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临床试验/NCT00968669
NCT00968669已完成2 期

A Phase 2b, Randomized Study to Evaluate the Efficacy and Safety of Subcutaneous MEDI-528 in Adults With Uncontrolled Asthma

MedImmune LLC57 个研究点 分布在 9 个国家目标入组 329 人开始时间: 2009年12月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
MedImmune LLC
入组人数
329
试验地点
57
主要终点
Change at Day 92 From Baseline in Mean Asthma Control Questionnaire (ACQ) Scores (Intent-toTreat Analysis)

研究概览

简要总结

To study the effectiveness and safety of multiple-doses of MEDI-528 on asthma control in adult participants with uncontrolled, moderate-to-severe, persistent asthma.

详细描述

The primary objective of this study is to evaluate the effect of multiple-dose subcutaneous (SC) administration of MEDI-528 on asthma control in adults with uncontrolled, moderate-to-severe, persistent asthma.

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
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 65 Years(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

结局指标

主要结局

Change at Day 92 From Baseline in Mean Asthma Control Questionnaire (ACQ) Scores (Intent-toTreat Analysis)

时间窗: Day 92

Change at Day 92 from baseline (Day 1, prior to dosing) in mean ACQ scores in pariticpants receiving 30, 100, or 300 mg MEDI-528 versus placebo (Intent-to-Treat Analysis). The 6-item ACQ is a participant-reported questionnaire assessing asthma symptoms (night-time waking, symptoms on waking, activity limitation, shortness of breath, wheezing) and daily rescue bronchodilator use. Participants were asked to recall how their asthma had been during the previous week. Questions were weighted equally and scored from 0 (totally controlled) to 6 (severely uncontrolled). The mean ACQ score is the mean of the responses. Mean scores of ≤ 0.75 indicate well-controlled asthma, scores between 0.76 and \< 1.5 indicate partly controlled asthma, and a score ≥ 1.5 indicates uncontrolled asthma. Individual changes of at least 0.5 are considered to be clinically meaningful.

次要结局

  • Weighted Asthma Exacerbation Rate Through Day 92 (Intent-to-Treat Analysis)(Days 1 - 92)
  • Weighted Asthma Exacerbation Rate Through Day 176 (Intent-to-Treat Analysis)(Days 1 - 176)
  • Proportion of Participants Experiencing at Least One Asthma Exacerbation Through Day 92 (Intent-to-Treat Analysis)(Days 1 - 92)
  • Proportion of Participants Experiencing at Least One Asthma Exacerbation Through Day 176 (Intent-to-Treat Analysis)(Days 1 - 176)
  • Time to First Asthma Exacerbation Through Day 92 (Intent-to-Treat Analysis)(Days 1 - 92)
  • Time to First Asthma Exacerbation Through Day 176 (Intent-to-Treat Analysis)(Days 1 - 176)
  • Change at Day 176 From Baseline in Mean Asthma Control Questionnaire Scores (Intent-to-Treat Analysis)(Day 176)
  • Proportion of Participants Achieving Mean Asthma Control Questionnaire (ACQ) Scores at Day 92 of < or = 0.75, > 0.75 to < 1.5, and > or = 1.5 (Intent-to-Treat Analysis)(Day 92)
  • Proportion of Participants Achieving Mean Asthma Control Questionnaire (ACQ) Scores at Day 176 of < or = 0.75, > 0.75 to < 1.5, and > or = 1.5 (Intent-to-Treat Analysis)(Day 176)
  • Time to First Observed Mean Asthma Control Questionnaire (ACQ) Change From Baseline > or = 0.5 Through Day 92 (Intent-to-Treat Analysis)(Days 1 - 92)
  • Time to First Observed Mean Asthma Control Questionnaire (ACQ) Change From Baseline > or = 0.5 Through Day 176 (Intent-to-Treat Analysis)(Days 1 - 176)
  • Change at Day 92 From Baseline in Forced Expiratory Volume in One Second (FEV1) (Intent-to-Treat Analysis)(Day 92)
  • Change at Day 176 From Baseline in Forced Expiratory Volume in One Second (FEV1) (Intent-to-Treat Analysis)(Day 176)
  • Proportion of Participants Who Had a Asthma Quality of Life Questionnaire - Standard (AQLQ[S]) Assessment Response at Day 85 (Intent-to-Treat Analysis)(Day 85)
  • Proportion of Participants Who Had a Asthma Quality of Life Questionnaire - Standard (AQLQ[S]) Assessment Response at Day 176 (Intent-to-Treat Analysis)(Day 176)
  • Proportion of Participants With Detectable Anti-drug Antibodies to MEDI-528(Days 1, 29, 57, 85, 127, 169, 176, 204,260, and 323)
  • First Dose Trough Concentration of MEDI-528(Day 15)
  • Day 169 Steady State Trough Concentration of MEDI-528(Day 169)
  • Half Life of MEDI-528(Days 1, 15, 29, 57, 85, 127, 169, 176, 204, 232, 260, 288, and 323)
  • Accumulation Ratio of Trough Concentrations of MEDI-528(Days 1, 15, 29, 57, 85, 127, 169, 176, 204, 232, 260, 288, and 323)

研究者

发起方
MedImmune LLC
申办方类型
Industry
责任方
Sponsor

研究点 (57)

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