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Infections & Beyond, Tuesday, June 22, 2021

机译:感染和超越,星期二,星期二,6月22日,2021年

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Introduction: Recurrent urinary tract infections (rUTI) affect 5–10% of women, resulting in enormously high use of antibiotics contributing to morbidity in individual patients and the massive rise of antimicrobial resistance. MV140 (Uromune?) is a polybacterial sublingual vaccine consisting of whole-cell inactivated bacteria (E. coli 25%, K. pneumoniae 25%, E. faecalis 25%, and P. vulgaris 25%) that has shown clinical benefit in observational studies of 1000 individuals.1 Confirmation of its clinical efficacy has awaited results from a randomized placebo-controlled trial (RCT). We present the late-breaking preliminary results of this RCT, which is presently in the analysis stage. Methods: A phase 3, multicenter, double-blind, parallel‐group RCT enrolled 240 women aged 18–75 with rUTI (≥5 uncomplicated UTI during the previous year). They were randomly allocated to receive placebo for six months or MV140 (active) for three or six months, in a 1:1:1 ratio. Primary and major secondary endpoints were number of UTIs and UTI-free rate in the nine-month study period following three months of intervention, respectively. Results: The median number of UTI episodes was 3.0 (interquartile range [IQR] 0.5–6.0] for placebo group compared to 0.0 (IQR 0.0–1.0] in both groups receiving MV140 (p0.001). A significant increase (over two-fold) in the UTI-free rate was observed (p0.001) in the treatment groups (55.7% and 58.0% in subjects receiving MV140 for three or six months, respectively) compared to the placebo group (25.0%). Only five subjects reported non-serious adverse reactions, two in the placebo group and three in the MV140 three-month group. Conclusions: The preliminary, late-breaking analysis of this first MV140 RCT shows clinical efficacy and safety in reducing the incidence and preventing recurrence of UTIs. Clinical use of this novel sublingual bacterial vaccine prophylaxis will offer women an effective evidence-based alternative to antibiotics in the management of rUTI.
机译:介绍:复发性尿路感染(RUTI)影响5-10%的女性,导致抗生素的巨大使用促进个体患者的发病率和抗微生物抗性的巨大升高。 MV140(尿道?)是由全细胞灭活的细菌(大肠杆菌25%,K.肺炎肺炎25%,E.粪便25%),在观察到临床益处研究& 1000个体.1确认其临床疗效至少已等待来自随机安慰剂对照试验(RCT)的结果。我们介绍了该RCT的延迟初步结果,目前在分析阶段。方法:第3阶段,多中心,双盲,并联群RCT注册了240名18-75岁的女性,RUTI(≥5在上一年中≥5个简单的UTI)。它们被随机分配给接收安慰剂六个月或MV140(活跃),为1:1:1的比例。主要和主要的次级终点分别是在介入三个月后的九个月的研究期间和UTI的汇率数量。结果:UTI剧集的中值为3.0(间隔范围[IQR] 0.5-6.0],用于安慰剂组相比,接受MV140的两个组(P <0.001)中的0.0(IQR 0.0-1.0]。显着增加(超过两组与安慰剂组相比,在治疗组中观察到(P <0.001)在治疗组中观察到(P <0.001)(分别接受MV140的受试者的58.0%,55.7%和58.0%)(25.0%)。只有五个科目报道了非严重的不良反应,两个在安慰剂组中,三个在MV140三个月的组中。结论:第一次MV140 RCT的初步,晚期分析显示临床疗效和安全性降低utis复发的临床疗效和安全性。这种新型舌下细菌疫苗预防的临床用途将为妇女提供有效的肌肉替代抗生素在罗迪管理中。

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