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临床试验/EUCTR2005-002207-16-GB
EUCTR2005-002207-16-GB进行中(未招募)1 期

A randomised controlled trial of Myfortic versus Mycophenolate Mofetil in the treatment of multi-system autoimmune disease. - MYFMAD

Cambridge University Hospitals NHS Foundation Trust0 个研究点目标入组 40 人开始时间: 2005年8月16日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
40

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

入选标准

  • Inclusion (requires all three)
  • i)Diagnosis of SLE or PSV
  • ii)Either: about to commence MMF, or established on MMF for at least three months but with inadequate disease control on MMF 2000mg/day or less
  • iii)Written informed consent
  • 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) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • b)Exclusion
  • i)Active infection (including hepatitis B, C, HIV and tuberculosis)
  • ii)Known hypersensitivity to MMF
  • iii)cancer or an individual history of cancer (other than resected basal cell skin carcinoma)
  • iv)Females who are pregnant, breast feeding, or at risk of pregnancy and not using a medically acceptable form of contraception
  • v)Any condition judged by the investigator that would cause the study to be detrimental to the patient
  • vi)Use of any investigational drug within four weeks of the baseline visit
  • vii)Patients who are planning to undergo elective surgery during the study period
  • viii)Age < 18 years

研究者

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