跳至主要内容
临床试验/EUCTR2006-003431-78-NL
EUCTR2006-003431-78-NL进行中(未招募)1 期

A Multicenter, Observational Study of the Long-term Safety of Infliximab (REMICADE®) in Subjects with Moderate to Severe Chronic Obstructive Pulmonary disease (COPD) - RESULTS COPD

Centocor BV0 个研究点目标入组 0 人开始时间: 2006年9月1日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
Centocor BV

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

  • All consenting subjects who received at least 1 dose of study agent in either the Centocor sponsored Phase 2 clinical study (C0168T54) or in the 2 Centocor-sponsored IIS studies (EU0016 C0168X09 and EU0073 C0168X57) of infliximab in subjects with COPD.
  • 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)
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Subjects who are unwilling to respond to requests for long-term safety information will be excluded.

研究者

发起方
Centocor BV

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