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临床试验/NCT03320265
NCT03320265终止2 期

Double-blind, Randomised, Placebo-controlled, Multicentre, Phase IIa Study to Investigate the Effect of PC-mAb on Arterial Inflammation in Subjects With Elevated Lipoprotein a

Athera Biotechnologies AB2 个研究点 分布在 2 个国家目标入组 10 人开始时间: 2017年10月11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
终止
入组人数
10
试验地点
2
主要终点
Monocyte function

研究概览

简要总结

Inflammation and abnormal amount of lipids in the blood are key factors for the development and progression of atherosclerosis (thickening of the artery wall) and cardiovascular disease. Lipoprotein (a) is a pro-inflammatory plasma lipoprotein that is believed to be a risk factor for cardiovascular diseases. Vascular inflammation generates a range of effects, including endothelial dysfunction and migration of white blood cells into the vessel wall, which results in increased risk of cardiovascular events.

This study is designed to assess the effects of multiple monthly intravenous infusions with the fully human antibody called PC-mAb, in subjects with elevated lipoprotein (a).

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
50 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

PC-mAb

Experimental

Phosphorylcholine human monoclonal antibody, i.v. infusions

干预措施: PC-mAb (Drug)

Placebo

Placebo Comparator

Placebo to PC-mAb, i.v. infusions

干预措施: Placebo (Drug)

结局指标

主要结局

Monocyte function

时间窗: From baseline (Day 1) to visit 11 (Day 85)

Change in transendothelial migration (TEM) in monocytes isolated from treated subjects

次要结局

  • Arterial inflammation(From baseline (Day 1) to visit 11 (Day 85))
  • Arterial stiffness(From baseline (Day 1) to visit 11 (Day 85))
  • Adverse events (AEs)/serious AEs (SAEs)(From baseline (Day 1) to visit 11 (Day 85))
  • Vital signs, height(At screening (Day -63 to -1))
  • Vital signs, body weight(At screening (Day -63 to -1), Day 1, Day 28, Day 56, Day 84 and end of study (Day 143))
  • Vital signs, blood pressure(At screening (Day -63 to -1), Day 1, Day 28, Day 56, Day 84 and end of study (Day 143))
  • Vital signs, hear rate(At screening (Day -63 to -1), Day 1, Day 28, Day 56, Day 84 and end of study (Day 143))
  • Vital signs, body temperature(At screening (Day -63 to -1), Day 1, Day 28, Day 56, Day 84 and end of study (Day 143))
  • Physical examination including review of all organ systems(At screening (Day -63 to -1), Day 1, Day 28, Day 56, Day 84 and end of study (Day 143))
  • Electrocardiogram (ECG), PR (PQ)(At screening (Day -63 to -1), Day 1, Day 28, Day 56, Day 84 and end of study (Day 143))
  • ECG, QRS(At screening (Day -63 to -1), Day 1, Day 28, Day 56, Day 84 and end of study (Day 143))
  • ECG, QT(At screening (Day -63 to -1), Day 1, Day 28, Day 56, Day 84 and end of study (Day 143))
  • ECG, QTcF(At screening (Day -63 to -1), Day 1, Day 28, Day 56, Day 84 and end of study (Day 143))

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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