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临床试验/NCT03027609
NCT03027609已完成2 期

Placebo-controlled, Double-blind, Randomized Study of Aerucin® as Adjunct Therapy to Antibiotics in the Treatment of P. Aeruginosa Pneumonia

Aridis Pharmaceuticals, Inc.11 个研究点 分布在 3 个国家目标入组 158 人开始时间: 2017年3月29日最近更新:
适应症
干预措施
相关药物

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

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

Experimental

One intravenous infusion of AR-105 20mg/'kg

干预措施: AR-105 (Drug)

Control

Placebo Comparator

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)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (11)

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