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两项三期随机多中心研究的设计,比较格派沙星与呋喃妥因治疗女性单纯性尿路感染的疗效

Design of Two Phase III, Randomized, Multicenter Studies Comparing Gepotidacin with Nitrofurantoin for the Treatment of Uncomplicated Urinary Tract Infection in Female Participants.

作者信息

Perry Caroline, Hossain Mohammad, Powell Marcy, Raychaudhuri Aparna, Scangarella-Oman Nicole, Tiffany Courtney, Xu Sherry, Dumont Etienne, Janmohamed Salim

机构信息

GSK, 1250 S. Collegeville Road, Collegeville, PA, 19426-0989, USA.

GSK, Research Triangle Park, NC, USA.

出版信息

Infect Dis Ther. 2022 Dec;11(6):2297-2310. doi: 10.1007/s40121-022-00706-9. Epub 2022 Oct 21.

Abstract

BACKGROUND

Uncomplicated urinary tract infections (uUTIs) are among the most common community-acquired infections for women worldwide. Treatment options are increasingly limited by antibiotic resistance; novel oral antibiotics are urgently needed. Gepotidacin is a novel, bactericidal, first-in-class triazaacenaphthylene antibiotic that inhibits bacterial deoxyribonucleic acid (DNA) replication by a distinct mechanism of action, which confers activity against most strains of target pathogens, such as Escherichia coli and Staphylococcus saprophyticus, including those resistant to current antibiotics. Here, we describe the designs of two near-identical phase III clinical trials (EAGLE-2 and EAGLE-3) evaluating gepotidacin for the treatment of uUTI.

METHODS

These are phase III, randomized, multicenter, parallel-group, double-blind, double-dummy, comparator-controlled, noninferiority studies, comparing the efficacy and safety of gepotidacin to nitrofurantoin in the treatment of uUTI. Eligible participants are women aged ≥ 12 years with ≥ 2 uUTI symptoms, randomized (1:1) to receive oral gepotidacin (1500 mg) plus placebo or nitrofurantoin (100 mg) plus placebo, twice daily for 5 days. The primary therapeutic endpoint is composite clinical and microbiological efficacy, with noninferiority comparisons made in individuals with a qualifying (≥ 10 colony-forming units/mL urine) nitrofurantoin-susceptible uropathogen.

RESULTS

These trials were designed in accordance with US Food and Drug Administration (2019) and European Medicines Agency (2018) guidance, particularly the composite endpoint and microbiological evaluability requirements. Across the trials ~ 5000 participants are planned to be enrolled from > 200 centers globally.

CONCLUSIONS

Gepotidacin represents an important potential treatment option being evaluated to address the need for novel oral antibiotics to treat uUTI. These trials are registered at ClinicalTrials.gov ( https://clinicaltrials.gov/ ) where the full protocols can be accessed under trial IDs: NCT04020341 (EAGLE-2) and NCT04187144 (EAGLE-3).

摘要

背景

单纯性尿路感染(uUTIs)是全球女性中最常见的社区获得性感染之一。治疗选择因抗生素耐药性而日益受限;迫切需要新型口服抗生素。格派沙星是一种新型的杀菌性三氮杂蒽醌类抗生素,是该类药物中的首个,它通过独特的作用机制抑制细菌脱氧核糖核酸(DNA)复制,对大多数目标病原体菌株具有活性,如大肠杆菌和腐生葡萄球菌,包括那些对现有抗生素耐药的菌株。在此,我们描述了两项评估格派沙星治疗uUTI的几乎相同的III期临床试验(EAGLE - 2和EAGLE - 3)的设计。

方法

这些是III期、随机、多中心、平行组、双盲、双模拟、对照药对照、非劣效性研究,比较格派沙星与呋喃妥因治疗uUTI的疗效和安全性。符合条件的参与者为年龄≥12岁、有≥2种uUTI症状的女性,随机(1:1)接受口服格派沙星(1500毫克)加安慰剂或呋喃妥因(100毫克)加安慰剂,每日两次,共5天。主要治疗终点是综合临床和微生物学疗效,在具有合格(≥10菌落形成单位/毫升尿液)的呋喃妥因敏感尿路病原体的个体中进行非劣效性比较。

结果

这些试验是根据美国食品药品监督管理局(2019年)和欧洲药品管理局(2018年)的指南设计的,特别是综合终点和微生物学可评估性要求。在这些试验中,计划从全球200多个中心招募约5000名参与者。

结论

格派沙星是一种正在评估的重要潜在治疗选择,以满足治疗uUTI对新型口服抗生素的需求。这些试验已在ClinicalTrials.gov(https://clinicaltrials.gov/)注册,在该网站可通过试验标识符NCT04020341(EAGLE - 2)和NCT04187144(EAGLE - 3)访问完整方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03c6/9669302/416e5f8157cf/40121_2022_706_Fig1_HTML.jpg

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