跳至主要内容
临床试验/NCT01584687
NCT01584687Unknown4 期

mRNA Expression as a Biomarker of Xolair (Omalizumab) Response

Instituto de Investigação em Imunologia0 个研究点目标入组 6 人开始时间: 2012年6月1日最近更新:
适应症

试验速览

阶段
4 期
发起方
入组人数
6
主要终点
Change of mRNA expression in leukocytes (real time-PCR)

研究概览

简要总结

Objectives: 1. Determine if mRNA expression could be use as a biomarker to predict and monitor the response to omalizumab in patients with difficult control asthma 2. Identify which genes are switched on and which are switched off by using Omalizumab.

Methods: This study is an open label clinical trial, with six patients. The patients will receive Omalizumab according to their age and weight (maximum dose: 375 mg every 15 days) for 4 months. There will be a run-in period of one month, when allergic asthma diagnosis will be confirmed and treatment will be optimized. Patients will be evaluated and will have blood sample collected on 3 occasions: in the beginning, 2 months after baseline and at the end of the study. Blood samples will always be collected one week after the last omalizumab dose. Primary outcome will be RNA expression of 20 genes measured by real time-PCR (high-affinity IgE receptor, IL-4, IL-5, IL-13, gama-IFN, quimokines, Fc epsilon, between others). Secondary outcomes will be ACT, ACQ and spirometry.

详细描述

Study rational: There is not a biomarker that can predict which patients will respond to Omalizumab and those who will not respond. Nowadays, the monitoring of therapeutic response to Omalizumab is based on clinical and spirometric data.

On the other hand, when a medication is administered, it has its main expected effect, but also acts on other targets with various direct and indirect effects. We do not know all the genes that are switched on and those that are switched off by the use of Omalizumab. For example, anti-IgE has been developed to block serum total IgE and thereby improve control of allergic asthma. However, the studies noted that Omalizumab also reduces the receptors FcepsilonRI, which may have implications for the treatment of autoimmune urticaria.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
12 Years 至 60 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • over 12 years
  • severe asthma not controlled despite medication
  • IgE between 70 and 1300 IU/ml and evidence of allergy clinical history and/or skin test or blood.

排除标准

  • previous use of omalizumab
  • smoke history

结局指标

主要结局

Change of mRNA expression in leukocytes (real time-PCR)

时间窗: At the end of the study (4months after baseline)

Patients will be evaluated and will have blood sample collected on 3 occasions: in the beginning, 2 months after baseline and at the end of the study. Blood samples will always be collected one week after the last omalizumab dose. Primary outcome will be RNA expression of 30 genes measured by real time-PCR.

次要结局

  • Change in the scores of questionnaires of asthma control(At the end of the study (4 months after baseline))

研究者

发起方
Instituto de Investigação em Imunologia
申办方类型
Other
责任方
Sponsor

相似试验