaventem 1930, Belgium.
Vet Parasitol. 2016 May 30;222:56-61. doi: 10.1016/j.vetpar.2016.02.017. Epub 2016 Feb 20.
The efficacy of the novel isoxazoline, sarolaner (Simparica™) was investigated in dogs with clinical signs consistent with sarcoptic mange and harbouring natural infestations of Sarcoptes scabiei. One placebo-controlled laboratory study and one multi-centred field study with a commercial comparator containing imidacloprid/moxidectin (Advocate(®) spot-on) were conducted. Oral or topical treatments were administered on Days 0 and 30. Up to 10 skin scrapings were taken for the assessment of S. scabiei infestations from each dog before treatment and on Days 14, 30, 44 and 60 in the laboratory study, and on Days 30 and 60 in the field study. In the laboratory study, efficacy was calculated based on the percent reduction of mean live mite counts compared to the placebo group. In the field study parasitological cure rate (% dogs free of mites) was determined and non-inferiority of sarolaner to the control product was assessed. In the laboratory study 44 mixed breed dogs were enrolled in four batches. Due to decreasing mite counts in the placebo treated dogs, immunosuppression with dexamethasone (0.4mg/kg three times per week for two weeks) was initiated in all dogs on study at that time (n=6) and those subsequently enrolled (n=14). In the field study, dogs were enrolled in a 2:1 ratio (sarolaner:comparator); 79 dogs were assessed for efficacy and safety, and an additional 45 dogs were assessed for safety only. There were no treatment related adverse events in either study. In the laboratory study, no mites were found on any sarolaner-treated dogs 14 days after the first treatment except for one dog that had a single mite on Day 44. In the field study, the parasitological cure rate was 88.7% and 100% in the sarolaner group and 84.6% and 96.0% in the imidacloprid/moxidectin group, on Days 30 and 60, respectively. Statistical analysis showed that sarolaner was non-inferior to imidacloprid/moxidectin at both time points. The clinical signs of sarcoptic mange, including hair loss, papules, pruritus, erythema, and scaling/crusting improved throughout the study. Sarolaner was safe, achieved 100% reduction in the numbers of S. scabiei detected and resulted in marked improvement of the clinical signs of sarcoptic mange in dogs following two monthly oral administrations.
在患有与疥螨病相符的临床症状且自然感染疥螨的犬只中,研究了新型异恶唑啉类药物沙罗拉纳(Simparica™)的疗效。开展了一项安慰剂对照实验室研究和一项多中心现场研究,后者使用含吡虫啉/莫昔克丁的市售对照产品(Advocate(®) 滴剂)。在第0天和第30天进行口服或局部治疗。在实验室研究中,治疗前以及治疗后第14、30、44和60天,从每只犬身上采集多达10份皮肤刮片,以评估疥螨感染情况;在现场研究中,在第30天和第60天进行采集。在实验室研究中,根据与安慰剂组相比平均活螨数量减少的百分比计算疗效。在现场研究中,确定寄生虫学治愈率(无螨犬只百分比),并评估沙罗拉纳相对于对照产品的非劣效性。在实验室研究中,44只混血犬分四批入组。由于安慰剂治疗的犬只螨数量减少,当时入组研究的所有犬只(n = 6)以及随后入组的犬只(n = 14)均开始用 地塞米松进行免疫抑制(0.4mg/kg,每周三次,持续两周)。在现场研究中,犬只按2:1的比例入组(沙罗拉纳:对照产品);79只犬只接受疗效和安全性评估,另外45只犬只仅接受安全性评估。两项研究均未出现与治疗相关的不良事件。在实验室研究中,首次治疗后14天,除一只在第44天发现有一只螨的犬只外,任何接受沙罗拉纳治疗的犬只均未发现螨。在现场研究中,沙罗拉纳组在第30天和第60天的寄生虫学治愈率分别为88.7%和100%,吡虫啉/莫昔克丁组分别为84.6%和96.0%。统计分析表明,在两个时间点沙罗拉纳均不劣于吡虫啉/莫昔克丁。在整个研究过程中,疥螨病的临床症状,包括脱毛、丘疹、瘙痒、红斑和脱屑/结痂均有所改善。沙罗拉纳安全有效,能使检测到的疥螨数量减少100%,且在每月口服两次后能显著改善犬只疥螨病的临床症状。