Department of Dermatology, Children's Hospital del Niño Jesús, Madrid, Spain.
Universitat Internacional de Catalunya, Barcelona, Spain.
Dermatology. 2020;236(3):199-207. doi: 10.1159/000504536. Epub 2020 Jan 20.
Ozenoxacin is a topical antibiotic approved in Europe to treat non-bullous impetigo in adults and children aged ≥6 months. This analysis evaluated the efficacy and safety of ozenoxacin in paediatric patients by age group.
Pooled data for patients aged 6 months to <18 years who had participated in a phase I or in two phase III clinical trials of ozenoxacin 1% cream were analysed by age group: 0.5-<2, 2-<6, 6-<12, and 12-<18 years.
The combined population comprised 529 patients with non-bullous impetigo treated with ozenoxacin (n = 239), vehicle (n = 201), or retapamulin as internal validation control (n = 89). Studies were well matched for extent and severity of impetigo and therapeutic schedule (twice daily application for 5 days). The clinical success rate after 5 days' treatment (day 6-7, end of therapy), and microbiological success rates after 3-4 days' treatment and at the end of therapy, were significantly higher with ozenoxacin than vehicle (p < 0.0001 for all comparisons). Clinical and bacterial eradication rates were higher with ozenoxacin than vehicle in each age group. No safety concerns were identified with ozenoxacin. One (0.3%) of 327 plasma samples exceeded the lower limit of quantification for ozenoxacin, but the low concentration indicated negligible systemic absorption.
This combined analysis supports the efficacy and safety of ozenoxacin administered twice daily for 5 days. Ozenoxacin 1% cream is a new option to consider for treatment of non-bullous impetigo in children aged 6 months to <18 years.
噁嗪酮是一种局部抗生素,在欧洲被批准用于治疗 6 个月及以上的成人和儿童非大疱性脓疱疮。本分析通过年龄组评估了噁嗪酮在儿科患者中的疗效和安全性。
对参加噁嗪酮 1%乳膏 I 期或两项 III 期临床试验的年龄在 6 个月至<18 岁的患者进行年龄组分析:0.5-<2 岁、2-<6 岁、6-<12 岁和 12-<18 岁。
患有非大疱性脓疱疮的合并人群包括 529 名接受噁嗪酮(n = 239)、赋形剂(n = 201)或 retapamulin 治疗的患者(n = 89)作为内部验证对照。研究在脓疱疮的严重程度和治疗方案(每天两次应用,持续 5 天)方面具有良好的匹配性。治疗后 5 天(第 6-7 天,治疗结束时)的临床治愈率,以及治疗后 3-4 天和治疗结束时的微生物学治愈率,均显著高于赋形剂(所有比较均为 p<0.0001)。在每个年龄组中,与赋形剂相比,噁嗪酮的临床和细菌清除率更高。噁嗪酮未出现安全性问题。327 份血浆样本中,只有 1 份(0.3%)超过噁嗪酮的定量下限,但低浓度表明全身吸收可忽略不计。
本联合分析支持每天两次应用 5 天的噁嗪酮的疗效和安全性。噁嗪酮 1%乳膏是治疗 6 个月至<18 岁儿童非大疱性脓疱疮的一种新选择。