Placebo-controlled, Double-blind, Randomized Study of Aerucin® as Adjunct Therapy to Antibiotics in the Treatment of P. Aeruginosa Pneumonia
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 158
- 试验地点
- 11
- 主要终点
- Clinical Cure on Day 21
研究概览
简要总结
Prospective, double-blind, randomized assessment of the efficacy, safety and pharmacokinetic of Aerucin® as adjunct treatment (in addition to standard of care antibiotics) for pneumonia caused by P. aeruginosa.
详细描述
This is a double-blind, randomized, placebo-controlled study of the human monoclonal antibody (mAb) AR-105 for the adjunctive therapeutic treatment of P. aeruginosa pneumonia in mechanically ventilated subjects. Subjects who are randomized will be treated with either standard of care (SOC) antibiotics plus placebo or SOC antibiotics plus AR-105. The study is being conducted at approximately 100 clinical sites across 17 countries. Subjects who meet all of the inclusion criteria and none of the exclusion criteria are screened by the microbiological culture test and/or rapid diagnostic test of an endotracheal aspirate to confirm the presence of an active P. aeruginosa infection. Following eligibility confirmation, the subject will be randomized in a 1:1 ratio to one of two treatment groups.
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
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
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
- •Informed consent
- •≥18 years of age, ≥ 20 years of age (Taiwan only),≥ 19 (S. Korea only)
- •pneumonia due to P. aeruginosa
- •mechanically-ventilated
- •intubated
- •APACHE II score between 10 and 35
- •Exclusion Criteria (main criteria):
- •being moribund
- •effective antibiotic therapy ≥48 hours
- •immunocompromised
- •underlying pulmonary disease that may preclude the assessment of a therapeutic response
排除标准
- 未提供
研究组 & 干预措施
AR-105
One intravenous infusion of AR-105 20mg/'kg
干预措施: AR-105 (Drug)
Control
Matching placebo
干预措施: Placebo (Drug)
结局指标
主要结局
Clinical Cure on Day 21
时间窗: 21 days following dosing
A summary of the number (%) of patients who were cured on or before Day 21 (micro-ITT population) is provided, by treatment group
次要结局
- Clinical Cure on Day 7(7 days following dosing)
- Clinical Cure on Day 14(14 days following dosing)
- Clinical Cure on Day 28(28 days following dosing)
