Phase 3, Randomized, Controlled Multicentric, Open-label Clinical Trial to Prove Non-Inferiority of Fosfomycin vs Meropenem or Ceftriaxone in the Treatment of Bacteriemic Urinary Infection Due to Multidrug Resistance in E.Coli
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 161
- 试验地点
- 22
- 主要终点
- Clinical and microbiological cure rate
研究概览
简要总结
Enterobacterieaceae (and specially Escherichia coli) showing resistance due to multidrug-resistant Escherichia coli, plasmid mediated AmpC or quinolone resistance caused by chromosomal mechanisms have spread worldwide during the last decades. This is important because many of these isolates are also resistant to other first-line agents such as fluoroquinolones or aminoglycosides, leaving few available options for therapy, and this condition is associated with increased morbidity- mortality and length of hospital stay. While carbapenems are considered the drugs of choice for multidrug-resistant Escherichia coli and AmpC producers, recent data suggests that certain alternatives may be suitable for some types of infections.
At the present time, finding therapeutic alternatives to carbapenems and cephalosporins for the treatment of invasive infections due to multidrug-resistant Escherichia coli is critical. Fosfomycin was discovered more than 40 years ago but was not investigated according to present standards, and thus is not used in clinical practice except in desperate situations. It is one of the so-considered neglected antibiotics with high potential interest for the future.
With the aim of demonstrate the clinical non-inferiority of intravenous fosfomycin compared to meropenem or ceftriaxone in the treatment of bacteraemic urinary tract infections caused by multidrug-resistant Escherichia coli . The investigators propose a "real practise" randomised, controlled, multicentre phase III clinical trial to compare the clinical and microbiological efficacy and safety of intravenous fosfomycin (4 grammes every 6 hours) with meropenem (1 gramme every 8 hours) or ceftriaxone (1 gramme every 24 hours) as targeted therapy of the previously specified infection; change to oral therapy according to predefined options is allowed in both arms after 5 days. Follow-up for the study is planned up to 60 days.
详细描述
The FOREST study is a phase 3, randomised, controlled, multicentric, open-label clinical trial to prove the noninferiority of fosfomycin versus meropenem in the targeted treatment of bacteraemic UTI due to ESBL-EC, designed as a real practice trial. It is a non-commercial, investigator-driven clinical study funded through a public competitive call by Instituto de Salud Carlos III, Spanish Ministry of Economy (PI13/01282).
The study is coordinated by investigators from Hospital Universitario Virgen Macarena in Seville, Spain; the sponsorship is performed by Fundación Pública Andaluza para la Gestión de la Investigación en Salud de Sevilla (FISEVI), of which the sponsor-scientific responsibilities are delegated to the CTU (Clinical Trial Unit-Hospital Universitario Virgen del Rocío, Seville, Spain). All participating patients or their relatives must give written informed consent before any study procedures occur, including the withdrawal of biological samples for the study.
The hypothesis to test is that intravenous fosfomycin is not inferior to meropenem for the targeted treatment of bacteraemic UTI caused by ESBL-EC in terms of efficacy.
The primary objective of the study is to demonstrate that intravenous fosfomycin is not inferior to meropenem for reaching clinical and microbiological cure 5-7 days after the completion of treatment.
Secondary objectives include comparing the early clinical and microbiological response, 30-day mortality, hospital stay, recurrence rate, safety and impact on intestinal colonisation by MDR Gram-negative bacilli, evaluation of the rate of resistance development to fosfomycin and blood level concentration of fosfomycin.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •≥18 years old hospitalized patients
- •Negative pregnancy test in fertile women
- •Episode of clinically-significant monomicrobial urinary BSI due to multidrug-resistant E.coli susceptible to fosfomycin and meropenem or ceftriaxone
- •Urinary sepsis with multidrug resistant E. coli isolation from the blood cultures, requires at least one clinical criteria and one of the following urinalysis criteria:
- •Clinical criteria
- •UTI symptoms (dysuriac, urgency, suprapubic pain or pollakiuria)
- •Lumbar back pain
- •Cost-vertebral angle tenderness
- •Altered mental status in people up to 70 years old
- •Intermittent or permanent indwelling foley catheter (or withdrawal during 24 hours previous) even without urinary symptoms urinalysis criteria
- •Urine dipstick test positive for either nitrites or leukocyte esterase
- •Positive urine culture - Signed informed consent form (ICF) executed prior to protocol screening assessments
排除标准
- •Polymicrobial bacteremia
- •No drainage of renal abscess or obstructive uropathy unresolved
- •Pregnant or careening women
- •Haematogenous infection
- •Other concomitant infection
- •Renal transplantation recipients
- •Polycystic kidney
- •Hypersensitivity and/or intolerance to meropenem or fosfomycin or ceftriaxone
- •Palliative care or life expectance < 90 days
- •Septic shock at time of randomization
- •New York Heart Association (NYHA) functional Class IV, hepatic cirrhosis or renal impairment receiving dialysis
- •Active empiric treatment >72 hours
- •Late randomization >24 hours after multidrug resistant.coli blood culture´s identification
- •Participation in other clinical trial with active treatment
研究组 & 干预措施
Fosfomycin sodium intravenous
4g every 6 hours iv (60 min infusion)
干预措施: Fosfomycin sodium intravenous (Drug)
Meropenem intravenous
1g every 8 hours (15-30 min infusion)
干预措施: Meropenem intravenous (Drug)
Ceftriaxone intravenous
1g every 24h (2-4 min)
干预措施: Ceftriaxone intravenous (Drug)
结局指标
主要结局
Clinical and microbiological cure rate
时间窗: Day 5-7 after end of treatment (test of cure)
Clinical Cure: Complete resolution of infection symptoms (bacteremia and/or urinary tract infection-UTI-), present at the day on which blood culture was drawn. Microbiological cure: Negative blood culture at day 5-7 after end of treatment. Besides this, if UTI was confirmed with a positive urine culture with the same microorganism than the blood culture, this culture should become negative.
次要结局
- Early microbiological response(within the first 5 days after treatment started)
- Safety of intravenous antibiotic administration in this indication(To the last visit, at 60 plus-minus 10 days (from the first day of study drugs administration))
- Early clinical response(After 5 -7 days of complete treatment (from the first day of study drugs administration))
- Length of hospital stay(At day 30 of follow-up)
- Recurrences (relapse and reinfection) rate(To the last visit, at 60 plus-minus 10 days (from the first day of study drugs administration))
- Mortality(At day 30 of follow-up)
- Fosfomycin steady-state plasma concentration(At 3 days after treatment started)
- Microbiota impact of study treatment bacilli(Screening, day 5-7, day 12)
- Safety of intravenous fosfomycin in this indication(To the last visit, at 60 plus-minus 10 days (from the first day of study drugs administration))
- Emergence of resistant clinical isolates of Escherichia coli to fosfomycin and meropenem(participants will be followed for the duration of fosfomycin, an expected average of 14 days)