跳至主要内容
临床试验/EUCTR2007-006764-29-FR
EUCTR2007-006764-29-FR进行中(未招募)不适用

A Randomized, double-blind, placebo-controlled pilot study of KB001 in mechanically-ventilated patients colonized with pseudomonas aeruginosa

KaloBios Pharmaceuticals, Inc.0 个研究点开始时间: 2008年1月31日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Provision of written informed consent obtained from patient or patient’s surrogate if unconscious or altered sensorium
  • 2. Age =18 years
  • 3. On mechanical ventilation and expected to remain mechanically ventilated for at least 3 days
  • 4. Documented pulmonary Pa colonization (> 10 colonies per plate by semi-quantitive culture or = 1000 CFU/mL by quantitative culture or PCR from ETA or = 100 CFU/mL by BAL)
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Patients with known chronic pulmonary infection with Pa (i.e., patients with cystic fibrosis)
  • 2. Patient currently diagnosed with PA VAP
  • 3. Change in systemic antibiotic therapy active against gram negative bacteria within 72 hours prior to screening culture used for documenting pulmonary Pa colonization for study entry
  • 4. Patients not expected to survive at least 3 days
  • 5. Patient expected to be transferred to another institution during the 28 day study period
  • 6. Women of childbearing potential with a positive serum pregnancy test
  • 7. Use of an investigational medication within 4 weeks prior to randomization
  • 8. Any other reason, which in the opinion of the Investigator would prevent the patient from completing participation in the study

研究者

发起方
KaloBios Pharmaceuticals, Inc.

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