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临床试验/NCT00879606
NCT00879606已完成2 期

Efficacy and Safety Evaluation of ALT-836 in Patients With Sepsis and Acute Lung Injury/Acute Respiratory Distress Syndrome

Altor BioScience20 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2009年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
150
试验地点
20
主要终点
Safety profile of the study drug

研究概览

简要总结

This is a prospective, randomized (1:1), double-blind, multi-center, Phase II clinical study to test the safety and efficacy of a recombinant chimeric anti-tissue factor antibody (ALT-836) versus placebo in patients with sepsis and acute lung injury/acute respiratory distress syndrome (ALI/ARDS). This study was divided into two parts and the first part of the study has been completed. In the first part of the study, sixty patients were randomized at a 1:1 ratio to receive one dose of the study drug or placebo. In the second part of the study, ninety patients will be randomized at a 1:1 ratio to receive a multi-dose treatment regimen of single doses every 72 hours up to a maximum of 4 doses of the study drug or placebo, provided there are no safety concerns.

详细描述

Tissue factor (TF)-dependent procoagulant activity and associated inflammatory processes may play a role in the severity and progression of ALI/ARDS. Recent studies demonstrated that TF levels were elevated in plasma and pulmonary edema fluid of ARDS/ALI patients compared to control patients with hydrostatic pulmonary edema. These higher plasma TF levels were correlated with increased mortality, fewer ventilation-free days, the presence of disseminated intravascular coagulation and the presence of sepsis in patients with ALI/ARDS, suggesting that systemic activation of coagulation may be clinically important in ALI/ARDS. Moreover, the pulmonary TF levels in patients with ALI/ARDS were found to range between 0.5 and 2 nM, approximately 100-fold higher than simultaneous plasma levels, suggesting an intra-alveolar source of TF. Thus, anti-TF antibody blockage of TF activity may therefore provide an effective therapeutic mechanism for the treatment of inflammatory disorders such as ALI and ARDS. This study will test the hypothesis that administration of anti-TF antibody (ALT-836) to septic patients with ALI/ARDS will improve the clinical outcome by shortening the duration of mechanical ventilation for these patients.

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

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

1

Experimental

Participants will be randomized to receive ALT-836.

干预措施: ALT-836 (Drug)

2

Placebo Comparator

Patients will be randomized to receive placebo.

干预措施: Placebo (Drug)

结局指标

主要结局

Safety profile of the study drug

时间窗: Throughout the 28 days following treatment

Number of ventilator-free days at Day 28

时间窗: Determined at Day 28

次要结局

  • Number of Non-pulmonary organ failure free days at Day 28(Determined at Day 28)
  • Mortality at Day 7, 14, 21, 28 and 60(Determined at Day 7, 14, 21, 28 and 60)
  • Length of hospitalization at Day 28(Determined at Day 28)
  • Immunogenicity(Throughout the 28 days following treatment)
  • Effects of the study drug and the etiology of the disease (i.e. pulmonary or extra-pulmonary origin)(Determined at Day 28)
  • Length of ICU stay at Day 28(Determined at Day 28)
  • Changes in physiological variables of lung injury(Throughout the 28 days following treatment)
  • Changes in disease severity and lung injury scores(Throughout the 28 days following treatment)
  • Pharmacokinetics & Pharmacodynamics(Throughout the 28 days following treatment)

研究者

发起方
Altor BioScience
申办方类型
Industry
责任方
Sponsor

研究点 (20)

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